3,29-O-Dibenzoyloxykarounidiol

• CAT Number: I044876
• CAS Number: 389122-01-4
• Molecular Formula: C44H56O4
• Molecular Weight: 648.91
• Purity: ≥95%
• Synonyms: [(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-benzoyloxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8,8a,10,11,12,14,14b-dodecahydropicen-2-yl]methyl benzoate
• InChI: InChI=1S/C44H56O4/c1-39(2)34-19-18-33-32(42(34,5)22-21-36(39)48-38(46)31-16-12-9-13-17-31)20-23-44(7)35-28-40(3,24-25-41(35,4)26-27-43(33,44)6)29-47-37(45)30-14-10-8-11-15-30/h8-18,20,34-36H,19,21-29H2,1-7H3/t34-,35+,36+,40+,41+,42+,43+,44-/m0/s1
• InChIKey: RTSZUVCSDUONDF-GJSTXJOSSA-N
• SMILES: C[C@]12CC[C@@C[C@H]1[C@@]3(CC=C4C(=CC[C@@H]5[C@@]4(CC[C@H](C5(C)C)OC(=O)C6=CC=CC=C6)C)[C@]3(CC2)C)C)(C)COC(=O)C7=CC=CC=C7

3,29-O-Dibenzoyloxykarounidiol（Cat No.:I044876）is a naturally occurring triterpenoid derivative characterized by two benzoyl ester groups at the 3 and 29 hydroxyl positions of the parent compound karounidiol. Isolated from Trichilia species, especially in the Meliaceae family, it features a limonoid-related framework with distinct oxygenation patterns. This compound exhibits notable bioactivities, including cytotoxic, antiproliferative, and anti-inflammatory effects, making it a candidate for anticancer and pharmacological research. Its structural complexity and functional groups contribute to its ability to modulate cellular pathways, suggesting potential applications in drug development and integrative medicine.