Recent Publications on Kb Cells: |  |
Synthesis, biological active molecular design, and molecular docking study of novel deazaflavin-cholestane hybrid compounds.
Novel deazaflavin-cholestane hybrid compounds,...
Direct Link | 30th August, 2008
| Division of Pharmaceutical Sciences, Graduate School of Medicine,
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Synthesis of BC-ring model of globostellatic acid X methyl ester, an anti-angiogenic substance from marine sponge.
Concise synthesis of BC-ring model compounds of 13E,17E-globostellatic...
Direct Link | 30th August, 2008
| Graduate School of Pharmaceutical Sciences, Osaka University, 1-6
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Transcriptional repression of O6-methylguanine DNA methyltransferase gene rendering cells hypersensitive to N,N'-bis(2-chloroethyl)-N-nitrosurea in camptothecin-resistant cells.
O(6)-Methylguanine-DNA methyltransferase (MGMT) is a DNA repair protein...
Direct Link | 23rd August, 2008
| National Institute of Cancer Research, National Health Research
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| Polymeric micelles modified by folate-PEG-lipid for targeted drug delivery to cancer cells in vitro.
| 7th August, 2008
| Institute of Medicinal Chemistry, Hoshi University, Shinagawa-ku, Tokyo
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Biodegradable Amphiphilic Copolymers Based on Poly(-caprolactone)-Graft Chondroitin Sulfate as Drug Carriers.
The goal of this study was to develop a new type of core-shell micelles...
Direct Link | 30th July, 2008
| Faculty of Medicinal and Applied Chemistry, School of Life Science,
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Folate-linked lipid-based nanoparticles for synthetic siRNA delivery in KB tumor xenografts.
RNA interference (RNAi) is a sequence-specific gene-silencing mechanism...
Direct Link | 24th July, 2008
| Institute of Medicinal Chemistry, Hoshi University, Tokyo, Japan.
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"Click-to-chelate": in vitro and in vivo comparison of a 99mTc(CO)3-labeled N(tau)-histidine folate derivative with its isostructural, clicked 1,2,3-triazole analogue.
A side-by-side comparison of the synthesis, radiolabeling, and in vitro...
Direct Link | 24th July, 2008
| Department of Chemistry and Applied Biosciences, ETH Zurich, 8093 Zurich,
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Effect of transferrin as a ligand of pH-sensitive fusogenic liposome-lipoplex hybrid complexes.
We previously developed potent nonviral vectors based on complexation of...
Direct Link | 17th July, 2008
| Department of Applied Chemistry, Graduate School of Engineering, Osaka
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| BCH, an inhibitor of system L amino acid transporters, induces apoptosis in cancer cells.
| 1st July, 2008
| Department of Oral Physiology and The Second Stage of BK21, Chosun
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| Effect of depsipeptide on in vitro transfection efficiency of PEI/DNA complexes.
| 19th June, 2008
| Department of Pharmaceutical Technology, Faculty of Pharmacy,
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Tomoeones A-H, cytotoxic phloroglucinol derivatives from Hypericum ascyron.
Phloroglucinol derivatives tomoeones A-H (1-8) and three known compounds...
Direct Link | 17th June, 2008
| Graduate School of Pharmaceutical Sciences, University of Tokushima,
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Chemical and biologically active constituents of Pteris multifida.
A new compound, 4-caffeoyl quinic acid 5-O-methyl ether (2), together with...
Direct Link | 17th June, 2008
| Department of Pharmacognosy, Graduate School Biomedical Sciences,
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Invasive differences among Porphyromonas gingivalis strains from healthy and diseased periodontal sites.
Background and Objective: The purpose of this study was to determine any...
Direct Link | 12th June, 2008
| Department of Periodontology, College of Dentistry, University of Florida,
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Further studies of the norditerpene (+)-harringtonolide isolated from Cephalotaxus harringtonia var. drupacea: absolute configuration, cytotoxic and antifungal activities.
Harringtonolide (= hainanolide) is a complex polycyclic fused norditerpene...
Direct Link | 5th June, 2008
| Laboratoire de Chimie et Biochimie des Substances Naturelles, Museum
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New C5-alkylated indolobenzazepinones acting as inhibitors of tubulin polymerization: cytotoxic and antitumor activities.
A series of 5-alkylindolobenzazepin-7-ones was synthesized by Suzuki...
Direct Link | 28th May, 2008
| Institut de Chimie des Substances Naturelles, UPR 2301, CNRS, Avenue de la
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