Required fields are marked with *

Verification code

Oleanolic acid

{PARAM:[Name]}({[CAS]})
Category Hepatitis C Virus (HCV)
CAS 508-02-1
Description Oleanolic Acid is a non-toxic, hepatoprotective triterpenoid found in Phytolacca Americana, which exerts antitumor and antiviral properties. Oleanolic Acid is a natural compound used in cosmetics material.
Quotation Now

Product Information

Synonyms Caryophyllin
Molecular Weight 456.7
Molecular Formula C30H48O3
Canonical SMILES CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C
InChI InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21-,22+,23-,27-,28+,29+,30-/m0/s1
InChIKey MIJYXULNPSFWEK-GTOFXWBISA-N
Purity >98%
Density 1.1 g/cm3
Solubility In vitro:
10 mM in DMSO
Appearance Powder
Application anti-inflammatory; antiulcer;
Storage Powder:
-20°C: 3 years
4°C: 2 years
In solvent:
-80°C: 6 months
-20°C: 1 month
Complexity 885
Exact Mass 456.36034539
In Vitro Oleanolic acid (OA) suppresses the proliferation of lung cancer cells in both dose- and time-dependent manners, along with an increase in miR-122 abundance. CCNG1 and MEF2D, two putative miR-122 targets, are found to be downregulated by OA treatment. OA induces Autophagy in normal tissue-derived cells without cytotoxicity. OA-induced Autophagy is shown to decrease the proliferation of KRAS-transformed normal cells and to impair their invasion and anchorage-independent growth.
PSA 116.45000
Target Autophagy; Endogenous Metabolite; HIV
XLogP3-AA 7.5

QC Data

TAKE YOUR NEXT STEPS

Get Started With Our Industry Experience And Client-Centric Focus!

Talk to Us

Copyright © 2025 BOC Sciences. All rights reserved.