VU6035406
VU6035406 is a functionally selective mAChR inhibitor, with mAChR IC50 values of 21 nM, 51 nM and 47 nM against human, rat and mouse targets, respectively. VU6035406 does not act as a P-glycoprotein substrate. VU6035406 shows extremely low inhibitory activity against cytochrome P450 1A2, 2C9, 2D6 and 3A4. VU6035406 can be used in the research of neurological and psychiatric disorders.
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- CAS No.: 2746405-41-2
- 화학식: C15H16ClN5O3S
- 분자량:381.84
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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mAChR5 21 |
mAChR5 51 nM (IC50, rat M5 (rM5) |
mAChR5 47 nM (IC50, mouse M5 (mM5)) |
VU6035406 potently inhibits human M5 muscarinic acetylcholine receptor-mediated calcium mobilization in hM5 CHO cells with an IC50 of 21 nM and exhibits >500-fold selectivity over human M1-M4 subtypes[1].
VU6035406 inhibits rat M5 muscarinic acetylcholine receptor-mediated calcium mobilization with an IC50 of 51 nM and exhibits high selectivity over rat M1-M4 subtypes[1].
VU6035406 inhibits mouse M5 muscarinic acetylcholine receptor-mediated calcium mobilization with an IC50 of 47 nM[1].
VU6035406 has a favorable CYP inhibition profile, with no significant inhibition of CYP1A2 or CYP2C9 and weak inhibition of CYP2D6 and CYP3A4[1].
VU6035406 has low to moderate predicted hepatic clearance across multiple species, favorable unbound fractions in plasma and brain, and moderate brain penetration in rats with a Kp,uu of 0.56[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 2746405-41-2
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분자량 381.84
-
화학식 C15H16ClN5O3S
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SMILES
O=S(C1=CN=C(C)O1)(N2CCC(CC2)C3=CN4N=CN=C4C=C3Cl)=O
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)