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AZ6102
Cat. No.:
OB0225WX-1706
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
AZ6102 is a potent TNKS1/2 inhibitor exhibiting 100-fold selectivity over other enzymes in the PARP family and a measured IC50 of 5 nM for Wnt pathway suppression in DLD-1 cells.
Synonym:
1645286-75-4; AZ-6102; AZ 6102; 2-(4-(6-((3R,5S)-3,5-dimethylpiperazin-1-yl)-4-methylpyridin-3-yl)phenyl)-7-methyl-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one; 4H-Pyrrolo[2,3-d]pyrimidin-4-one, 2-[4-[6-[(3R,5S)-3,5-dimethyl-1-piperazinyl]-4-methyl-3-pyridinyl]phenyl]-3,7-dihydro-7-methyl-, rel-; 2-(4-(6-(cis-3,5-Dimethylpiperazin-1-yl)-4-methylpyridin-3-yl)phenyl)-7-methyl-3H-pyrrolo[2,3-d]pyrimidin-4(7H)-one; 2-[4-[6-[(3R,5S)-3,5-dimethylpiperazin-1-yl]-4-methylpyridin-3-yl]phenyl]-7-methyl-3H-pyrrolo[2,3-d]pyrimidin-4-one; 2-(4-{6-[(3R,5S)-3,5-dimethylpiperazin-1-yl]-4-methylpyridin-3-yl}phenyl)-7-methyl-3H,4H,7H-pyrrolo[2,3-d]pyrimidin-4-one; 2-(4-(6-((3S,5R)-3,5-Dimethylpiperazin-1-yl)-4-methylpyridin-3-yl)phenyl)-7-methyl-3Hpyrrolo[2,3-d]pyrimidin-4(7H)-one
CAS No.:
1645286-75-4
Compound CID:
135905416
Formula:
C25H28N6
Formula Weight:
428.53
Specification
Targets&IC50:
TNKS2: 5 nM; TNKS1: 5 nM
Relative Density:
1.31 g/cm3
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
AZ6102 is utilized in biochemical assays as a dual inhibitor of tankyrase 1 and 2 to investigate the molecular mechanisms of axin stabilization in various neoplastic cell lines.
Library Information
Target:
PARP; Wnt/β-Catenin
Receptor:
PARP; TNKS1; TNKS2
Pathways:
DNA damage/DNA repair; Chromatin/Epigenetic; Cytoskeletal signaling; Stem cells
Plate Number:
AOCL-22
Plate Location:
g11
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
21.4 mg/mL; 50 mM
ALogP:
3.649
HBA_Count:
3
HBD_Count:
2
Rotatable Bond:
3





