Chemical Structure : Cilostazol
CAS No.: 73963-72-1
货号: PC-45282Not For Human Use, Lab Use Only.
Cilostazol (OPC 13013, OPC 21) is a potent, selective inhibitor of PDE3A with IC50 of 0.2 uM.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
50 mg | ¥580 | In stock | |
100 mg | ¥880 | In stock | |
500 mg | ¥1880 | In stock | |
1 g | Get quote |
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Cilostazol (OPC 13013, OPC 21) is a potent, selective inhibitor of PDE3A with IC50 of 0.2 uM.
Cilostazol (OPC 13013, OPC 21) inhibits platelet aggregation and has considerable antithrombotic effects in vivo.
Cilostazol (OPC 13013, OPC 21) relaxes vascular smooth muscle and inhibits mitogenesis and migration of vascular smooth muscle cells.
Cilostazol (OPC 13013, OPC 21) also upregulates autophagy via SIRT1 activation, has preventive effects on various central nervous system (CNS) diseases.
分子量 | 369.4607 | |
分子式 | C20H27N5O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
2(1H)-Quinolinone, 6-[4-(1-cyclohexyl-1H-tetrazol-5-yl)butoxy]-3,4-dihydro- |
1. Schrör K, et al. Diabetes Obes Metab. 2002 Mar;4 Suppl 2:S14-9.
2. Lee HR, et al. PLoS One. 2015 Aug 5;10(8):e0134486.
3. Qi DS, et al. Brain Res. 2016 Dec 15;1653:67-74.
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