Development of Tubulin-Polymerization Inhibitors Based on the Thalidomide Skeleton
スポンサーリンク
概要
- 論文の詳細を見る
We synthesized a series of compounds based on the potent tubulin-polymerization inhibitor 5-hydroxy-2-(2,6-diisopropylphenyl)-1H-isoindole-1,3-dione [5HPP-33 (3)], which is structurally derived from thalidomide (1), and investigated their inhibitory effects on tubulin polymerization. Direct interaction between 5HPP-33 (3) and α,β-tubulin heterodimer protein was demonstrated by means of a surface plasmon resonance study.
- 公益社団法人日本薬学会の論文
- 2007-06-01
著者
-
Aoyama Hiroshi
東京大学分子細胞生物学研究所
-
Aoyama Hiroshi
Univ. Tokyo Tokyo Jpn
-
Aoyama Hiroshi
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
-
Kagechika Hiroyuki
Graduate School Of Pharmaceutical Sciences The University Of Tokyo:research Foundation Itsuu Laborat
-
Kagechika Hiroyuki
Graduate School Of Biomedical Sci. Tokyo Medical And Dental Univ.
-
Nakamura Takanori
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
-
KOBAYASHI Hisayoshi
Institute of Molecular & Cellular Biosciences, The University of Tokyo
-
MIYACHI Hiroyuki
Institute of Molecular & Cellular Biosciences, The University of Tokyo
-
HASHIMOTO Yuichi
Institute of Molecular & Cellular Biosciences, The University of Tokyo
-
Hashimoto Yuichi
Univ. Tokyo Tokyo Jpn
-
Kobayashi H
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
-
Hashimoto Y
Univ. Tokyo Tokyo Jpn
-
Hashimoto Y
Graduate School Of Pharmaceutical Sciences Kyushu University
-
中山 太ニ
岡山大学薬学部薬剤学教室
-
MISAWA Takashi
Institute of Molecular and Cellular Biosciences, The University of Tokyo
-
NOGUCHI Tomomi
Institute of Molecular & Cellular Biosciences, The University of Tokyo
-
Miyachi Hiroyuki
Institute Of Molecular & Cellular Biosciences University Of Tokyo
-
Hashimoto Yuichi
Institute Of Molecular & Cellular Biosciences University Of Tokyo
-
Hashimoto Yuichi
Institute Of Molecular And Cellular Biosciences The Universityv Of Tokyo
-
Kobayashi Hisayoshi
Institute Of Molecular And Cellular Biosciences University Of Tokyo
-
Misawa Takashi
Institute Of Molecular And Cellular Biosciences The University Of Tokyo
-
Noguchi T
Medicinal Research Laboratories Taisho Pharmaceutical Co. Ltd.
-
Miyachi H
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
-
Miyachi Hiroyuki
Div. Of Pharmaceutical Sciences Graduate School Of Medicine Dentistry And Pharmaceutical Sciences Ok
-
Kagechika H
Tokyo Medical And Dental Univ. Tokyo Jpn
-
Noguchi-yachide Tomomi
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
-
Hashimoto Y
Institute Of Molecular & Cellular Biosciences The University Of Tokyo
関連論文
- Coordination of Divalent Metal Cation to Amide Group to Form Adduct Ion in FAB Mass Spectrometry: Implication of Zn^ in Enzymatic Hydrolysis of Amide Bond
- Determination of Endogenous Levels of Retinoic Acid Isomers in Type II Diabetes Mellitus Patients. Possible Correlation with HbAlc Values(Analytical Biochemistry)
- Isolation and Structural Characterization of Siderophores, Madurastatins, Produced by a Pathogenic Actinomadura madurae
- Asterobactin, a New Siderophore Group Antibiotic from Nocardia asteoides
- Glycosylative Inactivation of Chalcomycin and Tylosin by a Clinically Isolated Nocardia asteroides Strain
- Structures of ADP-Ribosylated Rifampicin and Its Metabolite : Intermediates of Rifampicin-ribosylation by Mycobacterium smegmatis DSM43756
- Isolation of salsolinol, a Tetrahydroisoquinoline alkaloid, from the marine sponge Xestospongia cf. vansoesti as a proteasome inhibitor
- Isolation of Salsolinol, a Tetrahydroisoquinoline Alkaloid, from the Marine Sponge Xestospongia cf. vansoesti as a Proteasome Inhibitor
- 1P084 サリドマイド・アナログの抗インフルエンザウイルス活性(蛋白質-機能(反応機構,生物活性など),第48回日本生物物理学会年会)
- Structure Determination of Ribosylated Rifampicin and Its Derivative:New Inactivated Metabolites of Rifampicin by Mycobacterial Strains
- Isolation and Structures of an Antifungal Antibiotic, Fusarielin A, and Related Compounds Produced by a Fusarium sp.
- (Cis)-PREFERENCE OF N, N'-DIMETHYL-N, N'-DIPHENYLGUANIDINE AND THE GUANIDINIUM SALT. CONSTRUCTION OF WATER-SOLUBLE AROMATIC LAYERED STRUCTURE
- STERICAL PRORERTIES OF N, N'-DIMETHYLUREA MOIETY ENHANCE FORMATION OF TRIPLY HYDROGEN-BONDED COMPLEXES
- Enhancing Effect of Tumor Promoters, Phorbol Esters and Teleocidins on Nuclear Receptor-Mediated Transcription
- Identification of Protein Disulfide Isomerase as a Phorbol Ester-Binding Protein
- Dicarba-closo-dodecaboranes as a Pharmacophore. Novel Potent Retinoidal Agonists
- Dicarba-closo-dodecaboranes as a Pharmacophore. Retinoidal Antagonists and Potential Agonists
- Photoaffinity Labeling of Tumor Promoter-Binding Protein (CN-TPBP) and Preparation of Affinity Sorbent Gels
- Brasiliquinones A, B and C, New Benz[a]anthraquinone Antibiotics from Nocardia brasiliensis I. Producing Strain, Isolation and Biological Activities of the Antibiotics
- α-Glucosidase Inhibitors with a 4, 5, 6, 7-Tetrachlorophthalimide Skeleton Pendanted with a Cycloalkyl or Dicarba-closo-dodecaborane Group
- α-Glucosidase Inhibitors with a Phthalimide Skeleton : Stucture-Activity Relationship Study
- Modulators of Tumor Necrosis Factor α Production Bearing Dicarba-closo-dodecaborane as a Hydrophobic Pharmacophore
- Latent Enamine Functionality of 5-Methyl-2,3-dihydropyrazines
- Novel Retinoidal Tropolone Derivatives. Bioisosteric Relationship of Tropolone Ring with Benzoic Acid Moiety in Retinoid Structure
- Retinoidal Pyrimidinecarboxylic Acids. Unexpected Diaza-Substituent Effects in Retinobenzoic Acids
- Retinoid X Receptor-Antagonistic Diazepinylbenzoic Acids
- Thiazolidinediones with Thyroid Hormone Receptor Agonistic Activity
- NOVEL THIAZOLIDINEDIONE DERIVATIVES WITH RETINOID SYNERGISTIC ACTIVITY
- POTENT RETINOID SYNERGISTS WITH A DIPHENYLAMINE SKELETON
- Polyenylidine Thiazolidine Derivatives with Retinoidal Activities
- Photoaffinity Labeling of the Ligand-Interacting Helix of the Retinoic Acid Receptor Alpha
- Evaluation of Differentiation-Inducing Activity of Retinoids on Human Leukemia Cell Lines HL-60 and NB4
- NOVEL AROMATIC UREA DERIVATIVES WITH DNA-BINDING ABILITY
- DEIODOTRIFLUOROMETHYLATION OF ETHYL 3,3', 5-TRIIODOTHYROACETATE. DIVERGENT DERIVATIZATION BASED ON THE COMBINATORIAL CONCEPT
- New-Type Inducers of Differentiation of HL-60 Leukemia Cells Suppress c-myc Expression(Medeicinal Chemistry,Chemical)
- Antitumor Activity of Brasilicardin A, a Novel Terpenoid Antibiotic from Nocardia brasiliensis
- A New Antifungal Macrolide Component, Brasilinolide B, Produced by Nocardia brasiliensis
- Production of Erythromycin E by Pathogenic Nocardia brasiliensis
- Brasilicardin A, a New Terpenoid Antibiotic from Pathogenic Nocardia brasilienesis: Fermentation, Isolation, and Biological Activity
- Brasilicardin A ; a New Terpenoid Antibiotic Produced by Nocardia brasiliensis
- Brasilinolide A, a New Macrolide Antibiotic Produced by Nocardia brasiliensis: Producing Strain, Isolation and Biological Activity
- Different Rifampicin Inactivation Mechanisms in Nocardia and Related Taxa
- A Synthetic Retinoid Am80 (Tamibarotene) Rescues the Memory Deficit Caused by Scopolamine in a Passive Avoidance Paradigm(Communications to the Editor)
- Design and Synthesis of Phthalimide-Based Fluorescent Liver X Receptor Antagonists
- Structural Development of Benzhydrol-Type 1'-Acetoxychavicol Acetate (ACA) Analogs as Human Leukemia Cell-Growth Inhibitors Based on Quantitative Structure-Activity Relationship (QSAR) Analysis
- Structure-Based Design and Synthesis of Fluorescent PPARα/δ Co-agonist and Its Application as a Probe for Fluorescent Polarization Assay of PPARδ Ligands
- Fusarielin A as an Anti-angiogenic and Anti-proliferative Agent : Basic Biological Characterization
- Structural Development of Liver X Receptor (LXR) Antagonists Derived from Thalidomide-Related Glucosidase Inhibitors
- Development of Tubulin-Polymerization Inhibitors Based on the Thalidomide Skeleton
- Hydrolyzed Metabolites of Thalidomide : Synthesis and TNF-α Production-Inhibitory Activity
- Mono- and Dihydroxylated Metabolites of Thalidomide : Synthesis and TNF-α Production-Inhibitory Activity
- Effects of Immunomodulatory Derivatives of Thalidomide (IMiDs) and Their Analogs on Cell-Differentiation, Cyclooxygenase Activity and Angiogenesis
- Enhancement of All-trans Retinoic Acid-Induced HL-60 Cell Differentiation by Thalidomide and Its Metabolites(Communication to the Editor)
- N-Phenylphthalimide-Type Cyclooxygenase (COX) Inhibitors Derived from Thalidomide : Substituent Effects on Subtype Selectivity
- Thalidomide as a Nitric Oxide Synthase Inhibitor and Its Structural Development
- Conversion of Ca^ Salt of an Organic Compound to Its Li^+ Salt to Simplify the Fast Atom Bombardment Mass Spectrum
- Coordination of Sodium Cation to an Oxygen Function and Olefinic Double Bond to Form Molecular Adduct Ion in Fast Atom Bombardment Mass Spectrometry
- Separation of Phosphatidylinositol 4-Phosphate from a Mixture with Phosphatidylserine and Phosphatidylinositol by Sep-Pak C_ Cartridge
- Potent Homophthalimide-Type Inhibitors of B16F10/L5 Mouse Melanoma Cell Invasion
- Collisionally Activated Dissociation of 13-Membered Peptides, Ustiloxins, and Phomopsins
- Structural Identification of a Major Cytokinin in Coconut Milk as 14-O-{3-O-[β-D-Galactopyranosyl-(1→2)-α-D-galactopyranosyl-(1→3)-α-L-arabinofuranosyl]-4-O-(α-L-arabinofuranosyl)-β-D-galactopyranosyl}trans-zeatin Riboside
- Liver X receptor (LXR) modulators with dibenz〔b,f〕〔1,4〕oxazepin-11-one, (Z)-dibenz〔b,f〕azocin-6-one, and 11,12-dihydrodibenz〔b,f〕azocin-6-one skeletons
- Enhancement of Chemically-Induced HL-60 Cell Differentiation by 3,3′-Diindolylmethane Derivatives
- meso-DNAs with Homopurine Sequences : Analysis of Their Interaction with Natural DNAs
- Synthesis and Anti-tubulin Activity of Ustiloxin D Derivatives
- Isolation and Structure of an Antimitotic Cyclic Peptide, Ustiloxin F: Chemical Interrelation with a Homologous Peptide, Ustiloxin B
- Interaction of Arenastatin A with Porcine Brain Tubulin
- INDUCER-SPECIFIC REGULATORS OF TUMOR NECROSIS FACTOR ALPHA PRODUCTION
- AUGMENTATION BY PHTHALIMIDES OF PHORBOL ESTER-INDUCED EXPRESSION OF TUMOR NECROSIS FACTOR ALPHA MESSAGE
- Location of Two Photoaffinity-Labeled Sites on the Ligand-Binding Domain of Retinoic Acid Receptor α
- Phenylphthalimides with Tumor Necrosis Factor Alpha Production-Enhancing Activity
- Development of Novel Chiral Urea Catalysts for the Hetero-Michael Reaction
- Specific Nonpeptide Inhibitors of Puromycin-Sensitive Aminopeptidase with a 2,4(1H,3H)-Quinazolinedione Skeleton
- Cyclooxygenase Inhibitors Derived from Thalidomide
- Asymmetric Synthesis of a 3-Acyltetronic Acid Derivative, RK-682, and Formation of Its Calcium Salt during Silica Gel Column Chromatography
- Anti-Androgenic Activity of Substituted Azo- and Azoxy-Benzene Derivatives
- Antiangiogenic Activity of Tumor Necrosis Factor-α Production Regulators Derived from Thalidomide
- Tumor Necrosis Factor-Alpha Production Enhancing Activity of Substituted 3'-Methylthalidomide : Influence of Substituents at the Phthaloyl Moiety on the Activity and Stereoselectivity
- Modification by Heme Oxygenase Inhibitor, Tin Protoporphyrin, of Cellular Differentiation of Human Myeloid Leukemia K562 Cell Line
- Tetrahydrobostrycin and 1-Deoxytetrahydrobostrycin, Two New Hexahydroanthrone Derivatives, from a Marine-derived Fungus Aspergillus sp.
- Four New Macrocyclic Trichothecenes from Two Strains of Marine-derived Fungi of the Genus Myrothecium
- Melophlins P, Q, R, and S : Four New Tetramic Acid Derivatives, from Two Palauan Marine Sponges of the Genus Melophlus
- Identification of Streptomyces and Kitasatospora strains from Thai soils with geldanamycin production strain
- Structure-Activity Relationship of Bis-Galloyl Derivatives Related to (-)-Epigallocatechin Gallate
- Manoalide derivatives from a marine sponge Luffariella sp. collected in Palau
- Three New Chlorine Containing Antibiotics from a Marine-derived Fungus Aspergillus ostianus Collected in Pohnpei
- A New Screening Method for Antimitotic Substances and Isolation of Glycolipids as Stimulators of Tubulin Polymerization from Okinawan Sponge Pseudoceratina sp.
- Isolation and Characterization of Bioactive Metabolites form Marine-Derived Filamentous Fungi Collected from Tropical and Sub-Tropical Coral Reefs
- Two New Pregnane Glycosides from Dioscorea futschauensis R. KUNTH
- Identification of Binding Proteins of Fusarielin A as Actin and Tubulin
- Inhibition of Restriction Enzymes EcoRI, BamHI and HindIII by Phenethylphenylphthalimides Derived from Thalidomide
- Paecilospirone, a Unique Spiro [chroman-2, 1' (3'H)-isobenzofuran] Derivative Isolated from Tropical Marine Fungus Paecilomyces sp.^H
- Phomopsidin, a New Inhibitor of Microtubule Assembly Produced by Phomopsis sp. isolated from Coral Reef in Pohnpei
- A Screening Method for Antimitotic and Antifungal Substances Using Conidia of Pyriculaia oryzae, Modification and Application to Tropical Marine Fungi
- Glycogen Phosphorylase a Inhibitors with a Phenethylphenylphthalimide Skeleton Derived from Thalidomide-Related α-Glucosidase Inhibitors and Liver X Receptor Antagonists
- Crystallization of bovine heart mitochondrial cytochrome c oxidase for X-ray diffraction at atomic resolution (2.8A)
- A mechanism of Cytochrome c Oxidase Proposed by the Crystal Structures at Different Oxidation and Ligand Binding States
- P-415 Target Protein Identification of Batzelladine A and D
- ILVIII-3 STRUCTURAL DEVELOPMENT STUDIES OF NUCLEAR RECEPTOR LIGANDS(Drug Discovery and Developments)
- Retinoic acids exert direct effects on T cells to suppress T_h1 development and enhance T_h2 development via retinoic acid receptors