Benzimidazole as deazapurine analogue for microbial transglycosylation

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Benzimidazole nucleosides are compounds with interesting pharmacological properties. Although chemical synthesis of these analogues has been carried out, only few derivatives have been obtained so far using biotransformations. We report herein the biocatalysed preparation of benzimidazole ribo- and...

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Detalles Bibliográficos
Autor principal: Bentancor, L.
Otros Autores: Trelles, J.A, Nóbile, M., Lewkowicz, E.S, Iribarren, A.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2004
Acceso en línea:Registro en Scopus
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Biblioteca Central Dr. Luis F. Leloir (FCEN) de Universidad de Buenos Aires
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024 7 |2 cas  |a benzimidazole, 51-17-2 
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100 1 |a Bentancor, L. 
245 1 0 |a Benzimidazole as deazapurine analogue for microbial transglycosylation 
260 |c 2004 
270 1 0 |m Lewkowicz, E.S.; Universidad Nacional de Quilmes, R.S. Peña 180, (1876) Bernal, Buenos Aires, Argentina; email: elewko@unq.edu.ar 
506 |2 openaire  |e Política editorial 
504 |a Cheng, J.B., Cooper, K., Duplantier, A.J., Eggler, J.F., Kraus, K.G., Marshall, S.C., Marfat, A., Umland, J.P., (1995) Bioorg. Med. Chem. Lett., 5, p. 1965 
504 |a Kugishima, H., Horie, T., Imafuku, K., (1994) J. Heterocyclic Chem., 31, p. 1557 
504 |a Ellingboe, J.W., Spinelli, W., Winkley, M.W., Nguyen, Y.T., Parsons, R.W., Moubarak, I.F., Kitzen, J.M., Bagli, J.F., (1992) J. Med. Chem., 35, p. 705 
504 |a Agrawal, S., Iyer, R.P., (1995) Curr. Opin. Biotechnol., 6, p. 12 
504 |a Salluja, S., Zou, R., Drach, J.C., Townsend, L.B., (1996) J. Med. Chem., 39, p. 881 
504 |a Townsend, L.B., Revankar, G.R., (1970) Chem. Rev., 70, p. 389 
504 |a Plosker, G.L., Noble, S., (1999) Drugs, 58, p. 325 
504 |a Zou, R., Kawashima, E., Freeman, G.A., Koszalka, G.W., Drach, J.C., Townsend, L.B., (2000) Nucleos. Nucleot. Nucleic Acids, 19, p. 125 
504 |a Migawa, M.T., Girardet, J.L., Walker, J.A., Koszalka, G.W., Chamberlain, S.D., Drach, J.C., Townsend, L.B., (1998) J. Med. Chem., 41, p. 1242 
504 |a Chen, J.J., Wei, Y., Drach, J.C., Townsend, L.B., (2000) J. Med. Chem., 43, p. 2449 
504 |a Garuti, L., Roberti, M., Gentilomi II, G., (2001) Farmaco, 56, p. 815 
504 |a Zou, R., Drach, J.C., Townsend, L.B., (1997) J. Med. Chem., 40, p. 811 
504 |a Gudmundson, K.S., Freeman, G.A., Drach, J.C., Townsend, L.B., (2000) J. Med. Chem., 43, p. 2473 
504 |a Mickhailopulo, I.A., Kazimierczuk, Z., Zinchenko, A.I., Barai, V.N., Romanova, V., Eroshevskaya, L.A., (1995) Nucleos. Nucleot., 14, p. 477 
504 |a Doskocil, J., Holy, A., (1977) Coll. Czech. Chem. Commun., 42, p. 370 
504 |a Lewkowicz, E., Martínez, N., Rogert, M.C., Porro, S., Iribarren, A.M., (2000) Biotechnol. Lett., 22, p. 1277 
504 |a Rogert, M.C., Trelles, J.A., Porro, S., Lewkowicz, E.S., Iribarren, A.M., (2002) Biocatal. Biotransform., 20, p. 347 
504 |a Trelles, J., Fernandez, M., Lewkowicz, E., Iribarren, A., Sinisterra, J.V., (2003) Tetrahedron Lett., 44, p. 2605 
504 |a Prasad, A.K., Trikha, S., Parmar, V.S., (1999) Bioorg. Chem., 27, p. 135 
504 |a Krenitzky, T., Koszalka, G., (1981) Biochemistry, 20, p. 3615 
520 3 |a Benzimidazole nucleosides are compounds with interesting pharmacological properties. Although chemical synthesis of these analogues has been carried out, only few derivatives have been obtained so far using biotransformations. We report herein the biocatalysed preparation of benzimidazole ribo- and 2′-deoxyribonucleosides by different microbial whole cells that afforded yields between 75 and 85%. © 2004 Elsevier B.V. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Secretaría de Ciencia y Técnica, Universidad Nacional de Río Cuarto 
536 |a Detalles de la financiación: This work was supported by Universidad Nacional de Quilmes and Secretarı́a de Ciencia y Técnica de la Nación, Argentina. AMI is research member of CONICET, Argentina. 
593 |a Universidad Nacional de Quilmes, R.S. Peña 180, (1876) Bernal, Buenos Aires, Argentina 
593 |a INGEBI, CONICET, Vuelta de Obligado 2490, (1428) Buenos Aires, Argentina 
690 1 0 |a BENZIMIDAZOLE 
690 1 0 |a MICROBIAL TRANSGLYCOSYLATION 
690 1 0 |a NUCLEOSIDE ANALOGUES 
690 1 0 |a WHOLE CELLS 
690 1 0 |a CELLS 
690 1 0 |a DERIVATIVES 
690 1 0 |a SYNTHESIS (CHEMICAL) 
690 1 0 |a BENZIMIDAZOLE 
690 1 0 |a BIOTRANSFORMATIONS 
690 1 0 |a PHARMACOLOGICAL PROPERTIES 
690 1 0 |a CATALYSIS 
690 1 0 |a BENZIMIDAZOLE 
690 1 0 |a BENZIMIDAZOLE 2' DEOXYRIBOSIDE 
690 1 0 |a BENZIMIDAZOLE RIBOSIDE 
690 1 0 |a PURINE DERIVATIVE 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a BACTERIAL CELL 
690 1 0 |a CATALYSIS 
690 1 0 |a CONFERENCE PAPER 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a DRUG SYNTHESIS 
690 1 0 |a DRUG TRANSFORMATION 
690 1 0 |a GLYCOSYLATION 
690 1 0 |a MICROORGANISM 
690 1 0 |a NONHUMAN 
700 1 |a Trelles, J.A. 
700 1 |a Nóbile, M. 
700 1 |a Lewkowicz, E.S. 
700 1 |a Iribarren, A.M. 
773 0 |d 2004  |g v. 29  |h pp. 3-7  |k n. 1-6  |p J. Mol. Catal. B Enzym.  |x 13811177  |w (AR-BaUEN)CENRE-5687  |t Journal of Molecular Catalysis B: Enzymatic 
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856 4 0 |u https://doi.org/10.1016/j.molcatb.2003.10.007  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_13811177_v29_n1-6_p3_Bentancor  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v29_n1-6_p3_Bentancor  |y Registro en la Biblioteca Digital 
961 |a paper_13811177_v29_n1-6_p3_Bentancor  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion 
999 |c 82178 

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