L-189

  Cat. No.:  DC8136   Featured
Chemical Structure
64232-83-3
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More than 5000 active chemicals with high quality for research!
Field of application
L-189 is a DNA ligase I, III and IV inhibitor (IC50 values are 5, 9 and 5 μM respectively) that blocks DNA binding (Ki = 5 μM for DNA ligase I).
Cas No.: 64232-83-3
Chemical Name: 6-Amino-5-(benzylideneamino)-2-sulfanyl-4-pyrimidinol
Synonyms: 4(1H)-Pyrimidinone,6-amino-2,3-dihydro-5-[(phenylmethylene)amino]-2-thioxo-;L189;L-189;6-Amino-2,3-dihydro-5-[(phenylmethylene)amino]-2-4(1H)-pyrimidineone;6-amino-5-(benzylideneamino)-2-sulfanyl-4-pyrimidinol;6-amino-5-(benzylideneamino)-2-sulfanylidene-1H-pyrimidin-4-one;(E)-6-amino-5-(benzylideneamino)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one;BCP15116;SBB100144;X3560;B7426;L 189;5-((1E)-2-phenyl-1-azavinyl)-6-amino-2-sulfanylpyrimidin-4-ol
SMILES: S=C1N([H])C(C(=C(N([H])[H])N1[H])/N=C(\[H])/C1C([H])=C([H])C([H])=C([H])C=1[H])=O
Formula: C11H10N4Os
M.Wt: 246.2883
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: L189 is a novel human DNA ligase inhibitor, inhibits hLigI/III/IV with IC50 of 5/9/5 μM.IC50 value: 5/9/5 μM (for hLigI/III/IV)Target: DNA ligasein vitro: L189 is a competitive inhibitor with respect to nicked DNA. L189 inhibits DNA ligases I, III and IV in DNA joining assays with purified proteins and in cell extract assays of DNA replication, base excision repair and non-homologous end joinging. L189 markedly increases killing of HCT116 colon cancer cells and the other cancer cell lines by ionizing radiation.
References: [1]. Xi Chen, Shijun Zhong, Xiao Zhu, et al. Rational Design of Human DNA Ligase Inhibitors that Target Cellular DNA Replication and Repair. Cancer Res 2008; 68: (9). May 1, 2008
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
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