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| | 19-HYDROXY-4-ANDROSTENE-3,17-DIONE Basic information |
| Product Name: | 19-HYDROXY-4-ANDROSTENE-3,17-DIONE | | Synonyms: | 19-HYDROXY-4-ANDROSTEN-3,17-DIONE;19-HYDROXY-4-ANDROSTENE-3,17-DIONE;19-HYDROXYANDROSTENDIONE;19-HYDROXYANDROSTENEDIONE;Androst-4-ene-3,17-dione, 19-hydroxy-;19-hydroxyandrost-4-ene-3,17-dione;4-ANDROSTENE-3,17-DIONE-19-0L;4-ANDROSTENE-3,17-DIONE-19-OL | | CAS: | 510-64-5 | | MF: | C19H26O3 | | MW: | 302.41 | | EINECS: | 208-116-5 | | Product Categories: | All Inhibitors;Inhibitors;Steroids | | Mol File: | 510-64-5.mol |  |
| | 19-HYDROXY-4-ANDROSTENE-3,17-DIONE Chemical Properties |
| Melting point | 168-169 °C(lit.) | | Boiling point | 485.4±45.0 °C(Predicted) | | density | 1.19±0.1 g/cm3(Predicted) | | storage temp. | Sealed in dry,Store in freezer, under -20°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 14.90±0.10(Predicted) | | form | Solid | | color | Off-White to Pale Yellow | | Optical Rotation | [α]/D +190±5°, c = 1 in chloroform | | BRN | 2567249 | | InChI | InChI=1S/C19H26O3/c1-18-8-7-16-14(15(18)4-5-17(18)22)3-2-12-10-13(21)6-9-19(12,16)11-20/h10,14-16,20H,2-9,11H2,1H3/t14-,15-,16-,18-,19+/m0/s1 | | InChIKey | XGUHPTGEXRHMQQ-BGJMDTOESA-N | | SMILES | C1(=O)C=C2[C@](CO)(CC1)[C@]1([H])[C@]([H])([C@@]3([H])[C@@](CC1)(C)C(=O)CC3)CC2 | | CAS DataBase Reference | 510-64-5(CAS DataBase Reference) | | NIST Chemistry Reference | 19-Hydroxyandrost-4-ene-3,17-dione(510-64-5) |
| | 19-HYDROXY-4-ANDROSTENE-3,17-DIONE Usage And Synthesis |
| Chemical Properties | Off-White Solid | | Uses | 19-Hydroxyandrostendione is a novel substituted estrogen as aromatase inhibitor. It induces neuroendocrine trans-differentiation of prostate cancer cells via an ectopic olactory receptor. | | Definition | ChEBI: 19-hydroxyandrost-4-ene-3,17-dione is a 19-hydroxy steroid, a 3-oxo steroid, a 17-oxo steroid and an androstanoid. It has a role as a mouse metabolite. | | IC 50 | Human Endogenous Metabolite | | Purification Methods | Recrystallise 19-hydroxy-4-androsten-3,17-dione from Me2CO/hexane or Et2O/hexane. It has UV with max at 242nm in EtOH or MeOH. The 19-acetoxy derivative has [] 26D +185o (CHCl3) and max 237.5nm in EtOH. [Ehrenstein & Dünnenberger J Org Chem 21 774 1956, Beilstein 8 IV2162.] |
| | 19-HYDROXY-4-ANDROSTENE-3,17-DIONE Preparation Products And Raw materials |
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