oleanolic acid

Oleanolic Acid (Caryophyllin) 是具有抗癌活性的一种天然产物。

Oleanolic acid hemiphthalate disodium salt is an anti-inflammatory agent.

4-Aza-Oleanolic acid methyl ester is a triterpenic derivative.

Oleanolic acid derivative 1 is a modified form of oleanolic acid.

Oleanolic acid derivative 2 is a derivative of oleanolic acid.

Compound J1 (3-Acetyl-28-N–(3–guanidinobutoxy)-oleanolic acid) 表现出优异的抗菌特性，并有效抗击革兰氏阳性菌和真菌。此化合物不仅能破坏细菌的细胞膜，还能插入DNA并与DNA促旋酶发生作用，从而增强其他抗生素的功效。此外，Compound J1 在小鼠的 MRSA 皮肤感染模型中显著减少了微生物数量，并加速了伤口的愈合。

Oleanolic acid-3-O-glucosyl(1-2)xylyl(1-3)glucosiduronic acid is a naturally occurring triterpene saponin.

Oleanolic acid acrylate (OAA) is an agonist of the serotonin (5-HT) receptor subtype 5-HT1A and a derivative of oleanolic acid. It is also a selective inhibitor of MAO-A with anti-depressant-like and anxiolytic activities.

18α-Oleanolic acid 是一种天然五环三萜酸，可从植物中提取。

Oleanolic acid 28-O-β-D-glucopyranoside (Beta-D-glucopyranosyl oleanolate) 是分离自Achyranthes bidentata 根中的一种皂苷。

Oleanolic acid 3-O-beta-D-glucosyl-(1->3)-alpha-L-rhamnosyl(1->2)-alpha-L-arabinoside is a natural product

3-O-Caffeoyl oleanolic acid exhibits in vitro cytotoxicity against the A549 cell line with the CC50 values of less than 20 ug mL.

Oleanolic acid-3-O-α-L-arabino pyranoside 是一种天然产物，可用作天然产物对照品，用于生命科学相关领域的研究，其产品编号为 TN8640。

3-o-β-D-glucopyranose-oleanolic acid-28-O-β-D-glucuronide 是一种天然产物，可用作天然产物对照品，用于生命科学相关领域的研究，其产品编号为 TN8866。

3-​O-​Acetyloleanolic acid 是从 Vigna sinensisK. 种子中提取得到的一种齐墩果醇酸，可诱导癌细胞凋亡并拥有抗血管生成作用。

3-Epioleanolic acid 是一种分离自马鞭草的有效成分，具有抗炎作用。

3-O-p-Coumaroyloleanolic acid 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN2976，CAS号为 151334-06-4。

OA-Br-1 是口服活性的PTP1B选择性抑制剂，IC50值为7.08 μM。它能够诱导细胞凋亡 (apoptosis) 并且具有广谱的抗癌细胞增殖活性。OA-Br-1 通过PTP1B PI3K AKT 信号通路在体内外对抗乳腺癌。

Fatsiaside C 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 T4069，CAS号为 60213-69-6。

α-Glucosidase-IN-3 是一种针对 α-葡萄糖苷酶和 α-淀粉酶的齐墩果酸肟酯衍生物，对α-葡萄糖苷酶的 IC50 值为 0.35 μM。

α-Glucosidase-IN-3是一种针对α-葡萄糖苷酶(IC50=1.28 µM)和α-淀粉酶(IC50=3.8 µM)的齐墩果酸肟酯衍生物。

Rehmannic acid and oleanolic acetate inhibit succinoxidase activity. Both Rehmannic acid and Icterogenin are potent uncouplers, abolishing the phosphate uptake, the respiration being inhibited by the former and increased by the latter.

Serratenediol demonstrates strong inhibitory effects on the Epstein-Barr virus early antigen (EBV-EA) activation without showing any cytotoxicity, its effects being stronger than that of a representative control, oleanolic acid. Serratenediol can promote

Terminolic acid (2α,6β,23-trihydroxyl oleanolic acid) 是一种从 Combretum racemosum 中分离得到的五环三萜糖苷，可通过与 IL-1β 和 IL-6 的受体活性位点结合抑制促炎细胞因子，并通过与 IL-4 受体结合位点结合增强抗炎细胞因子。它还表现出适度的抗菌活性。