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PHD-1-IN-1 是口服有效的缺氧诱导因子脯氨酰羟化酶结构域 1抑制剂,IC50为 0.034 μM。它与活性位 Fe2+具有独特的单齿结合相互作用,并诱导形成一个 “Arg367-out” 口袋。


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PHD-1-IN-1 是口服有效的缺氧诱导因子脯氨酰羟化酶结构域 1抑制剂,IC50为 0.034 μM。它与活性位 Fe2+具有独特的单齿结合相互作用,并诱导形成一个 “Arg367-out” 口袋。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 356 | In stock | |
| 5 mg | ¥ 893 | In stock | |
| 10 mg | ¥ 1,420 | In stock | |
| 25 mg | ¥ 2,570 | In stock | |
| 50 mg | ¥ 3,570 | In stock | |
| 100 mg | ¥ 4,910 | In stock | |
| 200 mg | ¥ 6,480 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 888 | In stock |
PHD-1-IN-1 相关产品
| 产品描述 | PHD-1-IN-1 is a potent inhibitor of hypoxia-inducible factor prolylhydroxylase domain-1 (PHD-1) enzyme(IC50 = 0.034 μM). |
| 靶点活性 | PHD1:0.034 μM |
| 体内活性 | Administration of PHD-1-IN-1 (3 mg/kg of p.o. or 0.5 mg/kg of i.v.) has a Cmax of 0.8 μM, a AUC of 176 ng?h/mL, Kp,uu of 1.11 and B/P of 0.95[1]. |
| 分子量 | 220.23 |
| 分子式 | C13H8N4 |
| CAS No. | 2009343-14-8 |
| Smiles | N#Cc1ccc(cc1)-c1cccc2ncnn12 |
| 密度 | no data available |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 11 mg/mL (49.95 mM), Sonication is recommended. | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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