目錄:MedChemExpress LLC>>生化試劑>> LLY-507 | MCE
CAS | 1793053-37-8 | 純度 | 98.47% |
---|---|---|---|
分子量 | 574.76 | 分子式 | C??H??N?O |
供貨周期 | 現貨 | 規格 | 5 mg |
貨號 | HY-19313 | 應用領域 | 醫療衛生,化工,生物產業,制藥 |
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CAS No. : 1793053-37-8
產品活性:LLY-507 is a potent and selective inhibitor of protein-lysine methyltransferase SMYD2. LLY-507 potently inhibits the ability of SMYD2 to methylate p53 peptide with an IC50 <15 nM. LLY-507 serves as a valuable chemical probe to aid in the dissection of SMYD2 function in cancer and other biological processes.
研究領域:Epigenetics
作用靶點:Histone Methyltransferase
In Vitro: LLY-507 is >100-fold selective for SMYD2 over 21 other methyltransferases including SMYD3.
LLY-507 binds to the substrate channel of SMYD2 and supports the selectivity of its inhibition.
LY-507 is able to potently inhibit the methylation of H4 peptide by SMYD2 enzyme with an IC50 of 31 nM.
LLY-507 (0.03-20 μM; 28 hours) inhibits SMYD2-mediated methylation of p53 Lys370 in U2OS cells, with an IC50 of 0.6 μM.
LLY-507 (0-20 μM; 3-7 days) inhibits the proliferation of several ESCC, HCC, and breast cancer cell lines.
相關產品:Bioactive Compound Library Plus | Epigenetics Compound Library | Histone Modification Research Compound Library | Anti-Cancer Compound Library | Reprogramming Compound Library | Chemical Probe Library | Anti-Breast Cancer Compound Library | Anti-Blood Cancer Compound Library | Targeted Diversity Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | PRMT5-IN-17 | EZM0414 | BIX-01294 | WDR5-IN-5 | PRMT5-IN-22 | Gambogenic acid | SGC707 | Dot1L-IN-7 | MS1943 | PRMT5-IN-21 | NSD3-IN-3 | DCLX069 | MAK683 | DS-437 | EPZ020411 | WDR5-IN-4 TFA | Amodiaquine dihydrochloride | Furamidine | SMYD3-IN-2 | UNC0642 | Chaetocin | UNC0646 | UNC0224 | EBI-2511 | BVT948 | MM-401 | CMP-5 | EPZ-719
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