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Volumn 9, Issue 7-8, 1999, Pages 631-642

Benzoxazoline and benzimidazoline derivatives as novel aldose reductase inhibitors, part 2: Lead optimization

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSE REDUCTASE INHIBITOR; IMIDAZOLINE DERIVATIVE; OXAZOLINE DERIVATIVE;

EID: 0033367146     PISSN: 10542523     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (12)
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    • Benzoxazoline and benzimidazoline derivatives as novel aldose reductase inhibitors, Part 1: Lead evolution
    • The previous paper in this issue
    • 1. Nakao, K.; Asao, M.; Shirai, H.; Saito, K.; Moriya, T.; Iwata, H; Matsumoto, M.; Matsuoka, Y.; Shimizu, R. Benzoxazoline and Benzimidazoline Derivatives as Novel Aldose Reductase Inhibitors, Part 1: Lead Evolution. Med. Chem. Res. The previous paper in this issue.
    • Med. Chem. Res.
    • Nakao, K.1    Asao, M.2    Shirai, H.3    Saito, K.4    Moriya, T.5    Iwata, H.6    Matsumoto, M.7    Matsuoka, Y.8    Shimizu, R.9
  • 2
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    • Comparative Molecular Field Analysis (CoMFA). 1. Effect of shape on binding of steroids to carrier proteins
    • 2. Cramer III, R. D.; Pattersn, D. E.; Bunce, J. D. Comparative Molecular Field Analysis (CoMFA). 1. Effect of Shape on Binding of Steroids to Carrier Proteins. J. Am. Chem. Soc. 1988, 110, 5959-5967.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5959-5967
    • Cramer R.D. III1    Pattersn, D.E.2    Bunce, J.D.3
  • 3
    • 0026645207 scopus 로고
    • Biological activities and quantitative structure-activity relationships of spiro[imidazolidine-4, 4'(1'H)-quinazoline]-2, 2', 5(3'H)-triones as aldose reductase inhibitors
    • 3. Yamagishi, M.; Yamada, Y.; Ozaki, K.; Asao, M.; Shimizu, R.; Suzuki, M.; Matsumoto, M.; Matsuoka, Y.; Matsumoto, K. Biological Activities and Quantitative Structure-Activity Relationships of Spiro[imidazolidine-4, 4'(1'H)-quinazoline]-2, 2', 5(3'H)-triones as Aldose Reductase Inhibitors. J. Med. Chem. 1992, 35, 2085-2094.
    • (1992) J. Med. Chem. , vol.35 , pp. 2085-2094
    • Yamagishi, M.1    Yamada, Y.2    Ozaki, K.3    Asao, M.4    Shimizu, R.5    Suzuki, M.6    Matsumoto, M.7    Matsuoka, Y.8    Matsumoto, K.9
  • 4
    • 0032858360 scopus 로고    scopus 로고
    • 3D-pharmacophore analyses of aldose reductase inhibitory spiroquinazolinones
    • 4. Nakao, K.; Asao, M.; Shirai, H.; Shimizu, R. 3D-Pharmacophore Analyses of Aldose Reductase Inhibitory Spiroquinazolinones. Drug Design and Discovery 1999, 16, 155-163.
    • (1999) Drug Design and Discovery , vol.16 , pp. 155-163
    • Nakao, K.1    Asao, M.2    Shirai, H.3    Shimizu, R.4
  • 5
    • 0025390935 scopus 로고
    • MOPAC: A semiempirical molecular orbital program
    • 5. Stewart, J. J. P. MOPAC: A Semiempirical Molecular Orbital Program. J. Comput.-Aided Mol. Design 1990, 4, 1-105.
    • (1990) J. Comput.-Aided Mol. Design , vol.4 , pp. 1-105
    • Stewart, J.J.P.1
  • 6
  • 7
    • 24444468650 scopus 로고
    • Ground states of molecules. 38. The MNDO method. Approximations and parameters
    • 7. Dewar, M. J. S.; Thiel, W. Ground States of Molecules. 38. The MNDO method. Approximations and Parameters. J. Am. Chem. Soc. 1977, 99, 4899-4907.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 4899-4907
    • Dewar, M.J.S.1    Thiel, W.2
  • 8
    • 0031570301 scopus 로고    scopus 로고
    • 'Specificity' pocket inferred from the crystal structures of the complexes of aldose reductase with the pharmaceutically important inhibitors tolrestat and sorbinil
    • 8. Urzhumtsev, A.; Tete-Favier, F.; Mitschler, A.; Barbanton, J.; Barth, P.; Urzhumtseva, L.; Biellmann, J.-F.; Podjamy, A. D.; Moras, D. A 'Specificity' Pocket Inferred from the Crystal Structures of the Complexes of Aldose Reductase with the Pharmaceutically Important Inhibitors Tolrestat and Sorbinil. Structure, 1997, 5, 601-612.
    • (1997) Structure , vol.5 , pp. 601-612
    • Urzhumtsev, A.1    Tete-Favier, F.2    Mitschler, A.3    Barbanton, J.4    Barth, P.5    Urzhumtseva, L.6    Biellmann, J.-F.7    Podjamy, A.D.8    Moras, D.A.9
  • 9
    • 0031727488 scopus 로고    scopus 로고
    • Molecular modeling studies of the binding modes of aldose reductase inhibitors at the active site of human aldose reductase
    • 9. Lee, Y. S.; Chen, Z.; Kador, P. F. Molecular Modeling Studies of the Binding Modes of Aldose Reductase Inhibitors at the Active Site of Human Aldose Reductase. Bioorg. Med. Chem. 1998, 6, 1811-1819.
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 1811-1819
    • Lee, Y.S.1    Chen, Z.2    Kador, P.F.3
  • 10
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    • SYBYL molecular modeling software. Tripos, Inc. 1699, S. Hanley Road, St. Louis, MO 63144-2913, U.S.A
    • 10. SYBYL molecular modeling software. Tripos, Inc. 1699, S. Hanley Road, St. Louis, MO 63144-2913, U.S.A.
  • 11
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    • HINT: A new method of empirical hydrophobic field calculation for CoMFA
    • 11. Kellogg, G. E.; Semus, S.; Abraham, D. J. HINT: A New Method of Empirical Hydrophobic Field Calculation for CoMFA. J. Comput.-Aided Mol. Design 1991, 5, 545-552.
    • (1991) J. Comput.-Aided Mol. Design , vol.5 , pp. 545-552
    • Kellogg, G.E.1    Semus, S.2    Abraham, D.J.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.