Chemical Structure : SEC inhibitor KL-2
CAS No.: 900308-51-2
货号: PC-35725Not For Human Use, Lab Use Only.
SEC inhibitor KL-2 is a peptidomimetic inhibitor of super elongation complex (SEC) and transcription elongation by Pol II, disrupts cyclin T1-AFF4 interaction (Ki=1.50 uM) within SEC.
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 5 mg | ¥1980 | In stock | |
| 10 mg | ¥2980 | In stock | |
| 25 mg | ¥4580 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote | 
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	SEC inhibitor KL-2 is a peptidomimetic inhibitor of super elongation complex (SEC) and transcription elongation by Pol II, disrupts cyclin T1-AFF4 interaction (Ki=1.50 uM) within SEC.
	SEC inhibitor KL-2 disrupts the interaction between the SEC scaffolding protein AFF4 and P-TEFb, resulting in impaired release of Pol II from promoter-proximal pause sites and a reduced average rate of processive transcription elongation.
	SEC inhibitor KL-2 attenuates the heat-shock response from Drosophila to human, reduces protein levels of SEC components AFF1 and AFF4, but not CDK9 or CCNT1 in HEK293T cells.
	SEC inhibitor KL-2 downregulates MYC and MYC-dependent transcriptional programs in mammalian cells and delays tumor progression in mouse xenograft models of MYC-driven cancer.
| 分子量 | 333.743 | |
| 分子式 | C17H13ClFNO3 | |
| 外观性状 | Solid | |
| 储存条件 | 
                            
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| Solubility | 
                             10 mM in DMSO  | 
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| Chemical Name/SMILES | 
                             N-(5-chloro-2-methylphenyl)-4-(4-fluorophenyl)-2,4-dioxobutanamide  | 
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1. Liang K, et al. Cell. 2018 Oct 18;175(3):766-779.e17.
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