In vitro cytotoxicity evaluation of some substituted isatin derivatives.
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Are the Traditional Medical Uses of Muricidae Molluscs Substantiated by Their Pharmacological Properties and Bioactive Compounds?Anti-Inflammatory Activity and Structure-Activity Relationships of Brominated Indoles from a Marine Mollusc.3-(2-Amino-1-methyl-4-oxo-4,5-dihydro-1H-imidazol-5-yl)-3-hydr-oxy-1-phenyl-indolin-2-one ethanol solvate.3-(2-Amino-1-methyl-4-oxo-4,5-dihydro-1H-imidazol-5-yl)-5-fluoro-3-hydr-oxy-1-methyl-indolin-2-one methanol hemisolvate.Schiff bases of indoline-2,3-dione (isatin) with potential antiproliferative activity.5-Chloro-benzothia-zole-2-spiro-3'-indolin-2'-one.[18F]- and [11C]-labeled N-benzyl-isatin sulfonamide analogues as PET tracers for apoptosis: synthesis, radiolabeling mechanism, and in vivo imaging study of apoptosis in Fas-treated mice using [11C]WC-98.Synthesis and biological evaluation of a novel class of isatin analogs as dual inhibitors of tubulin polymerization and Akt pathwayMarine compounds selectively induce apoptosis in female reproductive cancer cells but not in primary-derived human reproductive granulosa cellsrac-5-Bromo-N-benzyl-isatincreatinine ethanol monosolvate.Gastrointestinal and hepatotoxicity assessment of an anticancer extract from muricid molluscs.Natural product research in the Australian marine invertebrate Dicathais orbitaAmmonium chloride catalyzed synthesis of novel Schiff bases from spiro[indoline-3,4'-pyran]-3'-carbonitriles and evaluation of their antimicrobial and anti-breast cancer activities.Purified brominated indole derivatives from Dicathais orbita induce apoptosis and cell cycle arrest in colorectal cancer cell lines.Synthesis, activity, and pharmacophore development for isatin-beta-thiosemicarbazones with selective activity toward multidrug-resistant cells.6-bromoisatin found in muricid mollusc extracts inhibits colon cancer cell proliferation and induces apoptosis, preventing early stage tumor formation in a colorectal cancer rodent model.Apoptogenic metabolites in fractions of the Benthic diatom Cocconeis scutellum parva.Translationally controlled tumour protein TCTP is induced early in human colorectal tumours and contributes to the resistance of HCT116 colon cancer cells to 5-FU and oxaliplatin.Post SELECT: selenium on trial.N-Alkyl-Substituted Isatins Enhance P2X7 Receptor-Induced Interleukin-1β Release from Murine Macrophages.Simultaneous Assessment of the Efficacy and Toxicity of Marine Mollusc-Derived Brominated Indoles in an In Vivo Model for Early Stage Colon Cancer.An in vitro high-throughput assay for screening reproductive and toxic effects of anticancer compounds.In vitro assessment of the cytotoxic, apoptotic, and mutagenic potentials of isatin.An Updated Review on Marine Anticancer Compounds: The Use of Virtual Screening for the Discovery of Small-Molecule Cancer Drugs.Synthesis and in vitro evaluation of N-alkyl-3-hydroxy-3-(2-imino-3-methyl-5-oxoimidazolidin-4-yl)indolin-2-one analogs as potential anticancer agents.1-Benzyl-6-chloro-indoline-2,3-dione.6-Chloro-1-methyl-indoline-2,3-dione.Design, synthesis and anticonvulsant activity of some new 5,7-dibromoisatin semicarbazone derivatives.5-Fluoro-3-(2-phenyl-hydrazinyl-idene)indolin-2-oneDesign, synthesis and anticonvulsant activity of some new 6,8-halo-substituted-2h-[1,2,4]triazino[5,6-b]indole-3(5h)-one/-thione and 6,8-halo-substituted 5-methyl-2h-[1,2,4]triazino[5,6-b]indol-3(5h)-one/-thione.Bioactivity of the Murex Homeopathic Remedy and of Extracts from an Australian Muricid Mollusc against Human Cancer Cells.Ylide mediated carbonyl homologations for the preparation of isatin derivatives.Tetracyano isoindigo small molecules and their use in n-channel organic field-effect transistors.Brominated indoles from a marine mollusc inhibit inflammation in a murine model of acute lung injury.A New Protein Extract Inhibitor from Hypobranchial Purple Gland of Hexaplex trunculus, a Mediterranean Mollusk, Impairs the Motility of Human Glioblastoma U87 and the HeLa Cell Line of Cervical Carcinoma Cells.Allyl-isatin suppresses cell viability, induces cell cycle arrest, and promotes cell apoptosis in hepatocellular carcinoma HepG2 cells.Synthesis, Biological, and Computational Evaluation of Novel 1,3,5-Substituted Indolin-2-one Derivatives as Inhibitors of Src Tyrosine Kinase.QM study and conformational analysis of an isatin Schiff base as a potential cytotoxic agent.Bioactive Compounds Isolated from Neglected Predatory Marine Gastropods.Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies.
P2860
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P2860
In vitro cytotoxicity evaluation of some substituted isatin derivatives.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
In vitro cytotoxicity evaluation of some substituted isatin derivatives.
@en
type
label
In vitro cytotoxicity evaluation of some substituted isatin derivatives.
@en
prefLabel
In vitro cytotoxicity evaluation of some substituted isatin derivatives.
@en
P2093
P50
P1476
In vitro cytotoxicity evaluation of some substituted isatin derivatives
@en
P2093
John B Bremner
Julie M Locke
Kara L Vine
P304
P356
10.1016/J.BMC.2006.10.035
P407
P577
2006-10-20T00:00:00Z