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Volumn 59, Issue 2, 2016, Pages 687-706

Structure-Activity Relationship of Azaindole-Based Glucokinase Activators

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL] BENZOIC ACID METHYL ESTER; 2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]BENZENEPHOSPHONIC ACID 2,2 DIMETHYLPROPANEDIOL ESTER; 2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]BENZONITRILE; 2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN2 YL)ETHYL]BENZENEPHOSPHONIC ACID DIETHYL ESTER; 2 CHLORO 4 [2 CYCLOPNETYL 1 (1H PYRROLO[2,3 B]PYRDIIN 2 YL)ETHYL]PHENOL; 2 CHLORO 4 [2 CYCLOPPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]BENZYL ALCOHOL; 2 METHYLSULFUNYL 5 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]CHLOROBENZENE; 2 [4 [2 CYCLOPNETYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]PHENYL] 5,5 DIMETHYL 1,3 DIOXAPHOSPHINANE 2 OXIDE; 3 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]CHLOROBENZENE; 4 [2 CYCLOPNETYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]BROMOBENZENE; 5 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL] 2 METHYLSULFONYL CHLOROBENZENE; AZAINDOLE; ENZYME ACTIVATOR; GLUCOKINASE; INDOLE DERIVATIVE; O (2 METHOXYISOPROPYL) 2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]PHENOL; O ISOPROPYL 2 CHLORO 4 [2 CYCLOPENTYL 1 (1H PYRROLO[2,3 B]PYRIDIN 2 YL)ETHYL]PHENOL; PIRAGLIATIN; UNCLASSIFIED DRUG; 7-AZAINDOLE DIMER; ANTIDIABETIC AGENT; GLUCOSE;

EID: 84970934851     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/acs.jmedchem.5b01594     Document Type: Article
Times cited : (23)

References (34)
  • 1
    • 79960202841 scopus 로고    scopus 로고
    • Type 2 diabetes across generations: From pathophysiology to prevention and management
    • Nolan, C. J.; Damm, P.; Prentki, M. Type 2 diabetes across generations: from pathophysiology to prevention and management Lancet 2011, 378, 169-181 10.1016/S0140-6736(11)60614-4
    • (2011) Lancet , vol.378 , pp. 169-181
    • Nolan, C.J.1    Damm, P.2    Prentki, M.3
  • 3
    • 58149525327 scopus 로고    scopus 로고
    • Molecular Physiology of Mammalian Glucokinase
    • For a review, see
    • For a review, see: Iynedjian, P. B. Molecular Physiology of Mammalian Glucokinase Cell. Mol. Life Sci. 2009, 66, 27-42 10.1007/s00018-008-8322-9
    • (2009) Cell. Mol. Life Sci. , vol.66 , pp. 27-42
    • Iynedjian, P.B.1
  • 5
    • 0037624071 scopus 로고    scopus 로고
    • Allosteric activators of glucokinase: Potential role in diabetes therapy
    • Grimsby, J.; Sarabu, R.; Corbett, W. L.; Haynes, N. E.; Bizzarro, F. T.; Coffey, J. W.; Guertin, K. R.; Hilliard, D. W.; Kester, R. F.; Mahaney, P. E.; Marcus, L.; Qi, L.; Spence, C. L.; Tengi, J.; Magnuson, M. A.; Chu, C. A.; Dvorozniak, M. T.; Matschinsky, F. M.; Grippo, J. F. Allosteric activators of glucokinase: potential role in diabetes therapy Science 2003, 301, 370-373 10.1126/science.1084073
    • (2003) Science , vol.301 , pp. 370-373
  • 10
    • 84871717231 scopus 로고    scopus 로고
    • Discovery of a novel phenylethyl benzamide glucokinase activator for the treatment of type 2 diabetes mellitus
    • Park, K.; Lee, B. M.; Kim, Y. H.; Han, T.; Yi, W.; Lee, D. H.; Choi, H. H.; Chong, W.; Lee, C. H. Discovery of a novel phenylethyl benzamide glucokinase activator for the treatment of type 2 diabetes mellitus Bioorg. Med. Chem. Lett. 2013, 23, 537-542 10.1016/j.bmcl.2012.11.018
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 537-542
    • Park, K.1    Lee, B.M.2    Kim, Y.H.3    Han, T.4    Yi, W.5    Lee, D.H.6    Choi, H.H.7    Chong, W.8    Lee, C.H.9
  • 11
    • 84864401430 scopus 로고    scopus 로고
    • Investigation on the oxidation of aryl oxiranylmethanols and the synthesis of 2-aryl-N-thiazolyl-oxirane-2-carboxamides as glucokinase activators
    • Ye, N.; Xu, X.; Li, F.; Ning, M.; Liu, Z.; Cao, Y.; Leng, Y.; Zhang, A. Investigation on the oxidation of aryl oxiranylmethanols and the synthesis of 2-aryl-N-thiazolyl-oxirane-2-carboxamides as glucokinase activators Tetrahedron Lett. 2012, 53, 4738-4742 10.1016/j.tetlet.2012.06.111
    • (2012) Tetrahedron Lett. , vol.53 , pp. 4738-4742
    • Ye, N.1    Xu, X.2    Li, F.3    Ning, M.4    Liu, Z.5    Cao, Y.6    Leng, Y.7    Zhang, A.8
  • 14
    • 84862819984 scopus 로고    scopus 로고
    • Design, synthesis, and pharmacological evaluation of benzamide derivatives as glucokinase activators
    • Mao, W.; Ning, M.; Liu, Z.; Zhu, Q.; Leng, Y.; Zhang, A. Design, synthesis, and pharmacological evaluation of benzamide derivatives as glucokinase activators Bioorg. Med. Chem. 2012, 20, 2982-2991 10.1016/j.bmc.2012.03.008
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 2982-2991
    • Mao, W.1    Ning, M.2    Liu, Z.3    Zhu, Q.4    Leng, Y.5    Zhang, A.6
  • 19
    • 77957879376 scopus 로고    scopus 로고
    • Intrinsic electrophilicity of the 4-methylsulfonyl-2-pyridone scaffold in glucokinase activators: Role of glutathione-S-transferases and in vivo quantitation of a glutathione conjugate in rats
    • Litchfield, J.; Sharma, R.; Atkinson, K.; Filipski, K. J.; Wright, S. W.; Pfefferkorn, J. A.; Tan, B.; Kosa, R. E.; Stevens, B.; Tu, M.; Kalgutkar, A. S. Intrinsic electrophilicity of the 4-methylsulfonyl-2-pyridone scaffold in glucokinase activators: role of glutathione-S-transferases and in vivo quantitation of a glutathione conjugate in rats Bioorg. Med. Chem. Lett. 2010, 20, 6262-6267 10.1016/j.bmcl.2010.08.095
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 6262-6267
    • Litchfield, J.1    Sharma, R.2    Atkinson, K.3    Filipski, K.J.4    Wright, S.W.5    Pfefferkorn, J.A.6    Tan, B.7    Kosa, R.E.8    Stevens, B.9    Tu, M.10    Kalgutkar, A.S.11
  • 22
    • 77953131053 scopus 로고    scopus 로고
    • Design, synthesis, and pharmacological evaluation of N-(4-mono and 4,5-disubstituted thiazol-2-yl)-2-aryl-3-(tetrahydro-2H-pyran-4-yl)propanamides as glucokinase activators
    • Li, F.; Zhu, Q.; Zhang, Y.; Feng, Y.; Leng, Y.; Zhang, A. Design, synthesis, and pharmacological evaluation of N-(4-mono and 4,5-disubstituted thiazol-2-yl)-2-aryl-3-(tetrahydro-2H-pyran-4-yl)propanamides as glucokinase activators Bioorg. Med. Chem. 2010, 18, 3875-3884 10.1016/j.bmc.2010.04.038
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 3875-3884
    • Li, F.1    Zhu, Q.2    Zhang, Y.3    Feng, Y.4    Leng, Y.5    Zhang, A.6
  • 30
    • 84970938466 scopus 로고    scopus 로고
    • Fused Nitrogen Heterocyclic Compounds, Process of Preparation and Uses Thereof
    • WO 2011080755.
    • Dave, B.; Deshpande, A.; Kurhade, S.; Kobal, B.; Bhuniya, D.; Palle, V. Fused Nitrogen Heterocyclic Compounds, Process Of Preparation And Uses Thereof. WO 2011080755, Chem. Abstr. 155: 182037.
    • Chem. Abstr. , vol.155 , pp. 182037
    • Dave, B.1    Deshpande, A.2    Kurhade, S.3    Kobal, B.4    Bhuniya, D.5    Palle, V.6
  • 33
    • 1542791635 scopus 로고    scopus 로고
    • Structural basis for allosteric regulation of the monomeric allosteric enzyme human glucokinase
    • Kamata, K.; Mitsuya, M.; Nishimura, T.; Eiki, J.; Nagata, Y. Structural basis for allosteric regulation of the monomeric allosteric enzyme human glucokinase Structure 2004, 12, 429-438 10.1016/j.str.2004.02.005
    • (2004) Structure , vol.12 , pp. 429-438
    • Kamata, K.1    Mitsuya, M.2    Nishimura, T.3    Eiki, J.4    Nagata, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.