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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 | In Stock | |
| 5 mg | ¥ 1,760 | In Stock | |
| 10 mg | ¥ 2,980 | In Stock | |
| 25 mg | ¥ 4,930 | In Stock | |
| 50 mg | ¥ 6,890 | In Stock | |
| 100 mg | ¥ 9,480 | In Stock |
CALP2 acetate(261969-04-4 free base) 相关产品
| 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 |
| 颜色 | White |
| 物理性状 | Solid |
| Sequence | Val-Lys-Phe-Gly-Val-Gly-Phe-Lys-Val-Met-Val-Phe |
| Sequence Short | VKFGVGFKVMVF |
| 存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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