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Inhibitor Report for: 3-amino-4-phenyl-pyrrolidine-15B

General
Type Trifluoro, Pyrrolidine, Pyridine, Pyrimidine
Chemical_Nomenclature (3R,4S)-1-[6-(6-methoxypyridin-3-yl)pyrimidin-4-yl]-4-(2,4,5-trifluorophenyl)pyrrolidin-3-amine
Canonical SMILES COC1=NC=C(C=C1)C2=CC(=NC=N2)N3CC(C(C3)N)C4=CC(=C(C=C4F)F)F
InChI InChI=1S/C20H18F3N5O/c1-29-20-3-2-11(7-25-20)18-6-19(27-10-26-18)28-8-13(17(24)9-28)12-4-15(22)16(23)5-14(12)21/h2-7,10,13,17H,8-9,24H2,1H3/t13-,17+/m1/s1
InChIKey IFKWHPAWYJARQJ-DYVFJYSZSA-N
Other name(s) PZF ; CHEMBL237786 ; (3R,4S)-1-(6-(6-methoxypyridin-3-yl)pyrimidin-4-yl)-4-(2,4,5-trifluorophenyl)pyrrolidin-3-amine ; BDBM50221073 ; DB08445
________________________________________________________________________________________________
MW|401.39
Formula|C20H18F3N5O
CAS_number|
PubChem|24180585
UniChem|IFKWHPAWYJARQJ-DYVFJYSZSA-N
IUPHAR|
Wikipedia|

Target
Families | 3-amino-4-phenyl-pyrrolidine-15B ligand of proteins in family: DPP4N_Peptidase_S9
Stucture | 1 structure: 2QJR: Dipepdyl peptidase IV in complex with inhibitor PZF
Protein | human-DPP4

References:
Search PubMed for references concerning: 3-amino-4-phenyl-pyrrolidine-15B
    Title: (3R,4S)-4-(2,4,5-Trifluorophenyl)-pyrrolidin-3-ylamine inhibitors of dipeptidyl peptidase IV: synthesis, in vitro, in vivo, and X-ray crystallographic characterization
    Wright SW, Ammirati MJ, Andrews KM, Brodeur AM, Danley DE, Doran SD, Lillquist JS, Liu S, McClure LD and Cox ED <10 more author(s)>
    Ref: Bioorganic & Medicinal Chemistry Lett, 17:5638, 2007 : PubMed