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AZ 6102

Cat. No. M6477
AZ 6102 Structure
Size Price Availability Quantity
10mg USD 130  USD130 In stock
50mg USD 490  USD490 In stock
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Quality Control & Documentation
Biological Activity

AZ 6102 is a potent TNKS2 and TNKS1 inhibitor (IC50 values are 1 and 3 nM, respectively). Exhibits >100-fold selectivity for TNKS1/2 over PARP-1, PARP-2 and PARP-6. Inhibits Wnt signaling in DLD-1 cells (IC50 = 5 nM). Exhibits moderate oral bioavailability.

Chemical Information
Molecular Weight 428.53
Formula C25H28N6O
CAS Number 1645286-75-4
Form Solid
Solubility (25°C) DMSO 21.43 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Conway, et al. Bioorg Med Chem Lett. Synthesis of phenylglycine derivatives as potent and selective antagonists of group III metabotropic glutamate receptors.

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