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George Thalody

Showing results (1-10 of 12) with videos related to

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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 modelSvetlana 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 incontinencePiyasena 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 propertiesSvetlana 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 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|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.
Plos Genetics|May 10, 2006
Chemical genetics reveals an RGS/G-protein role in the action of a compoundKevin Fitzgerald, Svetlana Tertyshnikova, Lisa Moore, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 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 modelSvetlana 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 incontinencePiyasena 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 propertiesSvetlana 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 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|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.
Plos Genetics|May 10, 2006
Chemical genetics reveals an RGS/G-protein role in the action of a compoundKevin Fitzgerald, Svetlana Tertyshnikova, Lisa Moore, et al.
Pageof 2