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SU 10603

Cat. No. M42314
SU 10603 Structure
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Biological Activity

SU 10603 is a specific inhibitor of P45017α (P450c17; CYP17A1).

Chemical Information
Molecular Weight 257.71
Formula C15H12ClNO
CAS Number 786-97-0
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] Francesca Corsi et al. ACS Chem Neurosci. Targeting TSPO Reduces Inflammation and Apoptosis in an In Vitro Photoreceptor-Like Model of Retinal Degeneration

[2] C Cascio et al. J Steroid Biochem Mol Biol. Pathways of dehydroepiandrosterone formation in rat brain glia

[3] A Valencia-Sánchez et al. Arch Invest Med (Mex). [The (in vitro) inhibitor effect of SU-8000 and SU-10603 on 17 alpha-steroid-hydroxylase (17-alpha-OH-ase) in rat testis]

[4] D B Hales et al. J Biol Chem. Testosterone inhibits cAMP-induced de Novo synthesis of Leydig cell cytochrome P-450(17 alpha) by an androgen receptor-mediated mechanism

[5] L van Haren et al. Mol Cell Endocrinol. Measurement of steroidogenesis in rodent Leydig cells: a comparison between pregnenolone and testosterone production

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  Catalog
Abmole Inhibitor Catalog




Keywords: SU 10603 supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators


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