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CpCDPK1/TgCDPK1-IN-3

Cat. No. M41215
CpCDPK1/TgCDPK1-IN-3 Structure
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Quality Control & Documentation
Biological Activity

CpCDPK1/TgCDPK1-IN-3 is a CpCDPK1 and TgCDPK1 inhibitor with IC50 values of 0.003 and 0.0036 µM, respectively.

Chemical Information
Molecular Weight 306.37
Formula C17H18N6
CAS Number 1092788-87-8
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] Fanfan Shu et al. Front Microbiol. Characterization of Calcium-Dependent Protein Kinase 2A, a Potential Drug Target Against Cryptosporidiosis

[2] Jiayuan Su et al. Microorganisms. Comparative Characterization of CpCDPK1 and CpCDPK9, Two Potential Drug Targets Against Cryptosporidiosis

[3] Wenlin Huang et al. Antimicrob Agents Chemother. 5-Aminopyrazole-4-Carboxamide-Based Compounds Prevent the Growth of Cryptosporidium parvum

[4] Matthew A Hulverson et al. J Infect Dis. Bumped-Kinase Inhibitors for Cryptosporidiosis Therapy

[5] Jennifer D Artz et al. BMC Genomics. The Cryptosporidium parvum kinome

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  Catalog
Abmole Inhibitor Catalog




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