Acetyl podocarpic acid anhydride

• CAT Number: I011652
• CAS Number: 344327-48-6
• Molecular Formula: C38H46O7
• Molecular Weight: 614.77
• Purity: ≥95%
• Synonyms: [(1S,4aS,10aR)-6-acetyloxy-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbonyl] (1S,4aS,10aR)-6-acetyloxy-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylate
• InChI: InChI=1S/C38H46O7/c1-23(39)43-27-13-9-25-11-15-31-35(3,29(25)21-27)17-7-19-37(31,5)33(41)45-34(42)38(6)20-8-18-36(4)30-22-28(44-24(2)40)14-10-26(30)12-16-32(36)38/h9-10,13-14,21-22,31-32H,7-8,11-12,15-20H2,1-6H3/t31-,32-,35-,36-,37+,38+/m1/s1
• InChIKey: OUJQRQRBNRGQTC-SPGSYPTKSA-N
• SMILES: CC(=O)OC1=CC2=C(CC[C@@H]3[C@@]2(CCC[C@]3(C)C(=O)OC(=O)[C@]4(CCC[C@]5([C@H]4CCC6=C5C=C(C=C6)OC(=O)C)C)C)C)C=C1

Acetyl podocarpic acid anhydride（Cat No.:I011652）is a chemically modified derivative of podocarpic acid, a natural diterpenoid found in species of the Podocarpus genus. By forming an anhydride and introducing an acetyl group, this compound gains enhanced reactivity, making it useful in synthetic organic chemistry and medicinal chemistry research. It serves as an intermediate for developing anti-inflammatory, antimicrobial, or anticancer agents due to the bioactivity associated with podocarpic acid analogs. Researchers explore its structure–activity relationships to design novel therapeutics or bioactive molecules with improved pharmacological profiles and selectivity.