找到约 8 条 “Checkpoint” 相关结果 (用时 0.11 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
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M1676
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BIBR1532 | BIBR1532 | Checkpoint |
BIBR-1532 | |||
BIBR 1532是一种有效的,选择性的,非竞争性的端粒酶 telomerase 抑制剂,IC50为100 nM,也可通过抑制ATM/CHK1(ataxia-telangiectasia-mutated/Checkpoint kinase 1)通路发挥作用。BIBR1532 也是TERT抑制剂,TERT是端粒酶活性调节的限速酶。 | |||
M6104
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Ipilimumab | 伊匹木单抗;伊匹单抗 | Checkpoint |
MDX-010, BMS-734016;Yervoy | |||
Ipilimumab (MDX-010, BMS-734016,伊匹单抗)是一种全人源化的抗CTL antigen 4 (CTLA-4)的单克隆抗体,Ipilimumab是一种免疫检查点(Checkpoint)抑制剂。 | |||
M7986 | OM137 | OM137 | Others |
OM137 is an inhibitor of aurora kinases; inhibitor of spindle checkpoint. | |||
M10129
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CCT245737 | CCT245737 | Checkpoint |
SRA737; PNT-737 | |||
CCT245737是一种有效的,选择性的和口服活性的检查点激酶1(checkpoint kinase 1)抑制剂,对CHK1,CHK2和G2 check point abrogation 的IC50值分别为1.3 nM,2440 nM 和 30 nM。 | |||
M21002 | BOS172722 | BOS172722 | Others |
BOS172722 is a monopolar spindle 1 (MPS1) checkpoint inhibitor with IC50 of 11 nM, Ki of 0.11 nM. | |||
M30540 | Chk2-IN-1 | Chk2-IN-1 | Checkpoint |
Chk2-IN-1 (compound 1) 是一种有效和选择性的 checkpoint kinase 2 (Chk2) 抑制剂,抑制 Chk2 和 Chk1 的 IC50 值分别为 13.5 nM 和 220.4 nM。Chk2-IN-1 可引发强烈的共济失调毛细血管扩张突变 (ATM) 依赖性 Chk2 介导的辐射防护作用。 | |||
M40256 | Cryptomoscatone D2 | Cryptomoscatone D2 | Others |
Cryptomoscatone D2 是一种有效的 G2 检查点 (G2 checkpoint) 抑制剂。 | |||
M58881
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Recombinant Human CHK1 (BV) | 重组人CHK1 (BV) | Target Proteins |
Serine/threonine-protein kinase which is required for checkpoint-mediated cell cycle arrest and activation of DNA repair in response to the presence of DNA damage or unreplicated DNA |