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The following term was not found in PubMed: 7-difluoro-4-keto-quinoline-3-carboxylic-acid-ethyl-ester
Page 1
1-Allyl-6-nitro-1H-indazole.
Acta Crystallogr Sect E Struct Rep Online. 2012 Dec 1;68(Pt 12):o3368. doi: 10.1107/S1600536812046478. Epub 2012 Nov 17.
Acta Crystallogr Sect E Struct Rep Online. 2012.
PMID: 23476200
Free PMC article.
A green and efficient synthetic methodology towards the synthesis of 1-allyl-6-chloro-4-oxo-1,4-dihydroquinoline-3-carboxamide derivatives.
Gill MSA, Azzman N, Hassan SS, Shah SAA, Ahemad N.
Gill MSA, et al.
BMC Chem. 2022 Dec 8;16(1):111. doi: 10.1186/s13065-022-00902-1.
BMC Chem. 2022.
PMID: 36482476
Free PMC article.
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Synthesis and Pesticidal Activities of New Quinoxalines.
Liu XH, Yu W, Min LJ, Wedge DE, Tan CX, Weng JQ, Wu HK, Cantrell CL, Bajsa-Hirschel J, Hua XW, Duke SO.
Liu XH, et al.
J Agric Food Chem. 2020 Jul 15;68(28):7324-7332. doi: 10.1021/acs.jafc.0c01042. Epub 2020 Jun 30.
J Agric Food Chem. 2020.
PMID: 32530612
The compounds 2-(6-methoxy-2-oxo-3-phenylquinoxalin-1(2H)-yl)acetonitrile (3f) and 1-allyl-6-methoxy-3-phenylquinoxalin-2(1H)-one (3g) were the most active herbicides and fungicides. ...
The compounds 2-(6-methoxy-2-oxo-3-phenylquinoxalin-1(2H)-yl)acetonitrile (3f) and 1-allyl-6-methoxy-3-phenylquinoxalin …
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Antimicrobial activity of clavines.
Eich E, Eichberg D, Schwarz G, Clas F, Loos M.
Eich E, et al.
Arzneimittelforschung. 1985;35(12):1760-2.
Arzneimittelforschung. 1985.
PMID: 3913422
The most active compounds are 6-allyl-6-norfestuclavine (minimal inhibitory concentration (MIC) 30 micrograms/ml against Staphylococcus aureus), 1-propyl-6-norfestuclavine (MIC 60 micrograms/ml against Escherichia coli), 6-cyano-6-norfestuclavine (MIC 250 micrograms/ml against Ps …
The most active compounds are 6-allyl-6-norfestuclavine (minimal inhibitory concentration (MIC) 30 micrograms/ml against Staphylococcus aure …
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