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SR9186

Cat. No. M28250

All AbMole products are for research use only, cannot be used for human consumption.

SR9186 Structure
Synonym:

ML368

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Quality Control & Documentation
Biological Activity

SR9186 (ML368) is a potent CYP3A4 inhibitor with IC50 s for inhibition of midazolam → 1′hydroxymidazolam, testosterone → 6β-hydroxytestosterone, and vincristine → vincristine M1 of 9, 4, and 38 nM, respectively. SR-9186 inhibits liver-stage development of P. falciparum to block ivermectin metabolism.

Chemical Information
Molecular Weight 430.46
Formula C26H18N6O
CAS Number 1361414-26-7
Form Solid
Solubility (25°C) DMSO 31.25 mg/mL (ultrasonic and warming and heat to 60°C)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Joanna K Towles, et al. Drug Metab Dispos. Cytochrome P450 3A4 and CYP3A5-Catalyzed Bioactivation of Lapatinib

[2] Xiaohai Li, et al. Drug Metab Dispos. Discovery of a highly selective CYP3A4 inhibitor suitable for reaction phenotyping studies and differentiation of CYP3A4 and CYP3A5

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  Catalog
Abmole Inhibitor Catalog




Keywords: SR9186, ML368 supplier, Cytochrome P450 (e.g. CYP17), inhibitors, activators

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