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Results:
1-23
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Results: 23
Authors:
Maltais, R
Luu-The, V
Poirier, D
Citation: R. Maltais et al., Parallel solid-phase synthesis of 3 beta-peptido-3 alpha-hydroxy-5 alpha androstan-17-one derivatives for inhibition of type 3 17 beta-hydroxysteroiddehydrogenase, BIO MED CH, 9(12), 2001, pp. 3101-3111
Authors:
Poirier, D
Bydal, P
Tremblay, MR
Sam, KM
Luu-The, V
Citation: D. Poirier et al., Inhibitors of type II 17 beta-hydroxysteroid dehydrogenase, MOL C ENDOC, 171(1-2), 2001, pp. 119-128
Authors:
Ciobanu, LC
Boivin, RP
Luu-The, V
Poirier, D
Citation: Lc. Ciobanu et al., Synthesis and steroid sulphatase inhibitory activity of C19-and C21-steroidal derivatives bearing a benzyl-inhibiting group, EUR J MED C, 36(7-8), 2001, pp. 659-671
Authors:
Tremblay, MR
Lin, SX
Poirier, D
Citation: Mr. Tremblay et al., Chemical synthesis of 16 beta-propylaminoacyl derivatives of estradiol andtheir inhibitory potency on type 1 17 beta-hydroxy steroid dehydrogenase and binding affinity on steroid receptors, STEROIDS, 66(11), 2001, pp. 821-831
Authors:
Ciobanu, LC
Maltais, R
Poirier, D
Citation: Lc. Ciobanu et al., The sulfamate functional group as a new anchor for solid-phase organic synthesis, ORG LETT, 2(4), 2000, pp. 445-448
Authors:
Maltais, R
Tremblay, MR
Poirier, D
Citation: R. Maltais et al., Solid-phase synthesis of hydroxysteroid derivatives using the diethylsilyloxy linker, J COMB CHEM, 2(6), 2000, pp. 604-614
Authors:
Tremblay, MR
Poirier, D
Citation: Mr. Tremblay et D. Poirier, Solid-phase synthesis of phenolic steroids: From optimization studies to aconvenient procedure for combinatorial synthesis of biologically relevant estradiol derivatives, J COMB CHEM, 2(1), 2000, pp. 48-65
Authors:
Ngatcha, BT
Luu-The, V
Poirier, D
Citation: Bt. Ngatcha et al., Androsterone 3 beta-substituted derivatives as inhibitors of type 3 17 beta-hydroxysteroid dehydrogenase, BIOORG MED, 10(22), 2000, pp. 2533-2536
Authors:
Sam, KM
Labrie, F
Poirier, D
Citation: Km. Sam et al., N-butyl-N-methyl-11-(3 '-hydroxy-21 ',17 '-carbolactone-19 '-nor-17 'alpha-pregna-1 ',3 ',5 '(10 ')-trien-7 'alpha-yl)-undecanamide: an inhibitor of type 2 17 beta-hydroxysteroid dehydrogenase that does not have oestrogenic or androgenic activity, EUR J MED C, 35(2), 2000, pp. 217-225
Authors:
Berthiaume, D
Poirier, D
Citation: D. Berthiaume et D. Poirier, O-Methoxycarbonyl cyanohydrin as a new protective group for carbonyls, TETRAHEDRON, 56(33), 2000, pp. 5995-6003
Authors:
Godin, C
Provost, PR
Poirier, D
Blomquist, CH
Tremblay, Y
Citation: C. Godin et al., Separation by thin-layer chromatography of the most common androgen-derived C-19 steroids formed by mammalian cells (vol 64, pg 767, 1999), STEROIDS, 65(4), 2000, pp. 224-224
Authors:
Boivin, RP
Luu-The, V
Lachance, R
Labrie, F
Poirier, D
Citation: Rp. Boivin et al., Structure-activity relationships of 17 alpha-derivatives of estradiol as inhibitors of steroid sulfatase, J MED CHEM, 43(23), 2000, pp. 4465-4478
Authors:
Poirier, D
Ciobanu, LC
Maltais, R
Citation: D. Poirier et al., Steroid sulfatase inhibitors, EXPERT OP T, 9(8), 1999, pp. 1083-1099
Authors:
Tremblay, MR
Luu-The, V
Leblanc, G
Noel, P
Breton, E
Labrie, F
Poirier, D
Citation: Mr. Tremblay et al., Spironolactone-related inhibitors of type II 17 beta-hydroxysteroid dehydrogenase: Chemical synthesis, receptor binding affinities, and proliferativeantiproliferative activities, BIO MED CH, 7(6), 1999, pp. 1013-1023
Authors:
Tremblay, MR
Simard, J
Poirier, D
Citation: Mr. Tremblay et al., Parallel solid-phase synthesis of a model library of 7 alpha-alkylamide estradiol derivatives as potential estrogen receptor antagonists, BIOORG MED, 9(19), 1999, pp. 2827-2832
Authors:
Qiu, W
Zhu, DW
Azzi, A
Campbell, RL
Qi, H
Poirier, D
Lin, SX
Citation: W. Qiu et al., Two non-reactive ternary complexes of estrogenic 17 beta-hydroxysteroid dehydrogenase: crystallization and preliminary structural analysis, J STEROID B, 68(5-6), 1999, pp. 239-244
Authors:
Gaulin, C
Frigon, M
Poirier, D
Fournier, C
Citation: C. Gaulin et al., Transmission of calicivirus by a foodhandler in the pre-symptomatic phase of illness, EPIDEM INFE, 123(3), 1999, pp. 475-478
Authors:
Poirier, D
Berthiaume, D
Boivin, RP
Citation: D. Poirier et al., Unexpected formation of O-methoxycarbonyl cyanohydrin showing potential asa protective group of ketones, SYNLETT, (9), 1999, pp. 1423-1425
Solid-phase synthesis of phenolic steroids: Towards combinatorial libraries of estradiol derivatives
Authors:
Tremblay, MR
Poirier, D
Citation: Mr. Tremblay et D. Poirier, Solid-phase synthesis of phenolic steroids: Towards combinatorial libraries of estradiol derivatives, TETRAHEDR L, 40(7), 1999, pp. 1277-1280
Authors:
Ngatcha, BT
Poirier, D
Citation: Bt. Ngatcha et D. Poirier, Diastereoselective addition of organomagnesium reagents to 17 beta-TBDMS-dihydrotestosterone, SYN COMMUN, 29(7), 1999, pp. 1065-1074
17 alpha-Alkan (or alkyn) amide derivatives of estradiol as inhibitors of steroid-sulfatase activity
Authors:
Boivin, RP
Labrie, F
Poirier, D
Citation: Rp. Boivin et al., 17 alpha-Alkan (or alkyn) amide derivatives of estradiol as inhibitors of steroid-sulfatase activity, STEROIDS, 64(12), 1999, pp. 825-833
Authors:
Godin, C
Poirier, D
Blomquist, CH
Tremblay, Y
Citation: C. Godin et al., Separation by thin-layer chromatography of the most common androgen-derived C-19 steroids formed by mammalian cells, STEROIDS, 64(11), 1999, pp. 767-769
Authors:
Ciobanu, LC
Boivin, RP
Luu-The, V
Labrie, F
Poirier, D
Citation: Lc. Ciobanu et al., Potent inhibition of steroid sulfatase activity by 3-O-sulfamate 17 alpha-benzyl(or 4 '-tert-butylbenzyl)estra-1,3,5(10)-trienes: Combination of two substituents at positions C3 and C17 alpha of estradiol, J MED CHEM, 42(12), 1999, pp. 2280-2286
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