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Volumn 15, Issue 7, 2007, Pages 2631-2650

Design and synthesis of new potent dipeptidyl peptidase IV inhibitors with enhanced ex vivo duration

Author keywords

DPP IV inhibitor; Prolyl 2 cyanopyrrolidine

Indexed keywords

1 [[4 (1 AZEPANYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE; 1 [[4 (1 AZETIDINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (1 AZETIDINYLCARBONYL) 5 METHYL 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (1 AZOCANYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (1 PIPERIDINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (1 PYRROLIDINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (1,3 DIHYDRO 2H ISOINDOL 2 YLCARBONYL) 5 METHYL 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (2 HYDROXYETHYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE[7,7 DIMETHYL 2 OXOBICYCLO[2.2.1]HEPT 1 YL]METHANESULFONATE; 1 [[4 (4 MORPHOLINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (4 THIOMORPHOLINYLCARBONYL) 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[4 (HYDROXYMETHYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[5 METHYL 4 (1 PYRROLIDINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[5 METHYL 4 (4 MORPHOLINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 1 [[5 METHYL 4 (4 THIOMORPHOLINYLCARBONYL) 2 PYRROLIDINYL]CARBONYL] 2 PYRROLIDINECARBONITRILE 4 METHYLBENZENESULFONATE; 2 [5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] 3 PYRROLIDINYL] N,N DIMETHYLACETAMIDE 4 METHYLBENZENESULFONATE; 3 [5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] 3 PYRROLIDINYL] N,N DIMETHYLPROPANAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] 3 PYRROLIDINYL ACETIC ACID 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N ETHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N ETHYL N METHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N ETHYL N,2 DIMETHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N METHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N PROPYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N,N DIETHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N,N DIMETHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; 5 [[2 CYANO 1 PYRROLIDINYL]CARBONYL] N,N,2 TRIMETHYL 3 PYRROLIDINECARBOXAMIDE 4 METHYLBENZENESULFONATE; BENZYL 1 ( TERT BUTOXYCARBONYL) 4 [(4 METHYLBENZENESULFONYL)OXY] 2 PYRROLIDINECSRBOXYLATE; BENZYL 1 (TERT BUTOXYCARBONYL) 4 CYANO 2 PYRROLIDINECARBOXYLATE; DIPEPTIDYL PEPTIDASE IV INHIBITOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 33847617068     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2007.01.041     Document Type: Article
Times cited : (18)

References (20)
  • 13
    • 33847665656 scopus 로고    scopus 로고
    • Kondo, T.; Sugimoto, I.; Nekado, T.; Ochi, K.; Ohtani, T.; Tajima, Y.; Yamamoto, S.; Kawabata, K.; Nakai, H.; Toda, M. Bioorg. Med. Chem., in press, doi:10.1016/j.bmc.2007.01.033.
  • 15
    • 33847645452 scopus 로고    scopus 로고
    • note
    • Compound 64 was prepared by the following two methods. One of them is described in Section 2. The other is the same method as the reported one (Ezquerra et al. J. Org. Chem. 1995, 60, p 2925), which describes the established stereochemistry, starting with condensation reaction of the protected ethyl pyrroglutamate and 3-benzyloxypropionaldehyde. Products prepared by the above-described two methods showed an identical NMR. Based on the result, the stereochemistry of 4-position of 64 was determined to be 4β.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.