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Volumn 64, Issue 8, 1999, Pages 535-540

Nitrile hydratase from Rhodococcus erythropolis: Metabolization of steroidal compounds with a nitrile group

Author keywords

Microbial transformation; Nitrile hydratase; Progesterone receptor; Progestin; Steroid aromatization

Indexed keywords

DIENOGEST; ESTRANE DERIVATIVE; ESTROGEN RECEPTOR; NITRILE HYDRATASE; PROGESTERONE RECEPTOR;

EID: 0032859880     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(99)00028-8     Document Type: Article
Times cited : (15)

References (21)
  • 4
    • 0027321694 scopus 로고
    • Das endokrinologische Profil von Metaboliten des Gestagens Dienogest
    • Oettel M., Kaufmann G., Kurischko A. Das endokrinologische Profil von Metaboliten des Gestagens Dienogest. Pharmazie. 48:1993;541-545.
    • (1993) Pharmazie , vol.48 , pp. 541-545
    • Oettel, M.1    Kaufmann, G.2    Kurischko, A.3
  • 7
    • 0025155099 scopus 로고
    • Nitrilase-catalyzed production of pyrazinoic acid, an antimycobacterial agent, from cyanopyrazine by resting cells of Rhodococcus rhodochrous J1
    • Kobayashi M., Yanaka N., Nagasawa T., Yamada H. Nitrilase-catalyzed production of pyrazinoic acid, an antimycobacterial agent, from cyanopyrazine by resting cells of Rhodococcus rhodochrous J1. J Antibiot Tokyo. 43:1990;1316-1320.
    • (1990) J Antibiot Tokyo , vol.43 , pp. 1316-1320
    • Kobayashi, M.1    Yanaka, N.2    Nagasawa, T.3    Yamada, H.4
  • 8
    • 0028478144 scopus 로고
    • Enzyme-catalysed enantioselective hydrolysis of racemic naproxen nitrile
    • Effenberger F., Böhme J. Enzyme-catalysed enantioselective hydrolysis of racemic naproxen nitrile. Bioorg Med Chem. 2:1994;715-721.
    • (1994) Bioorg Med Chem , vol.2 , pp. 715-721
    • Effenberger, F.1    Böhme, J.2
  • 9
    • 0345221218 scopus 로고
    • Untersuchungen zur Bromierung/Dehydrobromierung von 17α-Cyanomethyl-17β-hydroxy-östr-5(10)-en-3-on
    • Menzenbach B., Hübner M., Ponsold K. Untersuchungen zur Bromierung/Dehydrobromierung von 17α-Cyanomethyl-17β-hydroxy-östr-5(10)-en-3-on. J Prakt Chemie. 326:1984;893-898.
    • (1984) J Prakt Chemie , vol.326 , pp. 893-898
    • Menzenbach, B.1    Hübner, M.2    Ponsold, K.3
  • 10
    • 0021178702 scopus 로고
    • Synthese potentieller Metaboliten der STS 557 (Dienogest). Teil 3: 17α-Hydroxymethyl-17β-hydroxyestra-4,9-dien-3-on
    • Menzenbach B., Hübner M., Sahm R., Ponsold K. Synthese potentieller Metaboliten der STS 557 (Dienogest). Teil 3 17α-Hydroxymethyl-17β-hydroxyestra-4,9-dien-3-on . Pharmazie. 39:1984;496-497.
    • (1984) Pharmazie , vol.39 , pp. 496-497
    • Menzenbach, B.1    Hübner, M.2    Sahm, R.3    Ponsold, K.4
  • 11
    • 25544464675 scopus 로고
    • Synthese potentieller Metaboliten der STS 557 (Dienogest). Teil 2: 17α-Cyanomethylestra-1,3,5(10),9(11)-tetraen-3,17β-diol
    • Hübner M., Menzenbach B., Röhrig H., Ponsold K. Synthese potentieller Metaboliten der STS 557 (Dienogest). Teil 2 17α-Cyanomethylestra-1,3,5(10),9(11)-tetraen-3,17β-diol . Pharmazie. 39:1984;496.
    • (1984) Pharmazie , vol.39 , pp. 496
    • Hübner, M.1    Menzenbach, B.2    Röhrig, H.3    Ponsold, K.4
  • 12
    • 0030985876 scopus 로고    scopus 로고
    • Preparation of 3-ketodesogestrel metabolites by microbial transformation and chemical synthesis
    • Groh H., Schön R., Ritzau M., Kasch H., Undisz K., Hobe G. Preparation of 3-ketodesogestrel metabolites by microbial transformation and chemical synthesis. Steroids. 62:1997;437-443.
    • (1997) Steroids , vol.62 , pp. 437-443
    • Groh, H.1    Schön, R.2    Ritzau, M.3    Kasch, H.4    Undisz, K.5    Hobe, G.6
  • 13
    • 0020385345 scopus 로고
    • Microbial transformation of 17α-cyanomethyl-17-hydroxy-4,9-estradien-3-one (STS 557) and 17α-cyanomethyl-19-nortestosterone by Mycobacterium smegmatis
    • Hobe G., Schön R., Hörhold C., Hübner M., Schade W., Schubert K. Microbial transformation of 17α-cyanomethyl-17-hydroxy-4,9-estradien-3-one (STS 557) and 17α-cyanomethyl-19-nortestosterone by Mycobacterium smegmatis. Steroids. 39:1982;399-409.
    • (1982) Steroids , vol.39 , pp. 399-409
    • Hobe, G.1    Schön, R.2    Hörhold, C.3    Hübner, M.4    Schade, W.5    Schubert, K.6
  • 17
    • 0019219057 scopus 로고
    • Species differences in biotransformation of 17α-cyanomethylestradiol 3-methyl ether
    • Hobe G., Schön R., Wehrberger K. Species differences in biotransformation of 17α-cyanomethylestradiol 3-methyl ether. Steroids. 36:1980;131-147.
    • (1980) Steroids , vol.36 , pp. 131-147
    • Hobe, G.1    Schön, R.2    Wehrberger, K.3
  • 19
    • 0023375253 scopus 로고
    • MTD calculations on quantitative structure-activity relationships of steroids binding to the progesterone receptor
    • Bohl M, Simon Z, Vlad A, Kaufmann G, Ponsold K. MTD calculations on quantitative structure-activity relationships of steroids binding to the progesterone receptor. Z. Naturforsch 1987;42c:935-40.
    • (1987) Z. Naturforsch , vol.42 C , pp. 935-940
    • Bohl, M.1    Simon, Z.2    Vlad, A.3    Kaufmann, G.4    Ponsold, K.5
  • 20
    • 0028176158 scopus 로고
    • Synthesis of (17α,20E/Z)iodovinyl testosterone and 19-nortestosterone derivatives as potential radioligands for androgen and progesterone receptors
    • Ali H., Rousseau J., van Lier J.E. Synthesis of (17α,20E/Z)iodovinyl testosterone and 19-nortestosterone derivatives as potential radioligands for androgen and progesterone receptors. J Steroid Biochem Mol Biol. 49:1994;15-29.
    • (1994) J Steroid Biochem Mol Biol , vol.49 , pp. 15-29
    • Ali, H.1    Rousseau, J.2    Van Lier, J.E.3
  • 21
    • 0020661301 scopus 로고
    • Influence of a 9-double bond on stereospecific microbial 4,5-reductions
    • Schubert K., Schumann G., Kaufmann G. Influence of a 9-double bond on stereospecific microbial 4,5-reductions. J Steroid Biochem. 18:1983;75-80.
    • (1983) J Steroid Biochem , vol.18 , pp. 75-80
    • Schubert, K.1    Schumann, G.2    Kaufmann, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.