1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)-
![1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)- Structure](CAS/20211123/GIF/2624131-45-7.gif)
- CAS No.
- 2624131-45-7
- Chemical Name:
- 1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)-
- Synonyms
- PW0787;PW0787, 10 mM in DMSO;GPR52,PW-0787,oral,PW0787,Inhibitor,PW 0787,brain-penetrant,selective,inhibit,psychostimulant,behavior;1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)-
- CBNumber:
- CB78896424
- Molecular Formula:
- C23H20F4N4O2
- Molecular Weight:
- 460.42
- MDL Number:
- MFCD33550902
- MOL File:
- 2624131-45-7.mol
1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)- 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 |
| pka | 14.18±0.20(Predicted) |
| color | Off-white to yellow |
1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)- Chemical Properties,Uses,Production
Uses
PW0787 is a potent, selective, orally active, and brain-penetrant GPR52 agonist (EC50=135 nM). PW0787 suppresses psychostimulant behavior[1].
Biological Activity
PW0787 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].
in vivo
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].
| Animal Model: | Na?ve male C57/BL6 mice weighing between 24 and 31 g |
| Dosage: | 0.3, 1, 3, or 10 mg/kg (dissolved in 0.9% saline containing 20% HP-β-CD with a final pH of the solution adjusted to 7.4) |
| Administration: | IP |
| Result: | Suppressed amphetamine (AMPH)-induced horizontal activity at both 3 mg/kg and 10 mg/kg doses. |
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.
1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)- Preparation Products And Raw materials
Raw materials
Preparation Products
1H-Indole-4-carboxamide, 1-[6-[[3-fluoro-5-(trifluoromethyl)phenyl]methyl]-4-pyrimidinyl]-2,3-dihydro-N-(2-hydroxyethyl)- Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 33024 | 60 |
| TargetMol Chemicals Inc. | +1-781-999-5354; +17819995354 | marketing@targetmol.com | United States | 32434 | 58 |
| TargetMol Chemicals Inc. | +1-781-999-5354; | support@targetmol.com | United States | 39031 | 58 |
| Shanghai YuanYe Biotechnology Co., Ltd. | 021-61312847; 18021002903 | 3008007409@qq.com | China | 71826 | 60 |
| Shanghai Chaolan Chemical Technology Center | 021-QQ：65489617 15618227136 | Sales@ATKchemical.com | China | 9979 | 58 |
| Shanghai Dongyang Biotechnology Co., Ltd. | 0512-0512-13601744364 13601744364 | chemsharker@126.com | China | 1000 | 58 |
| Bide Pharmatech Ltd. | 400-1647117 13681763483 | product02@bidepharm.com | China | 62320 | 58 |
| TargetMol Chemicals Inc. | 4008200310 | marketing@tsbiochem.com | China | 24989 | 58 |
| Aikon International Limited | 025-58859352 18921922613 | hywu@aikonchem.com | China | 10710 | 58 |
| Shanghai Yifei Biotechnology Co. , Ltd. | 021-65675885 18964387627 | customer_service@efebio.com | China | 11973 | 58 |
