-
1
-
-
0042844744
-
Natural products as sources of new drugs over the period 1981-2002
-
Newman, D. J.; Cragg, G. M.; Snader, K. M. Natural products as sources of new drugs over the period 1981-2002. J. Nat. Prod. 2003, 66, 1022-1037.
-
(2003)
J. Nat. Prod
, vol.66
, pp. 1022-1037
-
-
Newman, D.J.1
Cragg, G.M.2
Snader, K.M.3
-
2
-
-
14944383798
-
The evolving role of natural products in drug discovery
-
Koehn, F. E.; Carter, G. T. The evolving role of natural products in drug discovery. Nat. Rev. Drug Discovery 2005, 4, 206-220.
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, pp. 206-220
-
-
Koehn, F.E.1
Carter, G.T.2
-
3
-
-
33745784158
-
Charting biological and chemical space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds
-
Arve, L.; Voigt, T.; Waldmann, H. Charting biological and chemical space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds. QSAR Comb. Sci. 2006, 25, 449-456.
-
(2006)
QSAR Comb. Sci
, vol.25
, pp. 449-456
-
-
Arve, L.1
Voigt, T.2
Waldmann, H.3
-
4
-
-
0037119336
-
From protein domains to drug candidates: Natural products as guiding principles in the design and synthesis of compound libraries
-
Breinbauer, R.; Vetter, I. R.; Waldmann, H. From protein domains to drug candidates: Natural products as guiding principles in the design and synthesis of compound libraries. Angew. Chem., Int. Ed. 2002, 41, 2879-2890.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 2879-2890
-
-
Breinbauer, R.1
Vetter, I.R.2
Waldmann, H.3
-
5
-
-
5644294669
-
Current progress in natural product-like libraries for discovery screening
-
Tan, D. S. Current progress in natural product-like libraries for discovery screening. Comb. Chem. High Throughput Screening 2004, 7, 631-643.
-
(2004)
Comb. Chem. High Throughput Screening
, vol.7
, pp. 631-643
-
-
Tan, D.S.1
-
6
-
-
2942590399
-
Libraries from natural product-like scaffolds
-
Boldi, A. M. Libraries from natural product-like scaffolds. Curr. Opin. Chem. Biol. 2004, 8, 281-286.
-
(2004)
Curr. Opin. Chem. Biol
, vol.8
, pp. 281-286
-
-
Boldi, A.M.1
-
7
-
-
0141988625
-
Diversity oriented synthesis and branching reaction pathway to generate natural product-like compounds
-
Liao, Y.; Hu, Y.; Wu, J.; Zhu, Q.; Donovan, M.; Fathi, R.; Yang, Z. Diversity oriented synthesis and branching reaction pathway to generate natural product-like compounds. Curr. Med. Chem. 2003, 10, 2285-2316.
-
(2003)
Curr. Med. Chem
, vol.10
, pp. 2285-2316
-
-
Liao, Y.1
Hu, Y.2
Wu, J.3
Zhu, Q.4
Donovan, M.5
Fathi, R.6
Yang, Z.7
-
8
-
-
0037208308
-
Property distributions: Differences between drugs, natural products, and molecules from combinatorial chemistry
-
Feher, M.; Schmidt, J. M. Property distributions: Differences between drugs, natural products, and molecules from combinatorial chemistry. J. Chem. Inf. Comput. Sci. 2003, 43, 218-227.
-
(2003)
J. Chem. Inf. Comput. Sci
, vol.43
, pp. 218-227
-
-
Feher, M.1
Schmidt, J.M.2
-
9
-
-
33745785038
-
Meldrum's acid in multicomponent reactions: Applications to combinatorial and diversity-oriented synthesis
-
Gerencsér, J.; Dormán, G.; Darvas, F. Meldrum's acid in multicomponent reactions: Applications to combinatorial and diversity-oriented synthesis. QSAR Comb. Sci. 2006, 439-448.
-
(2006)
QSAR Comb. Sci
, pp. 439-448
-
-
Gerencsér, J.1
Dormán, G.2
Darvas, F.3
-
10
-
-
17144366282
-
Asymmetric multicomponent reactions (AMCRs): The new frontier
-
Ramón, D. J.; Miguel, Y. Asymmetric multicomponent reactions (AMCRs): The new frontier. Angew. Chem., Int. Ed. 2005, 44, 1602-1634.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 1602-1634
-
-
Ramón, D.J.1
Miguel, Y.2
-
11
-
-
0042745386
-
Recent advances in solution-phase multicomponent methodology for the synthesis of heterocyclic compounds
-
Orru, R. V. A.; de Greef, M. Recent advances in solution-phase multicomponent methodology for the synthesis of heterocyclic compounds. Synthesis 2003, 1471-1499.
-
(2003)
Synthesis
, pp. 1471-1499
-
-
Orru, R.V.A.1
de Greef, M.2
-
12
-
-
0037238724
-
Multicomponent reactions: Emerging chemistry in drug discovery. From xylocain to crixivan
-
Hulme, C.; Gore, V. Multicomponent reactions: Emerging chemistry in drug discovery. From xylocain to crixivan. Curr. Med. Chem. 2003, 10, 51-80.
-
(2003)
Curr. Med. Chem
, vol.10
, pp. 51-80
-
-
Hulme, C.1
Gore, V.2
-
13
-
-
0035030563
-
The multicomponent reactions and their libraries for natural and preparative chemistry
-
Ugi, I.; Heck, S. The multicomponent reactions and their libraries for natural and preparative chemistry. Comb. Chem. High Throughput Screening 2001, 4, 1-34.
-
(2001)
Comb. Chem. High Throughput Screening
, vol.4
, pp. 1-34
-
-
Ugi, I.1
Heck, S.2
-
14
-
-
0033019939
-
Discovery of new multicomponent reactions with combinatorial methods
-
Weber, L.; Illgen, K.; Almstetter, M. Discovery of new multicomponent reactions with combinatorial methods. Synlett 1999, 366-374.
-
(1999)
Synlett
, pp. 366-374
-
-
Weber, L.1
Illgen, K.2
Almstetter, M.3
-
15
-
-
0042469059
-
The generation of dihydropyrimidine libraries utilizing Biginelli multicomponent chemistry
-
For a recent review, see
-
For a recent review, see: Kappe, C. O. The generation of dihydropyrimidine libraries utilizing Biginelli multicomponent chemistry. QSAR Comb. Sci. 2003, 22, 630-645.
-
(2003)
QSAR Comb. Sci
, vol.22
, pp. 630-645
-
-
Kappe, C.O.1
-
16
-
-
0034618192
-
One-pot synthesis and biological evaluation of aspergillamides and analogues
-
Beck, B.; Hess, S.; Dömling, A. One-pot synthesis and biological evaluation of aspergillamides and analogues. Bioorg. Med. Chem. Lett. 2000, 10, 1701-1705.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 1701-1705
-
-
Beck, B.1
Hess, S.2
Dömling, A.3
-
17
-
-
0035362702
-
Combinatorial synthesis of nikkomycin analogues on solid support
-
For the synthesis of nikkomycin analogues utilizing the Ugi process on solid support, see
-
For the synthesis of nikkomycin analogues utilizing the Ugi process on solid support, see: Suda, A.; Ohta, A.; Sudoh, M.; Tsukuda, T.; Shimma, N. Combinatorial synthesis of nikkomycin analogues on solid support. Heterocycles 2001, 55, 1023-1028.
-
(2001)
Heterocycles
, vol.55
, pp. 1023-1028
-
-
Suda, A.1
Ohta, A.2
Sudoh, M.3
Tsukuda, T.4
Shimma, N.5
-
18
-
-
0032033637
-
Discovery of podophyllotoxins
-
Imbert, T. F. Discovery of podophyllotoxins. Biochimie 1998, 80, 207-222.
-
(1998)
Biochimie
, vol.80
, pp. 207-222
-
-
Imbert, T.F.1
-
19
-
-
0001635377
-
Podophyllotoxin derivatives: Drug discovery and development
-
Bohlin, L.; Rosen, B. Podophyllotoxin derivatives: Drug discovery and development. Drug Discovery Today 1996, 1, 343-351.
-
(1996)
Drug Discovery Today
, vol.1
, pp. 343-351
-
-
Bohlin, L.1
Rosen, B.2
-
20
-
-
0001571565
-
Inhibition of Topoisomerase-II by Vp-16-213 (Etoposide), Vm-26 (Teniposide), and structural congeners as an explanation for in vivo DNA breakage and cytotoxicity
-
Long, B. H.; Minocha, A. Inhibition of Topoisomerase-II by Vp-16-213 (Etoposide), Vm-26 (Teniposide), and structural congeners as an explanation for in vivo DNA breakage and cytotoxicity. Proc. Am. Assoc. Cancer Res. 1983, 24, 321-321.
-
(1983)
Proc. Am. Assoc. Cancer Res
, vol.24
, pp. 321-321
-
-
Long, B.H.1
Minocha, A.2
-
21
-
-
18744373344
-
Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents
-
You, Y. J. Podophyllotoxin derivatives: Current synthetic approaches for new anticancer agents. Curr. Pharm. Des. 2005, 11, 1695-1717.
-
(2005)
Curr. Pharm. Des
, vol.11
, pp. 1695-1717
-
-
You, Y.J.1
-
22
-
-
0033662352
-
Antitumor properties of podophyllotoxin and related compounds
-
Gordaliza, M.; Castro, M. A.; Corral, J. M. M.; San Feliciano, A. Antitumor properties of podophyllotoxin and related compounds. Curr. Pharm. Des. 2000, 6, 1811-1839.
-
(2000)
Curr. Pharm. Des
, vol.6
, pp. 1811-1839
-
-
Gordaliza, M.1
Castro, M.A.2
Corral, J.M.M.3
San Feliciano, A.4
-
23
-
-
0029904857
-
Chemoenzymatic and ring E-modular approach to the (-)-podophyllotoxin skeleton. Synthesis of 3′,4′,5′-tridemethoxy-(-)- podophyllotoxin
-
Berkowitz, D. B.; Maeng, J. -H.; Dantzig, A. H.; Shepard, R. L.; Norman, B. H. Chemoenzymatic and ring E-modular approach to the (-)-podophyllotoxin skeleton. Synthesis of 3′,4′,5′-tridemethoxy-(-)- podophyllotoxin. J. Am. Chem. Soc. 1996, 118, 9426-9427.
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 9426-9427
-
-
Berkowitz, D.B.1
Maeng, J.-H.2
Dantzig, A.H.3
Shepard, R.L.4
Norman, B.H.5
-
24
-
-
0030683597
-
A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans - Chinensin, justicidin B, and Taiwanin C
-
Hitotsuyanagi, Y.; Kobayashi, M.; Fukuyo, M.; Takeya, K.; Itokawa, H. A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans - Chinensin, justicidin B, and Taiwanin C. Tetrahedron Lett. 1997, 38, 8295-8296.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 8295-8296
-
-
Hitotsuyanagi, Y.1
Kobayashi, M.2
Fukuyo, M.3
Takeya, K.4
Itokawa, H.5
-
25
-
-
0034696048
-
4-Aza-2,3-dehydro-4-deoxypodophyllotoxins: Simple aza-podophyllotoxin analogues possessing potent cytotoxicity
-
Hitotsuyanagi, Y.; Fukuyo, M.; Tsuda, K.; Kobayashi, M.; Ozeki, A.; Itokawa, H.; Takeya, K. 4-Aza-2,3-dehydro-4-deoxypodophyllotoxins: Simple aza-podophyllotoxin analogues possessing potent cytotoxicity. Bioorg. Med. Chem. Lett. 2000, 10, 315-317.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 315-317
-
-
Hitotsuyanagi, Y.1
Fukuyo, M.2
Tsuda, K.3
Kobayashi, M.4
Ozeki, A.5
Itokawa, H.6
Takeya, K.7
-
26
-
-
0017656951
-
Non-enolizable podophyllotoxin derivatives
-
Gensler, W. J.; Murthy, C. D.; Trammell, M. H. Non-enolizable podophyllotoxin derivatives. J. Med. Chem. 1977, 20, 635-644.
-
(1977)
J. Med. Chem
, vol.20
, pp. 635-644
-
-
Gensler, W.J.1
Murthy, C.D.2
Trammell, M.H.3
-
27
-
-
0037136497
-
-
Tratrat, C.; Giorgi-Renault, S.; Husson, H. P. A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives. Org. Lett. 2002, 4, 3.187-3189.
-
Tratrat, C.; Giorgi-Renault, S.; Husson, H. P. A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives. Org. Lett. 2002, 4, 3.187-3189.
-
-
-
-
28
-
-
0001308948
-
-
Cassady, J. M, Douros, J. D, Eds, Academic; New York
-
Jardine, I. In Anticancer Agents Based on Natural Products; Cassady, J. M., Douros, J. D., Eds.; Academic; New York, 1980; pp 319-351.
-
(1980)
Anticancer Agents Based on Natural Products
, pp. 319-351
-
-
Jardine, I.1
-
30
-
-
0034618553
-
Subtype-selective N-methyl-D-aspartate receptor antagonists: Synthesis and biological evaluation of l-(heteroarylalkynyl)-4- benzylpiperidines
-
Wright, J. L.; Gregory, T. F.; Kesten, S. R.; Boxer, P. A.; Serpa, K. A.; Meltzer, L. T.; Wise, L. D. Subtype-selective N-methyl-D-aspartate receptor antagonists: Synthesis and biological evaluation of l-(heteroarylalkynyl)-4- benzylpiperidines. J. Med. Chem. 2000, 43, 3408-3419.
-
(2000)
J. Med. Chem
, vol.43
, pp. 3408-3419
-
-
Wright, J.L.1
Gregory, T.F.2
Kesten, S.R.3
Boxer, P.A.4
Serpa, K.A.5
Meltzer, L.T.6
Wise, L.D.7
-
31
-
-
33745276289
-
Estrogen receptor beta-subtype selective tetrahydrofluorenones: Use of a fused pyrazole as a phenol bioisostere
-
Wilkening, R. R.; Ratcliffe, R. W.; Fried, A. K.; Meng, D.; Sun, W.; Colwell, L.; Lambert, S.; Greenlee, M.; Nilsson, S.; Thorsell, A.; Mojena, M.; Tudela, C.; Frisch, K.; Chan, W.; Birzin, E. T.; Rohrer, S. P.; Hammond, M. L. Estrogen receptor beta-subtype selective tetrahydrofluorenones: Use of a fused pyrazole as a phenol bioisostere. Bioorg. Med. Chem. Lett. 2006, 16, 3896-3901.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 3896-3901
-
-
Wilkening, R.R.1
Ratcliffe, R.W.2
Fried, A.K.3
Meng, D.4
Sun, W.5
Colwell, L.6
Lambert, S.7
Greenlee, M.8
Nilsson, S.9
Thorsell, A.10
Mojena, M.11
Tudela, C.12
Frisch, K.13
Chan, W.14
Birzin, E.T.15
Rohrer, S.P.16
Hammond, M.L.17
-
32
-
-
33846934752
-
Structural simplification of bioactive natural products with multi-component synthesis: Dihydropyridopyrazole analogues of podophyllotoxin
-
For preliminary communication of this work, see
-
For preliminary communication of this work, see: Magedov, I. V.; Manpadi, M.; Rozhkova, E.; Przheval'skii, N. M.; Rogelj, S.; Shors, S. T.; Steelant, W. F. A.; Van slambrouck, S.; Kornienko, A. Structural simplification of bioactive natural products with multi-component synthesis: Dihydropyridopyrazole analogues of podophyllotoxin. Bioorg. Med. Chem. Lett. 2007, 17, 1381-1385.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 1381-1385
-
-
Magedov, I.V.1
Manpadi, M.2
Rozhkova, E.3
Przheval'skii, N.M.4
Rogelj, S.5
Shors, S.T.6
Steelant, W.F.A.7
Van slambrouck, S.8
Kornienko, A.9
-
33
-
-
0031878132
-
-
Quiroga, J.; Insuasty, B.; Hormaza, A.; Saitz, C.; Jullian, C. Synthesis of 4-aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-ones. J. Heterocycl. Chem. 1998, 35, 575-578.
-
(a) Quiroga, J.; Insuasty, B.; Hormaza, A.; Saitz, C.; Jullian, C. Synthesis of 4-aryl-4,7,8,9-tetrahydro-6H-pyrazolo[3,4-b]quinolin-5-ones. J. Heterocycl. Chem. 1998, 35, 575-578.
-
-
-
-
34
-
-
0035817055
-
-
Quiroga, J.; Mejía, D.; Insuasty, B.; Abonía, R.; Nogueras, M.; Sánchez, A.; Cobo, J.; Low, J. N. Regioselective synthesis of 4,7,8,9-tetrahydro-2H-pyrazolo[3,4-b]-quinolin-5(6H)-ones. Mechanism and structural analysis. Tetrahedron 2001, 57, 6947-6953.
-
Quiroga, J.; Mejía, D.; Insuasty, B.; Abonía, R.; Nogueras, M.; Sánchez, A.; Cobo, J.; Low, J. N. Regioselective synthesis of 4,7,8,9-tetrahydro-2H-pyrazolo[3,4-b]-quinolin-5(6H)-ones. Mechanism and structural analysis. Tetrahedron 2001, 57, 6947-6953.
-
-
-
-
35
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival - application to proliferation and cytotoxicity assays
-
Mosmann, T. Rapid colorimetric assay for cellular growth and survival - application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55-63.
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
-
36
-
-
35348884725
-
-
Although the antiproliferative effect of the tested compounds is generally much higher at 50 μM, the direct comparison of these data is impeded by limited solubility of a number of these compounds at this concentration
-
Although the antiproliferative effect of the tested compounds is generally much higher at 50 μM, the direct comparison of these data is impeded by limited solubility of a number of these compounds at this concentration.
-
-
-
-
37
-
-
0029043888
-
A novel assay for apoptosis - flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein-labeled annexin-V
-
Vermes, I.; Haanen, C.; Steffens-Nakken, H.; Reutelingsperger, C. A novel assay for apoptosis - flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein-labeled annexin-V J. Immunol. Methods 1995, 184, 39-51.
-
(1995)
J. Immunol. Methods
, vol.184
, pp. 39-51
-
-
Vermes, I.1
Haanen, C.2
Steffens-Nakken, H.3
Reutelingsperger, C.4
-
38
-
-
0026508561
-
Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages
-
Fadok, V. A.; Voelkler, D. R.; Campbell, P. A.; Cohen, J. J.; Bratton, D. L.; Henson, P. M. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J. Immunol. 1992, 148, 2207-2216.
-
(1992)
J. Immunol
, vol.148
, pp. 2207-2216
-
-
Fadok, V.A.1
Voelkler, D.R.2
Campbell, P.A.3
Cohen, J.J.4
Bratton, D.L.5
Henson, P.M.6
-
39
-
-
0031080192
-
Study of the apoptosis induced in vitro by antitumoral drugs on leukaemic cells
-
For example, see
-
For example, see: Vial, J. P.; Belloc, F.; Dumain, P.; Besnard, S.; Lacombe, F.; Boisseau, M. R.; Reiffers, J.; Bernard, P. Study of the apoptosis induced in vitro by antitumoral drugs on leukaemic cells. Leuk. Res. 1997, 21, 163-172.
-
(1997)
Leuk. Res
, vol.21
, pp. 163-172
-
-
Vial, J.P.1
Belloc, F.2
Dumain, P.3
Besnard, S.4
Lacombe, F.5
Boisseau, M.R.6
Reiffers, J.7
Bernard, P.8
-
40
-
-
23444440650
-
Discovery and structure-activity relationship of 3-aryl-5-aryl-1,2,4-oxadiazoles as a new series of apoptosis inducers and potential anticancer agents
-
Zhang, H.-Z.; Kasibhatla, S.; Kuemmerle, J.; Kemnitzer, W.; Ollis-Mason, K.; Qiu, L.; Crogan-Grundy, C.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery and structure-activity relationship of 3-aryl-5-aryl-1,2,4-oxadiazoles as a new series of apoptosis inducers and potential anticancer agents. J. Med. Chem. 2005, 48, 5215-5223.
-
(2005)
J. Med. Chem
, vol.48
, pp. 5215-5223
-
-
Zhang, H.-Z.1
Kasibhatla, S.2
Kuemmerle, J.3
Kemnitzer, W.4
Ollis-Mason, K.5
Qiu, L.6
Crogan-Grundy, C.7
Tseng, B.8
Drewe, J.9
Cai, S.X.10
-
41
-
-
25144441808
-
-
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G.; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
-
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G.; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
-
-
-
-
42
-
-
9744248288
-
-
Kemnitzer, W.; Drewe, J.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Biais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4aryl group. J. Med. Chem. 2004, 47, 6299-6310.
-
Kemnitzer, W.; Drewe, J.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Biais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4aryl group. J. Med. Chem. 2004, 47, 6299-6310.
-
-
-
|