About: 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

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About: 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 Goto Sponge NotDistinct Permalink

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rdf:type	skos:Concept http://linked.opendata.cz/ontology/domain/vavai/Vysledek
Description	Záměna oxo skupiny v 3-(4-alkylfenyl)-2H-1,3-benzoxazin-2,4(3H)-dionech často vede ke zvýšení aktivity vůči M. tuberculosis (cs) 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 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 (en)
Title	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 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 (en) 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 (cs)
skos:prefLabel	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 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 (en) 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 (cs)
skos:notation	RIV/00216208:11160/08:00109123!RIV09-MSM-11160___
http://linked.open...avai/riv/aktivita	S Z
http://linked.open...avai/riv/aktivity	S, Z(MSM0021620822)
http://linked.open...iv/cisloPeriodika	12
http://linked.open...vai/riv/dodaniDat	2009
http://linked.open...aciTvurceVysledku	Doležal, Rafael Waisser, Karel Kuneš, Jiří Matyk, Josef
http://linked.open.../riv/druhVysledku	J - Článek v odborném periodiku
http://linked.open...iv/duvernostUdaju	S - Úplné a pravdivé údaje nepodléhající ochraně podle zvláštních právních předpisů
http://linked.open...titaPredkladatele	Univerzita Karlova v Praze / Farmaceutická fakulta v Hradci Králové
http://linked.open...dnocenehoVysledku	370116
http://linked.open...ai/riv/idVysledku	RIV/00216208:11160/08:00109123
http://linked.open...riv/jazykVysledku	eng - angličtina
http://linked.open.../riv/klicovaSlova	antimycobacterial activity; antituberculotics; tuberculostatics; benzoxazine; thioxo group (en)
http://linked.open.../riv/klicoveSlovo	benzoxazine thioxo group antimycobacterial activity antituberculotics tuberculostatics
http://linked.open...odStatuVydavatele	DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV	[C9D10F56BD3D]
http://linked.open...i/riv/nazevZdroje	Archiv der Pharmazie
http://linked.open...in/vavai/riv/obor	FR
http://linked.open...ichTvurcuVysledku	4 (xsd:int)
http://linked.open...cetTvurcuVysledku	5 (xsd:int)
http://linked.open...UplatneniVysledku	2008
http://linked.open...v/svazekPeriodika	341
http://linked.open...iv/tvurceVysledku	Doležal, Rafael Kaustová, Jarmila Kuneš, Jiří Waisser, Karel Matyk, Josef
http://linked.open...ain/vavai/riv/wos	000261934000007
http://linked.open...n/vavai/riv/zamer	Research of new drug structures
issn	0365-6233
number of pages	4 (xsd:int)
http://localhost/t...ganizacniJednotka	11160
is http://linked.open...avai/riv/vysledek of	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 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 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 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

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