| Weight | 456.711 g/mol |
|---|---|
| Formula | C30H48O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
OLEANOLIC ACID (508-02-1)
Oleanane Triterpenes · Oleanol · Hederins
Score:
#1770 in Biochemistry
,
#3886 in Biology
,
#4896 in Chemistry
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- Sigma-Aldrich - OLEANOLIC ACID87.30 - 302.50 USD
- Fisher Scientific - Search for OLEANOLIC ACID
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- Pharmacology of oleanolic acid and ursolic acid (Journal of Ethnopharmacology, 1995)
- Oleanolic acid and ursolic acid: Research perspectives (Journal of Ethnopharmacology, 2005)
- Complete assignments of 1H and 13C NMR resonances of oleanolic acid, 18oleanolic acid, ursolic acid and their 11oxo derivatives (Magnetic Resonance in Chemistry, 2003)
- Pentacyclic Triterpenes of the Lupane, Oleanane and Ursane Group as Tools in Cancer Therapy (Planta Medica, 2009)
- Anti-AIDS agents. 30. Anti-HIV activity of oleanolic acid, pomolic acid, and structurally related triterpenoids. (Journal of Natural Products, 1998)
- Antiinflammatory activity of oleanolic acid in rats and mice (Journal of Pharmacy and Pharmacology, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Oleanane Triterpenes
- Oleanol
- Hederins
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SMILESCC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C
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InChIKeyMIJYXULNPSFWEK-UHFFFAOYSA-N
- Pubchem - OLEANOLIC ACID
- Wikipedia - oleanolic acid
Oleanolic acid or oleanic acid is a naturally occurring pentacyclic triterpenoid related to betulinic acid. It is widely distributed in food and plants where it exists as a free acid or as an aglycone of triterpenoid saponins.
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OLEANOLIC ACID
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