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ChemicalBook--->CAS DataBase List--->1644645-32-8

1644645-32-8

1644645-32-8 Structure

1644645-32-8 Structure
IdentificationBack Directory
[Name]

Benzonitrile, 3-chloro-5-[6-(5-fluoro-2-pyridinyl)-4-pyrimidinyl]-
[CAS]

1644645-32-8
[Synonyms]

HTL14242(HTL0014242)
3-Chloro-5-[6-(5-fluoro-2-pyridinyl)-4-pyrimidinyl]benzonitrile
Benzonitrile, 3-chloro-5-[6-(5-fluoro-2-pyridinyl)-4-pyrimidinyl]-
[Molecular Formula]

C16H8ClFN4
[MDL Number]

MFCD29089618
[MOL File]

1644645-32-8.mol
[Molecular Weight]

310.71
Chemical PropertiesBack Directory
[Boiling point ]

477.4±45.0 °C(Predicted)
[density ]

1.45±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 12.5 mg/mL (40.23 mM; Need ultrasonic)
[form ]

Solid
[pka]

-2.22±0.29(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

HTL14242 (HTL0014242) is an advanced and orally active mGlu5 NAM with a pKi?and a pIC50 of 9.3 and 9.2, respectively[1]. HTL14242 can be used for the research of parkinson’s disease[2].
[in vivo]

HTL14242 (oral administration; 1, 3, or 10 mg/kg; sacrificed 1 h postdose) emonstrates an excellent, dose-dependent occupancy of mGlu5?receptors from an oral dose, with an estimated ED50?of 0.3 mg/kg[1]. HTL14242 (oral administration; 1 mg/ml) exhibits an oral PK Profile, the t1/2, AUCinf?and F% are 6.5 hours, 3946 ng/h/mL and 80%, respectively in dog[1].

Animal Model:Dog (PK study)[1]
Dosage:3, 10 and 30 mg/kg
Administration:Oral administration; single dose
Result:Had a good PK characteristics in dogs.
[IC 50]

mGlu5
[storage]

Store at -20°C
[References]

[1] Kirstie A Bennett, et al. Structure-based Discovery and Development of Metabotropic Glutamate Receptor 5 Negative Allosteric Modulators. Adv Pharmacol. .?2020;88:35-58. DOI:10.1016/bs.apha.2020.03.001
[2] John A Christopher, et al. Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile). J Med Chem. .?2015 Aug 27;58(16):6653-64. DOI:10.1021/acs.jmedchem.5b00892
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