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CALP2 acetate 是一种钙调蛋白拮抗剂,对与 CaM EF-hand/Ca2+-结合位点具有高亲和力,Kd 为 7.9 µM。它有效抑制粘附和脱粒。它也是肺泡巨噬细胞的强激活剂。它抑制 CaM 依赖性磷酸二酯酶活性并增加细胞内 Ca2+ 浓度。
CALP2 acetate 是一种钙调蛋白拮抗剂,对与 CaM EF-hand/Ca2+-结合位点具有高亲和力,Kd 为 7.9 µM。它有效抑制粘附和脱粒。它也是肺泡巨噬细胞的强激活剂。它抑制 CaM 依赖性磷酸二酯酶活性并增加细胞内 Ca2+ 浓度。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 866 | 现货 | |
5 mg | ¥ 1,760 | 现货 | |
10 mg | ¥ 2,980 | 现货 | |
25 mg | ¥ 4,930 | 现货 | |
50 mg | ¥ 6,890 | 现货 | |
100 mg | ¥ 9,480 | 现货 |
产品描述 | CALP2 acetate is an antagonist of calmodulin showing high affinity for binding to the CaM EF-hand/Ca2+-binding site with a Kd of 7.9 µM. CALP2 acetate potently inhibits of adhesion and degranulation. CALP2 acetate is also a strong activator of alveolar macrophages. CALP2 acetate inhibits CaM-dependent phosphodiesterase activity and increases intracellular Ca2+ concentrations. |
靶点活性 | Calmodulin:7.9 µM(Kd) |
分子量 | 1357.7 |
分子式 | C68H104N14O13S |
Smiles | CC(C)[C@@H](C(N[C@@H](CCCCN)C(N[C@@H](Cc1ccccc1)C(NCC(N[C@@H](C(C)C)C(NCC(N[C@@H](Cc1ccccc1)C(N[C@@H](CCCCN)C(N[C@@H](C(C)C)C(N[C@@H](CCSC)C(N[C@@H](C(C)C)C(N[C@@H](Cc1ccccc1)C(O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)N |
密度 | no data available |
存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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