Bisnorcholenaldehyde

• CAT Number: R045507
• CAS Number: 3986-89-8
• Molecular Formula: C22H32O2
• Molecular Weight: 328.496
• Purity: ≥95%
• Synonyms: (20S)-3-Oxo-pregn-4-ene-20-carboxaldehyde;?3-Oxo-pregn-4-ene-20α-carboxaldehyde; (20S)-3-Oxopregn-4-ene-20-carboxaldehyde; 3-Oxo-23,24-dinorchol-4-en-22-al; 3-Oxopregn-4-ene-20-carboxaldehyde; Dinorcholenaldehyde; NSC 9738; U 3687
• Storage: Store at RT
• IUPAC Name: (2S)-2-[(8S,9S,10R,13S,14S,17R)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]propanal
• InChI: InChI=1S/C22H32O2/c1-14(13-23)18-6-7-19-17-5-4-15-12-16(24)8-10-21(15,2)20(17)9-11-22(18,19)3/h12-14,17-20H,4-11H2,1-3H3/t14-,17+,18-,19+,20+,21+,22-/m1/s1
• InChIKey: XVPJEGGIGJLDQK-HOFZUOGSSA-N
• SMILES: CC(C=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C

Bisnorcholenaldehyde is a steroidal compound derived from cholesterol. It lacks the characteristic four-carbon tail found in typical cholesterol molecules. This structural modification alters its biological activity and may confer unique properties. Bisnorcholenaldehyde is of interest in medicinal chemistry and drug development due to its potential pharmacological effects. Researchers explore its structure-activity relationships to understand its interactions with biological targets and its potential applications in treating various medical conditions.