出版と伝播
科学定期刊行物に研究成果を発表し、科学界に研究成果を伝播する予定である。 会議で研究結果を発表し、同業者と科学討論を行った。
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出版と伝播の学術論文
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Efficient synthesis of novel glutamate homologues and investigation of their affinity and selectivity profile at ionotropic glutamate receptors
関連化学物質
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(R)-2-(4-amino-4-carboxybut-1-en-1-yl)benzoic acid
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Kinetic characterisation of the FAD dependent monooxygenase TropB and investigation of its biotransformation potential
関連化学物質
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TVB-2640
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1,3-Benzenediol, 2,5-dimethyl-4-nitroso-
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NADPH
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Synthesis and biological evaluation of a diazepanone-based library of liposidomycins analogs as MraY inhibitors
関連化学物質
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(3S,6S,7R)-3-benzyloxymethyl-7-tertbutyldiphenylsilyloxymethyl-4-N-methyl-6-palmitoyloxy-1,4-diazepan-2-one
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Modelling Radical-initiated DNA Cleavage by Vinyl Epoxides
関連化学物質
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2-<2-(tert-butyldiphenylsiloxy)ethoxy>ethyl 2,3-epoxypent-4-enyl ether
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Synthesis and biological evaluation of quinazoline derivatives – A SAR study of novel inhibitors of ABCG2
関連化学物質
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4-phenoxy-2-phenylquinazoline
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Synthesis of novel coumarin and benzocoumarin derivatives and their biological and photophysical studies
関連化学物質
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N-(4-(hydroxymethyl)phenyl)-2-oxo-2H-chromene-3-carboxamide
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Synthesis, anticandidal activity and cytotoxicity of some tetrazole derivatives
関連化学物質
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1-(4-fluorophenyl)-2-[(1-methyl-1H-tetraazol-5-yl)sulfanyl]ethanone
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Design, synthesis and evaluation of novel thienopyrimidine-based agents bearing diaryl urea functionality as potential inhibitors of angiogenesis
関連化学物質
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1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-phenylurea
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Synthesis and evaluation of aminophosphinic acid derivatives as inhibitors of renal dipeptidase
関連化学物質
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2-[(1-tert-butoxycarbonylamino-2-cyclohexyl-ethyl)-methoxy-phosphinoylmethyl]-3-(4-iodo-phenyl)-acrylic acid methyl ester
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Design and synthesis of novel chiral dihydroimidazolium cyclophanes as N-heterocyclic carbene precatalysts
関連化学物質
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C37H29N2O2(1+)*Cl(1-)
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Pyrazole schiff base hybrids as anti-malarial agents: Synthesis, in vitro screening and computational study
関連化学物質
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1-(1,3-benzothiazol-2-yl)-3-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde
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