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  4. CGS 15435

CGS 15435 是一种有效的血栓烷 (TxA2) 合成酶抑制剂，IC50 为 1 nM， 比作用于环氧合酶，PGI2 合成酶和脂氧合酶的选择性高 100000 倍。

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CGS 15435 Chemical Structure

CGS 15435 Chemical Structure

CAS No. : 95853-92-2

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规格 价格 是否有货 数量
1 mg ￥3910
1 周
5 mg   询价  
10 mg   询价  

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CGS 15435 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

CGS 15435, a potent thromboxane (TxA2) synthetase inhibitor with an IC50 of 1 nM, has a selectivity for Tx synthetase 100000-fold greater than that for cyclooxygenase, PGI2 synthetase and lipoxygenase enzymes.

IC50 & Target[1]

TXA2

1 nM (IC50)

体外研究
(In Vitro)

CGS 15435 is a highly specific Tx synthetase inhibitor. CGS 15435 is only weakly effective as an inhibitor of PGE2 (Cyclooxygenase, IC50=1200 μM), prostacyclin (PGI2 synthetase, IC50=90 μM) or 5-Lipoxygenase (IC50=60 μM) product formation[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

CGS 15435 相关抗体:
体内研究
(In Vivo)

CGS 15435 has a long duration of action, since the increases in the plasma levels of TxB2 are prevented even at 24 h after CGS 15435 administration. CGS 15435 significantly inhibits TxB2 formation 4, 6, 12 and 24 h after dosing. Administration of CGS 15435 0.25 or 24 h prior to Arachidonic acid (AA) produced no increase in TxB2 in the surviving animals (4/4 and 5/6, respectively). The final TxB2 levels in the CGS15435A (0.25 and 24 h pretreatment) groups are significantly lower (P<0.05) than those seen in the AA or the Dazoxiben (2 h pretreatment) groups[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

356.85

Formula

C20H21ClN2O2
CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献
Kinase Assay
[1]

Thromboxane synthetase, cyclooxygenase, prostacyclin synthetase, and lipoxygenase enzymes are prepared. For the individual enzyme assays. [1-14C]Arachidonic acid (AA) is incubated with partially purified enzyme obtained from human platelets (thromboxane synthetase), sheep seminal vesicles (cyclooxygenase), bovine aorta (prostacyclin synthetase), and guinea-pig leukocytes (lipoxygenase). At the end of the incubation period, the products are extracted into ethyl acetate, the extracts are evaporated to dryness, the residues are redissolved in acetone, and these solutions are spotted on thin layer chromatography plates. The plates are developed in the appropriate solvents, scanned and radioactive spots corresponding to those of TxB2, PGE2, 6-keto PGFu, and 5-HETE, are scraped off and counted by a radiospectrometer. The IC50 values are determined by employing a range of concentrations of test compounds over the linear range of the assay and analyzed graphically. All determinations are done in duplicate and repeated once[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Administration
[1]

Rabbits[1]
Adult male New Zealand rabbits (2.3-3.5 kg) are anesthetized with sodium pentobarbital (30 mg/kg i.v.). The animals are tracheotomized and the left femoral artery and vein are cannulated for the recording of mean arterial blood pressure (MABP) and the injection of either vehicle or drug, respectively. The animals are allowed to stabilize for at least 15 rain prior to drug or vehicle administration. CGS 15435 and DAZ are dissolved in 2 mL of 0.5 M Tris buffer (pH 8.4) and injected i.v. over a 15 s period. CGS 15435 (8.6 μmol/kg; 3.1 mg/kg) is administered at 15 min (n=4) or 24 h (n=6) prior to AA.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.
参考文献

CGS 15435 相关分类

  • 摩尔计算器

  • 稀释计算器

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

CGS 1543595853-92-2CGS15435CGS-15435OthersInhibitorinhibitorinhibit

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目录号：
HY-100283
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