ML216

CAT: 0804-HY-12342-01Size: 5 mgDry Ice: NoHazardous: No
CAT#:0804-HY-12342-01Size:5 mg
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Description
ML216 (CID-49852229) is a potent, selective and cell permeable inhibitor of the DNA unwinding activity of BLM helicase with IC50s of 2.98 μM and 0.97 μM for BLMfull-length and BLM636-1298, respectively. ML216 inhibits ssDNA-dependent ATPase activity of BLM with a Ki of 1.76 μM. Antitumor avtivity[1][2].
CAS Number
[1430213-30-1]
Product Name Alternative
CID-49852229
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
DNA/RNA Synthesis
Type
Reference compound
Related Pathways
Cell Cycle/DNA Damage
Applications
Cancer-programmed cell death
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/ML216.html
Purity
99.89
Solubility
DMSO : 20 mg/mL (ultrasonic)
Smiles
O=C(NC1=CC=C(F)C(C(F)(F)F)=C1)NC2=NN=C(S2)C3=CC=NC=C3
Molecular Formula
C15H9F4N5OS
Molecular Weight
383.32
Precautions
H302, H315, H319, H335
References & Citations
[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.|[2]Banerjee T, et al. A new development in DNA repair modulation: discovery of a BLM helicase inhibitor. Cell Cycle. 2013 Mar 1;12 (5) :713-4.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported

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Alternative Products

CatalogName
MBS3846178-01ML216
A21754-25ML216 25mg
A21754-5ML216 5mg
A21754-10ML216 10mg
A21754-50ML216 50mg
A21754-100ML216 100mg
MBS130630-01ML216(CID-49852229)
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A21754-10mM-DML216 10mM * 1mL in DMSO
217222BLM Helicase Inhibitor, ML216 (ML-216, 1- (4-Fluoro-3- (trifluoromethyl) phenyl) -3- (5- (pyridin-4-yl) -1,3,4-thiadiazol-2-yl) urea)

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