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Showing results (51-60 of 60) with videos related to

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Bioorganic & Medicinal Chemistry Letters|September 3, 2013
Preparation of imidazoles as potent calcitonin gene-related peptide (CGRP) antagonistsGeorge Tora, Andrew P Degnan, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2007
An orally active corticotropin releasing factor 1 receptor antagonist from 8-aryl-1,3a,7,8-tetraaza-cyclopenta[a]indenesXiaojun Han, Rita Civiello, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2010
Discovery of 6-chloro-2-trifluoromethyl-7-aryl-7H-imidazo[1,2-a]imidazol-3-ylmethylamines, a novel class of corticotropin-releasing factor receptor type 1 (CRF1R) antagonistsDmitry Zuev, Vivekananda M Vrudhula, Jodi A Michne, et al.
Bioorganic & Medicinal Chemistry Letters|February 27, 2010
Design, synthesis and evaluation of constrained tetrahydroimidazopyrimidine derivatives as antagonists of corticotropin-releasing factor type 1 receptor (CRF1R)Vivekananda M Vrudhula, Bireshwar Dasgupta, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|May 2, 2013
Discovery of (R)-N-(3-(7-methyl-1H-indazol-5-yl)-1-(4-(1-methylpiperidin-4-yl)-1-oxopropan-2-yl)-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide (BMS-742413): a potent human CGRP antagonist with superior safety profile for the treatment of migraine through intranasal deliveryPrasad V Chaturvedula, Stephen E Mercer, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|June 26, 2012
The synthesis and SAR of calcitonin gene-related peptide (CGRP) receptor antagonists derived from tyrosine surrogates. Part 1Xiaojun Han, Rita L Civiello, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacyGene M Dubowchik, Jodi A Michne, Dmitry Zuev, et al.
Bioorganic & Medicinal Chemistry Letters|February 14, 2013
The synthesis and SAR of calcitonin gene-related peptide (CGRP) receptor antagonists derived from tyrosine surrogates. Part 2Xiaojun Han, Rita L Civiello, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|October 23, 2020
Azepino-indazoles as calcitonin gene-related peptide (CGRP) receptor antagonistsStephen E Mercer, Prasad V Chaturvedula, Charles M Conway, et al.
Journal of Medicinal Chemistry|July 31, 2008
Discovery of (R)-4-(8-fluoro-2-oxo-1,2-dihydroquinazolin-3(4H)-yl)-N-(3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-2-yl)piperidine-1-carboxamide (BMS-694153): a potent antagonist of the human calcitonin gene-related peptide receptor for migraine with rapid and efficient intranasal exposureAndrew P Degnan, Prasad V Chaturvedula, Charles M Conway, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

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Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Bioorganic & Medicinal Chemistry Letters|September 3, 2013
Preparation of imidazoles as potent calcitonin gene-related peptide (CGRP) antagonistsGeorge Tora, Andrew P Degnan, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2007
An orally active corticotropin releasing factor 1 receptor antagonist from 8-aryl-1,3a,7,8-tetraaza-cyclopenta[a]indenesXiaojun Han, Rita Civiello, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2010
Discovery of 6-chloro-2-trifluoromethyl-7-aryl-7H-imidazo[1,2-a]imidazol-3-ylmethylamines, a novel class of corticotropin-releasing factor receptor type 1 (CRF1R) antagonistsDmitry Zuev, Vivekananda M Vrudhula, Jodi A Michne, et al.
Bioorganic & Medicinal Chemistry Letters|February 27, 2010
Design, synthesis and evaluation of constrained tetrahydroimidazopyrimidine derivatives as antagonists of corticotropin-releasing factor type 1 receptor (CRF1R)Vivekananda M Vrudhula, Bireshwar Dasgupta, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|May 2, 2013
Discovery of (R)-N-(3-(7-methyl-1H-indazol-5-yl)-1-(4-(1-methylpiperidin-4-yl)-1-oxopropan-2-yl)-4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxamide (BMS-742413): a potent human CGRP antagonist with superior safety profile for the treatment of migraine through intranasal deliveryPrasad V Chaturvedula, Stephen E Mercer, Sokhom S Pin, et al.
Bioorganic & Medicinal Chemistry Letters|June 26, 2012
The synthesis and SAR of calcitonin gene-related peptide (CGRP) receptor antagonists derived from tyrosine surrogates. Part 1Xiaojun Han, Rita L Civiello, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacyGene M Dubowchik, Jodi A Michne, Dmitry Zuev, et al.
Bioorganic & Medicinal Chemistry Letters|February 14, 2013
The synthesis and SAR of calcitonin gene-related peptide (CGRP) receptor antagonists derived from tyrosine surrogates. Part 2Xiaojun Han, Rita L Civiello, Charles M Conway, et al.
Bioorganic & Medicinal Chemistry Letters|October 23, 2020
Azepino-indazoles as calcitonin gene-related peptide (CGRP) receptor antagonistsStephen E Mercer, Prasad V Chaturvedula, Charles M Conway, et al.
Journal of Medicinal Chemistry|July 31, 2008
Discovery of (R)-4-(8-fluoro-2-oxo-1,2-dihydroquinazolin-3(4H)-yl)-N-(3-(7-methyl-1H-indazol-5-yl)-1-oxo-1-(4-(piperidin-1-yl)piperidin-1-yl)propan-2-yl)piperidine-1-carboxamide (BMS-694153): a potent antagonist of the human calcitonin gene-related peptide receptor for migraine with rapid and efficient intranasal exposureAndrew P Degnan, Prasad V Chaturvedula, Charles M Conway, et al.
Pageof 6