| CAS NO: | 547-81-9 |
| 包装 | 价格(元) |
| 10mg | 电议 |
| 50mg | 电议 |
| 100mg | 电议 |
| Cas No. | 547-81-9 |
| 别名 | 异雌三醇,16-epi-Estriol; 16β,17β-Estriol |
| Canonical SMILES | C[C@@]12[C@](C[C@@H]([C@@H]2O)O)([H])[C@@]3([H])[C@@](CC1)([H])C4=CC=C(O)C=C4CC3 |
| 分子式 | C18H24O3 |
| 分子量 | 288.4 |
| 溶解度 | Ethanol: 1 mg/ml |
| 储存条件 | -20°C |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
| Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
| 半岛bd体育手机客户端 描述 | 16-Epiestriol is a metabolite of the endogenous estrogen estrone .1It is formed from estroneviaa 16β-hydroxy estrone intermediate by reduction of the C-17 ketone. 16-Epiestriol (200 ?g/ml) inhibits the growth of carbapenem-resistantA. baumannii.2It inhibits carrageenan-induced paw edema in rats when administered at a dose of 20 mg/kg.3Unlike hydrocortisone, 16-epiestriol (240 ?g/animal) does not increase plasma or liver glucose levels in adrenalectomized rats. 1.Brinton, L.A., Trabert, B., Anderson, G.L., et al.Serum estrogens and estrogen metabolites and endometrial cancer risk among postmenopausal womenCancer Epidemiol. Biomarkers Prev.25(7)1081-1089(2016) 2.Skariyachan, S., Muddebihalkar, A.G., Badrinath, V., et al.Natural epiestriol-16 act as potential lead molecule against prospective molecular targets of multidrug resistant Acinetobacter baumannii-Insight from in silico modelling and in vitro investigationsInfect. Genet. Evol.82104314(2020) 3.Latman, N.S., Kishore, V., and Bruot, B.C.16-Epiestriol: An anti-inflammatory steroid without glycogenic activityJ. Pharm. Sci.83(6)874-877(1994) |
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