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The Journal of Urology
|
January 25, 2003
Partially purified Grammostola spatulata venom inhibits stretch activated calcium signaling in bladder myocytes and improves bladder compliance in an in vitro rat whole bladder model
Svetlana Tertyshnikova, James A Matson, George Thalody, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
December 12, 2018
Assessing seizure liability using multi-electrode arrays (MEA)
Jingsong Fan, George Thalody, Jae Kwagh, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2002
The synthesis and structure-activity relationships of 1,3-diaryl 1,2,4-(4H)-triazol-5-ones: a new class of calcium-dependent, large conductance, potassium (maxi-K) channel opener targeted for urge urinary incontinence
Piyasena Hewawasam, Matthew Erway, George Thalody, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
December 21, 2004
BL-1249 [(5,6,7,8-tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties
Svetlana Tertyshnikova, Ronald J Knox, Mary Jane Plym, 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 delivery
Prasad 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 1
Xiaojun Han, Rita L Civiello, Charles M Conway, 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 2
Xiaojun 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 antagonists
Stephen 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 exposure
Andrew P Degnan, Prasad V Chaturvedula, Charles M Conway, et al.
Plos Genetics
|
May 10, 2006
Chemical genetics reveals an RGS/G-protein role in the action of a compound
Kevin Fitzgerald, Svetlana Tertyshnikova, Lisa Moore, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
The Journal of Urology
|
January 25, 2003
Partially purified Grammostola spatulata venom inhibits stretch activated calcium signaling in bladder myocytes and improves bladder compliance in an in vitro rat whole bladder model
Svetlana Tertyshnikova, James A Matson, George Thalody, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA
|
December 12, 2018
Assessing seizure liability using multi-electrode arrays (MEA)
Jingsong Fan, George Thalody, Jae Kwagh, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2002
The synthesis and structure-activity relationships of 1,3-diaryl 1,2,4-(4H)-triazol-5-ones: a new class of calcium-dependent, large conductance, potassium (maxi-K) channel opener targeted for urge urinary incontinence
Piyasena Hewawasam, Matthew Erway, George Thalody, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
December 21, 2004
BL-1249 [(5,6,7,8-tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine]: a putative potassium channel opener with bladder-relaxant properties
Svetlana Tertyshnikova, Ronald J Knox, Mary Jane Plym, 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 delivery
Prasad 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 1
Xiaojun Han, Rita L Civiello, Charles M Conway, 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 2
Xiaojun 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 antagonists
Stephen 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 exposure
Andrew P Degnan, Prasad V Chaturvedula, Charles M Conway, et al.
Plos Genetics
|
May 10, 2006
Chemical genetics reveals an RGS/G-protein role in the action of a compound
Kevin Fitzgerald, Svetlana Tertyshnikova, Lisa Moore, et al.
Page
of 2