메뉴 건너뛰기




Volumn 22, Issue 1, 2003, Pages 83-92

Comparative pharmacophore development for inhibitors of human and rat 5-α-reductase

Author keywords

5 reductase; Inhibitors; Pharmacophore; Structure activity relationships; Training set randomization; Variable weight pharmacophore

Indexed keywords

CRYSTAL STRUCTURE; DISEASES; DRUG THERAPY;

EID: 0038205810     PISSN: 10933263     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1093-3263(03)00138-4     Document Type: Article
Times cited : (20)

References (25)
  • 1
    • 0034743536 scopus 로고    scopus 로고
    • Steroid 5-α-reductases and 3α-hydroxysteroid dehydrogenases: Key enzymes in androgen metabolism
    • Jin Y., Penning T.M. Steroid 5-α-reductases and 3α-hydroxysteroid dehydrogenases: key enzymes in androgen metabolism. Best Pract. Res. Clin. Endocrinol. Metabol. 15:2001;79-94.
    • (2001) Best Pract. Res. Clin. Endocrinol. Metabol. , vol.15 , pp. 79-94
    • Jin, Y.1    Penning, T.M.2
  • 3
    • 0034745012 scopus 로고    scopus 로고
    • Clinical application of 5-α-reductase inhibitors
    • Cilotti A., Danza G., Serio M. Clinical application of 5-α-reductase inhibitors. J. Endocrinol. Invest. 24:2001;199-203.
    • (2001) J. Endocrinol. Invest. , vol.24 , pp. 199-203
    • Cilotti, A.1    Danza, G.2    Serio, M.3
  • 4
    • 0008699133 scopus 로고    scopus 로고
    • Prostate cancer: Horizons in the development of novel anti-cancer strategies
    • Papatsoris A.G., Papavassiliou A.G. Prostate cancer: horizons in the development of novel anti-cancer strategies. Curr. Med. Chem. 1:2001;47-70.
    • (2001) Curr. Med. Chem. , vol.1 , pp. 47-70
    • Papatsoris, A.G.1    Papavassiliou, A.G.2
  • 6
  • 8
    • 0001760102 scopus 로고    scopus 로고
    • Comparative QSAR analysis of 5-α-reductase inhibitors
    • Kurup A., Garg R., Hansch C. Comparative QSAR analysis of 5-α-reductase inhibitors. Chem. Rev. 100:2000;909-924.
    • (2000) Chem. Rev. , vol.100 , pp. 909-924
    • Kurup, A.1    Garg, R.2    Hansch, C.3
  • 10
    • 0034609834 scopus 로고    scopus 로고
    • Benz[c]quinolizin-3-ones: A novel class of potent and selective non-steroidal inhibitors of human steroid 5-α-reductase1
    • Guarna A., Machetti F., Occhiato E.G., Scarpi D., Comerci A., Danza G., Mancina R., Serio M., Hardy K. Benz[c]quinolizin-3-ones: a novel class of potent and selective non-steroidal inhibitors of human steroid 5-α-reductase1. J. Med. Chem. 43:2000;3718-3735.
    • (2000) J. Med. Chem. , vol.43 , pp. 3718-3735
    • Guarna, A.1    Machetti, F.2    Occhiato, E.G.3    Scarpi, D.4    Comerci, A.5    Danza, G.6    Mancina, R.7    Serio, M.8    Hardy, K.9
  • 11
    • 0036132203 scopus 로고    scopus 로고
    • 5-Phenyl substituted 1-methyl-2-pyridones and 4′-substituted biphenyl-4-carboxylic. Acids synthesis and evaluation as inhibitors of steroid-5-α-reductase type 1 and 2
    • Picard F., Schulz T., Hartmann R.W. 5-phenyl substituted 1-methyl-2-pyridones and 4′-substituted biphenyl-4-carboxylic. Acids synthesis and evaluation as inhibitors of steroid-5-α-reductase type 1 and 2. Bioorg. Med. Chem. Lett. 10:2002;437-448.
    • (2002) Bioorg. Med. Chem. Lett. , vol.10 , pp. 437-448
    • Picard, F.1    Schulz, T.2    Hartmann, R.W.3
  • 13
    • 0031788781 scopus 로고    scopus 로고
    • (1-Benzylindole-3-yl)alkanoic acids; Novel non-steroidal inhibitors of steroidal 5-α-reductase (I)
    • Sawada K., Hirai H., Golden P., Okada S., Sawada Y., Hashimoto M., Tanaka H. (1-Benzylindole-3-yl)alkanoic acids; novel non-steroidal inhibitors of steroidal 5-α-reductase (I). Chem. Pharm. Bull. 46:1998;1683-1687.
    • (1998) Chem. Pharm. Bull. , vol.46 , pp. 1683-1687
    • Sawada, K.1    Hirai, H.2    Golden, P.3    Okada, S.4    Sawada, Y.5    Hashimoto, M.6    Tanaka, H.7
  • 14
    • 0032895098 scopus 로고    scopus 로고
    • 4-(1-Benzoyl(indole-3-yl)butyric acids and FK 143: Novel non-steroidal inhibitors of steroid 5-α-reductase (II)
    • Sawada K., Golden P., Okada S., Kayakiri N., Sawada Y., Hashimoto M., Tanaka H. 4-(1-Benzoyl(indole-3-yl)butyric acids and FK 143: novel non-steroidal inhibitors of steroid 5-α-reductase (II). Chem. Pharm. Bull. 47:1999;481-491.
    • (1999) Chem. Pharm. Bull. , vol.47 , pp. 481-491
    • Sawada, K.1    Golden, P.2    Okada, S.3    Kayakiri, N.4    Sawada, Y.5    Hashimoto, M.6    Tanaka, H.7
  • 15
    • 0034071008 scopus 로고    scopus 로고
    • A novel class of inhibitors for human steroid 5-α-reductase: Synthesis and biological evaluation of indole derivatives (II)
    • Igarashi S., Inami H., Hara H., Fujii M., Koutoku H., Oritani H., Mase T. A novel class of inhibitors for human steroid 5-α-reductase: synthesis and biological evaluation of indole derivatives (II). Chem. Pharm. Bull. 48:2000;382-388.
    • (2000) Chem. Pharm. Bull. , vol.48 , pp. 382-388
    • Igarashi, S.1    Inami, H.2    Hara, H.3    Fujii, M.4    Koutoku, H.5    Oritani, H.6    Mase, T.7
  • 16
    • 0035829450 scopus 로고    scopus 로고
    • Novel lead generation through hypothetical pharmacophore three-dimensional database searching: Discovery of isoflavonoids as non-steroidal inhibitors of rat 5-α-reductase
    • Chen G.S., Chang C-S., Kan W.M., Chang C.-L., Wang K.C., Chern J.-W. Novel lead generation through hypothetical pharmacophore three-dimensional database searching: discovery of isoflavonoids as non-steroidal inhibitors of rat 5-α-reductase. J. Med Chem. 44:2001;3759-3763.
    • (2001) J. Med Chem. , vol.44 , pp. 3759-3763
    • Chen, G.S.1    Chang, C.-S.2    Kan, W.M.3    Chang, C.-L.4    Wang, K.C.5    Chern, J.-W.6
  • 17
    • 0027323620 scopus 로고
    • Finasteride: The first 5-alpha-reductase inhibitor
    • Sudduth S.L., Koronkowski M.J. Finasteride: the first 5-alpha-reductase inhibitor. Pharmacotherapy. 13:1993;309-325.
    • (1993) Pharmacotherapy , vol.13 , pp. 309-325
    • Sudduth, S.L.1    Koronkowski, M.J.2
  • 18
    • 0003675575 scopus 로고    scopus 로고
    • Hypogen: An automated system for generating 3D predictive pharmacophore models in pharmacophore perception, development, and use
    • O.F. Guner (Ed.), , International University Line, La Jolla, CA, Chapter 10
    • H. Li, J. Sutter, R. Hoffman, Hypogen: an automated system for generating 3D predictive pharmacophore models in pharmacophore perception, development, and use, in: O.F. Guner (Ed.), Drug Design, vol. 175, International University Line, La Jolla, CA, 2000 (Chapter 10).
    • (2000) Drug Design , pp. 175
    • Li, H.1    Sutter, J.2    Hoffman, R.3
  • 19
    • 0028984550 scopus 로고
    • Rat steroid 5-α-reductase kinetic characteristics: Extreme pH-dependancy of the type II isozyme in prostate and epididymis homogenates
    • Span P.N., Smals A.G.H., Sweep C.G.J., Benraad T.J. Rat steroid 5-α-reductase kinetic characteristics: extreme pH-dependancy of the type II isozyme in prostate and epididymis homogenates. J. Steroid Biochem. Metabol. 53:1995;185-192.
    • (1995) J. Steroid Biochem. Metabol. , vol.53 , pp. 185-192
    • Span, P.N.1    Smals, A.G.H.2    Sweep, C.G.J.3    Benraad, T.J.4
  • 20
    • 84986522856 scopus 로고
    • Poling: Promoting conformational variation
    • Smellie A., Teig S.L., Towbin P. Poling: promoting conformational variation. J. Comp. Chem. 16:1995;171-187.
    • (1995) J. Comp. Chem. , vol.16 , pp. 171-187
    • Smellie, A.1    Teig, S.L.2    Towbin, P.3
  • 21
    • 0029276206 scopus 로고
    • Analysis of conformational coverage. 1. Validation and estimation of coverage
    • Smellie A., Kahn S.D., Teig S.L. Analysis of conformational coverage. 1. Validation and estimation of coverage. J. Chem. Inf. Comp. Sci. 35:1995;285-294.
    • (1995) J. Chem. Inf. Comp. Sci. , vol.35 , pp. 285-294
    • Smellie, A.1    Kahn, S.D.2    Teig, S.L.3
  • 22
    • 0029277503 scopus 로고
    • Analysis of conformational coverage. 2. Applications of conformational models
    • Smellie A., Kahn S.D., Teig S.L. Analysis of conformational coverage. 2. Applications of conformational models. J. Chem. Inf. Comp. Sci. 35:1995;295-304.
    • (1995) J. Chem. Inf. Comp. Sci. , vol.35 , pp. 295-304
    • Smellie, A.1    Kahn, S.D.2    Teig, S.L.3
  • 24
    • 85031173923 scopus 로고    scopus 로고
    • http://www.accelrys.com/catalyst/cathypo.html.
  • 25
    • 12444267254 scopus 로고    scopus 로고
    • De novo ligand design
    • P.V.R. Schleyer, N.L. Allinger, T. Clark, J Gasteiger, P.A. Kollman, H.F. Schaefer III, P.R. Schreiner (Eds.), Wiley, Chichester, UK
    • H.J. Bohm, S. Fischer, De novo ligand design, in: P.V.R. Schleyer, N.L. Allinger, T. Clark, J Gasteiger, P.A. Kollman, H.F. Schaefer III, P.R. Schreiner (Eds.), Encycylopedia of Computational Chemistry, Wiley, Chichester, UK, 1998, pp. 657-663.
    • (1998) Encycylopedia of Computational Chemistry , pp. 657-663
    • Bohm, H.J.1    Fischer, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.