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Conivaptan impurity

CAS No.
1129433-63-1
Chemical Name:
Conivaptan impurity
Synonyms
Conivaptan-d4;N-[4-[(4,5-dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl-d4]-[1,1'-biphenyl]-2-carboxamide
CBNumber:
CB03144862
Molecular Formula:
C32H26N4O2
Molecular Weight:
498.59
MDL Number:
MOL File:
1129433-63-1.mol
Last updated:2023-05-21 10:59:17

Conivaptan impurity Properties

storage temp. Store at -20°C
solubility DMSO: soluble
form A solid

Conivaptan impurity price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 26455 Conivaptan-d4 1129433-63-1 500μg $194 2024-03-01 Buy
Cayman Chemical 26455 Conivaptan-d4 1129433-63-1 1mg $369 2024-03-01 Buy
AK Scientific 3226DC 2-Phenyl-N-[2,3,5,6-tetradeuterio-4-(2-methyl-4,5-dihydro-3H-imidazo[4,5-d][1]benzazepine-6-carbonyl)phenyl]benzamide 1129433-63-1 1mg $753 2021-12-16 Buy
Product number Packaging Price Buy
26455 500μg $194 Buy
26455 1mg $369 Buy
3226DC 1mg $753 Buy

Conivaptan impurity Chemical Properties,Uses,Production

Biological Activity

Conivaptan-d4 is intended for use as an internal standard for the quantification of conivaptan by GC- or LC-MS. Conivaptan is an antagonist of the arginine vasopressin (AVP) receptors V1A and V2 (Kis = 0.48 and 3.04 nM for rat liver V1A and kidney V2, respectively).1 It also competitively inhibits oxytocin binding to rat uterine oxytocin receptors (Ki = 44 nM) but has no effect on AVP binding to anterior pituitary V1B receptors at concentrations up to 100 μM in a radioligand binding assay. Conivaptan suppresses AVP-induced increases in intracellular calcium in vascular smooth muscle cells (VSMCs) in vitro and the pressor response in pithed rats. Conivaptan (0.01-0.3 mg/kg, i.v.) increases urine output and decreases urine osmolality in dehydrated conscious rats in a dose-dependent manner. It also reduces brain edema and blood-brain barrier disruption in a mouse experimental stroke model.2

References

1.Tahara, A., Tomura, Y., Wada, K.-I., et al.Pharmacological profile of YM087, a novel potent nonpeptide vasopressin V1A and V2 receptor antagonist, in vitro and in vivoJ. Pharmacol. Exp. Ther.282(1)301-308(1997) 2.Zeynalov, E., Jones, S.M., Seo, J.W., et al.Arginine-vasopressin receptor blocker conivaptan reduces brain edema and blood-brain barrier disruption after experimental stroke in micePLoS One10(8)e0136121(2015)

Conivaptan impurity Preparation Products And Raw materials

Raw materials

Preparation Products

Conivaptan impurity Suppliers

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Pharmacodia (Beijing) Co.,Ltd +86-400-851-9921 sales@pharmacodia.com China 2317 55
SHENZHEN PHYSTANDARD BIO-TECH CO.,LTD 0755-0755-0755-83725350 13380397412 3001280422@qq.com China 9924 58
Shanghai isotope chemical co.,ltd 021-021-51600108 13062666369 sales@chinaisotope.com China 4272 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
Hubei Moco Chemical Co., Ltd. 17386083646 2853567991@qq.com China 10469 58
Conivaptan-d4 N-[4-[(4,5-dihydro-2-methylimidazo[4,5-d][1]benzazepin-6(1H)-yl)carbonyl]phenyl-d4]-[1,1'-biphenyl]-2-carboxamide 1129433-63-1