CVN636 is a potent, orally active and selective mGluR7 allosteric agonist with an EC 50 value of 7 nM for hu mGluR7 . CVN636 has central nervous system (CNS) permeability
In Vivo
CVN636 (0.3-3 mg/kg; p.o.) reduces ethanol self-administration in msP rats . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: msP rat Dosage: 0.3, 1, and 3 mg/kg Administration: oral administration Result: Reduced alcohol self-administration in a dose-dependent.
IC50& Target:hu mGluR7 7 nM (EC 50 )
사양
생화학 및 생리적 메커니즘
CVN636 is a potent, orally active and selective mGluR7 allosteric agonist with an EC 50 value of 7 nM for hu mGluR7 . CVN636 has central nervous system (CNS) permeability.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.