Chemical Structure : Bezisterim
CAS No.: 1001100-69-1
货号: PC-21972Not For Human Use, Lab Use Only.
Bezisterim (HE3286, NE3107) is an orally bioavailable synthetic analogue of an active DHEA metabolite, displays both glucose-lowering and cholesterol-lowering effects, inhibits inflammatory NF-κB transcription, and confers oral bioavailability and blood-brain barrier permeability.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥1880 | In stock | |
| 10 mg | ¥2980 | In stock | |
| 25 mg | ¥4980 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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Bezisterim (HE3286, NE3107) is an orally bioavailable synthetic analogue of an active DHEA metabolite, displays both glucose-lowering and cholesterol-lowering effects, inhibits inflammatory NF-κB transcription, and confers oral bioavailability and blood-brain barrier permeability.
Bezisterim (HE3286) attenuates LPS- and TNFalpha-stimulated inflammation in primary murine macrophages.
Bezisterim (HE3286) downregulates inflammatory cytokine/chemokine expression in liver and adipose tissue of Zucker diabetic fatty rats.
| 分子量 | 330.47 | |
| 分子式 | C21H30O3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
17alpha-pregn-5-en-20-yne-3beta,7beta,17-triol |
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1. Kosiewicz MM, et al. Eur J Pharmacol. 2011 May 11;658(2-3):257-62.
2. Wang T, et al. J Pharmacol Exp Ther. 2010 Apr;333(1):70-80.
3. Offner H, et al. J Pharmacol Exp Ther. 2009 Jun;329(3):1100-9.
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