17-PA

17-PA 구조식 이미지
카스 번호:
694438-95-4
상품명:
17-PA
동의어(영문):
17-PA;17PA,17 PA;17-Phenyl-(3α,5α)-androst-16-en-3-ol;17-PHENYL-(3A,5A)-ANDROST-16-EN-3-OL;17-Phenyl-(3α,5α)-androst-16-en-3-ol;Androst-16-en-3-ol, 17-phenyl-, (3α,5α)-
CBNumber:
CB52453436
분자식:
C25H34O
포뮬러 무게:
350.54
MOL 파일:
694438-95-4.mol

17-PA 속성

저장 조건
Store at RT
용해도
<8.76mg/ml in DMSO; <17.53mg/ml in ethanol

안전

17-PA C화학적 특성, 용도, 생산

용도

17-PA is an antagonist of neurosteroid GABA potentiation.

생물학적 활성

Selective antagonist of neurosteroid potentiation and direct gating of GABA A receptors. Selectively reduces the effects of 5 α -reduced steroids compared to 5 β -reduced steroids and displays no effect on potentiation evoked by barbiturates and benzodiazepines. Attenuates 3 α ,5 α -THP-induced loss of righting reflex and total sleep time following i.c.v administration in rats.

효소 저해제

This selective neurosteroid antagonist (FW = 350.54 g/mol; CAS 694438- 95-4; Soluble to 25 mM in DMSO and to 50 mM in ethanol), also known as 17-PA, targets neurosteroid potentiation and directly gates GABAA receptors. 17-PA inhibition was also useful in demonstrating that ethanol modulates the interaction of the endogenous neurosteroid allopregnanolone with the α1β2γ2L GABAA receptor. 17-PA selectively reduces the effects of 5α-reduced steroids compared to 5β-reduced steroids and displays no effect on potentiation evoked by barbiturates and benzodiazepines. It also attenuates 3α,5α-THP-induced loss of righting reflex and total sleep time, following intracerebroventricular administration in rats.

17-PA 준비 용품 및 원자재

원자재

준비 용품


17-PA 공급 업체

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Shanghai Tachizaki Biomedical Research Center 18014399201
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