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ChemicalBook--->CAS DataBase List--->1160521-50-5

1160521-50-5

1160521-50-5 Structure

1160521-50-5 Structure
IdentificationBack Directory
[Name]

PDE4 (R)-(-)-RolipraM
[CAS]

1160521-50-5
[Synonyms]

PDE1-IN-1
ITI214 (free base)
PDE4 (R)-(-)-RolipraM
(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
Cyclopent[4,5]imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(2H)-one, 2-[[4-(6-fluoro-2-pyridinyl)phenyl]methyl]-5,6a,7,8,9,9a-hexahydro-5-methyl-3-(phenylamino)-, (6aR,9aS)-
[Molecular Formula]

C29H26FN7O
[MDL Number]

MFCD28385866
[MOL File]

1160521-50-5.mol
[Molecular Weight]

507.56
Chemical PropertiesBack Directory
[Boiling point ]

731.7±70.0 °C(Predicted)
[density ]

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

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

2.06±0.20(Predicted)
[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
[Uses]

ITI-214 free base is a potent, CNS-active, orally bioavailable PDE1 inhibitor (Ki of 58 pM) with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters and ion channels. ITI-214 free base inhibits recombinant full-length human PDE1A, PDE1B and PDE1C with Kis of 33 pM, 380 pM and 35 pM, respectively. ITI-214 free base shows efficacy in various animal models of motor and cognitive functions[1][2].
[in vivo]

ITI-214 significantly enhances memory performance in the test with a minimum effective dose of 3 mg/kg[1].

Animal Model:Male Sprague-Dawley rats[1]
Dosage:0.1-10 mg/kg
Administration:P.o.
Result:Significantly enhanced memory performance in the test with a minimum effective dose of 3 mg/kg.
[IC 50]

PDE1: 58 pM (Ki); PDE1A: 33 pM (Ki); PDE1B: 380 pM (Ki); PDE1C: 35 pM (Ki)
[References]

[1] Li P, et al. Discovery of Potent and Selective Inhibitors of Phosphodiesterase 1 for the Treatment of Cognitive Impairment Associated with Neurodegenerative and Neuropsychiatric Diseases. J Med Chem. 2016 Feb 11;59(3):1149-64. DOI:10.1021/acs.jmedchem.5b01751
[2] Lawrence Wennogle. Novel uses. From PCT Int. Appl. (2014), WO 2014145617 A2 20140918.
[3] Peng Li , et al. Salt crystals. From PCT Int. Appl. (2013), WO 2013192556 A2 20131227.
[4] Allen A. Fienberg, et al. Organic compounds. From PCT Int. Appl. (2010), WO 2010132127 A1 20101118.
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