ChemicalBook--->CAS DataBase List--->1642303-38-5

1642303-38-5

1642303-38-5 Structure

1642303-38-5 Structure
IdentificationBack Directory
[Name]

PDE1-IN-1 (phosphate)
[CAS]

1642303-38-5
[Synonyms]

ITI214
ITI-214 phosphate
PDE1-IN-1 (phosphate)
ITI-214 phosphate salt
ITI-214; ITI 214; ITI214; ITI-214 PHOSPHATE SALT.
(6AR,9aS)-2-(4-(6-fluoropyridin-2-yl)benzyl)-5-methyl-3-(phenylamino)-5,6a,7,8,9,9a-hexahydrocyclopenta[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one phosphate
[Molecular Formula]

C29H29FN7O5P
[MDL Number]

MFCD28385868
[MOL File]

1642303-38-5.mol
[Molecular Weight]

605.57
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:30.0(Max Conc. mg/mL);49.54(Max Conc. mM)
[form ]

A solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Description]

ITI214 is an inhibitor of phosphodiesterase 1 (PDE1; Ki = 0.058 nM). It is selective for PDE1 over PDE2A, -3B, -4A, -5A, -6, -7B, -8A, -9A, -10A, and -11A (Kis = 0.16-18 μM). ITI214 (3 and 6 mg/kg) enhances novel object recognition in rats. It increases prefrontal cortex cAMP and cGMP levels in mice when administered at a dose of 50 mg/kg. ITI214 (0.1, 3, and 10 mg/kg) reverses MK-801-induced decreases in spontaneous alteration in the T-maze continuous alternation task in mice.
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