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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
VU6019650 is a potent and selective orthosteric antagonist of M5 mAChR ( IC 50 =36 nM), can be used for opioid use disorder (OUD) relief. VU6019650 can cross blood brain barrier, potentially modulates the mesolimbic dopaminergic reward circuitry. VU601965
Appearance:Solid
IC50& Target:mAChR5|36 nM (IC|50|)
In Vitro:VU6019650 (0-10 μM) shows high selectivity for M5 (IC 50 =36 nM) over other subtypes (>100-fold selectivity against human M 1-4 ). VU6019650 (1 μM) blocks Oxo-M-induced activation of VTA neurons. VU6019650 exhibits brain penetrance with rat brai
In Vivo:VU6019650 (10-56.6mg/kg; i.p.; single dose) inhibits the rewarding effects of Oxycodone and reduces oxycodone self-administration in rats. Pharmacokinetic Analysis in ratsRoute Dose mg/kg) t (term) (min) MRT (min) Cl_obs (mL/min/kg) Vd ss (L/k
Biological Activity:VU6019650 is a potent and selective orthosteric antagonist of M5 mAChR ( IC 50 =36 nM), can be used for opioid use disorder (OUD) relief. VU6019650 can cross blood brain barrier, potentially modulates the mesolimbic dopaminergic reward circuitry. VU601965
| Canonical Smiles | O=S(C1=CC2=C(OCC2)C=C1)(N(CC[C@@H]3CSC4=NC=CN4C)C[C@@H]3F)=O |
|---|---|
| Molecular Weight | 411.51 |
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