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抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
T74298 Bcl-2-IN-5

Bcl-2-IN-5 是一种BCL-2抑制剂,对Bcl-2野生型、Bcl-2D103Y 和Bcl-2G101V 的IC50分别为 0.12 nM、0.14 nM 和 0.22 nM。Bcl-2-IN-5 抑制细胞生长,对 Bcl 2-G101V 敲入RS4; 11 和 RS4; 11 细胞的IC50值分别 0.2 nM 和 0.44 nM。
T69200 CGP74514A

CGP74514A is a CDK1 inhibitor with potential anticancer activity. In U937 cells, CGP74514A - induced apoptosis (5 microM) became apparent within 4 hr and approached 100% by 24 hr. The pan- caspase inhibitor Boc-fmk and the caspase-8 inhibitor lETD-fmk opposed CGP74514A -induced caspase-9 activation and PARP degradation, but not cytochrome c or Smac/DIABLO release. CGP74514A -mediated apoptosis was substantially blocked by ectopic expression of full-length Bel- 2, a loop-deleted mutant Bcl-2, and...

化合物

Bcl-2-IN-5
Cat.No: T74298
Synonym:
Target:
CGP74514A
Cat.No: T69200
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T5S2358 Dehydrocorydaline

Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine

BCL; PARP; p38 MAPK; Caspase; Parasite; Autophagy Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Proteases/Proteasome
Dehydrocorydaline (13-Methylpalmatine) 是一种生物碱。它调节Bax,Bcl-2蛋白表达,激活caspase-7,caspase-8,并使PARP 失活。它能增强p38 MAPK 活化,具有抗炎、抗癌等功效。它具有强大的抗疟疾作用,并具低细胞毒性。
T7027 EURYCOMANONE

东革阿里提取物,Pasakbumin A

Others Others
Eurycomanone (Pasakbumin A) 能够抑制雌激素生成过程中磷酸二酯酶和芳香酶的活性,促进精子生成。它对 HepG2 细胞具有细胞毒性,能够上调 p53 和 Bax 以及下调 Bcl-2 ,诱导细胞凋亡。它具有抗癌活性,在浓度范围内以剂量依赖性方式抑制 A549 肺癌细胞增殖 从 520 微克/毫升。

天然产物

Dehydrocorydaline
Cat.No: T5S2358
Synonym: Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine
Target: BCL, PARP, p38 MAPK, Caspase, Parasite, Autophagy
EURYCOMANONE
Cat.No: T7027
Synonym: 东革阿里提取物,Pasakbumin A
Target: Others
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