Oleanonic acid


CAS No. : 17990-42-0

(Synonyms: 3-Oxooleanolic acid)

17990-42-0
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Cat. No. : HY-N1487
M.Wt: 454.68
Formula: C30H46O3
Purity: >98 %
Solubility: H2O : ≥ mg/mL;DMSO : 50 mg/mL (ultrasonic)
Introduction of 17990-42-0 :

Oleanonic acid (3-Oxooleanolic acid) is an orally available triterpene that has anti-inflammatory and insecticidal properties. In vitro, oleanonic acid can improve oxidative stress, autophagy defects, ferroptosis, mitochondrial damage, and endoplasmic reticulum stress induced by Amyloid-β, and in vivo, it can alleviate myocardial hypertrophy in rats[1][2][3][4][5]. In Vitro:Oleanonic acid inhibits HIV-1 infection in PBMCs in vitro, with EC50 values for naturally infected PBMCs and monocytes/macrophages being 22.7 mM, 24.6 mM, and 57.4 mM, respectively. Furthermore, it can inhibit the production of leukotriene B4 by mouse peritoneal leukocytes, with an IC50 of 17 μM[2].
Oleanonic acid has strong anti-insect activity against Rhipicephalus (Kreyszig) and Amazon ticks, with IC50 values of 18.5 µM and 29.9 µM[3].
Oleanonic acid (0-45 μM, 24 h) inhibits the increase of NF-κB transcription activity in cardiomyocytes treated with phenylephrine (PE) and reduces the mRNA expression of hypertrophic genes like atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) in a dose-dependent manner[4].
Oleanonic acid (15 μM, 24 h) inhibits the phosphorylation of protein kinase Cζ (PKCζ) at the Thr410 site in cardiomyocytes, subsequently reducing NF-κB activation in PE-treated cardiomyocytes[4].
Oleanonic acid (1-5 μM, 48 h) reduces APP expression in SH-SY5Y cells, lessens damage induced by oxidative stress, repairs autophagy defects, and inhibits ferroptosis[5]. In Vivo:Oleanonic acid (15-45 mg/kg, oral, daily, 8 weeks) inhibits the PKCζ-NF-κB signaling pathway in rats and effectively improves cardiac hypertrophy[4].

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