-
1
-
-
84876002671
-
Natural Products: A Continuing Source of Novel Drug Leads
-
Cragg, G. M.; Newman, D. J. Natural Products: a Continuing Source of Novel Drug Leads Biochim. Biophys. Acta, Gen. Subj. 2013, 1830, 3670-3695 10.1016/j.bbagen.2013.02.008
-
(2013)
Biochim. Biophys. Acta, Gen. Subj.
, vol.1830
, pp. 3670-3695
-
-
Cragg, G.M.1
Newman, D.J.2
-
2
-
-
84858308226
-
Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
-
Newman, D. J.; Cragg, G. M. Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010 J. Nat. Prod. 2012, 75, 311-335 10.1021/np200906s
-
(2012)
J. Nat. Prod.
, vol.75
, pp. 311-335
-
-
Newman, D.J.1
Cragg, G.M.2
-
3
-
-
80053203292
-
Natural Products: An Evolving Role in Future Drug Discovery
-
Mishra, B. B.; Tiwari, V. K. Natural Products: an Evolving Role in Future Drug Discovery Eur. J. Med. Chem. 2011, 46, 4769-4807 10.1016/j.ejmech.2011.07.057
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 4769-4807
-
-
Mishra, B.B.1
Tiwari, V.K.2
-
4
-
-
84897443754
-
New Horizons for Old Drugs and Drug Leads
-
Cragg, G. M.; Grothaus, P. G.; Newman, D. J. New Horizons for Old Drugs and Drug Leads J. Nat. Prod. 2014, 77, 703-723 10.1021/np5000796
-
(2014)
J. Nat. Prod.
, vol.77
, pp. 703-723
-
-
Cragg, G.M.1
Grothaus, P.G.2
Newman, D.J.3
-
5
-
-
0032491014
-
Natural Products Analogs as Scaffolds for Supramolecular and Combinatorial Chemistry
-
Mink, D.; Mecozzi, S.; Rebek, J., Jr. Natural Products Analogs as Scaffolds for Supramolecular and Combinatorial Chemistry Tetrahedron Lett. 1998, 39, 5709-5712 10.1016/S0040-4039(98)01170-8
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 5709-5712
-
-
Mink, D.1
Mecozzi, S.2
Rebek, J.3
-
7
-
-
52449100159
-
Natural Products as Inspiration for the Development of Asymmetric Catalysis
-
Mohr, J. T.; Krout, M. R.; Stoltz, B. M. Natural Products as Inspiration for the Development of Asymmetric Catalysis Nature 2008, 455, 323-332 10.1038/nature07370
-
(2008)
Nature
, vol.455
, pp. 323-332
-
-
Mohr, J.T.1
Krout, M.R.2
Stoltz, B.M.3
-
8
-
-
33847748056
-
-
Eds. Wiley-Blackwell: Weinheim
-
Biopolymers for Medical and Pharmaceutical Applications: Humic Substances, Polyisoprenoids, Polyesters, and Polysaccharides; Steinbüchel, A.; Marchessault, R. H., Eds.; Wiley-Blackwell: Weinheim, 2005.
-
(2005)
Biopolymers for Medical and Pharmaceutical Applications: Humic Substances, Polyisoprenoids, Polyesters, and Polysaccharides
-
-
Steinbüchel, A.1
Marchessault, R.H.2
-
10
-
-
84890020560
-
Industrial Natural Product Chemistry for Drug Discovery and Development
-
Bauer, A.; Brönstrup, M. Industrial Natural Product Chemistry for Drug Discovery and Development Nat. Prod. Rep. 2014, 31, 35-60 10.1039/C3NP70058E
-
(2014)
Nat. Prod. Rep.
, vol.31
, pp. 35-60
-
-
Bauer, A.1
Brönstrup, M.2
-
11
-
-
0000096835
-
Click Chemistry: Diverse Chemical Function from a Few Good Reactions
-
Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click Chemistry: Diverse Chemical Function from a Few Good Reactions Angew. Chem., Int. Ed. 2001, 40, 2004-2021 10.1002/1521-3773(20010601)40:112004::AID-ANIE20043.0.CO;2-5
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
12
-
-
77949786732
-
In Situ Click Chemistry: Probing the Binding Landscapes of Biological Molecules
-
Mamidyala, S. K.; Finn, M. G. In Situ Click Chemistry: Probing the Binding Landscapes of Biological Molecules Chem. Soc. Rev. 2010, 39, 1252-1261 10.1039/b901969n
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1252-1261
-
-
Mamidyala, S.K.1
Finn, M.G.2
-
13
-
-
34447562439
-
In Situ Click Chemistry: A Powerful Means for Lead Discovery
-
Sharpless, K. B.; Manetsch, R. In Situ Click Chemistry: a Powerful Means for Lead Discovery Expert Opin. Drug Discovery 2006, 1, 525-538 10.1517/17460441.1.6.525
-
(2006)
Expert Opin. Drug Discovery
, vol.1
, pp. 525-538
-
-
Sharpless, K.B.1
Manetsch, R.2
-
14
-
-
0037099395
-
A Stepwise Huisgen Cycloaddition Process: Copper(I)-catalyzed Regioselective "Ligation" of Azides and Terminal Alkynes
-
Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A Stepwise Huisgen Cycloaddition Process: Copper(I)-catalyzed Regioselective "Ligation" of Azides and Terminal Alkynes Angew. Chem., Int. Ed. 2002, 41, 2596-2599 10.1002/1521-3773(20020715)41:142596::AID-ANIE25963.0.CO;2-4
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
15
-
-
0037012920
-
Peptidotriazoles on Solid Phase: (1,2,3)-Triazoles by Regiospecific Copper(I)-catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
-
Tornøe, C. W.; Christensen, C.; Meldal, M. Peptidotriazoles on Solid Phase: (1,2,3)-Triazoles by Regiospecific Copper(I)-catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides J. Org. Chem. 2002, 67, 3057-3064 10.1021/jo011148j
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3057-3064
-
-
Tornøe, C.W.1
Christensen, C.2
Meldal, M.3
-
16
-
-
34848920359
-
Peptidotriazoles: Copper(I)-catalyzed 1,3-Dipolar Cycloadditions on Solid-phase in Peptides
-
The first example of Cu(I) catalysed 1,3-Huisgen cycloaddition was reported in 2001 by Meldal; see; Lebl, M. Houghten, R. A. American Peptide Society and Kluwer Academic Publishers: San Diego
-
The first example of Cu(I) catalysed 1,3-Huisgen cycloaddition was reported in 2001 by Meldal; see Tornøe, C. W.; Meldal, M. Peptidotriazoles: Copper(I)-catalyzed 1,3-Dipolar Cycloadditions on Solid-phase in Peptides. Proc. Am. Pept. Symp. Lebl, M.; Houghten, R. A., Eds.; American Peptide Society and Kluwer Academic Publishers: San Diego, 2001; pp 263-264.
-
(2001)
Proc. Am. Pept. Symp.
, pp. 263-264
-
-
Tornøe, C.W.1
Meldal, M.2
-
17
-
-
0002490493
-
-
Padwa, A. Wiley: New York
-
Huisgen, R. 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley: New York, 1, 1984; pp 1-176.
-
(1984)
1,3-Dipolar Cycloaddition Chemistry
, vol.1
, pp. 1-176
-
-
Huisgen, R.1
-
18
-
-
47349098606
-
Ruthenium-catalyzed Azide-alkyne Cycloaddition: Scope and Mechanism
-
Boren, B. C.; Narayan, S.; Rasmussen, L. K.; Zhang, L.; Zhao, H.; Lin, Z.; Jia, G.; Fokin, V. V. Ruthenium-catalyzed Azide-alkyne Cycloaddition: Scope and Mechanism J. Am. Chem. Soc. 2008, 130, 8923-8930 10.1021/ja0749993
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 8923-8930
-
-
Boren, B.C.1
Narayan, S.2
Rasmussen, L.K.3
Zhang, L.4
Zhao, H.5
Lin, Z.6
Jia, G.7
Fokin, V.V.8
-
19
-
-
80053528741
-
Click Chemistry: 1,2,3-Triazoles as Pharmacophores
-
Agalave, S. G.; Maujan, S. R.; Pore, V. S. Click Chemistry: 1,2,3-Triazoles as Pharmacophores Chem.-Asian J. 2011, 6, 2696-2718 10.1002/asia.201100432
-
(2011)
Chem. - Asian J.
, vol.6
, pp. 2696-2718
-
-
Agalave, S.G.1
Maujan, S.R.2
Pore, V.S.3
-
20
-
-
34547272503
-
The Growing Applications of Click Chemistry
-
Moses, J. E.; Moorhouse, A. D. The Growing Applications of Click Chemistry Chem. Soc. Rev. 2007, 36, 1249-1262 10.1039/b613014n
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1249-1262
-
-
Moses, J.E.1
Moorhouse, A.D.2
-
21
-
-
51049094897
-
Cu-catalyzed Azide-alkyne Cycloaddition
-
Meldal, M.; Tornøe, C. W. Cu-catalyzed Azide-alkyne Cycloaddition Chem. Rev. 2008, 108, 2952-3015 10.1021/cr0783479
-
(2008)
Chem. Rev.
, vol.108
, pp. 2952-3015
-
-
Meldal, M.1
Tornøe, C.W.2
-
23
-
-
85043201023
-
-
Trost, B. M. Li, C.-J. Wiley-VCH: Weinheim
-
Schoffelen, S.; Meldal, M. Alkyne-Azide Reactions, in Modern Alkyne Chemistry; Trost, B. M.; Li, C.-J., Eds.; Wiley-VCH: Weinheim, 2014.
-
(2014)
Alkyne-Azide Reactions, in Modern Alkyne Chemistry
-
-
Schoffelen, S.1
Meldal, M.2
-
24
-
-
84861499417
-
The Impact of Click Chemistry in Medicinal Chemistry
-
Hou, J.; Liu, X.; Shen, J.; Zhao, G.; Wang, P. G. The Impact of Click Chemistry in Medicinal Chemistry Expert Opin. Drug Discovery 2012, 7, 489-501 10.1517/17460441.2012.682725
-
(2012)
Expert Opin. Drug Discovery
, vol.7
, pp. 489-501
-
-
Hou, J.1
Liu, X.2
Shen, J.3
Zhao, G.4
Wang, P.G.5
-
25
-
-
84867726453
-
I-Catalyzed Alkyne-Azide "Click" Cycloadditions from a Mechanistic and Synthetic Perspective
-
I-Catalyzed Alkyne-Azide "Click" Cycloadditions from a Mechanistic and Synthetic Perspective Eur. J. Org. Chem. 2006, 2006, 51-68 10.1002/ejoc.200500483
-
(2006)
Eur. J. Org. Chem.
, vol.2006
, pp. 51-68
-
-
Bock, V.D.1
Hiemstra, H.2
Van Maarseveen, J.H.3
-
26
-
-
84876676322
-
Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-catalyzed Azide-alkyne Cycloadditions
-
Worrell, B. T.; Malik, J. A.; Fokin, V. V. Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-catalyzed Azide-alkyne Cycloadditions Science 2013, 340, 457-460 10.1126/science.1229506
-
(2013)
Science
, vol.340
, pp. 457-460
-
-
Worrell, B.T.1
Malik, J.A.2
Fokin, V.V.3
-
27
-
-
39549111477
-
Click Chemistry Reactions in Medicinal Chemistry: Applications of the 1,3-Dipolar Cycloaddition between Azides and Alkynes
-
Tron, G. C.; Pirali, T.; Billington, R. A.; Canonico, P. L.; Sorba, G.; Genazzani, A. A. Click Chemistry Reactions in Medicinal Chemistry: Applications of the 1,3-Dipolar Cycloaddition Between Azides and Alkynes Med. Res. Rev. 2008, 28, 278-308 10.1002/med.20107
-
(2008)
Med. Res. Rev.
, vol.28
, pp. 278-308
-
-
Tron, G.C.1
Pirali, T.2
Billington, R.A.3
Canonico, P.L.4
Sorba, G.5
Genazzani, A.A.6
-
28
-
-
84877835595
-
Click Chemistry for Drug Development and Diverse Chemical-biology Applications
-
Thirumurugan, P.; Matosiuk, D.; Jozwiak, K. Click Chemistry for Drug Development and Diverse Chemical-biology Applications Chem. Rev. 2013, 113, 4905-4979 10.1021/cr200409f
-
(2013)
Chem. Rev.
, vol.113
, pp. 4905-4979
-
-
Thirumurugan, P.1
Matosiuk, D.2
Jozwiak, K.3
-
29
-
-
43449108552
-
Efficient Construction of Therapeutics, Bioconjugates, Biomaterials and Bioactive Surfaces Using Azide-alkyne "Click" Chemistry
-
Lutz, J. F.; Zarafshani, Z. Efficient Construction of Therapeutics, Bioconjugates, Biomaterials and Bioactive Surfaces Using Azide-alkyne "Click" Chemistry Adv. Drug Delivery Rev. 2008, 60, 958-970 10.1016/j.addr.2008.02.004
-
(2008)
Adv. Drug Delivery Rev.
, vol.60
, pp. 958-970
-
-
Lutz, J.F.1
Zarafshani, Z.2
-
30
-
-
47649133089
-
Click Chemistry and Medicinal Chemistry: A Case of "Cyclo-addiction"
-
Moorhouse, A. D.; Moses, J. E. Click Chemistry and Medicinal Chemistry: a Case of "Cyclo-addiction" ChemMedChem 2008, 3, 715-723 10.1002/cmdc.200700334
-
(2008)
ChemMedChem
, vol.3
, pp. 715-723
-
-
Moorhouse, A.D.1
Moses, J.E.2
-
31
-
-
0348109450
-
The Growing Impact of Click Chemistry on Drug Discovery
-
Kolb, H. C.; Sharpless, K. B. The Growing Impact of Click Chemistry on Drug Discovery Drug Discovery Today 2003, 8, 1128-1137 10.1016/S1359-6446(03)02933-7
-
(2003)
Drug Discovery Today
, vol.8
, pp. 1128-1137
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
32
-
-
84873122458
-
Click Reaction in Carbohydrate Chemistry: Recent Developments and Future Perspective
-
Kushwaha, D.; Dwivedi, P.; Kuanar, S. K.; Tiwari, V. K. Click Reaction in Carbohydrate Chemistry: Recent Developments and Future Perspective Curr. Org. Synth. 2013, 10, 90-135 10.2174/1570179411310010005
-
(2013)
Curr. Org. Synth.
, vol.10
, pp. 90-135
-
-
Kushwaha, D.1
Dwivedi, P.2
Kuanar, S.K.3
Tiwari, V.K.4
-
34
-
-
84862696152
-
Click Chemistry with Polymers, Dendrimers, and Hydrogels for Drug Delivery
-
Lallana, E.; Fernandez-Trillo, F.; Sousa-Herves, A.; Riguera, R.; Fernandez-Megia, E. Click Chemistry with Polymers, Dendrimers, and Hydrogels for Drug Delivery Pharm. Res. 2012, 29, 902-921 10.1007/s11095-012-0683-y
-
(2012)
Pharm. Res.
, vol.29
, pp. 902-921
-
-
Lallana, E.1
Fernandez-Trillo, F.2
Sousa-Herves, A.3
Riguera, R.4
Fernandez-Megia, E.5
-
35
-
-
82955165019
-
"Clicking" on/with Polymers: A Rapidly Expanding Field for the Straightforward Preparation of Novel Macromolecular Architectures
-
Kempe, K.; Krieg, A.; Becer, C. R.; Schubert, U. S. "Clicking" on/with Polymers: a Rapidly Expanding Field for the Straightforward Preparation of Novel Macromolecular Architectures Chem. Soc. Rev. 2012, 41, 176-191 10.1039/C1CS15107J
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 176-191
-
-
Kempe, K.1
Krieg, A.2
Becer, C.R.3
Schubert, U.S.4
-
36
-
-
80053495135
-
Fabrication and Functionalization of Hydrogels through "Click" Chemistry
-
Yigit, S.; Sanyal, R.; Sanyal, A. Fabrication and Functionalization of Hydrogels through "Click" Chemistry Chem.-Asian J. 2011, 6, 2648-2659 10.1002/asia.201100440
-
(2011)
Chem. - Asian J.
, vol.6
, pp. 2648-2659
-
-
Yigit, S.1
Sanyal, R.2
Sanyal, A.3
-
37
-
-
77949812304
-
Marrying Click Chemistry with Polymerization: Expanding the Scope of Polymeric Materials
-
Golas, P. L.; Matyjaszewski, K. Marrying Click Chemistry with Polymerization: Expanding the Scope of Polymeric Materials Chem. Soc. Rev. 2010, 39, 1338-1354 10.1039/B901978M
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1338-1354
-
-
Golas, P.L.1
Matyjaszewski, K.2
-
38
-
-
33846703461
-
"Click" Chemistry in Polymer and Materials Science
-
Binder, W. H.; Sachsenhofer, R. "Click" Chemistry in Polymer and Materials Science Macromol. Rapid Commun. 2007, 28, 15-54 10.1002/marc.200600625
-
(2007)
Macromol. Rapid Commun.
, vol.28
, pp. 15-54
-
-
Binder, W.H.1
Sachsenhofer, R.2
-
39
-
-
34548639157
-
Click Chemistry: Versatility and Control in the Hands of Materials Scientists
-
Nandivada, H.; Jiang, X.; Lahann, J. Click Chemistry: Versatility and Control in the Hands of Materials Scientists Adv. Mater. 2007, 19, 2197-2208 10.1002/adma.200602739
-
(2007)
Adv. Mater.
, vol.19
, pp. 2197-2208
-
-
Nandivada, H.1
Jiang, X.2
Lahann, J.3
-
41
-
-
34547482973
-
Clicking Polymers: A Straightforward Approach to Novel Macromolecular Architectures
-
Fournier, D.; Hoogenboom, R.; Schubert, U. S. Clicking Polymers: a Straightforward Approach to Novel Macromolecular Architectures Chem. Soc. Rev. 2007, 36, 1369-1380 10.1039/b700809k
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1369-1380
-
-
Fournier, D.1
Hoogenboom, R.2
Schubert, U.S.3
-
42
-
-
77949799806
-
Click Chemistry under Non-classical Reaction Conditions
-
Kappe, C. O.; Van Der Eycken, E. Click Chemistry under Non-classical Reaction Conditions Chem. Soc. Rev. 2010, 39, 1280-1290 10.1039/B901973C
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1280-1290
-
-
Kappe, C.O.1
Van Der Eycken, E.2
-
45
-
-
84855856535
-
Triterpenoids for Cancer Prevention and Treatment: Current Status and Future Prospects
-
Patlolla, J. M. R.; Rao, C. V. Triterpenoids for Cancer Prevention and Treatment: Current Status and Future Prospects Curr. Pharm. Biotechnol. 2012, 13, 147-155 10.2174/138920112798868719
-
(2012)
Curr. Pharm. Biotechnol.
, vol.13
, pp. 147-155
-
-
Patlolla, J.M.R.1
Rao, C.V.2
-
46
-
-
0027074951
-
Steroid Research at Syntex: "The Pill" and Cortisone
-
Djerassi, C. Steroid Research at Syntex: "the Pill" and Cortisone Steroids 1992, 57, 631-641 10.1016/0039-128X(92)90016-3
-
(1992)
Steroids
, vol.57
, pp. 631-641
-
-
Djerassi, C.1
-
47
-
-
77957155737
-
Trends for Diverse Production Strategies of Plant Medicinal Alkaloids
-
Yang, L.; Stöckigt, J. Trends for Diverse Production Strategies of Plant Medicinal Alkaloids Nat. Prod. Rep. 2010, 27, 1469-1479 10.1039/c005378c
-
(2010)
Nat. Prod. Rep.
, vol.27
, pp. 1469-1479
-
-
Yang, L.1
Stöckigt, J.2
-
49
-
-
77950521746
-
Cinchona Alkaloids in Asymmetric Organocatalysis
-
Marcelli, T.; Hiemstra, H. Cinchona Alkaloids in Asymmetric Organocatalysis Synthesis 2010, 8, 1229-1279 10.1055/s-0029-1218699
-
(2010)
Synthesis
, vol.8
, pp. 1229-1279
-
-
Marcelli, T.1
Hiemstra, H.2
-
50
-
-
79951680836
-
Recent Applications of Cinchona Alkaloids and Their Derivatives as Catalysts in Metal-free Asymmetric Synthesis
-
Yeboah, E. M. O.; Yeboah, S. O.; Singh, G. S. Recent Applications of Cinchona Alkaloids and Their Derivatives as Catalysts in Metal-free Asymmetric Synthesis Tetrahedron 2011, 67, 1725-1762 10.1016/j.tet.2010.12.050
-
(2011)
Tetrahedron
, vol.67
, pp. 1725-1762
-
-
Yeboah, E.M.O.1
Yeboah, S.O.2
Singh, G.S.3
-
51
-
-
84864668043
-
Resolution of Racemates and Enantioselective Analytics by Cinchona Alkaloids and Their Derivatives
-
Song, Ch. E. Wiley-VCH: Weinheim, Chapter 13
-
Kacprzak, K.; Gawroński, J. Resolution of Racemates and Enantioselective Analytics by Cinchona Alkaloids and Their Derivatives. In Cinchona Alkaloids in Synthesis and Catalysis, Song, Ch. E., Ed.; Wiley-VCH: Weinheim, 2009; Chapter 13.
-
(2009)
Cinchona Alkaloids in Synthesis and Catalysis
-
-
Kacprzak, K.1
Gawroński, J.2
-
52
-
-
34848865280
-
Bile Acid Scaffolds in Supramolecular Chemistry: The Interplay of Design and Synthesis
-
Davis, A. P. Bile Acid Scaffolds in Supramolecular Chemistry: the Interplay of Design and Synthesis Molecules 2007, 12, 2106-2122 10.3390/12082106
-
(2007)
Molecules
, vol.12
, pp. 2106-2122
-
-
Davis, A.P.1
-
53
-
-
77957789362
-
Steroid-based Anion Receptors and Transporters
-
Brotherhood, P. R.; Davis, A. P. Steroid-based Anion Receptors and Transporters Chem. Soc. Rev. 2010, 39, 3633-3647 10.1039/b926225n
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 3633-3647
-
-
Brotherhood, P.R.1
Davis, A.P.2
-
54
-
-
33750502923
-
Anion Binding and Transport by Steroid-based Receptors
-
Davis, A. P. Anion Binding and Transport by Steroid-based Receptors Coord. Chem. Rev. 2006, 250, 2939-2951 10.1016/j.ccr.2006.05.008
-
(2006)
Coord. Chem. Rev.
, vol.250
, pp. 2939-2951
-
-
Davis, A.P.1
-
55
-
-
0037227252
-
Development of Cholesterol-based Conjugates for Targeted Drug Delivery
-
Alanazi, F.; Halpern, D. S.; Lu, D. R. Development of Cholesterol-based Conjugates for Targeted Drug Delivery STP Pharm. Sci. 2003, 13, 27-35
-
(2003)
STP Pharm. Sci.
, vol.13
, pp. 27-35
-
-
Alanazi, F.1
Halpern, D.S.2
Lu, D.R.3
-
56
-
-
80053515989
-
Steroid/triterpenoid Functional Molecules Based on "Click Chemistry"
-
Hu, J.; Lu, J. R.; Ju, Y. Steroid/triterpenoid Functional Molecules Based on "Click Chemistry" Chem.-Asian J. 2011, 6, 2636-2647 10.1002/asia.201100378
-
(2011)
Chem. - Asian J.
, vol.6
, pp. 2636-2647
-
-
Hu, J.1
Lu, J.R.2
Ju, Y.3
-
57
-
-
84942505636
-
Chemistry and Biology of Cinchona Alkaloids
-
Ramawat, K. G. Merillon, J.-M. Springer
-
Kacprzak, K. Chemistry and Biology of Cinchona Alkaloids. In Handbook of Natural Products-Phytochemistry, Botany, Metabolism; Ramawat, K. G.; Merillon, J.-M., Eds.; Springer: 2013; pp 605-641.
-
(2013)
Handbook of Natural Products - Phytochemistry, Botany, Metabolism
, pp. 605-641
-
-
Kacprzak, K.1
-
58
-
-
0034063289
-
Synthesis of 10,11-Didehydro Cinchona Alkaloids and Key Derivatives
-
Braje, W. M.; Frackenpohl, J.; Schrake, O.; Wartchow, R.; Beil, W.; Hoffmann, H. M. R. Synthesis of 10,11-Didehydro Cinchona Alkaloids and Key Derivatives Helv. Chim. Acta 2000, 83, 777-792 10.1002/(SICI)1522-2675(20000412)83:4777::AID-HLCA7773.3.CO;2-N
-
(2000)
Helv. Chim. Acta
, vol.83
, pp. 777-792
-
-
Braje, W.M.1
Frackenpohl, J.2
Schrake, O.3
Wartchow, R.4
Beil, W.5
Hoffmann, H.M.R.6
-
59
-
-
39749164489
-
An Improved Synthesis of 10,11-Didehydro Cinchona Alkaloids
-
Kacprzak, K. M.; Lindner, W.; Maier, N. M. An Improved Synthesis of 10,11-Didehydro Cinchona Alkaloids Chirality 2008, 20, 441-445 10.1002/chir.20461
-
(2008)
Chirality
, vol.20
, pp. 441-445
-
-
Kacprzak, K.M.1
Lindner, W.2
Maier, N.M.3
-
60
-
-
33750492630
-
Highly Efficient Immobilization of Cinchona Alkaloid Derivatives to Silica Gel via Click Chemistry
-
Kacprzak, K. M.; Maier, N. M.; Lindner, W. Highly Efficient Immobilization of Cinchona Alkaloid Derivatives to Silica Gel via Click Chemistry Tetrahedron Lett. 2006, 47, 8721-8726 10.1016/j.tetlet.2006.10.018
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 8721-8726
-
-
Kacprzak, K.M.1
Maier, N.M.2
Lindner, W.3
-
61
-
-
79951720434
-
Triazolo-linked Cinchona Alkaloid Carbamate Anion Exchange-type Chiral Stationary Phases: Synthesis by Click Chemistry and Evaluation
-
Kacprzak, K. M.; Maier, N. M.; Lindner, W. Triazolo-linked Cinchona Alkaloid Carbamate Anion Exchange-type Chiral Stationary Phases: Synthesis by Click Chemistry and Evaluation J. Chromatogr. A 2011, 1218, 1452-1460 10.1016/j.chroma.2011.01.031
-
(2011)
J. Chromatogr. A
, vol.1218
, pp. 1452-1460
-
-
Kacprzak, K.M.1
Maier, N.M.2
Lindner, W.3
-
62
-
-
77956907286
-
Unexpected Enantioseparation of Mandelic Acids and Their Derivatives on 1,2,3-Triazololinked Quinine tert-Butyl Carbamate Anion Exchange-type Chiral Stationary Phase
-
Kacprzak, K. M.; Maier, N. M.; Lindner, W. Unexpected Enantioseparation of Mandelic Acids and Their Derivatives on 1,2,3-Triazololinked Quinine tert-Butyl Carbamate Anion Exchange-type Chiral Stationary Phase J. Sep. Sci. 2010, 33, 2590-2598 10.1002/jssc.201000393
-
(2010)
J. Sep. Sci.
, vol.33
, pp. 2590-2598
-
-
Kacprzak, K.M.1
Maier, N.M.2
Lindner, W.3
-
63
-
-
80052795489
-
Novel Pirkle-type Quinine 3,5-Dinitrophenylcarbamate Chiral Stationary Phase Implementing Click Chemistry
-
Kacprzak, K. M.; Lindner, W. Novel Pirkle-type Quinine 3,5-Dinitrophenylcarbamate Chiral Stationary Phase Implementing Click Chemistry J. Sep. Sci. 2011, 34, 2391-2396 10.1002/jssc.201100395
-
(2011)
J. Sep. Sci.
, vol.34
, pp. 2391-2396
-
-
Kacprzak, K.M.1
Lindner, W.2
-
64
-
-
84900627864
-
Novel Carbamoyl Type Quinine and Quinidine Based Chiral Anion Exchangers Implementing Alkyne-azide Cycloaddition Immobilization Chemistry
-
Hettegger, H.; Kohout, M.; Mimini, V.; Lindner, W. Novel Carbamoyl Type Quinine and Quinidine Based Chiral Anion Exchangers Implementing Alkyne-azide Cycloaddition Immobilization Chemistry J. Chromatogr. A 2014, 1337, 85-94 10.1016/j.chroma.2014.02.026
-
(2014)
J. Chromatogr. A
, vol.1337
, pp. 85-94
-
-
Hettegger, H.1
Kohout, M.2
Mimini, V.3
Lindner, W.4
-
65
-
-
23344445780
-
Fluorous Click Chemistry as a Practical Tagging Method
-
Kaleta, Z.; Egyed, O.; Soós, T. Fluorous Click Chemistry as a Practical Tagging Method Org. Biomol. Chem. 2005, 3, 2228-2230 10.1039/b504973c
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 2228-2230
-
-
Kaleta, Z.1
Egyed, O.2
Soós, T.3
-
66
-
-
77954303369
-
Simple Preparation of Dimeric Cinchona Alkaloid Derivatives on Polystyrene Supports and a Highly Enantioselective Catalytic Heterogeneous Dimerization of Ketenes
-
Jumde, R. P.; Mandoli, A.; De Lorenzi, F.; Pini, D.; Salvadori, P. Simple Preparation of Dimeric Cinchona Alkaloid Derivatives on Polystyrene Supports and a Highly Enantioselective Catalytic Heterogeneous Dimerization of Ketenes Adv. Synth. Catal. 2010, 352, 1434-1440 10.1002/adsc.201000165
-
(2010)
Adv. Synth. Catal.
, vol.352
, pp. 1434-1440
-
-
Jumde, R.P.1
Mandoli, A.2
De Lorenzi, F.3
Pini, D.4
Salvadori, P.5
-
67
-
-
84921628665
-
New Polymer-supported Mono- and bis-Cinchona Alkaloid Derivatives: Synthesis and Use in Asymmetric Organocatalyzed Reactions
-
Jumde, R. P.; Di Pietro, A.; Manariti, A.; Mandoli, A. New Polymer-supported Mono- and bis-Cinchona Alkaloid Derivatives: Synthesis and Use in Asymmetric Organocatalyzed Reactions Chem.-Asian J. 2015, 10, 397-404 10.1002/asia.201402924
-
(2015)
Chem. - Asian J.
, vol.10
, pp. 397-404
-
-
Jumde, R.P.1
Di Pietro, A.2
Manariti, A.3
Mandoli, A.4
-
68
-
-
84929466905
-
Comparison of Different Polymer- and Silica-supported 9-Amino-9-deoxy-epi-quinines as Recyclable Organocatalysts
-
Porta, R.; Coccia, F.; Annunziata, R.; Puglisi, A. Comparison of Different Polymer- and Silica-supported 9-Amino-9-deoxy-epi-quinines as Recyclable Organocatalysts ChemCatChem 2015, 7, 1490-1499 10.1002/cctc.201500106
-
(2015)
ChemCatChem
, vol.7
, pp. 1490-1499
-
-
Porta, R.1
Coccia, F.2
Annunziata, R.3
Puglisi, A.4
-
69
-
-
84925813799
-
A Polystyrene-supported 9-Amino(9-deoxy)epiquinine Derivative for Continuous Flow Asymmetric Michael Reactions
-
Izquierdo, J.; Ayats, C.; Henseler, A. H.; Pericàs, M. A. A Polystyrene-supported 9-Amino(9-deoxy)epiquinine Derivative for Continuous Flow Asymmetric Michael Reactions Org. Biomol. Chem. 2015, 13, 4204-4209 10.1039/C5OB00325C
-
(2015)
Org. Biomol. Chem.
, vol.13
, pp. 4204-4209
-
-
Izquierdo, J.1
Ayats, C.2
Henseler, A.H.3
Pericàs, M.A.4
-
70
-
-
84922680029
-
Solid Supported 9-Amino-9-deoxy-epi-quinine as Efficient Organocatalyst for Stereoselective Reactions in Batch and under Continuous Flow Conditions
-
Porta, R.; Benaglia, M.; Coccia, F.; Cozzi, F.; Puglisi, A. Solid Supported 9-Amino-9-deoxy-epi-quinine as Efficient Organocatalyst for Stereoselective Reactions in Batch and Under Continuous Flow Conditions Adv. Synth. Catal. 2015, 357, 377-383 10.1002/adsc.201400821
-
(2015)
Adv. Synth. Catal.
, vol.357
, pp. 377-383
-
-
Porta, R.1
Benaglia, M.2
Coccia, F.3
Cozzi, F.4
Puglisi, A.5
-
71
-
-
78651240030
-
Synthesis of 3′-Azido-3′-deoxythymidine (AZT) - Cinchona Alkaloid Conjugates via Click Chemistry: Toward Novel Fluorescent Markers and Cytostatic Agents
-
Baraniak, B.; Kacprzak, K.; Celewicz, L. Synthesis of 3′-Azido-3′-deoxythymidine (AZT)-Cinchona Alkaloid Conjugates via Click Chemistry: Toward Novel Fluorescent Markers and Cytostatic Agents Bioorg. Med. Chem. Lett. 2011, 21, 723-726 10.1016/j.bmcl.2010.11.127
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 723-726
-
-
Baraniak, B.1
Kacprzak, K.2
Celewicz, L.3
-
72
-
-
78649831810
-
Clickable 9-Azido-(9-deoxy)-Cinchona Alkaloids: Synthesis and Conformation
-
Kacprzak, K.; Gierczyk, B. Clickable 9-Azido-(9-deoxy)-Cinchona Alkaloids: Synthesis and Conformation Tetrahedron: Asymmetry 2010, 21, 2740-2745 10.1016/j.tetasy.2010.10.023
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 2740-2745
-
-
Kacprzak, K.1
Gierczyk, B.2
-
73
-
-
84877115441
-
Diastereoselective Corey-Chaykovsky 9-Epoxymethylation of Cinchona Alkaloids: Access to Chiral Scaffolds with Diverse Functionalities
-
Boratyński, P. J.; Skarzewski, J. Diastereoselective Corey-Chaykovsky 9-Epoxymethylation of Cinchona Alkaloids: Access to Chiral Scaffolds with Diverse Functionalities J. Org. Chem. 2013, 78, 4473-4482 10.1021/jo400465a
-
(2013)
J. Org. Chem.
, vol.78
, pp. 4473-4482
-
-
Boratyński, P.J.1
Skarzewski, J.2
-
74
-
-
31344479794
-
The Library of Cinchona Alkaloids-1,2,3-triazole Derivatives: Structure and Facile Access by "Click Chemistry"
-
Kacprzak, K.; Migas, M.; Plutecka, A.; Rychlewska, U.; Gawroński, J. The Library of Cinchona Alkaloids-1,2,3-triazole Derivatives: Structure and Facile Access by "Click Chemistry" Heterocycles 2005, 65, 1931-1938 10.3987/COM-05-10378
-
(2005)
Heterocycles
, vol.65
, pp. 1931-1938
-
-
Kacprzak, K.1
Migas, M.2
Plutecka, A.3
Rychlewska, U.4
Gawroński, J.5
-
75
-
-
84942500080
-
Antiproliferative Activity of Polyether Antibiotic - Cinchona Alkaloid Conjugates Obtained via Click Chemistry
-
Skiera, I.; Antoszczak, M.; Trynda, J.; Wietrzyk, J.; Boratyński, P.; Kacprzak, K.; Huczyński, A. Antiproliferative Activity of Polyether Antibiotic-Cinchona Alkaloid Conjugates Obtained via Click Chemistry Chem. Biol. Drug Des. 2015, 86, 911-917 10.1111/cbdd.12523
-
(2015)
Chem. Biol. Drug Des.
, vol.86
, pp. 911-917
-
-
Skiera, I.1
Antoszczak, M.2
Trynda, J.3
Wietrzyk, J.4
Boratyński, P.5
Kacprzak, K.6
Huczyński, A.7
-
76
-
-
0141631798
-
Fused Triazoles via Tandem Reactions of Activated Cinchona Alkaloids with Azide Ion. Second Cinchona Rearrangement Exemplified
-
Röper, S.; Franz, M. H.; Wartchow, R.; Hoffmann, H. M. Fused Triazoles via Tandem Reactions of Activated Cinchona Alkaloids with Azide Ion. Second Cinchona Rearrangement Exemplified Org. Lett. 2003, 5, 2773-2776 10.1021/ol034719y
-
(2003)
Org. Lett.
, vol.5
, pp. 2773-2776
-
-
Röper, S.1
Franz, M.H.2
Wartchow, R.3
Hoffmann, H.M.4
-
77
-
-
84862201122
-
Click Chemistry-derived Bivalent Quinine Inhibitors of P-glycoprotein-mediated Cellular Efflux
-
Kuriakose, J.; Hrycyna, C. A.; Chmielewski, J. Click Chemistry-derived Bivalent Quinine Inhibitors of P-glycoprotein-mediated Cellular Efflux Bioorg. Med. Chem. Lett. 2012, 22, 4410-4412 10.1016/j.bmcl.2012.04.125
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 4410-4412
-
-
Kuriakose, J.1
Hrycyna, C.A.2
Chmielewski, J.3
-
78
-
-
84973486031
-
-
Ramawat, K. G. Merillon, J.-M. Springer
-
Kacprzak, K. Chemistry and Biology of Camptothecin and Its Derivatives in Handbook of Natural Products-Phytochemistry, Botany, Metabolism; Ramawat, K. G.; Merillon, J.-M., Eds.; Springer, 2013; p 643-682.
-
(2013)
Chemistry and Biology of Camptothecin and Its Derivatives in Handbook of Natural Products - Phytochemistry, Botany, Metabolism
, pp. 643-682
-
-
Kacprzak, K.1
-
79
-
-
33846439358
-
Soluble Camptothecin Derivatives Prepared by Click Cycloaddition Chemistry on Functional Aliphatic Polyesters
-
Parrish, B.; Emrick, T. Soluble Camptothecin Derivatives Prepared by Click Cycloaddition Chemistry on Functional Aliphatic Polyesters Bioconjugate Chem. 2007, 18, 263-267 10.1021/bc060201d
-
(2007)
Bioconjugate Chem.
, vol.18
, pp. 263-267
-
-
Parrish, B.1
Emrick, T.2
-
80
-
-
84868524364
-
Synthesis of Water-soluble Camptothecin-polyoxetane Conjugates via Click Chemistry
-
Zolotarskaya, O. Y.; Wagner, A. F.; Beckta, J. M.; Valerie, K.; Wynne, K. J.; Yang, H. Synthesis of Water-soluble Camptothecin-polyoxetane Conjugates via Click Chemistry Mol. Pharmaceutics 2012, 9, 3403-3408 10.1021/mp3005066
-
(2012)
Mol. Pharmaceutics
, vol.9
, pp. 3403-3408
-
-
Zolotarskaya, O.Y.1
Wagner, A.F.2
Beckta, J.M.3
Valerie, K.4
Wynne, K.J.5
Yang, H.6
-
81
-
-
72449201610
-
Polymeric Phosphorylcholine-Camptothecin Conjugates Prepared by Controlled Free Radical Polymerization and Click Chemistry
-
Chen, X.; McRae, S.; Parelkar, S.; Emrick, T. Polymeric Phosphorylcholine-Camptothecin Conjugates Prepared by Controlled Free Radical Polymerization and Click Chemistry Bioconjugate Chem. 2009, 20, 2331-2341 10.1021/bc900339x
-
(2009)
Bioconjugate Chem.
, vol.20
, pp. 2331-2341
-
-
Chen, X.1
McRae, S.2
Parelkar, S.3
Emrick, T.4
-
82
-
-
32644453360
-
Copper-free Sonogashira Reaction using 7-Chloro Camptothecins
-
Luo, Y.; Gao, H.; Li, Y.; Huang, W.; Lu, W.; Zhang, Z. Copper-free Sonogashira Reaction using 7-Chloro Camptothecins Tetrahedron 2006, 62, 2465-2470 10.1016/j.tet.2006.01.001
-
(2006)
Tetrahedron
, vol.62
, pp. 2465-2470
-
-
Luo, Y.1
Gao, H.2
Li, Y.3
Huang, W.4
Lu, W.5
Zhang, Z.6
-
83
-
-
84894498565
-
Synthesis of 7-Triazole-substituted Camptothecin via Click Chemistry and Evaluation of in vitro Antitumor Activity
-
Wang, L.; Yuan, W.; Zhang, J.; Tong, L.; Luo, Y.; Chen, Y.; Lu, W.; Huang, Q. Synthesis of 7-Triazole-substituted Camptothecin via Click Chemistry and Evaluation of in vitro Antitumor Activity Chin. J. Chem. 2014, 32, 157-162 10.1002/cjoc.201300703
-
(2014)
Chin. J. Chem.
, vol.32
, pp. 157-162
-
-
Wang, L.1
Yuan, W.2
Zhang, J.3
Tong, L.4
Luo, Y.5
Chen, Y.6
Lu, W.7
Huang, Q.8
-
84
-
-
77951694589
-
Azides Derived from Colchicine and Their Use in Library Synthesis: A Practical Entry to New Bioactive Derivatives of an Old Natural Drug
-
Nicolaus, N.; Zapke, J.; Riesterer, P.; Neudörfl, J.-M.; Prokop, A.; Oschkinat, H.; Schmalz, H.-G. Azides Derived from Colchicine and Their Use in Library Synthesis: A Practical Entry to New Bioactive Derivatives of an Old Natural Drug ChemMedChem 2010, 5, 661-665 10.1002/cmdc.201000063
-
(2010)
ChemMedChem
, vol.5
, pp. 661-665
-
-
Nicolaus, N.1
Zapke, J.2
Riesterer, P.3
Neudörfl, J.-M.4
Prokop, A.5
Oschkinat, H.6
Schmalz, H.-G.7
-
85
-
-
79952774430
-
A Convenient Entry to New C-7-modified Colchicinoids Through Azide Alkyne [3 + 2] Cycloaddition: Application of Ring-contractive Rearangements
-
Nicolaus, N.; Reball, J.; Sitnikov, N.; Velder, J.; Termath, A.; Fedorov, A. Yu.; Schmalz, H.-G. A Convenient Entry to New C-7-modified Colchicinoids Through Azide Alkyne [3 + 2] Cycloaddition: Application of Ring-contractive Rearangements Heterocycles 2010, 82, 1585-1600 10.3987/COM-10-S(E)117
-
(2010)
Heterocycles
, vol.82
, pp. 1585-1600
-
-
Nicolaus, N.1
Reball, J.2
Sitnikov, N.3
Velder, J.4
Termath, A.5
Fedorov, A.Yu.6
Schmalz, H.-G.7
-
86
-
-
84884950953
-
Lipophilic Prodrugs of a Triazole-containing Colchicine Analogue in Liposomes: Biological Effects on Human Tumor Cells
-
Kuznetsova, N. R.; Svirshchevskaya, E. V.; Sitnikov, N. S.; Abodo, L.; Sutorius, H.; Zapke, J.; Velder, J.; Thomopoulou, P.; Oschkinat, H.; Prokop, A. et al. Lipophilic Prodrugs of a Triazole-containing Colchicine Analogue in Liposomes: Biological Effects on Human Tumor Cells Russ. J. Bioorg. Chem. 2013, 39, 543-552 10.1134/S1068162013050105
-
(2013)
Russ. J. Bioorg. Chem.
, vol.39
, pp. 543-552
-
-
Kuznetsova, N.R.1
Svirshchevskaya, E.V.2
Sitnikov, N.S.3
Abodo, L.4
Sutorius, H.5
Zapke, J.6
Velder, J.7
Thomopoulou, P.8
Oschkinat, H.9
Prokop, A.10
-
87
-
-
84863220848
-
Synthesis and Biological Evaluation of Novel Anticancer Bivalent Colchicine-tubulizine Hybrids
-
Malysheva, Y. B.; Combes, S.; Allegro, D.; Peyrot, V.; Knochel, P.; Gavryushin, A. E.; Fedorov, A. Y. Synthesis and Biological Evaluation of Novel Anticancer Bivalent Colchicine-tubulizine Hybrids Bioorg. Med. Chem. 2012, 20, 4271-4278 10.1016/j.bmc.2012.05.072
-
(2012)
Bioorg. Med. Chem.
, vol.20
, pp. 4271-4278
-
-
Malysheva, Y.B.1
Combes, S.2
Allegro, D.3
Peyrot, V.4
Knochel, P.5
Gavryushin, A.E.6
Fedorov, A.Y.7
-
88
-
-
79953228834
-
Synthesis, Biological Evaluation and Molecular Modeling of Novel Triazole-containing Berberine Derivatives as Acetylcholinesterase and β-amyloid Aggregation Inhibitors
-
Shi, A.; Huang, L.; Lu, C.; He, F.; Li, X. Synthesis, Biological Evaluation and Molecular Modeling of Novel Triazole-containing Berberine Derivatives as Acetylcholinesterase and β-amyloid Aggregation Inhibitors Bioorg. Med. Chem. 2011, 19, 2298-2305 10.1016/j.bmc.2011.02.025
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 2298-2305
-
-
Shi, A.1
Huang, L.2
Lu, C.3
He, F.4
Li, X.5
-
89
-
-
84905665478
-
Design, Synthesis, and Anticancer Activity of Novel Berberine Derivatives Prepared via CuAAC "Click" Chemistry as Potential Anticancer Agents
-
Jin, X.; Yan, T.-H.; Yan, L.; Li, Q.; Wang, R.-L.; Hu, Z.-L.; Jiang, Y.-Y.; Sun, Q.-Y.; Cao, Y.-B. Design, Synthesis, and Anticancer Activity of Novel Berberine Derivatives Prepared via CuAAC "Click" Chemistry as Potential Anticancer Agents Drug Des., Dev. Ther. 2014, 8, 1047-1059 10.2147/DDDT.S63228
-
(2014)
Drug Des., Dev. Ther.
, vol.8
, pp. 1047-1059
-
-
Jin, X.1
Yan, T.-H.2
Yan, L.3
Li, Q.4
Wang, R.-L.5
Hu, Z.-L.6
Jiang, Y.-Y.7
Sun, Q.-Y.8
Cao, Y.-B.9
-
90
-
-
78650240536
-
Click Chemistry and Biocatalysis for the Preparation of Pancratistatin Analogs
-
de la Sovera, V.; Bellomo, A.; Gonzalez, D. Click Chemistry and Biocatalysis for the Preparation of Pancratistatin Analogs Tetrahedron Lett. 2011, 52, 430-433 10.1016/j.tetlet.2010.11.084
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 430-433
-
-
De La Sovera, V.1
Bellomo, A.2
Gonzalez, D.3
-
91
-
-
84900986993
-
Design, Synthesis and Molecular Docking Studies of Novel N-Benzenesulfonyl-1,2,3,4-tetrahydroisoquinoline-based Triazoles with Potential Anticancer Activity
-
Pingaew, R.; Mandi, P.; Nantasenamat, C.; Prachayasittikul, S.; Ruchirawat, S.; Prachayasittikul, V. Design, Synthesis and Molecular Docking Studies of Novel N-Benzenesulfonyl-1,2,3,4-tetrahydroisoquinoline-based Triazoles with Potential Anticancer Activity Eur. J. Med. Chem. 2014, 81, 192-203 10.1016/j.ejmech.2014.05.019
-
(2014)
Eur. J. Med. Chem.
, vol.81
, pp. 192-203
-
-
Pingaew, R.1
Mandi, P.2
Nantasenamat, C.3
Prachayasittikul, S.4
Ruchirawat, S.5
Prachayasittikul, V.6
-
92
-
-
84873570152
-
Facile Synthesis of (1,2,3)-Triazole-Fused Isoindolines, Tetrahydroisoquinolines, Benzoazepines and Benzoazocines by Palladium-Copper Catalysed Heterocyclisation
-
Brahma, K.; Achari, B.; Chowdhury, C. Facile Synthesis of (1,2,3)-Triazole-Fused Isoindolines, Tetrahydroisoquinolines, Benzoazepines and Benzoazocines by Palladium-Copper Catalysed Heterocyclisation Synthesis 2013, 45, 545-555 10.1055/s-0032-1316839
-
(2013)
Synthesis
, vol.45
, pp. 545-555
-
-
Brahma, K.1
Achari, B.2
Chowdhury, C.3
-
93
-
-
80051889227
-
An Efficient Synthesis of a (-)-Physostigmine"s Library for Identifying Potential Anti-Alzheimer"s Agents
-
Wu, Y.; Wang, F.; Song, H.; Qin, Y. An Efficient Synthesis of a (-)-Physostigmine"s Library for Identifying Potential Anti-Alzheimer"s Agents Helv. Chim. Acta 2011, 94, 1496-1505 10.1002/hlca.201100020
-
(2011)
Helv. Chim. Acta
, vol.94
, pp. 1496-1505
-
-
Wu, Y.1
Wang, F.2
Song, H.3
Qin, Y.4
-
94
-
-
84885041416
-
Synthesis and Anticholinesterase Activity of (-)-Physostigmine Analogues with Modifications at C3α and C5
-
Wang, H. J.; Zhang, D.; Wang, F. S.; Wu, Y.; Song, H. Synthesis and Anticholinesterase Activity of (-)-Physostigmine Analogues with Modifications at C3α and C5 Chem. Res. Chin. Univ. 2013, 29, 888-893 10.1007/s40242-013-3066-y
-
(2013)
Chem. Res. Chin. Univ.
, vol.29
, pp. 888-893
-
-
Wang, H.J.1
Zhang, D.2
Wang, F.S.3
Wu, Y.4
Song, H.5
-
95
-
-
77949768135
-
Two Versatile and Parallel Approaches to Highly Symmetrical Open and Closed Natural Product-based Structures
-
Montenegro, H. E.; Ramírez-López, P.; de la Torre, M. C.; Asenjo, M.; Sierra, M. Two Versatile and Parallel Approaches to Highly Symmetrical Open and Closed Natural Product-based Structures Chem.-Eur. J. 2010, 16, 3798-3814 10.1002/chem.200903264
-
(2010)
Chem. - Eur. J.
, vol.16
, pp. 3798-3814
-
-
Montenegro, H.E.1
Ramírez-López, P.2
De La Torre, M.C.3
Asenjo, M.4
Sierra, M.5
-
96
-
-
79960362357
-
Flustramine Inspired Synthesis and Biological Evaluation of Pyrroloindoline Triazole Amides as Novel Inhibitors of Bacterial Biofilms
-
Bunders, C.; Cavanagh, J.; Melander, C. Flustramine Inspired Synthesis and Biological Evaluation of Pyrroloindoline Triazole Amides as Novel Inhibitors of Bacterial Biofilms Org. Biomol. Chem. 2011, 9, 5476-5481 10.1039/c1ob05605k
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 5476-5481
-
-
Bunders, C.1
Cavanagh, J.2
Melander, C.3
-
97
-
-
77958063689
-
Triazolyl Tryptoline Derivatives as β-Secretase Inhibitors
-
Jiaranaikulwanitch, J.; Boonyarat, C.; Fokin, V. V.; Vajragupta, O. Triazolyl Tryptoline Derivatives as β-Secretase Inhibitors Bioorg. Med. Chem. Lett. 2010, 20, 6572-6576 10.1016/j.bmcl.2010.09.043
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 6572-6576
-
-
Jiaranaikulwanitch, J.1
Boonyarat, C.2
Fokin, V.V.3
Vajragupta, O.4
-
98
-
-
79953212266
-
Synthesis and Biological Activity of 2-Aminoimidazole Triazoles Accessed by Suzuki-Miyaura Cross-coupling
-
Reyes, S.; Huigens, R. W., III; Su, Z.; Simon, M. L.; Melander, C. Synthesis and Biological Activity of 2-Aminoimidazole Triazoles Accessed by Suzuki-Miyaura Cross-coupling Org. Biomol. Chem. 2011, 9, 3041-3049 10.1039/c0ob00925c
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 3041-3049
-
-
Reyes, S.1
Huigens, R.W.2
Su, Z.3
Simon, M.L.4
Melander, C.5
-
99
-
-
82955165642
-
Evaluation of 4,5-Disubstituted-2-aminoimidazole-triazole Conjugates for Antibiofilm/antibiotic Resensitization Activity Against MRSA and Acinetobacter Baumannii
-
Su, Z.; Peng, L.; Worthington, R. J.; Melander, C. Evaluation of 4,5-Disubstituted-2-aminoimidazole-triazole Conjugates for Antibiofilm/antibiotic Resensitization Activity Against MRSA and Acinetobacter Baumannii ChemMedChem 2011, 6, 2243-2251 10.1002/cmdc.201100316
-
(2011)
ChemMedChem
, vol.6
, pp. 2243-2251
-
-
Su, Z.1
Peng, L.2
Worthington, R.J.3
Melander, C.4
-
100
-
-
84872686801
-
A Flexible Approach to 1,4-Di-substituted 2-Aminoimidazoles That Inhibit and Disperse Biofilms and Potentiate the Effects of β-Lactams Against Multi-drug Resistant Bacteria
-
Furlani, R. E.; Yeagley, A. A.; Melander, C. A Flexible Approach to 1,4-Di-substituted 2-Aminoimidazoles That Inhibit and Disperse Biofilms and Potentiate the Effects of β-Lactams Against Multi-drug Resistant Bacteria Eur. J. Med. Chem. 2013, 62, 59-70 10.1016/j.ejmech.2012.12.005
-
(2013)
Eur. J. Med. Chem.
, vol.62
, pp. 59-70
-
-
Furlani, R.E.1
Yeagley, A.A.2
Melander, C.3
-
101
-
-
80054755092
-
Designing 2-Aminoimidazole Alkaloids Analogs with Anti-biofilm Activities: Structure-activities Relationships of Polysubstituted Triazoles
-
Linares, D.; Bottzeck, O.; Pereira, O.; Praud-Tabariès, A.; Blache, Y. Designing 2-Aminoimidazole Alkaloids Analogs with Anti-biofilm Activities: Structure-activities Relationships of Polysubstituted Triazoles Bioorg. Med. Chem. Lett. 2011, 21, 6751-6755 10.1016/j.bmcl.2011.09.050
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 6751-6755
-
-
Linares, D.1
Bottzeck, O.2
Pereira, O.3
Praud-Tabariès, A.4
Blache, Y.5
-
102
-
-
77949280828
-
Synthesis of Triazolyl-Substituted 3-Aminopiperidines by Huisgen-1,3-Dipolar Cycloaddition - New Scaffolds for Combinatorial Chemistry
-
Schramm, H.; Saak, W.; Hoenke, C.; Christoffers, J. Synthesis of Triazolyl-Substituted 3-Aminopiperidines by Huisgen-1,3-Dipolar Cycloaddition-New Scaffolds for Combinatorial Chemistry Eur. J. Org. Chem. 2010, 2010, 1745-1753 10.1002/ejoc.200901458
-
(2010)
Eur. J. Org. Chem.
, vol.2010
, pp. 1745-1753
-
-
Schramm, H.1
Saak, W.2
Hoenke, C.3
Christoffers, J.4
-
103
-
-
79951850432
-
Synthesis of trans-4 Triazolyl-Substituted 3-Hydroxypiperidines
-
Harmsen, R. A. G.; Sydnes, L.; Törnroos, K. W.; Haug, B. E. Synthesis of trans-4 Triazolyl-Substituted 3-Hydroxypiperidines Synthesis 2011, 2011, 749-754 10.1055/s-0030-1259569
-
(2011)
Synthesis
, vol.2011
, pp. 749-754
-
-
Harmsen, R.A.G.1
Sydnes, L.2
Törnroos, K.W.3
Haug, B.E.4
-
104
-
-
66349095655
-
Synthesis of Novel 3-(1-(1-Substituted Piperidin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-5(4H)-one as Antifungal Agents
-
Sangshetti, J. N.; Nagawade, R. R.; Shinde, D. B. Synthesis of Novel 3-(1-(1-Substituted Piperidin-4-yl)-1H-1,2,3-triazol-4-yl)-1,2,4-oxadiazol-5(4H)-one as Antifungal Agents Bioorg. Med. Chem. Lett. 2009, 19, 3564-3567 10.1016/j.bmcl.2009.04.134
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3564-3567
-
-
Sangshetti, J.N.1
Nagawade, R.R.2
Shinde, D.B.3
-
105
-
-
84879482779
-
A Novel Amalgamation of 1,2,3-Triazoles, Piperidines and Thieno Pyridine Rings and Evaluation of Their Antifungal Activity
-
Darandale, S. N.; Mulla, N. A.; Pansare, D. N.; Sangshetti, J. N.; Shinde, D. B. A Novel Amalgamation of 1,2,3-Triazoles, Piperidines and Thieno Pyridine Rings and Evaluation of Their Antifungal Activity Eur. J. Med. Chem. 2013, 65, 527-532 10.1016/j.ejmech.2013.04.045
-
(2013)
Eur. J. Med. Chem.
, vol.65
, pp. 527-532
-
-
Darandale, S.N.1
Mulla, N.A.2
Pansare, D.N.3
Sangshetti, J.N.4
Shinde, D.B.5
-
106
-
-
84896766412
-
One-pot Synthesis of 3-Azido- and 3-Aminopiperidines by Intramolecular Cyclization of Unsaturated Amines
-
Ortiz, G. X., Jr.; Kang, B.; Wang, Q. One-pot Synthesis of 3-Azido- and 3-Aminopiperidines by Intramolecular Cyclization of Unsaturated Amines J. Org. Chem. 2014, 79, 571-581 10.1021/jo4022666
-
(2014)
J. Org. Chem.
, vol.79
, pp. 571-581
-
-
Ortiz, G.X.1
Kang, B.2
Wang, Q.3
-
107
-
-
79959684303
-
Thiopurine Derivatives Containing Triazole and Steroid: Synthesis, Antimalarial and Antileishmanial Activities
-
Corrales, R. C. N. R.; de Souza, N. B.; Pinheiro, L. S.; Abramo, C.; Coimbra, E. S.; Da Silva, A. D. Thiopurine Derivatives Containing Triazole and Steroid: Synthesis, Antimalarial and Antileishmanial Activities Biomed. Pharmacother. 2011, 65, 198-203 10.1016/j.biopha.2010.10.013
-
(2011)
Biomed. Pharmacother.
, vol.65
, pp. 198-203
-
-
Corrales, R.C.N.R.1
De Souza, N.B.2
Pinheiro, L.S.3
Abramo, C.4
Coimbra, E.S.5
Da Silva, A.D.6
-
108
-
-
79958753408
-
Novel Purine-based Fluoroaryl-1,2,3-triazoles as Neuroprotecting Agents: Synthesis, Neuronal Cell Culture Investigations, and CDK5 Docking Studies
-
Nair, N.; Kudo, W.; Smith, M. A.; Abrol, R.; Goddard, W. A., III; Reddy, V. P. Novel Purine-based Fluoroaryl-1,2,3-triazoles as Neuroprotecting Agents: Synthesis, Neuronal Cell Culture Investigations, and CDK5 Docking Studies Bioorg. Med. Chem. Lett. 2011, 21, 3957-3961 10.1016/j.bmcl.2011.05.019
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3957-3961
-
-
Nair, N.1
Kudo, W.2
Smith, M.A.3
Abrol, R.4
Goddard, W.A.5
Reddy, V.P.6
-
109
-
-
84901799830
-
Synthesis, Cytotoxicity, Antimicrobial and Anti-biofilm Activities of Novel Pyrazolo(3,4-b)pyridine and Pyrimidine Functionalized 1,2,3-Triazole Derivatives
-
Nagender, P.; Malla Reddy, G.; Naresh Kumar, R.; Poornachandra, Y.; Ganesh Kumar, C.; Narsaiah, B. Synthesis, Cytotoxicity, Antimicrobial and Anti-biofilm Activities of Novel Pyrazolo(3,4-b)pyridine and Pyrimidine Functionalized 1,2,3-Triazole Derivatives Bioorg. Med. Chem. Lett. 2014, 24, 2905-2908 10.1016/j.bmcl.2014.04.084
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 2905-2908
-
-
Nagender, P.1
Malla Reddy, G.2
Naresh Kumar, R.3
Poornachandra, Y.4
Ganesh Kumar, C.5
Narsaiah, B.6
-
110
-
-
84857511037
-
A New Cyclopamine Glucuronide Prodrug with Improved Kinetics of Drug Release
-
Renoux, B.; Legigan, T.; Bensalma, S.; Chadéneau, C.; Muller, J.-M.; Papot, S. A New Cyclopamine Glucuronide Prodrug with Improved Kinetics of Drug Release Org. Biomol. Chem. 2011, 9, 8459-8464 10.1039/c1ob06081c
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 8459-8464
-
-
Renoux, B.1
Legigan, T.2
Bensalma, S.3
Chadéneau, C.4
Muller, J.-M.5
Papot, S.6
-
111
-
-
38949179196
-
Synthesis and Anticancer Activity Studies of Cyclopamine Derivatives
-
Zhang, J.; Garrossian, M.; Gardner, D.; Garrossian, A.; Chang, Y.-T.; Kim, Y. K.; Chang, Ch.-W. T. Synthesis and Anticancer Activity Studies of Cyclopamine Derivatives Bioorg. Med. Chem. Lett. 2008, 18, 1359-1363 10.1016/j.bmcl.2008.01.017
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1359-1363
-
-
Zhang, J.1
Garrossian, M.2
Gardner, D.3
Garrossian, A.4
Chang, Y.-T.5
Kim, Y.K.6
Chang, Ch.-W.T.7
-
112
-
-
84858697862
-
Semi-synthesis of Bioactive Fluorescent Analogues of the Cytotoxic Marine Alkaloid Discorhabdin C
-
Lam, C. F. C.; Giddens, A. C.; Chand, N.; Webb, V. L.; Copp, B. R. Semi-synthesis of Bioactive Fluorescent Analogues of the Cytotoxic Marine Alkaloid Discorhabdin C Tetrahedron 2012, 68, 3187-3194 10.1016/j.tet.2012.02.052
-
(2012)
Tetrahedron
, vol.68
, pp. 3187-3194
-
-
Lam, C.F.C.1
Giddens, A.C.2
Chand, N.3
Webb, V.L.4
Copp, B.R.5
-
113
-
-
84894053007
-
Design, Synthesis, and Anti-tobacco Mosaic Virus (TMV) Activity of Glycoconjugates of Phenanthroindolizidines Alkaloids
-
Wu, M.; Han, G.; Meng, C.; Wang, Z.; Liu, Y.; Wang, Q. Design, Synthesis, and Anti-tobacco Mosaic Virus (TMV) Activity of Glycoconjugates of Phenanthroindolizidines Alkaloids Mol. Diversity 2014, 18, 25-37 10.1007/s11030-013-9484-4
-
(2014)
Mol. Diversity
, vol.18
, pp. 25-37
-
-
Wu, M.1
Han, G.2
Meng, C.3
Wang, Z.4
Liu, Y.5
Wang, Q.6
-
114
-
-
43749095416
-
Synthesis and Receptor Binding Properties of 2β-alkynyl and 2β-(1,2,3-Triazol)substituted 3β-(Substituted phenyl)tropane Derivatives
-
Jin, C.; Navarro, H. A.; Carroll, F. I. Synthesis and Receptor Binding Properties of 2β-alkynyl and 2β-(1,2,3-Triazol)substituted 3β-(Substituted phenyl)tropane Derivatives Bioorg. Med. Chem. 2008, 16, 5529-5535 10.1016/j.bmc.2008.04.008
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 5529-5535
-
-
Jin, C.1
Navarro, H.A.2
Carroll, F.I.3
-
115
-
-
84880039178
-
Synthesis of Novel Derivatives of Murrayafoline A and Their Inhibitory Effect on LPS-stimulated Production of Pro-inflammatory Cytokines in Bone Marrow-derived Dendritic Cells
-
Thuy, T. T. T.; Cuong, N. M.; Toan, T. Q.; Thang, N. N.; Tai, B. H.; Nhiem, N. X.; Hong, H.-J.; Kim, S.; Legoupy, S.; Koh, Y. S.; Kim, Y. H. Synthesis of Novel Derivatives of Murrayafoline A and Their Inhibitory Effect on LPS-stimulated Production of Pro-inflammatory Cytokines in Bone Marrow-derived Dendritic Cells Arch. Pharmacal Res. 2013, 36, 832-839 10.1007/s12272-013-0100-z
-
(2013)
Arch. Pharmacal Res.
, vol.36
, pp. 832-839
-
-
Thuy, T.T.T.1
Cuong, N.M.2
Toan, T.Q.3
Thang, N.N.4
Tai, B.H.5
Nhiem, N.X.6
Hong, H.-J.7
Kim, S.8
Legoupy, S.9
Koh, Y.S.10
Kim, Y.H.11
-
116
-
-
43049107992
-
Unearthing the Roots of the Terpenome
-
Christianson, D. W. Unearthing the Roots of the Terpenome Curr. Opin. Chem. Biol. 2008, 12, 141-150 10.1016/j.cbpa.2007.12.008
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 141-150
-
-
Christianson, D.W.1
-
117
-
-
3242785011
-
Isoprenoids: Remarkable Diversity of Form and Function
-
Holstein, S. A.; Hohl, R. J. Isoprenoids: Remarkable Diversity of Form and Function Lipids 2004, 39, 293-309 10.1007/s11745-004-1233-3
-
(2004)
Lipids
, vol.39
, pp. 293-309
-
-
Holstein, S.A.1
Hohl, R.J.2
-
118
-
-
0002503177
-
Bile Acids as Building Blocks of Supramolecular Hosts
-
Tamminen, J.; Kolehmainen, E. Bile Acids as Building Blocks of Supramolecular Hosts Molecules 2001, 6, 21-46 10.3390/60100021
-
(2001)
Molecules
, vol.6
, pp. 21-46
-
-
Tamminen, J.1
Kolehmainen, E.2
-
120
-
-
39149133975
-
Bile Acids as Building Blocks of Amphiphilic Polymers. Applications and Comparison with Other Systems
-
Durand, A. Bile Acids as Building Blocks of Amphiphilic Polymers. Applications and Comparison with Other Systems Collect. Czech. Chem. Commun. 2007, 72, 1553-1578 10.1135/cccc20071553
-
(2007)
Collect. Czech. Chem. Commun.
, vol.72
, pp. 1553-1578
-
-
Durand, A.1
-
121
-
-
14844358214
-
Bile Acid Derivatives as Enantiodifferentiating Host Molecules in Inclusion Processes
-
Bortolini, O.; Fantin, G.; Fogagnolo, M. Bile Acid Derivatives as Enantiodifferentiating Host Molecules in Inclusion Processes Chirality 2005, 17, 121-130 10.1002/chir.20126
-
(2005)
Chirality
, vol.17
, pp. 121-130
-
-
Bortolini, O.1
Fantin, G.2
Fogagnolo, M.3
-
122
-
-
50249180215
-
Bile Acids: Chemistry, Pathochemistry, Biology, Pathobiology, and Therapeutics
-
Hofmann, A. F.; Hagey, L. R. Bile Acids: Chemistry, Pathochemistry, Biology, Pathobiology, and Therapeutics Cell. Mol. Life Sci. 2008, 65, 2461-2483 10.1007/s00018-008-7568-6
-
(2008)
Cell. Mol. Life Sci.
, vol.65
, pp. 2461-2483
-
-
Hofmann, A.F.1
Hagey, L.R.2
-
123
-
-
0002148515
-
Bile Acids in Drug Discovery
-
Enhsen, A.; Kramer, W.; Wess, G. Bile Acids in Drug Discovery Drug Discovery Today 1998, 3, 409-418 10.1016/S1359-6446(96)10046-5
-
(1998)
Drug Discovery Today
, vol.3
, pp. 409-418
-
-
Enhsen, A.1
Kramer, W.2
Wess, G.3
-
124
-
-
34548458522
-
Exploitation of Bile Acid Transport Systems in Prodrug Design
-
Sievänen, E. Exploitation of Bile Acid Transport Systems in Prodrug Design Molecules 2007, 12, 1859-1889 10.3390/12081859
-
(2007)
Molecules
, vol.12
, pp. 1859-1889
-
-
Sievänen, E.1
-
125
-
-
77950808392
-
Bile Acids in Asymmetric Synthesis and Chiral Discrimination
-
Bortolini, O.; Fantin, G.; Fogagnolo, M. Bile Acids in Asymmetric Synthesis and Chiral Discrimination Chirality 2010, 22, 486-494 10.1002/chir.20769
-
(2010)
Chirality
, vol.22
, pp. 486-494
-
-
Bortolini, O.1
Fantin, G.2
Fogagnolo, M.3
-
126
-
-
84901281300
-
Synthesis and Evaluation of (18)F-Labeled Bile Acid Compound: A Potential PET Imaging Agent for FXR Related Diseases
-
Jia, L.; Jiang, D.; Hu, P.; Li, X.; Shi, H.; Cheng, D.; Zhang, L. Synthesis and Evaluation of (18)F-Labeled Bile Acid Compound: a Potential PET Imaging Agent for FXR Related Diseases Nucl. Med. Biol. 2014, 41, 495-500 10.1016/j.nucmedbio.2014.03.016
-
(2014)
Nucl. Med. Biol.
, vol.41
, pp. 495-500
-
-
Jia, L.1
Jiang, D.2
Hu, P.3
Li, X.4
Shi, H.5
Cheng, D.6
Zhang, L.7
-
127
-
-
24744463110
-
Synthesis of Bile Acid Dimers Linked with 1,2,3-Triazole Ring at C-3, C-11, and C-24 Positions
-
Aher, N. G.; Pore, V. S. Synthesis of Bile Acid Dimers Linked with 1,2,3-Triazole Ring at C-3, C-11, and C-24 Positions Synlett 2005, 14, 2155-2158 10.1055/s-2005-872223
-
(2005)
Synlett
, vol.14
, pp. 2155-2158
-
-
Aher, N.G.1
Pore, V.S.2
-
128
-
-
36148937894
-
Design, Synthesis, and Micellar Properties of Bile Acid Dimers and Oligomers Linked with a 1,2,3-Triazole Ring
-
Aher, N. G.; Pore, V. S.; Patil, S. P. Design, Synthesis, and Micellar Properties of Bile Acid Dimers and Oligomers Linked with a 1,2,3-Triazole Ring Tetrahedron 2007, 63, 12927-12934 10.1016/j.tet.2007.10.042
-
(2007)
Tetrahedron
, vol.63
, pp. 12927-12934
-
-
Aher, N.G.1
Pore, V.S.2
Patil, S.P.3
-
129
-
-
38149133668
-
Synthesis of 1,2,3-Triazole-containing Bile Acid Dimers and Properties of Inverse Micellar Mimic
-
Zhang, Z.; Ju, Y.; Zhao, Y. Synthesis of 1,2,3-Triazole-containing Bile Acid Dimers and Properties of Inverse Micellar Mimic Chem. Lett. 2007, 36, 1450-1451 10.1246/cl.2007.1450
-
(2007)
Chem. Lett.
, vol.36
, pp. 1450-1451
-
-
Zhang, Z.1
Ju, Y.2
Zhao, Y.3
-
130
-
-
84939417956
-
Synthesis of Isomeric Dimers of Deoxycholic Acid Derivatives Linked by 1,2,3-Triazole
-
Madrzak-Litwa, I.; Wojciechowska, A.; Paryzek, Z. Synthesis of Isomeric Dimers of Deoxycholic Acid Derivatives Linked by 1,2,3-Triazole Synth. Commun. 2015, 45, 1222-1230 10.1080/00397911.2015.1014116
-
(2015)
Synth. Commun.
, vol.45
, pp. 1222-1230
-
-
Madrzak-Litwa, I.1
Wojciechowska, A.2
Paryzek, Z.3
-
131
-
-
84894427282
-
Tripodal Bile Acid Architectures Based on a Triarylphosphine Oxide Core Obtained by Copper-Catalysed (1,3)-Dipolar Cycloaddition: Synthesis and Preliminary Aggregation Studies
-
Thota, B. N. S.; Savyasachi, A. J.; Lukashev, N.; Beletskaya, I.; Maitra, U. Tripodal Bile Acid Architectures Based on a Triarylphosphine Oxide Core Obtained by Copper-Catalysed (1,3)-Dipolar Cycloaddition: Synthesis and Preliminary Aggregation Studies Eur. J. Org. Chem. 2014, 2014, 1406-1415 10.1002/ejoc.201301443
-
(2014)
Eur. J. Org. Chem.
, vol.2014
, pp. 1406-1415
-
-
Thota, B.N.S.1
Savyasachi, A.J.2
Lukashev, N.3
Beletskaya, I.4
Maitra, U.5
-
132
-
-
77149169413
-
Molecular Pockets Derived from Cholic Acid as Chemosensors for Metal Ions
-
Zhang, J.; Luo, J.; Zhu, X. X.; Junk, M. J. N.; Hinderberger, D. Molecular Pockets Derived from Cholic Acid as Chemosensors for Metal Ions Langmuir 2010, 26, 2958-2962 10.1021/la9028996
-
(2010)
Langmuir
, vol.26
, pp. 2958-2962
-
-
Zhang, J.1
Luo, J.2
Zhu, X.X.3
Junk, M.J.N.4
Hinderberger, D.5
-
133
-
-
69249223458
-
2+ Ion and Their Logic Gate Behaviour
-
2+Ion and Their Logic Gate Behaviour Tetrahedron Lett. 2009, 50, 5842-5845 10.1016/j.tetlet.2009.08.007
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5842-5845
-
-
Kumar, A.1
Pandey, P.S.2
-
134
-
-
80054744508
-
Oligocholate Foldamers as Carriers for Hydrophilic Molecules Across Lipid Bilayers
-
Zhang, S.; Zhao, Y. Oligocholate Foldamers as Carriers for Hydrophilic Molecules Across Lipid Bilayers Chem.-Eur. J. 2011, 17, 12444-12451 10.1002/chem.201101510
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 12444-12451
-
-
Zhang, S.1
Zhao, Y.2
-
135
-
-
73949096670
-
Synthesis of Click Bile Acid Polymers and Their Application in Stabilization of Silver Nanoparticles Showing Iodide Sensing Property
-
Kumar, A.; Chhatra, R. K.; Pandey, P. S. Synthesis of Click Bile Acid Polymers and Their Application in Stabilization of Silver Nanoparticles Showing Iodide Sensing Property Org. Lett. 2010, 12, 24-27 10.1021/ol902351g
-
(2010)
Org. Lett.
, vol.12
, pp. 24-27
-
-
Kumar, A.1
Chhatra, R.K.2
Pandey, P.S.3
-
136
-
-
84868700776
-
Triazole-linked Polyamides and Polyesters Derived from Cholic Acid
-
Ivanysenko, O.; Strandman, S.; Zhu, X. X. Triazole-linked Polyamides and Polyesters Derived from Cholic Acid Polym. Chem. 2012, 3, 1962-1965 10.1039/c2py20168b
-
(2012)
Polym. Chem.
, vol.3
, pp. 1962-1965
-
-
Ivanysenko, O.1
Strandman, S.2
Zhu, X.X.3
-
137
-
-
69749086213
-
Copper-Catalyzed (1,3)-Dipolar Cycloaddition for the Synthesis of Macrocycles Containing Acyclic, Aromatic and Steroidal Moieties
-
Latyshev, G. V.; Baranov, M. S.; Kazantsev, A. V.; Averin, A. D.; Lukashev, N. V.; Beletskaya, I. P. Copper-Catalyzed (1,3)-Dipolar Cycloaddition for the Synthesis of Macrocycles Containing Acyclic, Aromatic and Steroidal Moieties Synthesis 2009, 2009, 2605-2615 10.1055/s-0029-1217400
-
(2009)
Synthesis
, vol.2009
, pp. 2605-2615
-
-
Latyshev, G.V.1
Baranov, M.S.2
Kazantsev, A.V.3
Averin, A.D.4
Lukashev, N.V.5
Beletskaya, I.P.6
-
138
-
-
80055084220
-
Synthesis of a Bile Acid-Based Click-Macrocycle and Its Application in Selective Recognition of Chloride Ion
-
Chhatra, R. K.; Kumar, A.; Pandey, P. S. Synthesis of a Bile Acid-Based Click-Macrocycle and Its Application in Selective Recognition of Chloride Ion J. Org. Chem. 2011, 76, 9086-9089 10.1021/jo201161n
-
(2011)
J. Org. Chem.
, vol.76
, pp. 9086-9089
-
-
Chhatra, R.K.1
Kumar, A.2
Pandey, P.S.3
-
139
-
-
38749094503
-
Anion Recognition by 1,2,3-Triazolium Receptors:Application of Click Chemistry in Anion Recognition
-
Kumar, A.; Pandey, P. S. Anion Recognition by 1,2,3-Triazolium Receptors:Application of Click Chemistry in Anion Recognition Org. Lett. 2008, 10, 165-168 10.1021/ol702457w
-
(2008)
Org. Lett.
, vol.10
, pp. 165-168
-
-
Kumar, A.1
Pandey, P.S.2
-
140
-
-
84891762733
-
A Click Chemistry Approach to Secosteroidal Macrocycles
-
Ibrahim-Ouali, M.; Hamze, K. A Click Chemistry Approach to Secosteroidal Macrocycles Steroids 2014, 80, 102-110 10.1016/j.steroids.2013.12.002
-
(2014)
Steroids
, vol.80
, pp. 102-110
-
-
Ibrahim-Ouali, M.1
Hamze, K.2
-
141
-
-
84890790070
-
Straightforward Synthesis of Cholic Acid Stabilized Loop Mimetics
-
Clemmen, A.; Boutton, C.; Vanlandschoot, P.; Wittelsberger, A.; Borghmans, I.; Coppens, A.; Casteels, P.; Madder, A. Straightforward Synthesis of Cholic Acid Stabilized Loop Mimetics Tetrahedron Lett. 2014, 55, 423-429 10.1016/j.tetlet.2013.11.046
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 423-429
-
-
Clemmen, A.1
Boutton, C.2
Vanlandschoot, P.3
Wittelsberger, A.4
Borghmans, I.5
Coppens, A.6
Casteels, P.7
Madder, A.8
-
142
-
-
84555189821
-
Shortcut Access to Peptidosteroid Conjugates: Building Blocks for Solid-phase Bile Acid Scaffold Decoration by Convergent Ligation
-
Verzele, D.; Figaroli, S.; Madder, A. Shortcut Access to Peptidosteroid Conjugates: Building Blocks for Solid-phase Bile Acid Scaffold Decoration by Convergent Ligation Molecules 2011, 16, 10168-10186 10.3390/molecules161210168
-
(2011)
Molecules
, vol.16
, pp. 10168-10186
-
-
Verzele, D.1
Figaroli, S.2
Madder, A.3
-
143
-
-
33749986728
-
Design and Synthesis of Fluconazole/bile acid Conjugate Using Click Reaction
-
Pore, V. S.; Aher, N. G.; Kumar, M.; Shukla, P. K. Design and Synthesis of Fluconazole/bile acid Conjugate Using Click Reaction Tetrahedron 2006, 62, 11178-11186 10.1016/j.tet.2006.09.021
-
(2006)
Tetrahedron
, vol.62
, pp. 11178-11186
-
-
Pore, V.S.1
Aher, N.G.2
Kumar, M.3
Shukla, P.K.4
-
144
-
-
53549097892
-
Synthesis and Biological Evaluation of Bile Acid Dimers Linked with 1,2,3-Triazole and bis-β-Lactam
-
Vatmurge, N. S.; Hazra, B. G.; Pore, V. S.; Shirazi, F.; Deshpande, M. V.; Kadreppa, S.; Chattopadhyay, S.; Gonnade, R. G. Synthesis and Biological Evaluation of Bile Acid Dimers Linked with 1,2,3-Triazole and bis-β-Lactam Org. Biomol. Chem. 2008, 6, 3823-3830 10.1039/b809221d
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 3823-3830
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Deshpande, M.V.5
Kadreppa, S.6
Chattopadhyay, S.7
Gonnade, R.G.8
-
145
-
-
40749106101
-
Synthesis and Antimicrobial Activity of β-Lactam-bile Acid Conjugates Linked via Triazole
-
Vatmurge, N. S.; Hazra, B. G.; Pore, V. S.; Shirazi, F.; Chavan, P. S.; Deshpande, M. V. Synthesis and Antimicrobial Activity of β-Lactam-bile Acid Conjugates Linked via Triazole Bioorg. Med. Chem. Lett. 2008, 18, 2043-2047 10.1016/j.bmcl.2008.01.102
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 2043-2047
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Chavan, P.S.5
Deshpande, M.V.6
-
146
-
-
79959782009
-
Design and Synthesis of Bile Acid-peptide Conjugates Linked via Triazole Moiety
-
Sokolova, N. V.; Latyshev, G. V.; Lukashev, N. V.; Nenajdenko, V. G. Design and Synthesis of Bile Acid-peptide Conjugates Linked via Triazole Moiety Org. Biomol. Chem. 2011, 9, 4921-4926 10.1039/c0ob01188f
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 4921-4926
-
-
Sokolova, N.V.1
Latyshev, G.V.2
Lukashev, N.V.3
Nenajdenko, V.G.4
-
147
-
-
84903318522
-
Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications
-
Sokolova, N. V.; Nenajdenko, V. G. Azidoisocyanides, New Bifunctional Reagents for Multicomponent Reactions and Biomolecule Modifications Chem. Nat. Compd. 2014, 50, 197-213 10.1007/s10600-014-0914-z
-
(2014)
Chem. Nat. Compd.
, vol.50
, pp. 197-213
-
-
Sokolova, N.V.1
Nenajdenko, V.G.2
-
149
-
-
84916214199
-
Man-Made Cytotoxic Steroids: Exemplary Agents for Cancer Therapy
-
Bansal, R.; Acharya, P. C. Man-Made Cytotoxic Steroids: Exemplary Agents for Cancer Therapy Chem. Rev. 2014, 114, 6986-7005 10.1021/cr4002935
-
(2014)
Chem. Rev.
, vol.114
, pp. 6986-7005
-
-
Bansal, R.1
Acharya, P.C.2
-
150
-
-
84892821933
-
Synthesis of Steroidal Dendrimers Modified by "Click" Chemistry with PAMAM Dendrons as Unimolecular Micelles
-
Soto-Castro, D.; Magana-Vergara, N. E.; Farfán, N.; Santillan, R. Synthesis of Steroidal Dendrimers Modified by "Click" Chemistry with PAMAM Dendrons as Unimolecular Micelles Tetrahedron Lett. 2014, 55, 1014-1019 10.1016/j.tetlet.2013.12.066
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 1014-1019
-
-
Soto-Castro, D.1
Magana-Vergara, N.E.2
Farfán, N.3
Santillan, R.4
-
151
-
-
84857031226
-
A Facile "Click" Approach to Novel 15β-Triazolyl-5α-androstane Derivatives, and an Evaluation of Their Antiproliferative Activities in vitro
-
Kádár, Z.; Molnár, J.; Schneider, G.; Zupkó, I.; Frank, E. A Facile "Click" Approach to Novel 15β-Triazolyl-5α-androstane Derivatives, and an Evaluation of Their Antiproliferative Activities in vitro Bioorg. Med. Chem. 2012, 20, 1396-1402 10.1016/j.bmc.2012.01.008
-
(2012)
Bioorg. Med. Chem.
, vol.20
, pp. 1396-1402
-
-
Kádár, Z.1
Molnár, J.2
Schneider, G.3
Zupkó, I.4
Frank, E.5
-
152
-
-
79960445267
-
Synthesis of Novel Steroidal 17α-Triazolyl Derivatives via Cu(I)-catalyzed Azide-alkyne Cycloaddition, and an Evaluation of Their Cytotoxic Activity in vitro
-
Frank, E.; Molnár, J.; Zupkó, I.; Kádár, Z.; Wölfling, J. Synthesis of Novel Steroidal 17α-Triazolyl Derivatives via Cu(I)-catalyzed Azide-alkyne Cycloaddition, and an Evaluation of Their Cytotoxic Activity in vitro Steroids 2011, 76, 1141-1148 10.1016/j.steroids.2011.05.002
-
(2011)
Steroids
, vol.76
, pp. 1141-1148
-
-
Frank, E.1
Molnár, J.2
Zupkó, I.3
Kádár, Z.4
Wölfling, J.5
-
153
-
-
81255128918
-
Efficient Approach to Novel 1α-Triazolyl-5α-androstane Derivatives as Potent Antiproliferative Agents
-
Kádár, Z.; Baji, A.; Zupkó, I.; Bartók, T.; Wölfling, J.; Frank, E. Efficient Approach to Novel 1α-Triazolyl-5α-androstane Derivatives as Potent Antiproliferative Agents Org. Biomol. Chem. 2011, 9, 8051-8057 10.1039/c1ob06086d
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 8051-8057
-
-
Kádár, Z.1
Baji, A.2
Zupkó, I.3
Bartók, T.4
Wölfling, J.5
Frank, E.6
-
154
-
-
79959627028
-
Synthesis and in vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives
-
Kádár, Z.; Kovács, D.; Frank, E.; Schneider, G.; Huber, J.; Zupkó, I.; Bartók, T.; Wölfling, J. Synthesis and in vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives Molecules 2011, 16, 4786-4806 10.3390/molecules16064786
-
(2011)
Molecules
, vol.16
, pp. 4786-4806
-
-
Kádár, Z.1
Kovács, D.2
Frank, E.3
Schneider, G.4
Huber, J.5
Zupkó, I.6
Bartók, T.7
Wölfling, J.8
-
155
-
-
77955926541
-
D-ring Substituted 1,2,3-Triazolyl 20-Keto Pregnenanes as Potential Anticancer Agents: Synthesis and Biological Evaluation
-
Banday, A. H.; Shameem, S. A.; Gupta, B. D.; Kumar, H. M. S. D-ring Substituted 1,2,3-Triazolyl 20-Keto Pregnenanes as Potential Anticancer Agents: Synthesis and Biological Evaluation Steroids 2010, 75, 801-804 10.1016/j.steroids.2010.02.015
-
(2010)
Steroids
, vol.75
, pp. 801-804
-
-
Banday, A.H.1
Shameem, S.A.2
Gupta, B.D.3
Kumar, H.M.S.4
-
156
-
-
84888120103
-
Click Chemistry Decoration of Amino Sterols as Promising Strategy to Developed New Leishmanicidal Drugs
-
Porta, E. O. J.; Carvalho, P. B.; Avery, M. A.; Tekwani, B. L.; Labadie, G. R. Click Chemistry Decoration of Amino Sterols as Promising Strategy to Developed New Leishmanicidal Drugs Steroids 2014, 79, 28-36 10.1016/j.steroids.2013.10.010
-
(2014)
Steroids
, vol.79
, pp. 28-36
-
-
Porta, E.O.J.1
Carvalho, P.B.2
Avery, M.A.3
Tekwani, B.L.4
Labadie, G.R.5
-
157
-
-
84900831753
-
Synthesis of Novel 1,2,3-Triazolyl Derivatives of Pregnane, Androstane and D-Homoandrostane. Tandem "Click" Reaction/Cu-catalyzed D-Homo Rearrangement
-
Kotovshchikov, Y. N.; Latyshev, G. V.; Lukashev, N. V.; Beletskaya, I. P. Synthesis of Novel 1,2,3-Triazolyl Derivatives of Pregnane, Androstane and D-Homoandrostane. Tandem "Click" Reaction/Cu-catalyzed D-Homo Rearrangement Org. Biomol. Chem. 2014, 12, 3707-3720 10.1039/C4OB00404C
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 3707-3720
-
-
Kotovshchikov, Y.N.1
Latyshev, G.V.2
Lukashev, N.V.3
Beletskaya, I.P.4
-
158
-
-
78049472036
-
Preparation and Preliminary Bioevaluation of 99mTc(CO)3-11β-Progesterone Derivative Prepared via Click Chemistry Route
-
Dhyani, M. V.; Satpati, D.; Korde, A.; Dev Sarma, H.; Kumar, Ch.; Banerjee, S. Preparation and Preliminary Bioevaluation of 99mTc(CO)3-11β-Progesterone Derivative Prepared via Click Chemistry Route Nucl. Med. Biol. 2010, 37, 997-1004 10.1016/j.nucmedbio.2010.05.005
-
(2010)
Nucl. Med. Biol.
, vol.37
, pp. 997-1004
-
-
Dhyani, M.V.1
Satpati, D.2
Korde, A.3
Dev Sarma, H.4
Kumar, Ch.5
Banerjee, S.6
-
159
-
-
80054694552
-
Synthesis and Preliminary Bioevaluation of 99mTc(CO)3-17a-Triazolylandrost-4-ene-3-one Derivative Prepared via Click Chemistry Route
-
Dhyani, M. V.; Satpati, D.; Korde, A.; Banerjee, S. Synthesis and Preliminary Bioevaluation of 99mTc(CO)3-17a-Triazolylandrost-4-ene-3-one Derivative Prepared via Click Chemistry Route Cancer Biother.Radiopharm. 2011, 26, 539-545 10.1089/cbr.2011.0966
-
(2011)
Cancer Biother.Radiopharm.
, vol.26
, pp. 539-545
-
-
Dhyani, M.V.1
Satpati, D.2
Korde, A.3
Banerjee, S.4
-
160
-
-
84861199309
-
Synthesis of Ferrocene-labeled Steroids via Copper-catalyzed Azide-alkyne Cycloaddition. Reactivity Difference between 2β-, 6β- and 16β-Azido-androstanes
-
Féher, K.; Balogh, J.; Csók, Z.; Kégl, T.; Kollár, L.; Skoda-Földes, R. Synthesis of Ferrocene-labeled Steroids via Copper-catalyzed Azide-alkyne Cycloaddition. Reactivity Difference Between 2β-, 6β- and 16β-Azido-androstanes Steroids 2012, 77, 738-744 10.1016/j.steroids.2012.04.005
-
(2012)
Steroids
, vol.77
, pp. 738-744
-
-
Féher, K.1
Balogh, J.2
Csók, Z.3
Kégl, T.4
Kollár, L.5
Skoda-Földes, R.6
-
161
-
-
84867365233
-
Convergent Synthesis of a Steroidal Antiestrogen-mitomycin C Hybrid Using "Click" Chemistry
-
Hanson, R. N.; Hua, E.; Labaree, D.; Hochberg, R. B.; Proffitt, K.; Essigmann, J. M.; Croy, R. G. Convergent Synthesis of a Steroidal Antiestrogen-mitomycin C Hybrid Using "Click" Chemistry Org. Biomol. Chem. 2012, 10, 8501-8508 10.1039/c2ob25902h
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 8501-8508
-
-
Hanson, R.N.1
Hua, E.2
Labaree, D.3
Hochberg, R.B.4
Proffitt, K.5
Essigmann, J.M.6
Croy, R.G.7
-
162
-
-
84873049158
-
Preparation, Preliminary Screening of New Types of Steroid Conjugates and Their Activities on Steroid Receptors
-
Jurášek, M.; Džubák, P.; Sedlák, D.; Dvořáková, H.; Hajdúch, M.; Bartuněk, P.; Drašar, P. Preparation, Preliminary Screening of New Types of Steroid Conjugates and Their Activities on Steroid Receptors Steroids 2013, 78, 356-361 10.1016/j.steroids.2012.11.016
-
(2013)
Steroids
, vol.78
, pp. 356-361
-
-
Jurášek, M.1
Džubák, P.2
Sedlák, D.3
Dvořáková, H.4
Hajdúch, M.5
Bartuněk, P.6
Drašar, P.7
-
163
-
-
77955343889
-
An Efficient Approach to the Discovery of Potent Inhibitors Against Glycosyltransferases
-
Hosoguchi, K.; Maeda, T.; Furukawa, J.; Shinohara, Y.; Hinou, H.; Sekiguchi, M.; Togame, H.; Takemoto, H.; Kondo, H.; Nishimura, S. An Efficient Approach to the Discovery of Potent Inhibitors Against Glycosyltransferases J. Med. Chem. 2010, 53, 5607-5619 10.1021/jm100612r
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5607-5619
-
-
Hosoguchi, K.1
Maeda, T.2
Furukawa, J.3
Shinohara, Y.4
Hinou, H.5
Sekiguchi, M.6
Togame, H.7
Takemoto, H.8
Kondo, H.9
Nishimura, S.10
-
164
-
-
84866077273
-
17α-Ethynylestradiol Peptide Labeling by "Click" Chemistry
-
Bol'shakov, O. I.; Lebedyeva, I. O.; Katritzky, A. R. 17α-Ethynylestradiol Peptide Labeling by "Click" Chemistry Synthesis 2012, 44, 2926-2932 10.1055/s-0032-1316702
-
(2012)
Synthesis
, vol.44
, pp. 2926-2932
-
-
Bol'Shakov, O.I.1
Lebedyeva, I.O.2
Katritzky, A.R.3
-
165
-
-
85027928389
-
Synthesis of Peptide Conjugates of Mestranol by a 1,3-Dipolar Cycloaddition Click Reaction
-
Sokolova, N. V.; Nenajdenko, V. G. Synthesis of Peptide Conjugates of Mestranol by a 1,3-Dipolar Cycloaddition Click Reaction Chem. Heterocycl. Compd. 2012, 48, 903-906 10.1007/s10593-012-1074-3
-
(2012)
Chem. Heterocycl. Compd.
, vol.48
, pp. 903-906
-
-
Sokolova, N.V.1
Nenajdenko, V.G.2
-
167
-
-
84890957694
-
Click Chemistry Inspired Highly Facile Synthesis of Triazolyl Ethisterone Glycoconjugates
-
Kumar, D.; Mishra, K. B.; Mishra, B. B.; Mondal, S.; Tiwari, V. K. Click Chemistry Inspired Highly Facile Synthesis of Triazolyl Ethisterone Glycoconjugates Steroids 2014, 80, 71-79 10.1016/j.steroids.2013.11.022
-
(2014)
Steroids
, vol.80
, pp. 71-79
-
-
Kumar, D.1
Mishra, K.B.2
Mishra, B.B.3
Mondal, S.4
Tiwari, V.K.5
-
168
-
-
49449098341
-
Lipid-conjugated Oligonucleotides via "Click Chemistry" Efficiently Inhibit Hepatitis C Virus Translation
-
Godeau, G.; Staedel, C.; Barthélémy, P. Lipid-conjugated Oligonucleotides via "Click Chemistry" Efficiently Inhibit Hepatitis C Virus Translation J. Med. Chem. 2008, 51, 4374-4376 10.1021/jm800518u
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4374-4376
-
-
Godeau, G.1
Staedel, C.2
Barthélémy, P.3
-
169
-
-
53549099104
-
Synthesis of a Side Chain Liquid Crystalline Polymer Containing the Cholesteryl Moiety via ROP and "Click" Chemistry
-
Cui, Z.; Zhang, Y.; He, S. Synthesis of a Side Chain Liquid Crystalline Polymer Containing the Cholesteryl Moiety via ROP and "Click" Chemistry Colloid Polym. Sci. 2008, 286, 1553-1559 10.1007/s00396-008-1916-9
-
(2008)
Colloid Polym. Sci.
, vol.286
, pp. 1553-1559
-
-
Cui, Z.1
Zhang, Y.2
He, S.3
-
170
-
-
77954610087
-
Synthesis and Characterization of Novel Cholesterol Based Mesogenic Compounds Using "Click" Chemistry
-
Majumdar, K. C.; Mondal, S.; Sinha, R. K. Synthesis and Characterization of Novel Cholesterol Based Mesogenic Compounds Using "Click" Chemistry New J. Chem. 2010, 34, 1255-1260 10.1039/b9nj00744j
-
(2010)
New J. Chem.
, vol.34
, pp. 1255-1260
-
-
Majumdar, K.C.1
Mondal, S.2
Sinha, R.K.3
-
171
-
-
84873808770
-
Synthesis and Characterization of Cholesterol-(1,2,3-triazole)-PEG via Click Chemistry
-
Xu, W.; Luo, B.; Li, C.; Yang, J.; Zhou, C. Synthesis and Characterization of Cholesterol-(1,2,3-triazole)-PEG via Click Chemistry Adv. Mater. Res. 2013, 647, 499-503 10.4028/www.scientific.net/AMR.647.499
-
(2013)
Adv. Mater. Res.
, vol.647
, pp. 499-503
-
-
Xu, W.1
Luo, B.2
Li, C.3
Yang, J.4
Zhou, C.5
-
172
-
-
84885173308
-
"Click" Synthesized Sterol-based Cationic Lipids as Gene Carriers, and the Effect of Skeletons and Headgroups on Gene Delivery
-
Sheng, R.; Luo, T.; Sun, J.; Wang, Z.; Cao, A.; Li, H. "Click" Synthesized Sterol-based Cationic Lipids as Gene Carriers, and the Effect of Skeletons and Headgroups on Gene Delivery Bioorg. Med. Chem. 2013, 21, 6366-6377 10.1016/j.bmc.2013.08.047
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 6366-6377
-
-
Sheng, R.1
Luo, T.2
Sun, J.3
Wang, Z.4
Cao, A.5
Li, H.6
-
173
-
-
84884194029
-
Efficient Synthesis of Novel A-Ring-substituted 1,2,3-Triazolylcholestane Derivatives via Catalytic Azide-alkyne Cycloaddition
-
Kádár, Z.; Frank, E.; Schneider, G.; Molnár, J.; Zupkó, I.; Kóti, J.; Schönecker, B.; Wölfling, J. Efficient Synthesis of Novel A-Ring-substituted 1,2,3-Triazolylcholestane Derivatives via Catalytic Azide-alkyne Cycloaddition Arkivoc 2012, iii, 279-296
-
(2012)
Arkivoc
, vol.3
, pp. 279-296
-
-
Kádár, Z.1
Frank, E.2
Schneider, G.3
Molnár, J.4
Zupkó, I.5
Kóti, J.6
Schönecker, B.7
Wölfling, J.8
-
174
-
-
84872769330
-
Ursane-type Pentacyclic Triterpenoids as Useful Platforms to Discover Anticancer Drugs
-
Salvador, J. A.; Moreira, V. M.; Gonçalves, B. M.; Leal, A. S.; Jing, Y. Ursane-type Pentacyclic Triterpenoids as Useful Platforms to Discover Anticancer Drugs Nat. Prod. Rep. 2012, 29, 1463-1479 10.1039/c2np20060k
-
(2012)
Nat. Prod. Rep.
, vol.29
, pp. 1463-1479
-
-
Salvador, J.A.1
Moreira, V.M.2
Gonçalves, B.M.3
Leal, A.S.4
Jing, Y.5
-
175
-
-
84867055462
-
Synthetic Oleanane Triterpenoids: Multifunctional Drugs with a Broad Range of Applications for Prevention and Treatment of Chronic Disease
-
Liby, K. T.; Sporn, M. B. Synthetic Oleanane Triterpenoids: Multifunctional Drugs with a Broad Range of Applications for Prevention and Treatment of Chronic Disease Pharmacol. Rev. 2012, 64, 972-1003 10.1124/pr.111.004846
-
(2012)
Pharmacol. Rev.
, vol.64
, pp. 972-1003
-
-
Liby, K.T.1
Sporn, M.B.2
-
176
-
-
73349109760
-
Triterpenoids as New Promising Anticancer Drugs
-
Petronelli, A.; Pannitteri, G.; Testa, U. Triterpenoids as New Promising Anticancer Drugs Anti-Cancer Drugs 2009, 20, 880-892 10.1097/CAD.0b013e328330fd90
-
(2009)
Anti-Cancer Drugs
, vol.20
, pp. 880-892
-
-
Petronelli, A.1
Pannitteri, G.2
Testa, U.3
-
177
-
-
70349525363
-
Plant-derived Triterpenoids and Analogues as Antitumor and Anti-HIV agents
-
Kuo, R.-Y.; Qian, K.; Morris-Natschke, S. L.; Lee, K.-H. Plant-derived Triterpenoids and Analogues as Antitumor and Anti-HIV agents Nat. Prod. Rep. 2009, 26, 1321-1344 10.1039/b810774m
-
(2009)
Nat. Prod. Rep.
, vol.26
, pp. 1321-1344
-
-
Kuo, R.-Y.1
Qian, K.2
Morris-Natschke, S.L.3
Lee, K.-H.4
-
178
-
-
84964199238
-
Triterpenoids
-
See also other reviews of the authors published in this journal since 2001
-
Hill, R. A.; Connolly, J. D. Triterpenoids Nat. Prod. Rep. 2015, 32, 273-327 See also other reviews of the authors published in this journal since 2001. 10.1039/C4NP00101J
-
(2015)
Nat. Prod. Rep.
, vol.32
, pp. 273-327
-
-
Hill, R.A.1
Connolly, J.D.2
-
179
-
-
65249125749
-
Synthesis of Glucoconjugates of Oleanolic Acid as Inhibitors of Glycogen Phosphorylase
-
Cheng, K.; Liu, J.; Liu, X.; Li, H.; Sun, H.; Xie, J. Synthesis of Glucoconjugates of Oleanolic Acid as Inhibitors of Glycogen Phosphorylase Carbohydr. Res. 2009, 344, 841-850 10.1016/j.carres.2009.02.012
-
(2009)
Carbohydr. Res.
, vol.344
, pp. 841-850
-
-
Cheng, K.1
Liu, J.2
Liu, X.3
Li, H.4
Sun, H.5
Xie, J.6
-
180
-
-
77954615525
-
Tethered Derivatives of D-Glucose and Pentacyclic Triterpenes for Homo/heterobivalent Inhibition of Glycogen Phosphorylase
-
Cheng, K.; Liu, J.; Sun, H.; Bokor, E.; Czifrák, K.; Kónya, B.; Tóth, M.; Docsa, T.; Gergely, P.; Somsák, L. Tethered Derivatives of D-Glucose and Pentacyclic Triterpenes for Homo/heterobivalent Inhibition of Glycogen Phosphorylase New J. Chem. 2010, 34, 1450-1464 10.1039/b9nj00602h
-
(2010)
New J. Chem.
, vol.34
, pp. 1450-1464
-
-
Cheng, K.1
Liu, J.2
Sun, H.3
Bokor, E.4
Czifrák, K.5
Kónya, B.6
Tóth, M.7
Docsa, T.8
Gergely, P.9
Somsák, L.10
-
181
-
-
77949669520
-
Synthesis of Oleanolic Acid Dimers as Inhibitors of Glycogen Phosphorylase
-
Cheng, K.; Liu, J.; Sun, H.; Xie, J. Synthesis of Oleanolic Acid Dimers as Inhibitors of Glycogen Phosphorylase Chem. Biodiversity 2010, 7, 690-697 10.1002/cbdv.200900086
-
(2010)
Chem. Biodiversity
, vol.7
, pp. 690-697
-
-
Cheng, K.1
Liu, J.2
Sun, H.3
Xie, J.4
-
182
-
-
84879063655
-
Development of Oleanane-Type Triterpenes as a New Class of HCV Entry Inhibitors
-
Yu, F.; Wang, Q.; Zhang, Z.; Peng, Y.; Qiu, Y.; Shi, Y.; Zheng, Y.; Xiao, S.; Wang, H.; Huang, X. et al. Development of Oleanane-Type Triterpenes as a New Class of HCV Entry Inhibitors J. Med. Chem. 2013, 56, 4300-4319 10.1021/jm301910a
-
(2013)
J. Med. Chem.
, vol.56
, pp. 4300-4319
-
-
Yu, F.1
Wang, Q.2
Zhang, Z.3
Peng, Y.4
Qiu, Y.5
Shi, Y.6
Zheng, Y.7
Xiao, S.8
Wang, H.9
Huang, X.10
-
183
-
-
84896536482
-
Development of Bivalent Oleanane-type Triterpenes as Potent HCV Entry Inhibitors
-
Yu, F.; Peng, Y.; Wang, Q.; Shi, Y.; Si, L.; Wang, H.; Zheng, Y.; Lee, E.; Xiao, S.; Yu, M.; Li, Y.; Zhang, C.; Tang, H.; Wang, C.; Zhang, L.; Zhou, D. Development of Bivalent Oleanane-type Triterpenes as Potent HCV Entry Inhibitors Eur. J. Med. Chem. 2014, 77, 258-268 10.1016/j.ejmech.2014.03.017
-
(2014)
Eur. J. Med. Chem.
, vol.77
, pp. 258-268
-
-
Yu, F.1
Peng, Y.2
Wang, Q.3
Shi, Y.4
Si, L.5
Wang, H.6
Zheng, Y.7
Lee, E.8
Xiao, S.9
Yu, M.10
Li, Y.11
Zhang, C.12
Tang, H.13
Wang, C.14
Zhang, L.15
Zhou, D.16
-
184
-
-
84880781906
-
1,2,3-Triazole-Substituted Oleanolic Acid Derivatives: Synthesis and Antiproliferative Activity
-
Pertino, M. W.; Lopez, C.; Theoduloz, C.; Schmeda-Hirschmann, G. 1,2,3-Triazole-Substituted Oleanolic Acid Derivatives: Synthesis and Antiproliferative Activity Molecules 2013, 18, 7661-7674 10.3390/molecules18077661
-
(2013)
Molecules
, vol.18
, pp. 7661-7674
-
-
Pertino, M.W.1
Lopez, C.2
Theoduloz, C.3
Schmeda-Hirschmann, G.4
-
185
-
-
79960401541
-
Synthesis and Anion Recognition of a Novel Oleanolic Acid-based Cyclic Dimer
-
Hu, J.; Li, R.; Lu, J.; Ju, Y. Synthesis and Anion Recognition of a Novel Oleanolic Acid-based Cyclic Dimer Tetrahedron Lett. 2011, 52, 4211-4214 10.1016/j.tetlet.2011.06.022
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 4211-4214
-
-
Hu, J.1
Li, R.2
Lu, J.3
Ju, Y.4
-
186
-
-
76649106073
-
Betulinic Acid, a Natural Compound with Potent Anticancer Effects
-
Mullauer, F. B.; Kessler, J. H.; Medema, J. P. Betulinic Acid, a Natural Compound with Potent Anticancer Effects Anti-Cancer Drugs 2010, 21, 215-227 10.1097/CAD.0b013e3283357c62
-
(2010)
Anti-Cancer Drugs
, vol.21
, pp. 215-227
-
-
Mullauer, F.B.1
Kessler, J.H.2
Medema, J.P.3
-
187
-
-
33744459230
-
Betulinic Acid Derivatives as Anticancer Agents: Structure Activity Relationship
-
Mukherjee, R.; Kumar, V.; Srivastava, S. K.; Agarwal, S. K.; Burman, A. C. Betulinic Acid Derivatives as Anticancer Agents: Structure Activity Relationship Anti-Cancer Agents Med. Chem. 2006, 6, 271-279 10.2174/187152006776930846
-
(2006)
Anti-Cancer Agents Med. Chem.
, vol.6
, pp. 271-279
-
-
Mukherjee, R.1
Kumar, V.2
Srivastava, S.K.3
Agarwal, S.K.4
Burman, A.C.5
-
188
-
-
33747802067
-
Pharmacological Properties of the Ubiquitous Natural Product Betulin
-
Alakurtti, S.; Mäkelä, T.; Koskimies, S.; Yli-Kauhaluoma, J. Pharmacological Properties of the Ubiquitous Natural Product Betulin Eur. J. Pharm. Sci. 2006, 29, 1-13 10.1016/j.ejps.2006.04.006
-
(2006)
Eur. J. Pharm. Sci.
, vol.29
, pp. 1-13
-
-
Alakurtti, S.1
Mäkelä, T.2
Koskimies, S.3
Yli-Kauhaluoma, J.4
-
189
-
-
84862784033
-
Anti-AIDS Agents 88. Anti-HIV Conjugates of Betulin and Betulinic Acid with AZT Prepared via Click Chemistry
-
Bori, I. D.; Hung, H.-Y.; Qian, K.; Chen, C.-H.; Morris-Natschke, S. L.; Lee, K.-H. Anti-AIDS Agents 88. Anti-HIV Conjugates of Betulin and Betulinic Acid with AZT Prepared via Click Chemistry Tetrahedron Lett. 2012, 53, 1987-1989 10.1016/j.tetlet.2012.02.022
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 1987-1989
-
-
Bori, I.D.1
Hung, H.-Y.2
Qian, K.3
Chen, C.-H.4
Morris-Natschke, S.L.5
Lee, K.-H.6
-
190
-
-
84907225755
-
Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics
-
Wang, C.; Lu, L.; Na, H.; Li, X.; Wang, Q.; Jiang, X.; Xu, X.; Yu, F.; Zhang, T.; Li, J. et al. Conjugation of a Nonspecific Antiviral Sapogenin with a Specific HIV Fusion Inhibitor: A Promising Strategy for Discovering New Antiviral Therapeutics J. Med. Chem. 2014, 57, 7342-7354 10.1021/jm500763m
-
(2014)
J. Med. Chem.
, vol.57
, pp. 7342-7354
-
-
Wang, C.1
Lu, L.2
Na, H.3
Li, X.4
Wang, Q.5
Jiang, X.6
Xu, X.7
Yu, F.8
Zhang, T.9
Li, J.10
-
191
-
-
84875976313
-
Synthesis of 3-O-Propargylated Betulinic Acid and its 1,2,3-Triazoles as Potential Apoptotic Agents
-
Majeed, R.; Sangwan, P. L.; Chinthakindi, P. K.; Khan, I.; Dangroo, N. A.; Thota, N.; Hamid, A.; Sharma, P. R.; Saxena, A. K.; Koul, S. Synthesis of 3-O-Propargylated Betulinic Acid and its 1,2,3-Triazoles as Potential Apoptotic Agents Eur. J. Med. Chem. 2013, 63, 782-792 10.1016/j.ejmech.2013.03.028
-
(2013)
Eur. J. Med. Chem.
, vol.63
, pp. 782-792
-
-
Majeed, R.1
Sangwan, P.L.2
Chinthakindi, P.K.3
Khan, I.4
Dangroo, N.A.5
Thota, N.6
Hamid, A.7
Sharma, P.R.8
Saxena, A.K.9
Koul, S.10
-
192
-
-
84885855301
-
Synthesis and Study of Mutagenic Properties of Lupane Triterpenoids Containing 1,2,3-Triazole Fragments in the C-30 Position
-
Antimonova, A. N.; Petrenko, N. I.; Shakirov, M. M.; Rybalova, T. V.; Frolova, T. S.; Shul"ts, E. E.; Kukina, T. P.; Sinitsyna, O. I.; Tolstikov, G. A. Synthesis and Study of Mutagenic Properties of Lupane Triterpenoids Containing 1,2,3-Triazole Fragments in the C-30 Position Chem. Nat. Compd. 2013, 49, 657-664 10.1007/s10600-013-0702-1
-
(2013)
Chem. Nat. Compd.
, vol.49
, pp. 657-664
-
-
Antimonova, A.N.1
Petrenko, N.I.2
Shakirov, M.M.3
Rybalova, T.V.4
Frolova, T.S.5
Shul'ts, E.E.6
Kukina, T.P.7
Sinitsyna, O.I.8
Tolstikov, G.A.9
-
193
-
-
84885581343
-
Betulonic Acid-peptide Conjugates: Synthesis and Evaluation of Anti-inflammatory Activity
-
Govdi, A. I.; Vasilevsky, S. F.; Sokolova, V.; Sorokina, I. V.; Tolstikova, T. G.; Nenajdenko, V. G. Betulonic Acid-peptide Conjugates: Synthesis and Evaluation of Anti-inflammatory Activity Mendeleev Commun. 2013, 23, 260-261 10.1016/j.mencom.2013.09.007
-
(2013)
Mendeleev Commun.
, vol.23
, pp. 260-261
-
-
Govdi, A.I.1
Vasilevsky, S.F.2
Sokolova, V.3
Sorokina, I.V.4
Tolstikova, T.G.5
Nenajdenko, V.G.6
-
194
-
-
78650512271
-
Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry
-
Vasilevsky, S. F.; Govdi, A. I.; Sorokina, I. V.; Tolstikova, T. G.; Baev, D. S.; Tolstikov, G. A.; Mamatuyk, V.; Alabugin, I. V. Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry Bioorg. Med. Chem. Lett. 2011, 21, 62-65 10.1016/j.bmcl.2010.11.072
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 62-65
-
-
Vasilevsky, S.F.1
Govdi, A.I.2
Sorokina, I.V.3
Tolstikova, T.G.4
Baev, D.S.5
Tolstikov, G.A.6
Mamatuyk, V.7
Alabugin, I.V.8
-
195
-
-
79959766022
-
3 Molecule with Three Glycyrrhetinic Acid Units and Self-Assembly Properties
-
3Molecule with Three Glycyrrhetinic Acid Units and Self-Assembly Properties Chin. J. Chem. 2011, 29, 1139-1142 10.1002/cjoc.201190213
-
(2011)
Chin. J. Chem.
, vol.29
, pp. 1139-1142
-
-
Hu, J.1
Yu, L.2
Zhang, M.3
Ju, Y.J.4
-
197
-
-
84869082314
-
A Dual-responsive Macrocycle Based on Glycyrrhetinic acid
-
Hu, J.; Wu, J.; Lu, J.; Ju, Y. A Dual-responsive Macrocycle Based on Glycyrrhetinic acid Tetrahedron Lett. 2012, 53, 6705-6709 10.1016/j.tetlet.2012.09.118
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 6705-6709
-
-
Hu, J.1
Wu, J.2
Lu, J.3
Ju, Y.4
-
198
-
-
84905905997
-
Synthesis and Evaluation of Triazole Linked Glycosylated 18β-Glycyrrhetinic Acid Derivatives as Anticancer Agents
-
Parida, P. K.; Sau, A.; Ghosh, T.; Jana, K.; Biswas, K.; Raha, S.; Misra, A. K. Synthesis and Evaluation of Triazole Linked Glycosylated 18β-Glycyrrhetinic Acid Derivatives as Anticancer Agents Bioorg. Med. Chem. Lett. 2014, 24, 3865-3868 10.1016/j.bmcl.2014.06.054
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 3865-3868
-
-
Parida, P.K.1
Sau, A.2
Ghosh, T.3
Jana, K.4
Biswas, K.5
Raha, S.6
Misra, A.K.7
-
199
-
-
84866913755
-
2-Adrenergic Receptor-Gs Signaling by Changing the Location of Gαs in Lipid Rafts
-
2-Adrenergic Receptor-Gs Signaling by Changing the Location of Gαs in Lipid Rafts PLoS One 2012, 7 e44921 10.1371/journal.pone.0044921
-
(2012)
PLoS One
, vol.7
, pp. e44921
-
-
Shi, Q.1
Hou, Y.2
Hou, J.3
Pan, P.4
Liu, Z.5
Jiang, M.6
Gao, J.7
Bai, G.8
-
200
-
-
84893489417
-
A Novel Approach for Fluorescent Visualization of Glycyrrhetic Acid on a Cell with a Quantum Dot
-
Hou, J.; Shi, Q.; Cao, M.; Pan, P.; Ge, G.; Fan, X.; Bai, G.; Xin, Y. A Novel Approach for Fluorescent Visualization of Glycyrrhetic Acid on a Cell with a Quantum Dot Biochemistry (Moscow) 2014, 79, 25-30 10.1134/S0006297914010040
-
(2014)
Biochemistry (Moscow)
, vol.79
, pp. 25-30
-
-
Hou, J.1
Shi, Q.2
Cao, M.3
Pan, P.4
Ge, G.5
Fan, X.6
Bai, G.7
Xin, Y.8
-
201
-
-
79952900480
-
Molecular Activities, Biosynthesis and Evolution of Triterpenoid Saponins
-
Augustin, J. M.; Kuzina, V.; Andersen, S. B.; Bak, S. Molecular Activities, Biosynthesis and Evolution of Triterpenoid Saponins Phytochemistry 2011, 72, 435-457 10.1016/j.phytochem.2011.01.015
-
(2011)
Phytochemistry
, vol.72
, pp. 435-457
-
-
Augustin, J.M.1
Kuzina, V.2
Andersen, S.B.3
Bak, S.4
-
202
-
-
80052401813
-
"Click" Synthesis of Triazole-based Spirostan Saponin Analogs
-
Pérez-Labrada, K.; Brouard, I.; Morera, C.; Estévez, F.; Bermejo, J.; Rivera, D. G. "Click" Synthesis of Triazole-based Spirostan Saponin Analogs Tetrahedron 2011, 67, 7713-7727 10.1016/j.tet.2011.08.003
-
(2011)
Tetrahedron
, vol.67
, pp. 7713-7727
-
-
Pérez-Labrada, K.1
Brouard, I.2
Morera, C.3
Estévez, F.4
Bermejo, J.5
Rivera, D.G.6
-
203
-
-
84873739522
-
Synthesis and Conformational Study of Triazole-linked bis-Spirostanic Conjugates
-
Pérez-Labrada, K.; Morera, C.; Brouard, I.; Llerena, R.; Rivera, D. G. Synthesis and Conformational Study of Triazole-linked bis-Spirostanic Conjugates Tetrahedron Lett. 2013, 54, 1602-1606 10.1016/j.tetlet.2013.01.058
-
(2013)
Tetrahedron Lett.
, vol.54
, pp. 1602-1606
-
-
Pérez-Labrada, K.1
Morera, C.2
Brouard, I.3
Llerena, R.4
Rivera, D.G.5
-
204
-
-
82955237594
-
Click Chemistry: An Efficient Synthesis of Heterocycles Substituted with Steroids, Saponins, and Digitalis Analogues
-
Deobald, A. M.; Camargo, L. R. S.; Alves, D.; Zukerman-Schpector, J.; Corrêa, A. G.; Paixa'o, M. W. Click Chemistry: An Efficient Synthesis of Heterocycles Substituted with Steroids, Saponins, and Digitalis Analogues Synthesis 2011, 2011, 4003-4010 10.1055/s-0031-1289606
-
(2011)
Synthesis
, vol.2011
, pp. 4003-4010
-
-
Deobald, A.M.1
Camargo, L.R.S.2
Alves, D.3
Zukerman-Schpector, J.4
Corrêa, A.G.5
Paixa'o, M.W.6
-
205
-
-
84904490673
-
Preparation of Selectively Protected Protoescigenin Derivatives for Synthesis of Escin Analogs and Neoglycoconjugates
-
Jatczak, K.; Gruza, M.; Filip, K.; Cmoch, P.; Grynkiewicz, G. Preparation of Selectively Protected Protoescigenin Derivatives for Synthesis of Escin Analogs and Neoglycoconjugates Cent. Eur. J. Chem. 2014, 12, 1222-1231 10.2478/s11532-014-0572-9
-
(2014)
Cent. Eur. J. Chem.
, vol.12
, pp. 1222-1231
-
-
Jatczak, K.1
Gruza, M.2
Filip, K.3
Cmoch, P.4
Grynkiewicz, G.5
-
206
-
-
3242785011
-
Isoprenoids: Remarkable Diversity of Form and Function
-
Holstein, S. A.; Hohl, R. J. Isoprenoids: Remarkable Diversity of Form and Function Lipids 2004, 39, 293-309 10.1007/s11745-004-1233-3
-
(2004)
Lipids
, vol.39
, pp. 293-309
-
-
Holstein, S.A.1
Hohl, R.J.2
-
207
-
-
25844446180
-
The Allylic Azide Rearrangement: Achieving Selectivity
-
Feldman, A. K.; Colasson, B.; Sharpless, K. B.; Fokin, V. V. The Allylic Azide Rearrangement: Achieving Selectivity J. Am. Chem. Soc. 2005, 127, 13444-13445 10.1021/ja050622q
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13444-13445
-
-
Feldman, A.K.1
Colasson, B.2
Sharpless, K.B.3
Fokin, V.V.4
-
208
-
-
60249090089
-
Synthesis of a Polyprenyl-type Library Containing 1,4-Disubstituted-1,2,3-triazoles with Anti-biofilm Activities Against Pseudoalteromonas sp
-
Praud-Tabaries, A.; Dombrowsky, L.; Bottzek, O.; Briand, J.-F.; Blache, Y. Synthesis of a Polyprenyl-type Library Containing 1,4-Disubstituted-1,2,3-triazoles with Anti-biofilm Activities Against Pseudoalteromonas sp Tetrahedron Lett. 2009, 50, 1645-1648 10.1016/j.tetlet.2009.01.125
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1645-1648
-
-
Praud-Tabaries, A.1
Dombrowsky, L.2
Bottzek, O.3
Briand, J.-F.4
Blache, Y.5
-
209
-
-
79951722365
-
Targeting Bacterial Biofilms: Design of a Terpenoid-like Library as Non-toxic Anti-biofilm Compounds
-
Sall, C.; Dombrowsky, L.; Bottzeck, O.; Praud-Tabariès, A.; Blache, Y. Targeting Bacterial Biofilms: Design of a Terpenoid-like Library as Non-toxic Anti-biofilm Compounds Bioorg. Med. Chem. Lett. 2011, 21, 1493-1497 10.1016/j.bmcl.2010.12.134
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 1493-1497
-
-
Sall, C.1
Dombrowsky, L.2
Bottzeck, O.3
Praud-Tabariès, A.4
Blache, Y.5
-
210
-
-
84921325836
-
Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications
-
Palsuledesai, C. C.; Distefano, M. D. Protein Prenylation: Enzymes, Therapeutics, and Biotechnology Applications ACS Chem. Biol. 2015, 10, 51-62 10.1021/cb500791f
-
(2015)
ACS Chem. Biol.
, vol.10
, pp. 51-62
-
-
Palsuledesai, C.C.1
Distefano, M.D.2
-
211
-
-
84872346257
-
Triazole-based Inhibitors of Geranylgeranyltransferase II
-
Zhou, X.; Hartman, S. V.; Born, E. J.; Smits, J. P.; Holstein, S. A.; Wiemer, D. F. Triazole-based Inhibitors of Geranylgeranyltransferase II Bioorg. Med. Chem. Lett. 2013, 23, 764-766 10.1016/j.bmcl.2012.11.089
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 764-766
-
-
Zhou, X.1
Hartman, S.V.2
Born, E.J.3
Smits, J.P.4
Holstein, S.A.5
Wiemer, D.F.6
-
212
-
-
84899456383
-
Geranyl and Neryl Triazole Bisphosphonates as Inhibitors of Geranylgeranyl Diphosphate Synthase
-
Zhou, X.; Ferree, S. D.; Wills, V. S.; Born, E. J.; Tong, H.; Wiemer, D. F.; Holstein, S. A. Geranyl and Neryl Triazole Bisphosphonates as Inhibitors of Geranylgeranyl Diphosphate Synthase Bioorg. Med. Chem. 2014, 22, 2791-2798 10.1016/j.bmc.2014.03.014
-
(2014)
Bioorg. Med. Chem.
, vol.22
, pp. 2791-2798
-
-
Zhou, X.1
Ferree, S.D.2
Wills, V.S.3
Born, E.J.4
Tong, H.5
Wiemer, D.F.6
Holstein, S.A.7
-
213
-
-
84866644783
-
Synthesis of Farnesol Analogues Containing Triazoles in Place of Isoprenes through "Click Chemistry"
-
Subramanian, T.; Parkin, S.; Spielmann, H. P. Synthesis of Farnesol Analogues Containing Triazoles in Place of Isoprenes through "Click Chemistry" Synlett 2012, 23, 2539-2543 10.1055/s-0031-1290461
-
(2012)
Synlett
, vol.23
, pp. 2539-2543
-
-
Subramanian, T.1
Parkin, S.2
Spielmann, H.P.3
-
214
-
-
84855907701
-
S-Farnesyl-Thiopropionic Acid Triazoles as Potent Inhibitors of Isoprenylcysteine Carboxyl Methyltransferase
-
Bergman, J. A.; Hahne, K.; Song, J.; Hrycyna, C. A.; Gibbs, R. A. S-Farnesyl-Thiopropionic Acid Triazoles as Potent Inhibitors of Isoprenylcysteine Carboxyl Methyltransferase ACS Med. Chem. Lett. 2012, 3, 15-19 10.1021/ml200106d
-
(2012)
ACS Med. Chem. Lett.
, vol.3
, pp. 15-19
-
-
Bergman, J.A.1
Hahne, K.2
Song, J.3
Hrycyna, C.A.4
Gibbs, R.A.5
-
215
-
-
77953893928
-
Copper-free Click Chemistry Bioorthogonal Reagents for Tagging Azides
-
Baskin, J. M.; Bertozzi, C. R. Copper-free Click Chemistry Bioorthogonal Reagents for Tagging Azides Aldrichimica Acta 2010, 43, 15-23
-
(2010)
Aldrichimica Acta
, vol.43
, pp. 15-23
-
-
Baskin, J.M.1
Bertozzi, C.R.2
-
216
-
-
70649096244
-
A Novel Approach to Tag and Identify Geranylgeranylated Proteins
-
Chan, L. N.; Hart, C.; Guo, L.; Nyberg, T.; Davies, B. S. J.; Fong, L. G.; Young, S. G.; Agnew, B. J.; Tamanoi, F. A Novel Approach to Tag and Identify Geranylgeranylated Proteins Electrophoresis 2009, 30, 3598-3606 10.1002/elps.200900259
-
(2009)
Electrophoresis
, vol.30
, pp. 3598-3606
-
-
Chan, L.N.1
Hart, C.2
Guo, L.3
Nyberg, T.4
Davies, B.S.J.5
Fong, L.G.6
Young, S.G.7
Agnew, B.J.8
Tamanoi, F.9
-
217
-
-
33846333918
-
Selective Labeling of Proteins by Using Protein Farnesyltransferase
-
Duckworth, B. P.; Zhang, Z.; Hosokawa, A.; Distefano, M. D. Selective Labeling of Proteins by Using Protein Farnesyltransferase ChemBioChem 2007, 8, 98-105 10.1002/cbic.200600340
-
(2007)
ChemBioChem
, vol.8
, pp. 98-105
-
-
Duckworth, B.P.1
Zhang, Z.2
Hosokawa, A.3
Distefano, M.D.4
-
218
-
-
34250015570
-
Evaluation of an Alkyne-containing Analogue of Farnesyl Diphosphate as a Dual Substrate for Protein-prenyltransferases
-
Hosokawa, A.; Wollack, J. W.; Zhang, Z.; Chen, L.; Barany, G.; Distefano, M. D. Evaluation of an Alkyne-containing Analogue of Farnesyl Diphosphate as a Dual Substrate for Protein-prenyltransferases Int. J. Pept. Res. Ther. 2007, 13, 345-354 10.1007/s10989-007-9090-3
-
(2007)
Int. J. Pept. Res. Ther.
, vol.13
, pp. 345-354
-
-
Hosokawa, A.1
Wollack, J.W.2
Zhang, Z.3
Chen, L.4
Barany, G.5
Distefano, M.D.6
-
219
-
-
78349284828
-
Evaluation of Alkyne-Modified Isoprenoids as Chemical Reporters of Protein Prenylation
-
DeGraw, A. J.; Palsuledesai, C.; Ochocki, J. D.; Dozier, J. K.; Lenevich, S.; Rashidian, M.; Distefano, M. D. Evaluation of Alkyne-Modified Isoprenoids as Chemical Reporters of Protein Prenylation Chem. Biol. Drug Des. 2010, 76, 460 10.1111/j.1747-0285.2010.01037.x
-
(2010)
Chem. Biol. Drug Des.
, vol.76
, pp. 460
-
-
DeGraw, A.J.1
Palsuledesai, C.2
Ochocki, J.D.3
Dozier, J.K.4
Lenevich, S.5
Rashidian, M.6
Distefano, M.D.7
-
220
-
-
84879730573
-
Prenylome Profiling Reveals S-farnesylation is Crucial for Membrane Targeting and Antiviral Activity of ZAP Long-isoform
-
Charron, G.; Li, M. M. H.; MacDonald, M. R.; Hang, H. C. Prenylome Profiling Reveals S-farnesylation is Crucial for Membrane Targeting and Antiviral Activity of ZAP Long-isoform Proc. Natl. Acad. Sci. U. S. A. 2013, 110, 11085-11090 10.1073/pnas.1302564110
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 11085-11090
-
-
Charron, G.1
Li, M.M.H.2
MacDonald, M.R.3
Hang, H.C.4
-
221
-
-
80051786364
-
Evaluation of a Cell Penetrating Prenylated Peptide Lacking an Intrinsic Fluorophore via in situ Click Reaction
-
Ochocki, J. D.; Mullen, D. G.; Wattenberg, E. V.; Distefano, M. D. Evaluation of a Cell Penetrating Prenylated Peptide Lacking an Intrinsic Fluorophore via in situ Click Reaction Bioorg. Med. Chem. Lett. 2011, 21, 4998-5001 10.1016/j.bmcl.2011.04.138
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 4998-5001
-
-
Ochocki, J.D.1
Mullen, D.G.2
Wattenberg, E.V.3
Distefano, M.D.4
-
222
-
-
67651120082
-
Synthesis and Application of Photoaffinity Probe Containing an Intact Isoprenoid Chain
-
Li, L.; Tang, W.; Zhao, Z. K. Synthesis and Application of Photoaffinity Probe Containing an Intact Isoprenoid Chain Bioorg. Med. Chem. Lett. 2009, 19, 4824-4826 10.1016/j.bmcl.2009.06.037
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4824-4826
-
-
Li, L.1
Tang, W.2
Zhao, Z.K.3
-
223
-
-
84887747556
-
Simultaneous Dual Protein Labeling Using a Triorthogonal Reagent
-
Rashidian, M.; Kumarapperuma, S. C.; Gabrielse, K.; Fegan, A.; Wagner, C. R.; Distefano, M. D. Simultaneous Dual Protein Labeling Using a Triorthogonal Reagent J. Am. Chem. Soc. 2013, 135, 16388-16396 10.1021/ja403813b
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 16388-16396
-
-
Rashidian, M.1
Kumarapperuma, S.C.2
Gabrielse, K.3
Fegan, A.4
Wagner, C.R.5
Distefano, M.D.6
-
224
-
-
84896861606
-
1,2,3-Triazole-Containing Derivatives of Rupestonic Acid: Click-chemical Synthesis and Antiviral Activities Against Influenza Viruses
-
He, Y.-W.; Dong, C.-Z.; Zhao, J.-Y.; ma, L.-L.; Li, Y.-H.; Aisa, H. A. 1,2,3-Triazole-Containing Derivatives of Rupestonic Acid: Click-chemical Synthesis and Antiviral Activities Against Influenza Viruses Eur. J. Med. Chem. 2014, 76, 245-255 10.1016/j.ejmech.2014.02.029
-
(2014)
Eur. J. Med. Chem.
, vol.76
, pp. 245-255
-
-
He, Y.-W.1
Dong, C.-Z.2
Zhao, J.-Y.3
Ma, L.-L.4
Li, Y.-H.5
Aisa, H.A.6
-
225
-
-
84901924951
-
Natural Sesquiterpene Lactones as Renewable Chemical Materials for New Medicinal Products
-
Adekenov, S. M. Natural Sesquiterpene Lactones as Renewable Chemical Materials for New Medicinal Products Eurasian Chem.-Technol. J. 2015, 15, 163-174 10.18321/ectj220
-
(2015)
Eurasian Chem.-Technol. J.
, vol.15
, pp. 163-174
-
-
Adekenov, S.M.1
-
226
-
-
80054071903
-
Perspectives on Sesquiterpene Lactones in Inflammation and Cancer
-
Merfort, I. Perspectives on Sesquiterpene Lactones in Inflammation and Cancer Curr. Drug Targets 2011, 12, 1560-1573 10.2174/138945011798109437
-
(2011)
Curr. Drug Targets
, vol.12
, pp. 1560-1573
-
-
Merfort, I.1
-
227
-
-
84893723977
-
Click Chemistry Inspired Facile Synthesis and Bioevaluation of Novel Triazolyl Analogs of Ludartin
-
Lone, S. H.; Bhat, K. A.; Majeed, R.; Hamid, A.; Khuroo, M. A. Click Chemistry Inspired Facile Synthesis and Bioevaluation of Novel Triazolyl Analogs of Ludartin Bioorg. Med. Chem. Lett. 2014, 24, 1047-1051 10.1016/j.bmcl.2014.01.018
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 1047-1051
-
-
Lone, S.H.1
Bhat, K.A.2
Majeed, R.3
Hamid, A.4
Khuroo, M.A.5
-
228
-
-
84902192717
-
Design and Synthesis of Novel 1,2,3-Triazole Derivatives of Coronopilin as Anti-cancer Compounds
-
Khazir, J.; Hyder, I.; Gayatri, J. L.; Yandrati, L. P.; Nalla, N.; Chasoo, G.; Mahajan, A.; Saxena, A. K.; Alam, M. S.; Qazi, G. N.; Kumar, H. M. S. Design and Synthesis of Novel 1,2,3-Triazole Derivatives of Coronopilin as Anti-cancer Compounds Eur. J. Med. Chem. 2014, 82, 255-262 10.1016/j.ejmech.2014.05.053
-
(2014)
Eur. J. Med. Chem.
, vol.82
, pp. 255-262
-
-
Khazir, J.1
Hyder, I.2
Gayatri, J.L.3
Yandrati, L.P.4
Nalla, N.5
Chasoo, G.6
Mahajan, A.7
Saxena, A.K.8
Alam, M.S.9
Qazi, G.N.10
Kumar, H.M.S.11
-
229
-
-
84916942936
-
Diterpenoids of Terrestrial Origin
-
Hanson, J. R. Diterpenoids of Terrestrial Origin Nat. Prod. Rep. 2015, 32, 76 10.1039/C4NP00108G
-
(2015)
Nat. Prod. Rep.
, vol.32
, pp. 76
-
-
Hanson, J.R.1
-
230
-
-
84863946239
-
-
Nat. Prod. Rep. 2012, 29, 890. 10.1039/c2np20051a
-
(2012)
Nat. Prod. Rep.
, vol.29
, pp. 890
-
-
-
231
-
-
84055186954
-
-
Nat. Prod. Rep. 2011, 28, 1755. 10.1039/c1np90021h
-
(2011)
Nat. Prod. Rep.
, vol.28
, pp. 1755
-
-
-
232
-
-
70349504182
-
-
Nat. Prod. Rep. 2009, 26, 1156. 10.1039/b807311m
-
(2009)
Nat. Prod. Rep.
, vol.26
, pp. 1156
-
-
-
233
-
-
84871880840
-
Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin
-
Wilbon, P. A.; Chu, F.; Tang, C. Progress in Renewable Polymers from Natural Terpenes, Terpenoids, and Rosin Macromol. Rapid Commun. 2013, 34, 8-37 10.1002/marc.201200513
-
(2013)
Macromol. Rapid Commun.
, vol.34
, pp. 8-37
-
-
Wilbon, P.A.1
Chu, F.2
Tang, C.3
-
234
-
-
84874905056
-
Controlled Polymerization of Next-Generation Renewable Monomers and beyond
-
Yao, K.; Tang, C. Controlled Polymerization of Next-Generation Renewable Monomers and Beyond Macromolecules 2013, 46, 1689-1712 10.1021/ma3019574
-
(2013)
Macromolecules
, vol.46
, pp. 1689-1712
-
-
Yao, K.1
Tang, C.2
-
235
-
-
79958862934
-
Degradable Rosin-ester-caprolactone Graft Copolymers
-
Yao, K.; Wang, J.; Zhang, W.; Lee, J. S.; Wang, C.; Chu, F.; He, X.; Tang, C. Degradable Rosin-ester-caprolactone Graft Copolymers Biomacromolecules 2011, 12, 2171-2177 10.1021/bm200460u
-
(2011)
Biomacromolecules
, vol.12
, pp. 2171-2177
-
-
Yao, K.1
Wang, J.2
Zhang, W.3
Lee, J.S.4
Wang, C.5
Chu, F.6
He, X.7
Tang, C.8
-
236
-
-
84894620086
-
Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid
-
Pertino, M. W.; Verdugo, V.; Theoduloz, C.; Schmeda-Hirschmann, G. Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid Molecules 2014, 19, 2523-2535 10.3390/molecules19022523
-
(2014)
Molecules
, vol.19
, pp. 2523-2535
-
-
Pertino, M.W.1
Verdugo, V.2
Theoduloz, C.3
Schmeda-Hirschmann, G.4
-
237
-
-
50249167106
-
A Click Chemistry Approach to Pleuromutilin Conjugates with Nucleosides or Acyclic Nucleoside Derivatives and Their Binding to the Bacterial Ribosome
-
Lolk, L.; Pøhlsgaard, J.; Jepsen, A. S.; Hansen, L. H.; Nielsen, H.; Steffansen, S. I.; Sparving, L.; Nielsen, A. B.; Vester, B.; Nielsen, P. A Click Chemistry Approach to Pleuromutilin Conjugates with Nucleosides or Acyclic Nucleoside Derivatives and Their Binding to the Bacterial Ribosome J. Med. Chem. 2008, 51, 4957-4967 10.1021/jm800261u
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4957-4967
-
-
Lolk, L.1
Pøhlsgaard, J.2
Jepsen, A.S.3
Hansen, L.H.4
Nielsen, H.5
Steffansen, S.I.6
Sparving, L.7
Nielsen, A.B.8
Vester, B.9
Nielsen, P.10
-
238
-
-
84863242788
-
A Click Chemistry Approach to Pleuromutilin Derivatives, Part 2: Conjugates with Acyclic Nucleosides and Their Ribosomal Binding and Antibacterial Activity
-
Dreier, I.; Kumar, S.; Søndergaard, H.; Rasmussen, M. L.; Hansen, L. H.; List, N. H.; Kongsted, J.; Vester, B.; Nielsen, P. A Click Chemistry Approach to Pleuromutilin Derivatives, Part 2: Conjugates with Acyclic Nucleosides and Their Ribosomal Binding and Antibacterial Activity J. Med. Chem. 2012, 55, 2067-2077 10.1021/jm201266b
-
(2012)
J. Med. Chem.
, vol.55
, pp. 2067-2077
-
-
Dreier, I.1
Kumar, S.2
Søndergaard, H.3
Rasmussen, M.L.4
Hansen, L.H.5
List, N.H.6
Kongsted, J.7
Vester, B.8
Nielsen, P.9
-
239
-
-
84893724606
-
A Click Chemistry Approach to Pleuromutilin Derivatives. Part 3: Extended Footprinting Analysis and Excellent MRSA Inhibition for a Derivative with an Adenine Phenyl Side Chain
-
Dreier, I.; Hansen, L. H.; Nielsen, P.; Vester, B. A Click Chemistry Approach to Pleuromutilin Derivatives. Part 3: Extended Footprinting Analysis and Excellent MRSA Inhibition for a Derivative with an Adenine Phenyl Side Chain Bioorg. Med. Chem. Lett. 2014, 24, 1043-1046 10.1016/j.bmcl.2014.01.019
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 1043-1046
-
-
Dreier, I.1
Hansen, L.H.2
Nielsen, P.3
Vester, B.4
-
240
-
-
84878343968
-
Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects
-
Pertino, M. W.; Theoduloz, C.; Bastías, M.; Schmeda-Hirschmann, G. Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects Molecules 2013, 18, 5936-5953 10.3390/molecules18055936
-
(2013)
Molecules
, vol.18
, pp. 5936-5953
-
-
Pertino, M.W.1
Theoduloz, C.2
Bastías, M.3
Schmeda-Hirschmann, G.4
-
241
-
-
84880183745
-
Derivatives of Grindelic Acid: From a Non-active Natural Diterpene to Synthetic Antitumor Derivatives
-
Reta, G. F.; Chiaramello, A. I.; Garcia, C.; León, L. G.; Martin, V. S.; Padrón, J. M.; Tonn, C. E.; Donadel, O. J. Derivatives of Grindelic Acid: From a Non-active Natural Diterpene to Synthetic Antitumor Derivatives Eur. J. Med. Chem. 2013, 67, 28-38 10.1016/j.ejmech.2013.06.013
-
(2013)
Eur. J. Med. Chem.
, vol.67
, pp. 28-38
-
-
Reta, G.F.1
Chiaramello, A.I.2
Garcia, C.3
León, L.G.4
Martin, V.S.5
Padrón, J.M.6
Tonn, C.E.7
Donadel, O.J.8
-
242
-
-
84880554110
-
Overcoming Synthetic Challenges of Oridonin A-Ring Structural Diversification: Regio- and Stereoselective Installation of Azides and 1,2,3-Triazoles at the C-1, C-2, or C-3 Position
-
Ding, C.; Zhang, Y.; Chen, H.; Wild, Ch.; Wang, T.; White, M. A.; Shen, Q.; Zhou, J. Overcoming Synthetic Challenges of Oridonin A-Ring Structural Diversification: Regio- and Stereoselective Installation of Azides and 1,2,3-Triazoles at the C-1, C-2, or C-3 Position Org. Lett. 2013, 15, 3718-3721 10.1021/ol4015865
-
(2013)
Org. Lett.
, vol.15
, pp. 3718-3721
-
-
Ding, C.1
Zhang, Y.2
Chen, H.3
Wild, Ch.4
Wang, T.5
White, M.A.6
Shen, Q.7
Zhou, J.8
-
243
-
-
60449110147
-
Synthesis and Biological Evaluation of C-12 Triazole and Oxadiazole Analogs of Salvinorin A
-
Yang, L.; Xu, W.; Chen, F.; Liu-Chen, L.-Y.; Ma, Z.; Lee, D. Y. W. Synthesis and Biological Evaluation of C-12 Triazole and Oxadiazole Analogs of Salvinorin A Bioorg. Med. Chem. Lett. 2009, 19, 1301-1304 10.1016/j.bmcl.2009.01.078
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 1301-1304
-
-
Yang, L.1
Xu, W.2
Chen, F.3
Liu-Chen, L.-Y.4
Ma, Z.5
Lee, D.Y.W.6
-
244
-
-
77956148100
-
A Solanesol-derived Scaffold for Multimerization of Bioactive Peptides
-
Alleti, R.; Rao, V.; Xu, L.; Gillies, R. J.; Mash, E. A. A Solanesol-derived Scaffold for Multimerization of Bioactive Peptides J. Org. Chem. 2010, 75, 5895-5903 10.1021/jo101043m
-
(2010)
J. Org. Chem.
, vol.75
, pp. 5895-5903
-
-
Alleti, R.1
Rao, V.2
Xu, L.3
Gillies, R.J.4
Mash, E.A.5
|