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| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Basic Description
| Synonyms | 3β,5α-Tetrahydrodeoxycorticosterone; Epiallopregnanolone |
|---|---|
| Storage Temp | Room temperature |
| Shipped In | Normal |
| Product Description | 3β,21-Dihydroxy-5α-pregnan-20-one is a sterol derivative that is structurally related to other progesterone-type sterols that have been shown to be neuroactive and are thought to regulate various physiological functions. One study showed that some neuroactive steroids can sensitize GABA receptors to its corresponding ligand - gamma-amino butyric acid. |
Associated Targets(Human)
G6PD Tchem Glucose-6-phosphate 1-dehydrogenase (1 Activities)
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
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CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
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CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
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G6PD Tchem Glucose-6-phosphate 1-dehydrogenase (778 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP1A1 Tchem Cytochrome P450 1A (45 Activities)
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Names and Identifiers
| IUPAC Name | 2-hydroxy-1-[(3S,5S,8R,9S,10S,13S,14S,17S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone |
|---|---|
| INCHI | InChI=1S/C21H34O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h13-18,22-23H,3-12H2,1-2H3/t13-,14-,15-,16-,17-,18+,20-,21-/m0/s1 |
| InChi Key | CYKYBWRSLLXBOW-VTBMCCKRSA-N |
| Canonical SMILES | CC12CCC(CC1CCC3C2CCC4(C3CCC4C(=O)CO)C)O |
| Isomeric SMILES | C[C@]12CC[C@@H](C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4C(=O)CO)C)O |
| WGK Germany | 3 |
| PubChem CID | 11877475 |
| Molecular Weight | 334.49 |
Certificates
Certificate of Analysis(COA)
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Safety and Hazards(GHS)
| WGK Germany | 3 |
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