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  7. 17-PA, Tocris Bioscience™

17-PA, Tocris Bioscience™

Catalog Number p-4783680
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Quantity:
10 mg
50 mg
This item is not returnable. View return policy
694438-95-4
C25H34O
350.546
SINAMTXBCYKFDL-WBJZGETLSA-N
17-phenyl-3?,5?-androst-16-en-3-ol, 3alpha,5alpha-17-phenylandrost-16-en-3-ol, 3alpha,5alpha-17-phenylandrosta-16-ene-3-ol
25068278
(3R,5S,8R,9S,10S,13S,14S)-10,13-dimethyl-17-phenyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
CC12CCC(CC1CCC3C2CCC4(C3CC=C4C5=CC=CC=C5)C)O
This item is not returnable. View return policy
694438-95-4
C25H34O
350.546
SINAMTXBCYKFDL-WBJZGETLSA-N
17-phenyl-3?,5?-androst-16-en-3-ol, 3alpha,5alpha-17-phenylandrost-16-en-3-ol, 3alpha,5alpha-17-phenylandrosta-16-ene-3-ol
25068278
(3R,5S,8R,9S,10S,13S,14S)-10,13-dimethyl-17-phenyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
CC12CCC(CC1CCC3C2CCC4(C3CC=C4C5=CC=CC=C5)C)O

Description

Antagonist of neurosteroid potentiation and direct gating of GABAA

Selective antagonist of neurosteroid potentiation and direct gating of GABAA receptors. Selectively reduces the effects of 5α-reduced steroids compared to 5β-reduced steroids and displays no effect on potentiation evoked by barbiturates and benzodiazepines. Attenuates 3α,5α-THP-induced loss of righting reflex and total sleep time following i.c.v administration in rats.
Quantity 10 mg
Formula Weight 350.54
Percent Purity >99%
Chemical Name or Material 17-PA

Safety and Handling

Recommended Storage Store at Room Temperature
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