Prasugrel binds to the platelet receptor for adenosine diphosphate (ADP). It is an inhibitor of platelet aggregation
Type : Drug, Not AlphaBeta Hydrolase target, Acetate, Cyclopropyl, Antiplatlet
Chemical_Nomenclature : [5-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-6,7-dihydro-4H-thieno[3,2-c]pyridin-2-yl] acetate
Canonical SMILES : CC(=O)OC1=CC2=C(S1)CCN(C2)C(C3=CC=CC=C3F)C(=O)C4CC4
InChI : InChI=1S\/C20H20FNO3S\/c1-12(23)25-18-10-14-11-22(9-8-17(14)26-18)19(20(24)13-6-7-13)15-4-2-3-5-16(15)21\/h2-5,10,13,19H,6-9,11H2,1H3
InChIKey : DTGLZDAWLRGWQN-UHFFFAOYSA-N
Other name(s) : Effient || Efient || CS-747
MW : 373.4
Formula : C20H20FNO3S
CAS_number : 150322-43-3
PubChem : 6918456
UniChem : DTGLZDAWLRGWQN-UHFFFAOYSA-N
Structures : No structure
Families : Carb_B_Chordata, Arylacetamide_deacetylase
Title : Role of human AADAC on hydrolysis of eslicarbazepine acetate and effects of AADAC genetic polymorphisms on hydrolase activity - Hirosawa_2021_Drug.Metab.Dispos__ |
Author(s) : Hirosawa K , Fukami T , Tashiro K , Sakai Y , Kisui F , Nakano M , Nakajima M |
Ref : Drug Metabolism & Disposition: The Biological Fate of Chemicals , : , 2021 |
Abstract : |
PubMedSearch : Hirosawa_2021_Drug.Metab.Dispos__ |
PubMedID: 33446525 |
Gene_locus related to this paper: human-AADAC |
Title : Arylacetamide Deacetylase is Responsible for Activation of Prasugrel in Human and Dog - Kurokawa_2016_Drug.Metab.Dispos_44_409 |
Author(s) : Kurokawa T , Fukami T , Yoshida T , Nakajima M |
Ref : Drug Metabolism & Disposition: The Biological Fate of Chemicals , 44 :409 , 2016 |
Abstract : |
PubMedSearch : Kurokawa_2016_Drug.Metab.Dispos_44_409 |
PubMedID: 26718653 |
Title : A comparison of the metabolism of clopidogrel and prasugrel - Laizure_2010_Expert.Opin.Drug.Metab.Toxicol_6_1417 |
Author(s) : Laizure SC , Parker RB |
Ref : Expert Opin Drug Metab Toxicol , 6 :1417 , 2010 |
Abstract : |
PubMedSearch : Laizure_2010_Expert.Opin.Drug.Metab.Toxicol_6_1417 |
PubMedID: 20839914 |
Title : The biotransformation of prasugrel, a new thienopyridine prodrug, by the human carboxylesterases 1 and 2 - Williams_2008_Drug.Metab.Dispos_36_1227 |
Author(s) : Williams ET , Jones KO , Ponsler GD , Lowery SM , Perkins EJ , Wrighton SA , Ruterbories KJ , Kazui M , Farid NA |
Ref : Drug Metabolism & Disposition: The Biological Fate of Chemicals , 36 :1227 , 2008 |
Abstract : |
PubMedSearch : Williams_2008_Drug.Metab.Dispos_36_1227 |
PubMedID: 18372401 |