Highly active potential antituberculotics: 3-(4-alkylphenyl)-4-thioxo-2H-1,3-benzoxazine-2(3H)-ones and 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-dithiones substituted in ring-B by halogen
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F08%3A00109123" target="_blank" >RIV/00216208:11160/08:00109123 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Highly active potential antituberculotics: 3-(4-alkylphenyl)-4-thioxo-2H-1,3-benzoxazine-2(3H)-ones and 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-dithiones substituted in ring-B by halogen
Original language description
The replacement of the oxo group bythioxo group of 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-diones often led to an improvement in the antimycobacterial activity against M. tuberculosis
Czech name
Vysoce účinná poteciální antituberkulotika: 3-(4-alkylfenyl)-4-thioxo-2H-1,3-benzoxazin-2(3H)-ony a 3-(4-alkylfenyl)-2H-1,3-benzoxazin-2,4(3H)-dithiony halogenem substituované v kruhu B
Czech description
Záměna oxo skupiny v 3-(4-alkylfenyl)-2H-1,3-benzoxazin-2,4(3H)-dionech často vede ke zvýšení aktivity vůči M. tuberculosis
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FR - Pharmacology and apothecary chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach
Others
Publication year
2008
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Archiv der Pharmazie
ISSN
0365-6233
e-ISSN
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Volume of the periodical
341
Issue of the periodical within the volume
12
Country of publishing house
DE - GERMANY
Number of pages
4
Pages from-to
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UT code for WoS article
000261934000007
EID of the result in the Scopus database
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