CAS 10070-48-1

Lup-20(29)-ene-3,16-diol, (3β,16β)-

Description:

Lup-20(29)-ene-3,16-diol, also known by its CAS number 10070-48-1, is a triterpenoid compound derived from the lupane family of natural products. This substance is characterized by its tetracyclic structure, which includes a fused cyclopentane and cyclohexane ring system. The presence of hydroxyl groups at the 3 and 16 positions contributes to its chemical reactivity and potential biological activity. Triterpenoids like this compound are often found in various plants and have been studied for their pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. The stereochemistry of the compound, indicated by the (3β,16β) configuration, plays a crucial role in its interaction with biological targets. Additionally, lupane derivatives are of interest in the field of natural product chemistry and may have applications in herbal medicine and therapeutic development. Overall, Lup-20(29)-ene-3,16-diol represents a significant compound within the realm of phytochemistry and natural product research.

Formula: C₃₀H₅₀O₂

InChI: InChI=1S/C30H50O2/c1-18(2)19-11-14-28(6)24(32)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1

InChI key: InChIKey=AJBZENLMTKDAEK-SKESNUHASA-N

SMILES: C[C@]12[C@@]3(C)[C@@]([C@@]4([C@@](C)([C@@H](O)C3)CC[C@H]4C(C)=C)[H])(CC[C@@]1([C@]5(C)[C@@](CC2)(C(C)(C)[C@@H](O)CC5)[H])[H])[H]

Synonyms:

• Calenduladiol
• Lup-20(30)-ene-3β,16β-diol
• Lup-20(29)-ene-3,16-diol, (3β,16β)-
• NSC 133914
• Thurberin

Calenduladiol

Controlled Product

CAS: 10070-48-1

Calenduladiol is a bioactive compound, which is a phytochemical extracted from the Calendula officinalis plant. This compound has been isolated from the natural resin of the plant's flowers, where it plays a role in the plant's defense and healing mechanisms. The mode of action of Calenduladiol involves modulation of inflammatory pathways through the inhibition of pro-inflammatory cytokines and the promotion of tissue repair. It interacts with cellular receptors to attenuate inflammatory cascades and enhance regenerative processes.

Formula: C₃₀H₅₀O₂

Purity: Min. 95%

Molecular weight: 442.7 g/mol

Ref: 3D-KAA07048