17-PA

CAS No.
694438-95-4
Chemical Name:
17-PA
Synonyms
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
Molecular Formula:
C25H34O
Molecular Weight:
350.54
MDL Number:
MFCD09971119
MOL File:
694438-95-4.mol
Last updated:2023-05-18 11:31:09

17-PA Properties

storage temp. Store at RT
solubility <8.76mg/ml in DMSO; <17.53mg/ml in ethanol

17-PA price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Tocris 2681 17-PA ≥99%(HPLC) 694438-95-4 10 $217 2021-12-16 Buy
Tocris 2681 17-PA ≥99%(HPLC) 694438-95-4 50 $870 2021-12-16 Buy
Usbiological 254348 17-PA 694438-95-4 10mg $579 2021-12-16 Buy
TRC P133880 17-PA 694438-95-4 25mg $365 2021-12-16 Buy
ApexBio Technology B7151 17-PA 694438-95-4 10mg $408 2021-12-16 Buy
Product number Packaging Price Buy
2681 10 $217 Buy
2681 50 $870 Buy
254348 10mg $579 Buy
P133880 25mg $365 Buy
B7151 10mg $408 Buy

17-PA Chemical Properties,Uses,Production

Uses

17-PA is an antagonist of neurosteroid GABA potentiation.

Biological Activity

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.

Enzyme inhibitor

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 Preparation Products And Raw materials

Raw materials

Preparation Products

17-PA Suppliers

Global( 18)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8449 60
Shanghai Rechem science Co., Ltd. 21-31433387 15618786686 sales@rechemscience.com China 2983 58
BOC Sciences -- info@bocsci.com USA 0 65
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
JinOu Biomedical (Nanjing) Co., Ltd. 13000000000 jinoupharma@163.com China 11732 58
TargetMol Chemicals Inc. 4008200310 marketing@tsbiochem.com China 24131 58
Shanghai Tachizaki Biomedical Research Center 18014399201 sales@chemlab-tachizaki.com China 2488 58

694438-95-4(17-PA)Related Search:

17-PA 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)- 17-Phenyl-(3α,5α)-androst-16-en-3-ol 17PA,17 PA 694438-95-4 C25H34O