INDEX NAME NOT YET ASSIGNED

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Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:INDEX NAME NOT YET ASSIGNED
CAS:2624131-45-7
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
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Products Intro: Product Name:PW0787
CAS:2624131-45-7
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 15618227136
Email: info@SuperLan-chem.com
Products Intro: Product Name:PW0787
CAS:2624131-45-7
Purity:98% Package:5MG;10MG;50MG;100MG,1G,5G,100G
Company Name: Shanghai Dongyang Biotechnology Co., Ltd.  
Tel: 0512-0512-13601744364 13601744364
Email: chemsharker@126.com
Products Intro: Product Name:PW0787
CAS:2624131-45-7
Purity:98% Package:1g 5g 10g 25g 50g 100g
Company Name: Bide Pharmatech Ltd.  
Tel: 400-1647117 15221909166
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Products Intro: Product Name:1-(6-(3-Fluoro-5-(trifluoromethyl)benzyl)pyrimidin-4-yl)-N-(2-hydroxyethyl)indoline-4-carboxamide
CAS:2624131-45-7
Purity:98+% Package:25mg;50mg;100mg Remarks:BD01465654
INDEX NAME NOT YET ASSIGNED Basic information
Product Name:INDEX NAME NOT YET ASSIGNED
Synonyms:PW0787;GPR52,PW-0787,oral,PW0787,Inhibitor,PW 0787,brain-penetrant,selective,inhibit,psychostimulant,behavior
CAS:2624131-45-7
MF:C23H20F4N4O2
MW:460.43
EINECS:
Product Categories:
Mol File:2624131-45-7.mol
INDEX NAME NOT YET ASSIGNED Structure
INDEX NAME NOT YET ASSIGNED Chemical Properties
Boiling point 605.1±55.0 °C(Predicted)
density 1.388±0.06 g/cm3(Predicted)
storage temp. 4°C, protect from light
solubility DMSO : 50 mg/mL (108.60 mM; Need ultrasonic)
form Solid
pka14.18±0.20(Predicted)
color Off-white to yellow
Safety Information
MSDS Information
INDEX NAME NOT YET ASSIGNED Usage And Synthesis
Biological ActivityPW0787 is a potent, selective, orally active, and brain-penetrant GPR52 agonist (EC50=135 nM). PW0787 suppresses psychostimulant behavior[1]. PW0787 (0.3, 1, 3, or 10 mg/kg; IP) displays antipsychotic-like activity by significantly inhibiting amphetamine-induced hyperlocomotor behavior in mice[1].PW0787 is evaluated in rats after a single dose of 20 mg/kg by oral (PO) or 10 mg/kg by intravenous (IV) administration. PW0787 has excellent plasma exposure after PO (AUC0-inf = 13,749 ng?h/mL) and IV dosing (AUC0-inf=9030 ng?h/mL), as well as high maximum serum concentration following PO (Cmax=3407 ng/mL) and IV administration (Cmax=6726 ng/mL). Additionally, PW0787 displays good volume of plasma distribution (Vss=1.5 L/kg) and acceptable plasma clearance (CL=1.1 L/h/kg) after 10 mg/kg IV. Excellent oral bioavailability (F) with the value of 76% is observed[1].
References[1]. Wang P, et al. Discovery of Potent and Brain-Penetrant GPR52 Agonist that Suppresses Psychostimulant Behavior. J Med Chem. 2020;63(22):13951-13972.
INDEX NAME NOT YET ASSIGNED Preparation Products And Raw materials
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