CAS NO: | 511-96-6 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
20mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Gitogenin is a natural steroid isolated from the whole plant ofTribulus longipetalus. Gitogenin is a selective inhibitor ofUDP-glucuronosyltransferase 1A4 (UGT1A4)and enzymeα-glucosidasewithIC50values of 0.69 μM (use trifluoperazine as a substrate) and 37.2 μM, respectively, and does not inhibit the activities of major humancytochrome P450isoforms[1][2]. | ||||||||||||||||
IC50& Target | IC50: 0.69 μM (UDP-glucuronosyltransferase 1A4)[1]; IC50: 37.2 μM (α-glucosidase)[2] | ||||||||||||||||
体外研究 (In Vitro) | When tamoxifen is used as the substrate metabolized by UGT1A4 in HLMs, Gitogenin exhibits potent inhibition of tamoxifen, with anIC50value of 6.13 μM. Similarly, for midazolam as the substrate of UGT1A4, theIC50value is 5.7 μM. In addition, when olanzapine is used as a substrate of UGT1A4, theIC50value is determined as 6.0 μM. Finally, we also evaluats Gitogenin for asenapine glucuronidation mediated by UGT1A4, and similar inhibition effect is observed, with anIC50value of 22.0 μM[1]. | ||||||||||||||||
体内研究 (In Vivo) | Stimulation of growth hormone release is investigated on rat pituitary cells in vitro. Gitogenin (20 μg/mL) shows rat growth-hormone (rGH) release stimulating activities (26.1 ng/mL)[3]. | ||||||||||||||||
分子量 | 432.64 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C27H44O4 | ||||||||||||||||
CAS 号 | 511-96-6 | ||||||||||||||||
结构分类 |
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来源 |
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 1.85 mg/mL(4.28 mM;ultrasonic and warming and heat to 60℃) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |