ML216

Modify Date: 2024-01-24 06:15:28

ML216 Structure
ML216 structure
Common Name ML216
CAS Number 1430213-30-1 Molecular Weight 383.323
Density 1.6±0.1 g/cm3 Boiling Point N/A
Molecular Formula C15H9F4N5OS Melting Point N/A
MSDS N/A Flash Point N/A

 Use of ML216


ML216(CID-49852229) is a potent inhibitor of the DNA unwinding activity of BLM helicase; showing similar IC50s of 3.0 and 0.97 μM for full length BLM and BLM636–1298 respectively.IC50 value: 3.0/0.97 uM(Full length/636–1298 BLM)Target: BLM helicase inhibitorML216 shows cell-based activity, and can induce sister chromatid exchanges, enhance to the toxicity of aphidicolin and exert anti-proliferative activity in cells expressing BLM, but not in those lacking BLM.

 Names

Name 1-[4-Fluoro-3-(trifluoromethyl)phenyl]-3-[5-(4-pyridinyl)-1,3,4-t hiadiazol-2-yl]ure
Synonym More Synonyms

 ML216 Biological Activity

Description ML216(CID-49852229) is a potent inhibitor of the DNA unwinding activity of BLM helicase; showing similar IC50s of 3.0 and 0.97 μM for full length BLM and BLM636–1298 respectively.IC50 value: 3.0/0.97 uM(Full length/636–1298 BLM)Target: BLM helicase inhibitorML216 shows cell-based activity, and can induce sister chromatid exchanges, enhance to the toxicity of aphidicolin and exert anti-proliferative activity in cells expressing BLM, but not in those lacking BLM.
Related Catalog
References

[1]. Nguyen GH, et al. A small molecule inhibitor of the BLM helicase modulates chromosome stability in human cells. Chem Biol. 2013 Jan 24;20(1):55-62.

 Chemical & Physical Properties

Density 1.6±0.1 g/cm3
Molecular Formula C15H9F4N5OS
Molecular Weight 383.323
Exact Mass 383.046387
PSA 114.76000
LogP 4.11
Index of Refraction 1.641
Storage condition 2-8℃

 Synonyms

Urea, N-[4-fluoro-3-(trifluoromethyl)phenyl]-N'-[5-(4-pyridinyl)-1,3,4-thiadiazol-2-yl]-
1-[4-Fluoro-3-(trifluoromethyl)phenyl]-3-[5-(4-pyridinyl)-1,3,4-thiadiazol-2-yl]urea
ML216