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813452-18-5

813452-18-5 Structure

813452-18-5 Structure
IdentificationBack Directory
[Name]

(S)-1-((2S,3S,11bS)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-3-yl)-4-(fluoromethyl)pyrrolidin-2-one
[CAS]

813452-18-5
[Synonyms]

R1579
R-1579
RG1579
RG-1579
RO-4876904
Camegliptin
CARMEGLIPTIN
RO-4876904-001
2-Pyrrolidinone, 1-[(2S,3S,11bS)-2-amino-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizin-3-yl]-4-(fluoromethyl)-, (4S)-
(S)-1-((2S,3S,11bS)-2-amino-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-3-yl)-4-(fluoromethyl)pyrrolidin-2-one
[Molecular Formula]

C20H28FN3O3
[MDL Number]

MFCD16038044
[MOL File]

813452-18-5.mol
[Molecular Weight]

377.45
Chemical PropertiesBack Directory
[Boiling point ]

546.5±50.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[pka]

9.44±0.40(Predicted)
Hazard InformationBack Directory
[Uses]

Carmegliptin (RO-4876904) is an orally active, potent and long-acting dipeptidyl peptidase IV inhibitor. Carmegliptin is also a substrate of P-glycoprotein that synergizes with Verapamil (HY-14275). Carmegliptin improves insulin sensitivity and reduces hepatic glucose production in hyperglycemic mice. Carmegliptin is promising for research of type 2 diabetes, hypertension and cardiovascular disease[1][2].
[IC 50]

DPP-4
[References]

[1] Mattei P, et al. Discovery of carmegliptin: a potent and long-acting dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1109-13. DOI:10.1016/j.bmcl.2009.12.024
[2] Kuhlmann O, et al. Interaction potential of Carmegliptin with P-glycoprotein (Pgp) transporter in healthy volunteers. J Drug Assess. 2014 Mar 3;3(1):28-37. DOI:10.3109/21556660.2014.900065
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