SR9186 (ML368) is a selective CYP3A4 inhibitor with IC50 values of 9, 4, and 38 nM for Midazolam 1-hydroxymidazolam, Testosterone 6beta-hydroxytestosterone, and Vincristine Vincristine M1, respectively. SR-9186 inhibits the development of hepatic-stage P. falciparum and blocks ivermectin metabolism. SR-9186 can be used in breast cancer research[1][2].
Molecular Weight:
430.46
Purity:
98.06
CAS Number:
[1361414-26-7]
Formula:
C26H18N6O
Target:
Cytochrome P450,Parasite
Application Notes:
MCE Product type: Reference compound
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