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BMS-207940

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For Research Use Only | Not For Clinical Use
CATAP210891046
CAS210891-04-6
Structure
MDL NumberMFCD05260689
Molecular Weight536.64
InChI KeyORJRYNKVKJAJPY-UHFFFAOYSA-N
Description≥98% (HPLC)
SolubilityDMSO: 20 mg/mL, clear
Assay≥98% (HPLC)
Colorwhite to beige
Formpowder
Size5MG, 25MG
Storage Conditionsroom temp
1

11 C-BMS-5p and 18 F-FBzBMS: radiolabeled analogs of BMS-207940, a potent and selective antagonist of endothelin receptor subtype A

Arvind Chopra

PMID: 23833790

1

Biphenylsulfonamide Endothelin Receptor Antagonists. 4. Discovery of N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]- 2-yl]methyl]-N,3,3-trimethylbutanamide (BMS-207940), a Highly Potent and Orally Active ET(A) Selective Antagonist

Natesan Murugesan, Zhengxiang Gu, Steven Spergel, Marian Young, Ping Chen, Arvind Mathur, Leslie Leith, Mark Hermsmeier, Eddie C-K Liu, Rongan Zhang, Eileen Bird, Tom Waldron, Anthony Marino, Barry Koplowitz, etc.

J Med Chem. 2003 Jan 2;46(1):125-37.

PMID: 12502366

1

BMS-193884 and BMS-207940 Bristol-Myers Squibb

Martin Hulpke-Wette, Reiner Buchhorn

Curr Opin Investig Drugs. 2002 Jul;3(7):1057-61.

PMID: 12186267

1

Simulation of the Impact of Atropisomer Interconversion on Plasma Exposure of Atropisomers of an Endothelin Receptor Antagonist

Y S Zhou, L K Tay, D Hughes, S Donahue

J Clin Pharmacol. 2004 Jul;44(7):680-8.

PMID: 15199072

1

Synthesis and in Vivo Evaluation of Novel PET Radioligands for Imaging the endothelin-A Receptor

William B Mathews, Natesan Murugesan, Jinsong Xia, Ursula Scheffel, John Hilton, Hayden T Ravert, Robert F Dannals, Zsolt Szabo

J Nucl Med. 2008 Sep;49(9):1529-36.

PMID: 18703610

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