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CGS 15435是一种有效的血栓素(TxA2)合成酶抑制剂(IC50: 1 nM)。CGS 15435作用于 PGI2合成酶、环氧合酶和脂合酶比作用于血栓素合成酶选择性低得多。
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CGS 15435是一种有效的血栓素(TxA2)合成酶抑制剂(IC50: 1 nM)。CGS 15435作用于 PGI2合成酶、环氧合酶和脂合酶比作用于血栓素合成酶选择性低得多。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,380 | 现货 | |
5 mg | ¥ 3,340 | 现货 | |
10 mg | ¥ 4,670 | 现货 | |
25 mg | ¥ 6,900 | 现货 | |
50 mg | ¥ 9,360 | 现货 | |
100 mg | ¥ 12,400 | 现货 |
产品描述 | CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50: 1 nM). CGS 15435 acts on PGI2 synthase, cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase. |
靶点活性 | TXA2:1 nM |
体外活性 | CGS 15435 inhibited the formation of PGE2 (IC50:1200 μM), PGI2 synthetase (IC50:90 μM) and 5-lipoxygenase (IC50:60 μM).[1] |
体内活性 | The effect of CGS 15435 was long lasting, as the increase of plasma TxB2 levels was prevented even 24 hours after the administration of CGS 15435. CGS 15435 inhibited the formation of TxB2 significantly at 4, 6, 12 and 24 h after administration. Administration of CGS 15435 0.25 or 24 h before arachidonic acid (AA) did not increase TxB2 in surviving animals (4/4 and 5/6, respectively). The final TxB2 level in CGS15435A(pretreatment for 0.25 and 24 h) groups was significantly lower than that in arachidonic acid (AA) and daxibon (pretreatment for 2 h) groups.[1] |
分子量 | 356.85 |
分子式 | C20H21ClN2O2 |
CAS No. | 95853-92-2 |
Smiles | C(CCCCC(O)=O)C1=C(N(C)C=2C1=CC(Cl)=CC2)C=3C=CC=NC3 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||
溶解度信息 | DMSO: 3.57 mg/mL (10 mM) | ||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||
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