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  • Search Condition : Filter (MeSH = Quantitative Structure-Activity Relationship)
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Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-4(RCB1902) Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts.
Human and Animal Cells B16 melanoma 4A5(RCB0557) Structural Requirements of Alkylglyceryl-l-Ascorbic Acid Derivatives for Melanogenesis Inhibitory Activity.
Human and Animal Cells CHO-K1(RCB0285) Asp73-dependent and -independent regulation of the affinity of ligands for human histamine H1 receptors by Na.
Human and Animal Cells LLC-GA5-CoL150(RCB0871) Feature importance of machine learning prediction models shows structurally active part and important physicochemical features in drug design.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Antitumor Effects and Tumor-specificity of Guaiazulene-3-Carboxylate Derivatives Against Oral Squamous Cell Carcinoma In Vitro.
Human and Animal Cells HSC-4(RCB1902) , HSC-2(RCB1945) , HSC-3(RCB1975) , HL60(RCB0041) Evaluation of cytotoxiciy and tumor-specificity of licorice flavonoids based on chemical structure.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of 2-Arylazolylchromones and 2-Triazolylchromones.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of Azulene Amide Derivatives.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of 3-(N-Cyclicamino)chromone Derivatives.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) Quantitative Structure-Cytotoxicity Relationship of Pyrano[4,3-b]chromones.
Human and Animal Cells HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of 2-(N-cyclicamino)chromone Derivatives.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of Cinnamic Acid Phenetyl Esters.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of Newly Synthesized Piperic Acid Esters.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of Aurones.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-Cytotoxicity Relationship of Chalcones.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative Structure-cytotoxicity Relationship of 3-Benzylidenechromanones.
Human and Animal Cells LLC-GA5-CoL150(RCB0871) Structure-activity relationships of dibenzoylhydrazines for the inhibition of P-glycoprotein-mediated quinidine transport.
Human and Animal Cells Ca9-22(RCB1976) , HSC-2(RCB1945) , HSC-3(RCB1975) , HSC-4(RCB1902) Quantitative structure-cytotoxicity relationship of phenylpropanoid amides.
General Microbes JCM 1662 , JCM 1657 Synthesis, antibacterial, antioxidant activity and QSAR studies of novel 2-arylidenehydrazinyl-4-arylthiazole analogues.
Human and Animal Cells HSC-4(RCB1902) , HSC-2(RCB1945) , HSC-3(RCB1975) Quantitative structure-activity relationship (QSAR) analysis of tumor-specificity of 1,2,3,4-tetrahydroisoquinoline derivatives.