ChemicalBook--->CAS DataBase List--->1642187-96-9

1642187-96-9

1642187-96-9 Structure

1642187-96-9 Structure
IdentificationBack Directory
[Name]

2-(3-Chloro-4-fluorophenyl)-N-(1-methylethyl)-6-[3-(4-morpholinyl)propoxy]-4-oxo-pyrido[2,3-d]pyrimidine-3(4H)-acetamide hydrochloride
[CAS]

1642187-96-9
[Synonyms]

TASP 0390325
2-(3-Chloro-4-fluorophenyl)-N-(1-methylethyl)-6-[3-(4-morpholinyl)propoxy]-4-oxo-pyrido[2,3-d]pyrimidine-3(4H)-acetamide hydrochloride
[Molecular Formula]

C25H30Cl2FN5O4
[MDL Number]

MFCD30742933
[MOL File]

1642187-96-9.mol
[Molecular Weight]

554.44
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

TASP 0390325 is a vasopressin V1B receptor antagonist, which has antidepressant and anxiolytic therapeutic potential.
[in vivo]

TASP0390325 blocks the anterior pituitary V1B receptor in vivo. Oral administration of TASP0390325 antagonized the increase in plasma ACTH levels induced by CRF/dDAVP in rats, indicating that TASP0390325 blocks the anterior pituitary V1B receptor in vivo. TASP0390325 (1 mg/kg) significantly antagonizes CRF/dDAVP-induced plasma ACTH in rats[1].
Oral administration of TASP0390325 also exerts antidepressant effects in two models of depression (a forced swimming test and an olfactory bulbectomy model)[1].

Animal Model:Male Sprague-Dawley (SD) rats (211-246 g)[1]
Dosage:0.3 and 1 mg/kg (TASP0390325 is suspended in 0.5% methylcellulose 400)
Administration:Oral administration
Result:Antagonized the increase in plasma ACTH levels induced by CRF/dDAVP in rats at a dose of 1 mg/kg. In contrast, 0.3 and 1.0 mg/kg itself did not significantly affect basal ACTH levels.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

2-(3-Chloro-4-fluorophenyl)-N-(1-methylethyl)-6-[3-(4-morpholinyl)propoxy]-4-oxo-pyrido[2,3-d]pyrimidine-3(4H)-acetamide hydrochloride(1642187-96-9)1HNMR
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