Oleanonic Acid (CAS 17990-42-0)
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Oleanonic acid is a triterpenoid compound that has interest in various fields of research due to its unique structure and properties. In plant science, it is studied for its role in plant defense mechanisms and as a precursor in the biosynthesis of other biologically active triterpenoids. Chemists investigate oleanonic acid for its potential as a starting material in the synthesis of complex organic molecules, taking advantage of its rigid, polycyclic framework. The compound′s presence in certain plant species makes it a point of focus in botanical studies, particularly in relation to plants′ adaptive responses to environmental stressors. Additionally, oleanonic acid is utilized in material sciences, where researchers explore its incorporation into novel compounds with potential industrial applications, such as natural product-based catalysts and new materials with unique characteristics derived from its hydrophobicity and stability.
Oleanonic Acid (CAS 17990-42-0) References
- Oleanonic acid, a 3-oxotriterpene from Pistacia, inhibits leukotriene synthesis and has anti-inflammatory activity. | Giner-Larza, EM., et al. 2001. Eur J Pharmacol. 428: 137-43. PMID: 11779030
- Two new pentacyclic triterpenoids from Lantana camara LINN. | Begum, S., et al. 2008. Chem Pharm Bull (Tokyo). 56: 1317-20. PMID: 18758109
- Oxidation of oleanolic acid ofAvicennia officinalis leaves to oleanonic acid in the natural environment of Sunderban mangrove ecosystem. | Misra, S., et al. 1985. J Chem Ecol. 11: 339-42. PMID: 24309965
- Constituents of the roots and leaves of Ekebergia capensis and their potential antiplasmodial and cytotoxic activities. | Irungu, BN., et al. 2014. Molecules. 19: 14235-46. PMID: 25211004
- Nematicidal triterpenoids from Lantana camara. | Begum, S., et al. 2015. Chem Biodivers. 12: 1435-42. PMID: 26363887
- A simple and reliable analytical method based on HPLC-UV to determine oleanonic acid content in Chios gum mastic for quality control. | Jin, Y., et al. 2017. Arch Pharm Res. 40: 49-56. PMID: 27858280
- Synthesis and Cytotoxic Activity of Triterpenoid Thiazoles Derived from Allobetulin, Methyl Betulonate, Methyl Oleanonate, and Oleanonic Acid. | Borkova, L., et al. 2017. ChemMedChem. 12: 390-398. PMID: 28084676
- Oleanonic acid ameliorates pressure overload-induced cardiac hypertrophy in rats: The role of PKCζ-NF-κB pathway. | Gao, H., et al. 2018. Mol Cell Endocrinol. 470: 259-268. PMID: 29138023
- Repeated dose (90 days) oral toxicity study of ursolic acid in Han-Wistar rats. | Geerlofs, L., et al. 2020. Toxicol Rep. 7: 610-623. PMID: 32435599
- Herb-drug interaction between Styrax and warfarin: Molecular basis and mechanism. | Zhang, F., et al. 2020. Phytomedicine. 77: 153287. PMID: 32739573
- wSDTNBI: a novel network-based inference method for virtual screening. | Wu, Z., et al. 2022. Chem Sci. 13: 1060-1079. PMID: 35211272
- Screening of Botanical Drugs against SARS-CoV-2 Entry Reveals Novel Therapeutic Agents to Treat COVID-19. | Cao, J., et al. 2022. Viruses. 14: PMID: 35215943
- Hypoglycaemic activity of Oleanonic acid, a 3-oxotriterpenoid isolated from Aidia Genipiflora (DC.) Dandy, involves inhibition of carbohydrate metabolic enzymes and promotion of glucose uptake. | Harley, BK., et al. 2022. Biomed Pharmacother. 149: 112833. PMID: 35316751
- Metabolite and Gene Expression Analysis Underlying Temporal and Spatial Accumulation of Pentacyclic Triterpenoids in Jujube. | Wen, C., et al. 2022. Genes (Basel). 13: PMID: 35627208
- Triterpenoid pyrazines and pyridines - Synthesis, cytotoxicity, mechanism of action, preparation of prodrugs. | Hodoň, J., et al. 2022. Eur J Med Chem. 243: 114777. PMID: 36174412
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Oleanonic Acid, 250 mg | sc-478580 | 250 mg | $380.00 |