Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Želmíra Odlerová"'
Autor:
Zbynek Svoboda, Jiri Janota, Milan Slosarek, Zelmira Odlerova, Katarina Kralova, Jiri Kunes, Karel Waisser, Lenka Kubicova
Publikováno v:
Molecules, Vol 5, Iss 5, Pp 714-726 (2000)
A set of N,N'-diarylalkanediamides was synthesized. The compounds were tested for their antimycobacterial and antialgal activity. The antimycobacterial activity of N,N'-diarylalkanediamides depends on the lipophilicity of the respective acid. Antimyc
Externí odkaz:
https://doaj.org/article/be84fe7b9ecc4605a511aa44dc9c9cc2
Publikováno v:
Collection of Czechoslovak Chemical Communications. 63:698-712
Fifteen novel substituted azachalcone derivatives and their bis substituted analogs were prepared from 3,5-diacetyl-2,6-dimethylpyridine by the Claisen-Schmidt condensation. The influence of the reaction conditions on the yield of mono- and bischalco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26bd6e7dfa2034c8e899c21aa61a9ddd
https://doi.org/10.1135/cccc19980698
https://doi.org/10.1135/cccc19980698
Publikováno v:
Collection of Czechoslovak Chemical Communications. 62:510-515
A series of thirty 2,3-dithiabicyclo[3.3.0]octa-4,8-diene derivatives was examined for antimycobacterial activity against Mycobacterium tuberculosis, M. kansasii, M. avium, and M. fortuitum. The structure-activity relationships were analysed by Free-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a4048bac2ce3477b111909851c35127
https://doi.org/10.1135/cccc19970510
https://doi.org/10.1135/cccc19970510
Publikováno v:
Scopus-Elsevier
On the basis of a preliminary study of the antimycobacterial activity of thiobenzanilides, a group of 4'-isopropyl- and 4'-butylthiobenzanilides have been synthesized and tested against Mycobacterium tuberculosis, Mycobacterium kansasii, Mycobacteriu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c86bd3b18da1950f913b7054b84c73ba
https://doi.org/10.1135/cccc19971503
https://doi.org/10.1135/cccc19971503
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:791-798
A series of 5-alkylthio-1-aryltetrazoles 1-14 was prepared by alkylation of the corresponding 1-aryltetrazole-5-thiols with alkyl bromides in the cyclohexane-aqueous potassium hydroxide system. The new compounds were evaluated for their activity agai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e85a80b0beca975e26508b3a7e43e446
https://doi.org/10.1135/cccc19960791
https://doi.org/10.1135/cccc19960791
Autor:
Karel Waisser, Želmíra Odlerová, Vera Klimesova, Miloš Macháček, Martin Svoboda, Vladimír Buchta
Publikováno v:
Archiv der Pharmazie. 329:438-442
A series of 4-alkylthiopyridine-2-carbothioamides have been prepared and evaluated in vitro for antimicrobial activity. Chemical structures have been demonstrated by IR and 1H NMR data and by elemental analysis. The antimycobacterial activity of thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dde8dd8286c7cd20275b485db3c5d1c
https://doi.org/10.1002/ardp.19963291003
https://doi.org/10.1002/ardp.19963291003
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:1109-1114
Homolytic alkylation of 6-chloro-2-pyrazinecarbonitrile by alkanoic acid and subsequent partial hydrolysis afforded 5-alkyl-6-chloro-2-pyrazinecarboxamides 1a-1e. Reaction of amides 1a-1e by Lawesson's reagent afforded corresponding thioamides 2a-2e.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4955be2bb6343156dc1989a7e5ce32e
https://doi.org/10.1135/cccc19961109
https://doi.org/10.1135/cccc19961109
Publikováno v:
Collection of Czechoslovak Chemical Communications. 61:1102-1108
A series of N-substituted 3-amino-5-thiocarbamoyl-2-pyrazinecarboxamides was prepared. The structure of compounds was confirmed by elemental analysis, IR and 1H NMR spectra. The results of in vitro antifugal and antimycobacterial susceptibility testi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d40e8c5ae9bcfd67819d5227546edd23
https://doi.org/10.1135/cccc19961102
https://doi.org/10.1135/cccc19961102
Publikováno v:
Collection of Czechoslovak Chemical Communications. 60:1236-1241
Nucleophilic substitution of 3-chloro-5-cyano-2-pyrazinecarboxamide by substituted anilines afforded substituted 3-arylamino-5-cyano-2-pyrazinecarboxamides I-X. The structures of compounds were confirmed by elemental analysis, UV, IR and 1H NMR spect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd12988baec9e4111ebdda3c2177491e
https://doi.org/10.1135/cccc19951236
https://doi.org/10.1135/cccc19951236
Publikováno v:
Collection of Czechoslovak Chemical Communications. 59:234-238
Oxidation of 1-aryltetrazole-5-thiols afforded bis(1-aryltetrazol-5-yl) disulfides. The compounds were tested for antimycobacterial activity against Mycobacterium tuberculosis, M. kansasii, M. avium and M. fortuitum. In the case of M. tuberculosis, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efbde9d90ab603f03c3aadb32b198d91
https://doi.org/10.1135/cccc19940234
https://doi.org/10.1135/cccc19940234