grade
analytical standard
Quality Level
assay
≥98.5% (HPLC)
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
292 °C (dec.) (lit.)
application(s)
food and beverages
format
neat
SMILES string
[H][C@@]12CC[C@]3(C)[C@]([H])(CC=C4[C@]5([H])[C@@H](C)[C@H](C)CC[C@@]5(CC[C@@]34C)C(O)=O)[C@@]1(C)CC[C@H](O)C2(C)C
InChI
1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1
InChI key
WCGUUGGRBIKTOS-GPOJBZKASA-N
General description
熊果酸属于三萜类化合物,广泛存在于草药、食品和其他植物中。它可能具有药理活性,如心脏保护、镇痛、强心、镇静和滋补作用。
Application
有关合适仪器技术的更多信息,请参考产品′s分析证书。如需进一步支持,请联系技术服务。
Biochem/physiol Actions
三萜类化合物存在于苹果等各类水果中,它是一种心脏保护剂和抗肿瘤剂。由于它能够抑制淀粉样蛋白β和CD36受体之间的相互作用,因此在研究中被用作潜在的阿尔茨海默氏病治疗剂。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
580.5 °F
flash_point_c
304.7 °C
ppe
Eyeshields, Gloves, type N95 (US)
Pharmacology of oleanolic acid and ursolic acid
Liu J
Journal of Ethnopharmacology, 49, 57-68 (1995)
Jin-Feng Hu et al.
Journal of natural products, 69(1), 118-120 (2006-01-31)
One new (1) and four known (2-5) ursene triterpenes with potent inhibition of the formation of the bacterial biofilm Pseudomonas aeruginosa PA01 were obtained from Diospyros dendo using a high-throughput natural products chemistry procedure. These compounds were isolated as mass-limited
Huang-Yao Tu et al.
Bioorganic & medicinal chemistry, 17(20), 7265-7274 (2009-09-18)
Twenty-three ursolic acid (1) derivatives 2-24 including nine new 1 derivatives 5, 7-11, 20-22 were synthesized and evaluated for cytotoxicities against NTUB1 cells (human bladder cancer cell line). Compounds 5 and 17 with an isopropyl ester moiety at C-17-COOH and
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 89797-25MG-F | 04061833278444 |
| 89797-5MG-F | 04061833077047 |