Results 1 to 10 of about 171,741 (166)
Nickel-Catalyzed Intermolecular Cyclization of 2-Bromobenzamide: A General Strategy for Synthesizing 6(5H)-Phenanthridinone Derivatives [PDF]
Molecules6(5H)-phenanthridinone derivatives, as an important class of alkaloids, have broad application value in drug development and functional material synthesis.
Xinsheng Xiao +6 more
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Sydnone derivatives as synthons for novel bismesoionic compounds. Synthesis of 3-(2-sulphido-1,3,4-thiadiazolium-4-carbonylphenyl) sydnones and 4-[4-(2-sulphido-1,3,4-thiadiazolium)benzoyl]- 1,3,4-thi [PDF]
Journal of the Serbian Chemical Society, 2006 Some hitherto unknown novel bismesoionic compounds, 3-[4/3 (5H/substituted- 2-sulphido-1,3,4-thiadiazolium-4 carbonyl)phenyl]sydnones 5a–d and 6a-d and 4-[4 (5H/substituted-2-sulphido-1,3,4-thiadiazolium)benzoyl] (5H/substituted-1,3,4-thiadiazolium- 2 ...
Jogul Johnson J., Badami Bharati V.
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Seeds, 2023 The aim of this study was to find the optimal gibberellic acid (GA3) and copper sulfate (CuSO4·5H2O) concentrations to reduce the number of seeds and increase the quality of Bac Son mandarin fruit.
Nguyen Quoc Hung +4 more
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Scientific Opinion on Flavouring Group Evaluation 217, Revision 1 (FGE.217Rev1). Consideration of genotoxic potential for ?,?-unsaturated ketones and precursors from chemical subgroup 4.1 of FGE.19: Lactones [PDF]
EFSA Journal, 2013 The Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids of the European Food Safety Authority was requested to evaluate the genotoxic potential of 12 flavouring substances from subgroup 4.1 of FGE.19 in the Flavouring Group ...
EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
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The Antifungal Action Mode of N-Phenacyldibromobenzimidazoles
Molecules, 2021 Our study aimed to characterise the action mode of N-phenacyldibromobenzimidazoles against C. albicans and C. neoformans. Firstly, we selected the non-cytotoxic most active benzimidazoles based on the structure–activity relationships showing that the ...
Monika Staniszewska +6 more
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Журнал органічної та фармацевтичної хімії, 2020 Aim. To synthesize, prove the structure and study the analgesic and anti-inflammatory activities of 3-(het)-aryl-2-(6,7,8,9-tetrahydro-5H-[1,2,4]triazolo[4,3-a]azepin-3-yl)acrylonitrile derivatives. Results and discussion.
Serhii A. Demchenko +7 more
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Polyketides from the Halotolerant Fungus Myrothecium sp. GS-17
Molecules, 2013 Two new polyketides, myrothecol (1) and 5-hydroxy-3-methyl-4-(1- hydroxylethyl)-furan-2(5H)-one (2), were isolated from the fermentation broth of the halotolerant fungus Myrothecium sp.
Tao Liu +8 more
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Scientific Reports, 2021 The chemical resistance of drugs against any change in their composition and studying the rate of multiwell-multichannel reactions in the liquid phase, respectively, are the important challenges of pharmacology and chemistry.
Hamed Douroudgari, Morteza Vahedpour
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Pakistan Journal of Pharmaceutical Sciences, 2022 Pyrimidine 2, 4, 6-trione derivatives are known to have L-type calcium channel blockade activity due to which they are quite effective in cardiovascular diseases along with cancer, epilepsy and inflammatory disorders.
A computational approach Nadeem Irshad +3 more
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Cytotoxicity of 3,4-dihalogenated 2(5H)-furanones
Journal of Pharmacy and Pharmacology, 2004 Abstract Mucohalogen acids have been used for the preparation of a variety of 3,4-dihalogenated 2(5H)-furanones. In one synthetic step the carbamates 2a-c and the pseudoanhydrides 4a-e were prepared using isocyanates and acid anhydrides.
Eric, Lattmann +5 more
openaire +2 more sources