D-Ethyl gonendione

CAS: 21800-83-9

Ref. 3D-FE23047

Produktinformation

• Name: D-Ethyl gonendione
• Synonyme: 13-Ethyl-gon-4-ene-3,17-dione(+)-13-Ethylgon-4-ene-3,17-dione(+)-13-b-Ethylgon-4-ene-3,17-dione, (+)-13-Ethylgon-4-ene-3,17-dione, (+)-13β-Ethylgon-4-ene-3,17-dione, (8R,9S,10R,13S,14S)-13-ethyl-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione (non-preferred name), (8R,9S,10R,14S)-13-Ethyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione, (8R,9S,10R,14S)-13-ethyl-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione (non-preferred name), 13-Ethyl-gon-4-ene-3,17-dione, 13β-Ethylgon-4-en-3,17-dione, 18-Methyl-19-norandrost-4-ene-3,17-dione, 18-Methyl-estr-4-ene-3,17-dione, 18-Methylestr-4-ene-3,17-dione, 18a-Homo-19-norandrost-4-ene-3,17-dione, Gon-4-ene-3,17-dione, 13-ethyl-

Beschreibung

D-Ethyl gonendione is a metabolite of the sex hormones testosterone and estrogen. It has been shown to inhibit the growth of anisopliae and metarhizium by reducing their uptake. D-Ethyl gonendione also inhibits the growth of pastoris and microbial transformation as well as inhibiting the uptake of solubilized compounds. The compound has been shown to be metabolized through a number of metabolic transformations, including hydroxylation by cytochrome p450 enzymes, which is necessary for its activity as a contraceptive. D-Ethyl gonendione also binds to DNA, specifically to dinucleotide phosphate, which may account for some of its activity.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 286.41 g/mol
• Formel: C₁₉H₂₆O₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C19H26O2/c1-2-19-10-9-15-14-6-4-13(20)11-12(14)3-5-16(15)17(19)7-8-18(19)21/h11,14-17H,2-10H2,1H3/t14-,15+,16+,17-,19-/m0/s1
• InChI Key: InChIKey=SBLHOJQRZNGHLQ-ATIFRJIPSA-N
• SMILES: CC[C@]12CC[C@@H]3[C@H]4CCC(=O)C=C4CC[C@H]3[C@@H]1CCC2=O