Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Aldo Trani"'
Publikováno v:
Journal of Antimicrobial Chemotherapy. 36:1061-1065
Purpuromycin and its semi-synthetic derivative MDL 63,604 had in-vitro activity similar to that of amphotericin B against isolates of Candida albicans. MDL 63,604 had activity similar to that of metronidazole against Trichomonas vaginalis. Both compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15744f6f8e4c0a5da1b845d96d39d111
https://doi.org/10.1093/jac/36.6.1061
https://doi.org/10.1093/jac/36.6.1061
Autor:
Aldo Trani, Angelo Borghi, C. Quarta, Pietro Ferrari, Giancarlo Lancini, L. F. Zerilli, M. T. De Pietro
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07c0a6a6f0be61ee2c134104786731dc
https://doi.org/10.1002/chin.199652282
https://doi.org/10.1002/chin.199652282
Publikováno v:
ChemInform. 29
A novel product, isolated from a culture broth of Actinoplanes ianthinogenes fermented for producing purpuromycin, was purified and its structure established on the basis of physico-chemical data and chemical reactions. The new product resulted to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4032d38bbb7388e6f70081c42bbb98d
https://doi.org/10.1002/chin.199803252
https://doi.org/10.1002/chin.199803252
Publikováno v:
Scopus-Elsevier
A series of O56-substituted carboxyester or carboxyamide derivatives of deglucoteicoplanin (TD) was prepared by condensation of the 56-hydroxyl function with various alkylating agents of general formula RBr, where R represents functional groups with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76588e2260caa34d271bce688448c588
https://doi.org/10.7164/antibiotics.45.1633
https://doi.org/10.7164/antibiotics.45.1633
Autor:
Jürgen Kettenring, Marisa Berti, Rosa Pallanza, Bruno Cavalleri, Aldo Trani, Adriano Malabarba, Erminio Gerli
Publikováno v:
The Journal of Antibiotics. 43:1107-1121
The synthesis and the biological properties of a series of N15-alkyl and N15, N15-dialkyl derivatives of teicoplanin A2, its pseudoaglycones and aglycone are described. The alkylation of the terminal amino group did not affect the ability of these te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::704cc2054436650775699f148eddb48d
https://doi.org/10.7164/antibiotics.43.1107
https://doi.org/10.7164/antibiotics.43.1107
Publikováno v:
The Journal of antibiotics. 51(9)
The structure of a product, isolated during the synthesis of the semisynthetic glycopeptide MDL 63,246, was elucidated on the basis of spectroscopic methods and proved to be a novel glycopeptide containing a 3-oxazolin-5-one ring between positions 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b51ee175a49e564371eeb713316419c
https://pubmed.ncbi.nlm.nih.gov/9820238
https://pubmed.ncbi.nlm.nih.gov/9820238
Publikováno v:
The Journal of antibiotics. 50(8)
A novel product, isolated from a culture broth of Actinoplanes ianthinogenes fermented for producing purpuromycin, was purified and its structure established on the basis of physico-chemical data and chemical reactions. The new product resulted to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::639496dc184b2e14609e59f89bd5e3e4
https://pubmed.ncbi.nlm.nih.gov/9315079
https://pubmed.ncbi.nlm.nih.gov/9315079
Autor:
F Ripamonti, Romeo Ciabatti, Gianbattista Panzone, Aldo Trani, Beth P. Goldstein, Clelia Dallanoce
Publikováno v:
Journal of medicinal chemistry. 40(6)
Purpuromycin (1) is an antibiotic with a broad spectrum of antimicrobial activity, encompassing bacteria, fungi, and protozoa, particularly those involved in vaginal infections. With the aim of enhancing the solubility and reducing the serum binding,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f5fc7bc6a75ab14795c2db01cf99896
https://pubmed.ncbi.nlm.nih.gov/9083486
https://pubmed.ncbi.nlm.nih.gov/9083486
Autor:
Romeo Ciabatti, Pietro Ferrari, Enrico Selva, Paolo Tavecchia, Clelia Dallanoce, Marazzi Alessandra Maria, Aldo Trani, Ismaela Ciciliato
Publikováno v:
The Journal of antibiotics. 49(12)
New N-acyl derivatives of 1-N-desmethyl goldinamine were obtained from degradation of kirromycin. Periodate-oxidation of these derivatives provided new aldehydic fragments that were further elaborated. Both N-phenyl ureido and N-phthalimido derivativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6018447caf2e732a68f70c4389f78a87
https://pubmed.ncbi.nlm.nih.gov/9031671
https://pubmed.ncbi.nlm.nih.gov/9031671
Autor:
Rosetta Pallanza, Romeo Ciabatti, Aldo Trani, Pietro Ferrari, Marisa Berti, Adriano Malabarba
Publikováno v:
The Journal of antibiotics. 43(11)
The condensation of the terminal carboxyl group of the deglucoteicoplanin (TD) with various substituted hydrazines produced hydrazide derivatives having different physico-chemical properties. This chemical modification of the carboxyl function does n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c33c5b6e6a2851473acd1f89616ea0a
https://pubmed.ncbi.nlm.nih.gov/2272922
https://pubmed.ncbi.nlm.nih.gov/2272922