-
3
-
-
0032862255
-
Steroids from sponges: Recent reports
-
A. Aiello, E. Fattorusso, and M. Menna Steroids from sponges: recent reports Steroids 64 1999 687 714
-
(1999)
Steroids
, vol.64
, pp. 687-714
-
-
Aiello, A.1
Fattorusso, E.2
Menna, M.3
-
4
-
-
57249093635
-
Marine polar steroids
-
V.A. Stonick Marine polar steroids Russ Chem Rev 70 2001 673 715
-
(2001)
Russ Chem Rev
, vol.70
, pp. 673-715
-
-
Stonick, V.A.1
-
6
-
-
0027425393
-
Blancasterol, a cytotoxic 9,11-secosteroid isolated from the northeastern pacific marine sponge Pleraplysilla sp.
-
J. Pika, and R.J. Andersen Blancasterol, a cytotoxic 9,11-secosteroid isolated from the northeastern pacific marine sponge Pleraplysilla sp. Tetrahedron 49 1993 8757 8760
-
(1993)
Tetrahedron
, vol.49
, pp. 8757-8760
-
-
Pika, J.1
Andersen, R.J.2
-
7
-
-
15444341432
-
New secosteroids from a Gorgonian of the genus Muricella
-
Y. Seo, K.W. Cho, H. Chung, H.S. Lee, and J. Shin New secosteroids from a Gorgonian of the genus Muricella J Nat Prod 61 1998 1441 1443
-
(1998)
J Nat Prod
, vol.61
, pp. 1441-1443
-
-
Seo, Y.1
Cho, K.W.2
Chung, H.3
Lee, H.S.4
Shin, J.5
-
8
-
-
0031881663
-
New metabolites from the sponge Spongia agaricina
-
A. Rueda, E. Zubia, M.J. Ortega, J.L. Carballo, and J. Salva New metabolites from the sponge Spongia agaricina J Nat Prod 61 1998 258 261
-
(1998)
J Nat Prod
, vol.61
, pp. 258-261
-
-
Rueda, A.1
Zubia, E.2
Ortega, M.J.3
Carballo, J.L.4
Salva, J.5
-
9
-
-
0028295195
-
Euryspongiols: Ten new highly hydroxylated 9,11-secosteroids with antihistaminic activity from the sponge Euryspongia sp stereochemistry and reduction
-
J. Dopeso, E. Quinoa, R. Riguera, C. Debitus, and P.R. Berquist Euryspongiols: ten new highly hydroxylated 9,11-secosteroids with antihistaminic activity from the sponge Euryspongia sp. stereochemistry and reduction Tetrahedron 50 1994 3813 3828
-
(1994)
Tetrahedron
, vol.50
, pp. 3813-3828
-
-
Dopeso, J.1
Quinoa, E.2
Riguera, R.3
Debitus, C.4
Berquist, P.R.5
-
10
-
-
0031977402
-
A bioactive secosterol with an unusual A- and B-ring oxygenation pattern isolated from an Indonesian soft coral Lobophytum sp.
-
L.A. Morris, E.M. Christie, M. Jaspars, and L.P. Van Ofwegen A bioactive secosterol with an unusual A- and B-ring oxygenation pattern isolated from an Indonesian soft coral Lobophytum sp. J Nat Prod 61 1998 538 541
-
(1998)
J Nat Prod
, vol.61
, pp. 538-541
-
-
Morris, L.A.1
Christie, E.M.2
Jaspars, M.3
Van Ofwegen, L.P.4
-
11
-
-
0017259625
-
Synthesis of beta, gamma-acetylenic 3-oxo steroids of the 5,10-seco series
-
F.H. Batzold, and C.H. Robinson Synthesis of beta, gamma-acetylenic 3-oxo steroids of the 5,10-seco series J Org Chem 41 1976 313 317
-
(1976)
J Org Chem
, vol.41
, pp. 313-317
-
-
Batzold, F.H.1
Robinson, C.H.2
-
12
-
-
0017699156
-
The substrate specificity and stereochemistry, reversibility and inhibition of the 3-oxo steroid delta 4-delta 5-isomerase component of cholesterol oxidase
-
A.G. Smith, and C.J.W. Brooks The substrate specificity and stereochemistry, reversibility and inhibition of the 3-oxo steroid delta 4-delta 5-isomerase component of cholesterol oxidase Biochem J 167 1977 121 129
-
(1977)
Biochem J
, vol.167
, pp. 121-129
-
-
Smith, A.G.1
Brooks, C.J.W.2
-
13
-
-
0018742170
-
Selective inhibition by secosteroids of 5α-reductase activity in human sex skin fibroblasts
-
N.A. Zerhouni, M. Maes, C. Sultan, S. Rothwell, and C.J. Migeon Selective inhibition by secosteroids of 5α-reductase activity in human sex skin fibroblasts Steroids 33 1979 277 285
-
(1979)
Steroids
, vol.33
, pp. 277-285
-
-
Zerhouni, N.A.1
Maes, M.2
Sultan, C.3
Rothwell, S.4
Migeon, C.J.5
-
14
-
-
0019453362
-
Irreversible inactivation of delta 5-3-ketosteroid isomerase of Pseudomonas testosteroni by acetylenic suicide substrates. Mechanism of formation and properties of the steroid-enzyme adduct
-
T.M. Penning, D.F. Covey, and P. Talalay Irreversible inactivation of delta 5-3-ketosteroid isomerase of Pseudomonas testosteroni by acetylenic suicide substrates. Mechanism of formation and properties of the steroid-enzyme adduct J Biol Chem 256 1981 6842 6850
-
(1981)
J Biol Chem
, vol.256
, pp. 6842-6850
-
-
Penning, T.M.1
Covey, D.F.2
Talalay, P.3
-
15
-
-
0020002255
-
Inactivation of Δ5-3-ketosteroid isomerase(s) from beef adrenal cortex by β,γ-acetylenic ketosteroids
-
T.M. Penning Inactivation of Δ5-3-ketosteroid isomerase(s) from beef adrenal cortex by β,γ-acetylenic ketosteroids Steroids 39 1982 301 311
-
(1982)
Steroids
, vol.39
, pp. 301-311
-
-
Penning, T.M.1
-
16
-
-
0023091465
-
Contraceptive steroid treatment affects steroid binding proteins and the percentage of free 17β-estradiol and testosterone in the cynomolgus monkey (Macaca fascicularis)
-
M.H. Vazquez, J.G. Tezon, and J.A. Blaquier Contraceptive steroid treatment affects steroid binding proteins and the percentage of free 17β-estradiol and testosterone in the cynomolgus monkey (Macaca fascicularis) J Steroid Biochem 28 1987 227 234
-
(1987)
J Steroid Biochem
, vol.28
, pp. 227-234
-
-
Vazquez, M.H.1
Tezon, J.G.2
Blaquier, J.A.3
-
17
-
-
37049075115
-
Synthesis of 1,10-seco-5α-estr-1-ynes: Potential mechanism-based inhibitors of 3α- and 3β-hydroxysteroid dehydrogenases
-
Y. Hu, and D.F. Covey Synthesis of 1,10-seco-5α-estr-1-ynes: potential mechanism-based inhibitors of 3α- and 3β-hydroxysteroid dehydrogenases J Chem Soc Perkin Trans 1 1993 417 422
-
(1993)
J Chem Soc Perkin Trans 1
, pp. 417-422
-
-
Hu, Y.1
Covey, D.F.2
-
18
-
-
84891789419
-
Ergosteroids syntheses and biological activity of seco-steroids related to dehydroepiandrosterone
-
I.L. Reich, H. Lardy, Y. Wei, P. Marwah, N. Kneer, D.R. Powell, and H.J. Reich Ergosteroids syntheses and biological activity of seco-steroids related to dehydroepiandrosterone Steroids 63 542 1998 53
-
(1998)
Steroids
, vol.63
, Issue.542
, pp. 53
-
-
Reich, I.L.1
Lardy, H.2
Wei, Y.3
Marwah, P.4
Kneer, N.5
Powell, D.R.6
Reich, H.J.7
-
19
-
-
57949104006
-
Synthesis, HIV-RT inhibitory activity and SAR of 1-benzyl-1H-1,2,3- triazole derivatives of carbohydrates
-
F.C. Silva, M.C.B.V. Souza, I.I.P. Frugulhetti, H.C. Castro, S.L.O. Souza, T.M.L. Souza, D.Q. Rodrigues, A.M.T. Souza, P.A. Abreu, F. Passamani, C.R. Rodrigues, and V.F. Ferreira Synthesis, HIV-RT inhibitory activity and SAR of 1-benzyl-1H-1,2,3-triazole derivatives of carbohydrates Eur J Med Chem 44 2009 373 383
-
(2009)
Eur J Med Chem
, vol.44
, pp. 373-383
-
-
Silva, F.C.1
Souza, M.C.B.V.2
Frugulhetti, I.I.P.3
Castro, H.C.4
Souza, S.L.O.5
Souza, T.M.L.6
Rodrigues, D.Q.7
Souza, A.M.T.8
Abreu, P.A.9
Passamani, F.10
Rodrigues, C.R.11
Ferreira, V.F.12
-
20
-
-
24744461365
-
4-Aryl-1,2,3-triazole: A novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivo
-
L.S. Kallander, Q. Lu, W. Chen, T. Tomaszek, G. Yang, D. Tew, T.D. Meek, G.A. Hofmann, C.K. Schulz-Pritchard, W.W. Smith, C.A. Janson, M.D. Ryan, G.F. Zhang, K.O. Johanson, R.B. Kirkpatrick, T.F. Ho, P.W. Fisher, M.R. Mattern, R.K. Johnson, M.J. Hansbury, J.D. Winkler, K.W. Ward, D.F. Veber, and S.K. Thompson 4-Aryl-1,2,3-triazole: a novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivo J Med Chem 48 2005 5644 5647
-
(2005)
J Med Chem
, vol.48
, pp. 5644-5647
-
-
Kallander, L.S.1
Lu, Q.2
Chen, W.3
Tomaszek, T.4
Yang, G.5
Tew, D.6
Meek, T.D.7
Hofmann, G.A.8
Schulz-Pritchard, C.K.9
Smith, W.W.10
Janson, C.A.11
Ryan, M.D.12
Zhang, G.F.13
Johanson, K.O.14
Kirkpatrick, R.B.15
Ho, T.F.16
Fisher, P.W.17
Mattern, M.R.18
Johnson, R.K.19
Hansbury, M.J.20
Winkler, J.D.21
Ward, K.W.22
Veber, D.F.23
Thompson, S.K.24
more..
-
21
-
-
77956186207
-
Synthesis of novel sulfanilamide-derived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities
-
X.L. Wang, K. Wan, and C.H. Zhou Synthesis of novel sulfanilamide-derived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities Eur J Med Chem 45 2010 4631 4633
-
(2010)
Eur J Med Chem
, vol.45
, pp. 4631-4633
-
-
Wang, X.L.1
Wan, K.2
Zhou, C.H.3
-
22
-
-
33750602935
-
Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives
-
M.S. Costa, N. Boechat, E.A. Rangel, F.C. Silva, A.M.T. Souza, C.R. Rodrigues, H.C. Castro, I.N. Junior, M.C.S. Lourenço, S.M.S.V. Wardell, and V.F. Ferreira Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives Bioorg Med Chem 14 2006 8644 8653
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 8644-8653
-
-
Costa, M.S.1
Boechat, N.2
Rangel, E.A.3
Silva, F.C.4
Souza, A.M.T.5
Rodrigues, C.R.6
Castro, H.C.7
Junior, I.N.8
Lourenço, M.C.S.9
Wardell, S.M.S.V.10
Ferreira, V.F.11
-
23
-
-
0000956115
-
Cooperative interactions of the catalytic nucleophile and the catalytic acid in the inhibition of β-glycosidases. Calculations and their validation by comparative kinetic and structural studies of the inhibition of glycogen phosphorylase b
-
T.D. Heightman, A. Vasella, K.E. Tsitsanou, S.E. Zographos, V.T. Skamnaki, and N.G. Oikonomakos Cooperative interactions of the catalytic nucleophile and the catalytic acid in the inhibition of β-glycosidases. Calculations and their validation by comparative kinetic and structural studies of the inhibition of glycogen phosphorylase b Helv Chim Acta 81 1998 853 864
-
(1998)
Helv Chim Acta
, vol.81
, pp. 853-864
-
-
Heightman, T.D.1
Vasella, A.2
Tsitsanou, K.E.3
Zographos, S.E.4
Skamnaki, V.T.5
Oikonomakos, N.G.6
-
24
-
-
0038299192
-
Triazole carboxylic acids as anionic sugar mimics? Inhibition of glycogen phosphorylase by a d-glucotriazole carboxylate
-
T.M. Krulle, C.D. Fuente, L. Pickering, R.T. Aplin, K.E. Tsitsanou, S.E. Zographos, N.G. Oikonomakos, R.J. Nash, R.C. Griffiths, and G.W. Fleet Triazole carboxylic acids as anionic sugar mimics? Inhibition of glycogen phosphorylase by a d-glucotriazole carboxylate Tetrahedron Asymmetry 8 1997 3807 3820
-
(1997)
Tetrahedron Asymmetry
, vol.8
, pp. 3807-3820
-
-
Krulle, T.M.1
Fuente, C.D.2
Pickering, L.3
Aplin, R.T.4
Tsitsanou, K.E.5
Zographos, S.E.6
Oikonomakos, N.G.7
Nash, R.J.8
Griffiths, R.C.9
Fleet, G.W.10
-
25
-
-
33847733975
-
1,2,3-Triazoles as peptide bond isosteres: Synthesis and biological evaluation of cyclotetrapeptide mimics
-
V.D. Bock, D. Speijer, H. Hiemstra, and J.H. van Maarseveen 1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics Org Biomol Chem 5 2007 971 975
-
(2007)
Org Biomol Chem
, vol.5
, pp. 971-975
-
-
Bock, V.D.1
Speijer, D.2
Hiemstra, H.3
Van Maarseveen, J.H.4
-
26
-
-
79959376326
-
Click-generated triazole ureas as ultrapotent in vivo-active serine hydrolase inhibitors
-
A. Adibekian, B.R. Martin, C. Wang, K.L. Hsu, D.A. Bachovchin, S. Niessen, H. Hoover, and B.F. Cravatt Click-generated triazole ureas as ultrapotent in vivo-active serine hydrolase inhibitors Nat Chem Biol 7 2011 469 478
-
(2011)
Nat Chem Biol
, vol.7
, pp. 469-478
-
-
Adibekian, A.1
Martin, B.R.2
Wang, C.3
Hsu, K.L.4
Bachovchin, D.A.5
Niessen, S.6
Hoover, H.7
Cravatt, B.F.8
-
27
-
-
0036127307
-
Biotransformation reactions of five-membered aromatic heterocyclic rings
-
D.K. Dalvie, A.S. Kalgulkar, S.C. Khojasteh-Bakht, R.S. Obach, and J.P. O'Donnell Biotransformation reactions of five-membered aromatic heterocyclic rings Chem Res Toxicol 15 2002 269 299
-
(2002)
Chem Res Toxicol
, vol.15
, pp. 269-299
-
-
Dalvie, D.K.1
Kalgulkar, A.S.2
Khojasteh-Bakht, S.C.3
Obach, R.S.4
O'Donnell, J.P.5
-
28
-
-
9644268752
-
Biotransformation reactions of five-membered aromatic heterocyclic rings
-
W.S. Horne, M.K. Yadav, C.D. Stout, and M.R. Ghadiri Biotransformation reactions of five-membered aromatic heterocyclic rings J Am Chem Soc 126 2004 15366 15367
-
(2004)
J Am Chem Soc
, vol.126
, pp. 15366-15367
-
-
Horne, W.S.1
Yadav, M.K.2
Stout, C.D.3
Ghadiri, M.R.4
-
29
-
-
40749106101
-
Synthesis and antimicrobial activity of β-lactam-bile acid conjugates linked via triazole
-
N.S. Vatmurge, B.G. Hazra, V.S. Pore, F. Shirazi, P.S. Chavan, and M.V. Deshpande Synthesis and antimicrobial activity of β-lactam-bile acid conjugates linked via triazole Bioorg Med Chem Lett 18 2008 2043 2047
-
(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
-
30
-
-
53549097892
-
Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam
-
N.S. Vatmurge, B.G. Hazra, V.S. Pore, F. Shirazi, P.S. Chavan, M.V. Deshpande, S. Kadreppa, and S. Chattopadhyay Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-β-lactam Bioorg Med Chem Lett 6 2008 3823 3830
-
(2008)
Bioorg Med Chem Lett
, vol.6
, pp. 3823-3830
-
-
Vatmurge, N.S.1
Hazra, B.G.2
Pore, V.S.3
Shirazi, F.4
Chavan, P.S.5
Deshpande, M.V.6
Kadreppa, S.7
Chattopadhyay, S.8
-
31
-
-
0037025285
-
Synthesis of four cholic acid-based CSPs containing 2-naphthoyl carbamate and 3,5-dinitrophenylcarbamate moieties and their evaluation in the HPLC resolution of racemic compounds
-
A. Iuliano, I. Pieraccini, G. Félix, and P. Salvadori Synthesis of four cholic acid-based CSPs containing 2-naphthoyl carbamate and 3,5-dinitrophenylcarbamate moieties and their evaluation in the HPLC resolution of racemic compounds Tetrahedron Asymmetry 13 2002 1265 1275
-
(2002)
Tetrahedron Asymmetry
, vol.13
, pp. 1265-1275
-
-
Iuliano, A.1
Pieraccini, I.2
Félix, G.3
Salvadori, P.4
-
33
-
-
84942705127
-
Nomenclature of Steroids
-
G.P. Moss Nomenclature of Steroids Pure Appl Chem 61 1989 1783 1822
-
(1989)
Pure Appl Chem
, vol.61
, pp. 1783-1822
-
-
Moss, G.P.1
-
34
-
-
0037099395
-
Stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B.A. Sharpless Stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes Angew Chem Int Ed 41 2002 2596 2599
-
(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.A.4
-
35
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
-
C.W. Tornoe, C. Christensen, and M. Meldal 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 67 2002 2057
-
(2002)
J Org Chem
, vol.67
, pp. 2057
-
-
Tornoe, C.W.1
Christensen, C.2
Meldal, M.3
-
36
-
-
33947493431
-
Recent applications of the CuI-catalysed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in carbohydrate chemistry
-
S. Dedola, S.A. Nepogodiev, and R.A. Field Recent applications of the CuI-catalysed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in carbohydrate chemistry Org Biomol Chem 5 2007 1006 1017
-
(2007)
Org Biomol Chem
, vol.5
, pp. 1006-1017
-
-
Dedola, S.1
Nepogodiev, S.A.2
Field, R.A.3
-
38
-
-
78149469867
-
Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis
-
V. Aragão Leoneti, V.L. Campo, A.S. Gomes, R.A. Field, and I. Carvalho Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis Tetrahedron 66 2010 9475 9492
-
(2010)
Tetrahedron
, vol.66
, pp. 9475-9492
-
-
Aragão Leoneti, V.1
Campo, V.L.2
Gomes, A.S.3
Field, R.A.4
Carvalho, I.5
-
39
-
-
78751650598
-
Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols
-
M. Ibrahim-Ouali, K. Hamze, and L. Rocheblave Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols Steroids 76 2011 324 330
-
(2011)
Steroids
, vol.76
, pp. 324-330
-
-
Ibrahim-Ouali, M.1
Hamze, K.2
Rocheblave, L.3
-
40
-
-
0001687625
-
Steroids and related products. Reduction of ester to ethers
-
G.R. Pettit, and D.M. Piatak Steroids and related products. Reduction of ester to ethers J Org Chem 27 1962 2127 2130
-
(1962)
J Org Chem
, vol.27
, pp. 2127-2130
-
-
Pettit, G.R.1
Piatak, D.M.2
-
41
-
-
0035813244
-
Microwave assisted organic synthesis: A review
-
P. Lidstrom, J. Tierney, B. Wathey, and J. Westman Microwave assisted organic synthesis: a review Tetrahedron 57 45 2001 9225 9283
-
(2001)
Tetrahedron
, vol.57
, Issue.45
, pp. 9225-9283
-
-
Lidstrom, P.1
Tierney, J.2
Wathey, B.3
Westman, J.4
-
42
-
-
0344880114
-
Quantitative dealkylation of alkyl esters via treatment with trimethylsilyl iodide. A new method for ester hydrolysis
-
M.F. Jung, and M.A. Lyster Quantitative dealkylation of alkyl esters via treatment with trimethylsilyl iodide. A new method for ester hydrolysis J Am Chem Soc 99 3 1977 968 969
-
(1977)
J Am Chem Soc
, vol.99
, Issue.3
, pp. 968-969
-
-
Jung, M.F.1
Lyster, M.A.2
-
43
-
-
0003686469
-
Synthetic methods and reactions. Transformations with chlorotrimethylsilane/sodium iodide, a convenient in situ iodotrimethylsilane reagent
-
G.A. Olah, S.C. Narang, B.G.B. Gupta, and R. Malhotra Synthetic methods and reactions. Transformations with chlorotrimethylsilane/sodium iodide, a convenient in situ iodotrimethylsilane reagent J Org Chem 44 8 1979 1247 1251
-
(1979)
J Org Chem
, vol.44
, Issue.8
, pp. 1247-1251
-
-
Olah, G.A.1
Narang, S.C.2
Gupta, B.G.B.3
Malhotra, R.4
-
44
-
-
0000110991
-
Selective oxidation with N-bromosuccinimide. Cholic acid
-
T.L. Fieser, and S. Rajagopalan Selective oxidation with N-bromosuccinimide. Cholic acid J Am Chem Soc 71 1949 3935 3938
-
(1949)
J Am Chem Soc
, vol.71
, pp. 3935-3938
-
-
Fieser, T.L.1
Rajagopalan, S.2
|