Total Synthesis, Structural Revision, and Biological Evaluation of Calafianin, a Marine Spiroisoxazoline from the Sponge, Aplysina gerardogreeni
スポンサーリンク
概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 2006-01-15
著者
-
Tomoda Hiroshi
School Of Pharmaceutical Sciences Kitasato University
-
Nishiyama Shigeru
Department Of Chemistry Faculty Of Science And Technology Keio University
-
Obata Rika
Department Of Chemistry Faculty Of Science And Technology Keio University
-
OGAMINO Takahisa
Department of Chemistry, Faculty of Science and Technology, Keio University
-
Ogamino Takahisa
Department Of Chemistry Faculty Of Science And Technology Keio University
-
Nishiyama Shigeru
Department Of Chemistry Faculty Of Science And Technology Keio Univerisity
-
Nishiyama Shigeru
Dep. Of Chemistry Keio Univ.
-
Nishiyama Shigeru
Department of Applied Chemistry, Faculty of Engineering, Keio University
関連論文
- Total Synthesis of Malformin C, an Inhibitor of Bleomycin-Induced G2 Arrest
- Fungal Malformins Inhibit Bleomycin-Induced G2 Checkpoint in Jurkat Cells(Highlighted paper selected by Editor-in-chief,Biochemistry)
- Lariatins, Novel Anti-mycobacterial Peptides with a Lasso Structure, Produced by Rhodococcus jostii K01-B0171
- Citrinamides, New Potentiators of Antifungal Miconazole Activity, Produced by Penicillium sp. FKI-1938
- Tensyuic Acids, New Antibiotics Produced by Aspergillus niger FKI-2342
- Fungal Citridone D Having a Novel Phenylfuropyridine Skeleton
- Tensidols, New Potentiators of Antifungal Miconazole Activity, Produced by Aspergillus niger FKI-2342
- P-527 CHEMICAL STUDY OF CITRIDONES, POTENTIATORS OF ANTI-FUNGAL MICONAZOLE ACTIVITY
- Citridones, New Potentiators of Antifungal Miconazole Activity, Produced by Penicillium sp. FKI-1938 : II. Structure Elucidation
- Citridones, New Potentiators of Antifungal Miconazole Activity, Produced by Penicillium sp. FKI-1938 : I. Taxonomy, Fermentation, Isolation and Biological Properties
- Simaomicin α, a polycyclic xanthone, induces G_1 arrest with suppression of retinoblastoma protein phosphorylation
- Anti-atherosclerotic Activity of Triacsin C, an Acyl-CoA Synthetase Inhibitor
- Verticipyrone, a New NADH-fumarate Reductase Inhibitor, Produced by Verticillium sp. FKI-1083
- Paecilaminol, a New NADH-Fumarate Reductase Inhibitor, Produced by Paecilomyces sp. FKI-0550
- Selective Inhibition of Acyl-CoA : cholesterol Acyltransferase 2 Isozyme by Flavasperone and Sterigmatocystin from Aspergillus Species
- Selectivity of Pyripyropene Derivatives in Inhibition toward Acyl-CoA : cholesterol Acyltransferase 2 Isozyme
- P-523 SELECTIVITY OF BEAUVERIOLIDE ANALOGS, ACAT INHIBITORS, TO THE ISOZYMES
- Total Synthesis of (+)-Tanikolide, Using Regioselective Elimination of a Vicinal Dibromoalkane
- Structure Elucidation of Fungal Sespendole, an Inhibitor of Lipid Droplet Synthesis in Macrophages
- Sespendole, a New Inhibitor of Lipid Droplet Synthesis in Macrophages, Produced by Pseudobotrytis terrestris FKA-25
- Efficient Route to (S)-Azetidine-2-carboxylic Acid
- Yaequinolones, New Insecticidal Antibiotics Produced by Penicillium sp. FKI-2140 : I. Taxonomy, Fermentation, Isolation and Biological Activity
- New Insecticidal Antibiotics, Hydroxyfungerins A and B, Produced by Metarhizium sp. FKI-1079
- Stemphones, Novel Potentiators of Imipenem Activity against Methicillin-resistant Staphylococcus aureus, Produced by Aspergillus sp. FKI-2136
- New Sesquicillins, Insecticidal Antibiotics Produced by Albophoma sp. FKI-1778
- Spylidone, a Novel Inhibitor of Lipid Droplet Accumulation in Mouse Macrophages Produced by Phoma sp. FKI-1840
- Inhibition of Lipid Droplet Accumulation in Mouse Macrophages by Stemphone Derivatives
- Structure-activity Relationships of Stemphones, Potentiators of Imipenem Activity against Methicillin-resistant Staphylococcus aureus
- P-539 ISOBISVERTINOL, A NOVEL INHIBITOR OF LIPID DROPLET ACCUMULATION IN MOUSE MACROPHAGES PRODUCED BY Aspergillus sp. FKI-1746
- Yaequinolones, New Insecticidal Antibiotics Produced by Penicillium sp. FKI-2140 : II. Structural Elucidation
- Selectivity of Microbial Acyl-CoA : cholesterol Acyltransferase Inhibitors toward Isozymes
- Molecular Target of Decursins in the Inhibition of Lipid Droplet Accumulation in Macrophages(Pharmacognosy)
- Inhibition of Lipid Droplet Accumulation in Macrophages by Triterpenoids Produced from Torametes orientaris(Pharmacognosy)
- Synthetic Study on a 26-Membered Macrolide, Amphidinolide B: Synthesis of the C_1-C_13 Fragment
- Absolute Configuration of (+)-Aureothin: A Toxic Metabolite Possessing γ-Pyrone Unit
- Structural Revision of Griseulin, a Bioactive Pyrone Possessing a Nitrophenyl Unit
- Efficient Synthesis of the Optically Active Cyclopentane Derivative, A Versatile Intermediate Toward the Euphorbia Diterpenes
- P-540 SECONDARY METABOLITE PRODUCED BY A RARE FUNGUS, CALDARIOMYCES SP. FKA-35, ISOLATED FROM SUBTROPICAL SOIL
- Short-Step and Scalable Synthesis of (±)-Cytoxazone
- Synthetic Studies on Ceratospongamides, Cyclic Heptapeptides Containing Thiazole and Oxazoline Units : Total Synthesis of cis, cis-Ceratospongamide
- P-525 Efficient production of the anti-HIV protein actinohivin in recombinant Streptomyces strain
- Biomimetic Syntheses of Isodityrosine Natural Products, and an Approach to Chemistry and Molecular Recognition of Secoaglucovancomycin and Related Oligopeptides
- Synthetic Studies on Polypropionate-Derived 4-Pyrone-Containing Marine Natural Products
- The Synthesis and Biological Activity of Pyranonaphthoquione Derivatives from Streptomyces sp. and Their Related Substances
- Total Synthesis, Structural Revision, and Biological Evaluation of Calafianin, a Marine Spiroisoxazoline from the Sponge, Aplysina gerardogreeni
- Biosynthesis of Sespendole
- Efficient Synthesis of Propargylic Ethers under the DBU Conditions and Its Application to Natural Products Synthesis
- Synthesis of Chroman Derivatives by the Ring Expansion Reaction of Spirodienones, and an Assessment of their Plant Growth Inhibition
- Conversion of 3-O-Substituted 1, 2-Dibromoalkanes into 2-Bromo-1-alkenes by the Selective Elimination : Its Application to Total Synthesis of 12-Oxygenated Tremetones
- Asymmetric Synthesis of the Polyol Subunit of the Macrolide Antibiotic, Ossamycin : A Unique Approach Utilizing Stereochemical Specificity
- P-162 SYNTHETIC STUDIES ON CHLOROQUINOCIN, A POTENTIAL ANTIBIOTIC AGAINST GRAM-POSITIVE BACTERIA
- P-280 Synthesis of Glutarimide Antibiotics Streptimidone and its Analogues as NF-κB Activation Inhibitors
- Expression of two human acyl-CoA : diacylglycerol acyltransferase isozymes in yeast and selectivity of microbial inhibitors toward the isozymes
- Total synthesis of amidepsine B and revision of its absolute configuration
- Staphylotrichum boninense, a new hyphomycete (Chaetomiaceae) from soils in the Bonin Islands, Japan
- 広範囲な生物活性を示すキサントン型天然有機化合物マンゴスチン類の酸化反応
- Application of Electrochemically Generated Hypervalent Iodine Oxidant to Natural Products Synthesis
- Chemical modification of neamine. 5. Preparation of amino-deoxyneamines.
- Synthesis of stachyose tetradecaacetate and an isomer.
- Synthesis of (2-chloroethyl)-nitrosourea derivatives of carbohydrate.
- Total syntheses of (.+-.)-aerothionin, (.+-.)-homoaerothionin, and (.+-.)-aerophobin-1.
- Aminocyclitols. XXVI. A Synthesis of Aminocyclopentanetetrols
- Modification of aminocyclitol antibiotics. 6. Preparation of 5-deoxykanamycin B.
- Synthesis of Carbocydic Adenosine Analogs: 9-(2′,3′,4′,5′-Tetrahydroxycyclopentyl)adenines
- Synthesis of tetrahydrospectinomycin.