Conivaptan hydrochloride

Discontinued Product

6830 has been discontinued.

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说明: Very high affinity vasopressin V1A and V2 antagonist; orally bioavailable
化学名: N-[4-[(4,5-Dihydro-2-methylimidazo[4,5-d][benzazepin-6(1H)-yl)carbonyl]phenyl-[1,1'-biphenyl]-2-carboxamide hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献
评论
文献 (1)

生物活性 for Conivaptan hydrochloride

Conivaptan hydrochloride is a very high affinity vasopressin V1A and V2 antagonist (Ki values are 0.61 and 0.66 - 3.04 nM, respectively). Inhibits vasopressin-induced pressor responses in rats without altering blood pressure, and increases urine flow while decreasing urine osmolality. Orally bioavailable.

化合物库 for Conivaptan hydrochloride

Conivaptan hydrochloride is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for Conivaptan hydrochloride

分子量 535.04
公式 C32H26N4O2.HCl
储存 Desiccate at RT
纯度 ≥98% (HPLC)
CAS Number 168626-94-6
PubChem ID 151171
InChI Key IKENVDNFQMCRTR-UHFFFAOYSA-N
Smiles CC1=NC2=C(C3=CC=CC=C3N(C(C4=CC=C(C=C4)NC(C5=C(C6=CC=CC=C6)C=CC=C5)=O)=O)CC2)N1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

产品说明书 for Conivaptan hydrochloride

参考文献 for Conivaptan hydrochloride

参考文献是支持产品生物活性的出版物。

Tahara et al (1997) Pharmacological profile of YM087, a novel potent nonpeptide vasopressin V1A and V2 receptor antagonist, in vitro and in vivo. J.Pharmacol.Exp.Ther. 282 301 PMID: 9223568

Yatsu et al (1997) Pharmacological profile of YM087, a novel nonpeptide dual vasopressin V1A and V2 receptor antagonist, in dogs. Eur.J.Pharmacol. 321 225 PMID: 9063692

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关键词: Conivaptan hydrochloride, Conivaptan hydrochloride supplier, conivaptan, HCl, very, high, affinity, vasopressin, V1A, V2, antagonists, antagonism, AVP, orally, bioavailable, Vasopressin, Receptors, 6830, Tocris Bioscience

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