Anagliptin

Anagliptin is an orally available, potent, selective inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity. Compared to vildagliptin, anagliptin caused longer lasting inhibition of DPP-4 activity

General

Type : Drug,Cyanide,Pyrrolidine,Gliptin,Pyrimidine,Carboxamide,Pyrazole

Chemical_Nomenclature : N-[2-[[2-[(2S)-2-cyanopyrrolidin-1-yl]-2-oxoethyl]amino]-2-methylpropyl]-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxamide

Canonical SMILES : CC1=NN2C=C(C=NC2=C1)C(=O)NCC(C)(C)NCC(=O)N3CCCC3C#N

InChI : InChI=1S\/C19H25N7O2\/c1-13-7-16-21-9-14(11-26(16)24-13)18(28)22-12-19(2,3)23-10-17(27)25-6-4-5-15(25)8-20\/h7,9,11,15,23H,4-6,10,12H2,1-3H3,(H,22,28)\/t15-\/m0\/s1

InChIKey : LDXYBEHACFJIEL-HNNXBMFYSA-N

Other name(s) : Suiny,UNII-K726J96838,CHEMBL1929396,CHEMBL1929387,Anagliptin HCl


MW : 383.45

Formula : C19H25N7O2

CAS_number : 739366-20-2

PubChem : 44513473

UniChem : LDXYBEHACFJIEL-HNNXBMFYSA-N

IUPHAR :

Wikipedia :

Target

Families : Anagliptin ligand of proteins in family: DPP4N_Peptidase_S9

Stucture : 3WQH Crystal Structure of human DPP-IV in complex with Anagliptin

Protein : human-DPP4

References (2)

Title : Anagliptin, a potent dipeptidyl peptidase IV inhibitor: its single-crystal structure and enzyme interactions - Watanabe_2015_J.Enzyme.Inhib.Med.Chem_30_981
Author(s) : Watanabe YS , Yasuda Y , Kojima Y , Okada S , Motoyama T , Takahashi R , Oka M
Ref : J Enzyme Inhib Med Chem , 30 :981 , 2015
Abstract : Watanabe_2015_J.Enzyme.Inhib.Med.Chem_30_981
ESTHER : Watanabe_2015_J.Enzyme.Inhib.Med.Chem_30_981
PubMedSearch : Watanabe_2015_J.Enzyme.Inhib.Med.Chem_30_981
PubMedID: 26147347
Gene_locus related to this paper: human-DPP4

Title : Discovery and pharmacological characterization of N-[2-({2-[(2S)-2-cyanopyrrolidin-1-yl]-2-oxoethyl}amino)-2-methylpropyl]-2-methyl pyrazolo[1,5-a]pyrimidine-6-carboxamide hydrochloride (anagliptin hydrochloride salt) as a potent and selective DPP-IV inhibitor - Kato_2011_Bioorg.Med.Chem_19_7221
Author(s) : Kato N , Oka M , Murase T , Yoshida M , Sakairi M , Yamashita S , Yasuda Y , Yoshikawa A , Hayashi Y , Makino M , Takeda M , Mirensha Y , Kakigami T
Ref : Bioorganic & Medicinal Chemistry , 19 :7221 , 2011
Abstract : Kato_2011_Bioorg.Med.Chem_19_7221
ESTHER : Kato_2011_Bioorg.Med.Chem_19_7221
PubMedSearch : Kato_2011_Bioorg.Med.Chem_19_7221
PubMedID: 22019046