567-03-3
Chemical Structure
Tetrahydrodeoxycorticosterone
Synonym(s): Tetrahydro-11-deoxycorticosterone
- CAS No.: 567-03-3
- Formula:C21H34O3
- Molecular Weight:334.49
IUPAC Name: 2-hydroxy-1-((3R,5R,8R,9S,10S,13S,14S,17S)-3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethan-1-one
InChIKey: CYKYBWRSLLXBOW-DATPGIFZSA-N
SMILES: C[C@@]12[C@@H](C(CO)=O)CC[C@@]1([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC2
Biological Activity: Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Tetrahydrodeoxycorticosterone | 99.45% | Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Tetrahydrodeoxycorticosterone-d3 | 99.53% | Tetrahydrodeoxycorticosterone-d3 is the deuterium labeled Tetrahydrodeoxycorticosterone. Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
-
Similarity Score 1.00
HY-1234893α,21-Dihydroxy-5α-pregnan-20-one -
Similarity Score 1.00
HY-123489S3α,21-Dihydroxy-5α-pregnan-20-one-d3 -
Similarity Score 1.00
HY-124463Epiallopregnanolone -
Similarity Score 0.83
HY-148156Hydroxydione -
Similarity Score 0.83
HY-W7438705α-Dihydrodeoxycorticosterone -
Similarity Score 0.82
HY-117979Alphadolone -
Similarity Score 0.82
HY-W588255Tetrahydro-11-dehydrocorticosterone -
Similarity Score 0.81
HY-1133645α-Tetrahydrocorticosterone -
Similarity Score 0.81
HY-113422Tetrahydrocorticosterone -
Explore the MedChemAI to find more analogs
References
- [1]. Hua-Jun Feng, et al. Comparison of αβδ and αβγ GABA A receptors: Allosteric modulation and identification of subunit arrangement by site-selective general anesthetics. Pharmacol Res. 2018 Jul;133:289-300. [Content Brief]
- [2]. Roger F Butterworth. Neurosteroids in hepatic encephalopathy: Novel insights and new therapeutic opportunities. J Steroid Biochem Mol Biol. 2016 Jun;160:94-7. [Content Brief]
