VU0469650

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Company Name: Shanghai Beckham Medical Technology Co., Ltd  
Tel: 13816613772
Email: huahero21@sina.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com
Company Name: Jinan Yaoyan Pharmaceutical Co., Ltd.  
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Email: jnyaoyan@163.com
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774 400-920-5774
Email: sales@glpbio.cn
Company Name: Nanjing Meihao Pharmaceutical Technology Co., Ltd.  
Tel: meitaochem@126.com
Email: meitaochem@126.com

VU0469650 manufacturers

  • VU 0469650
  • VU 0469650 pictures
  • $37.00
  • 2026-07-14
  • CAS:1443748-47-7
  • Purity: 98.03%
  • Supply Ability: 10g
VU0469650 Basic information
Product Name:VU0469650
Synonyms:3-[(3R)-3-Methyl-4-(tricyclo[3.3.1.13,7]dec-1-ylcarbonyl)-1-piperazinyl]-2-pyridinecarbonitrile hydrochloride;VU 0469650 hydrochloride;3-[(3R)-3-METHYL-4-[(4-METHYLADAMANTAN-1-YL)CARBONYL]PIPERAZIN-1-YL]PYRIDINE-2-CARBONITRILE;VU0469650;CID73755207;2-Pyridinecarbonitrile, 3-[(3R)-3-methyl-4-(tricyclo[3.3.1.13,7]dec-1-ylcarbonyl)-1-piperazinyl]-;VU 0469650 HCl;VU0469650|||VU 0469650|||VU-0469650|||VU 0469650 HCl
CAS:1443748-47-7
MF:C22H28N4O
MW:364.48
EINECS:
Product Categories:
Mol File:1443748-47-7.mol
VU0469650 Structure
VU0469650 Chemical Properties
Boiling point 584.7±50.0 °C(Predicted)
density 1.25±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 100 mM,Ethanol: 50 mM
pka1.42±0.12(Predicted)
form Solid
color Off-white to light yellow
Optical Rotation[α]/D -41 to -51°, c =1 in methanol
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
VU0469650 Usage And Synthesis
UsesVU 0469650 Hydrochloride is potent and selective negative allosteric modulators of metabotropic glutamate receptor 1 (mGlu1).
Biological ActivityVU0469650 is a brain-penetrant, potent and selective metabotropic glutamate receptor 1 (mGlu1) negative allosteric modulator (NAM). VU0469650 selectively inhibits glu-induced Ca2+ influx in human mGluR1-expressing HEK 293A (EC50 = 99 nM with [Glu] = EC20 for 1.9 min, then EC100 for 1.7 min; inactive against cells expressing human mGlu2-8 at 10 μM) with no affinity toward a panel of 68 clinically relevant GPCRs, ion channels, kinases, and transporters. Prior administration of VU0469650 in mice in vivo (60 mg/kg i.p.) modulates the antipsychotic activity of M4 muscarinic receptor PAM VU0467154 and th at of the M1/M4 agonist xanomeline.
in vivo

VU0469650 (male Sprague-Dawley rats, 0.2 mg/kg, IV, once) exhibits moderate to high clearance, a moderate volume of distribution, and a half-life of approximately 1 hour[1].
VU0469650 (male Sprague-Dawley rats, 10 mg/kg, IP, once) shows an excellent selectivity profile and good exposure in both plasma and brain samples[1].

IC 50mGluR 1: 99 nM (IC50)
storageStore at +4°C
VU0469650 Preparation Products And Raw materials
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