Both Enantiomers of 8-Hydroxyhexadecanoic Acid Inhibit the Spore Germination of Lygodium japonicum
スポンサーリンク
概要
著者
-
Sugai Takeshi
Department Of Agricultural Chemistry The University Of Tokyo
-
Mori Kenji
Department Of Agricultural Chemistry College Of Science And Technology The University Of Tokyo
-
SUGAI Takeshi
Department of Agricultural Chemistry, The University of Tokyo
関連論文
- C-type Natriuretic Peptide, a Novel Antifibrotic Agent, Attenuates Cardiac Remodeling and Improves Left Ventricular Dysfunction in Dilated Cardiomyopathy(Cardiovascular Pharmacology, Basic/Clinical 1 (H), The 69th Annual Scientific Meeting of the Japanese
- Calcineurin-NFAT Pathway-Dependent Cardiac Remodeling in Mice Deficient for GC-A, a Receptor for Atrial and Brain Natriuretic Peptides(Cardiac Hypertrophy 1 (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Interaction between C-Type Natriuretic Peptide and Endothelin-1 in Hypertrophic Response of Cultured Rat Cardiac Myocytes
- Endogenous Endothelin-1 Secreted from Cultured Rat Cardiac Nonmyocytes Inhibits Doxorubicin-Induced Cardiac Myocyte Apoptosis via ERK-Dependent CREB Activation
- A case of Kabuki syndrome presenting West syndrome
- Stereoselective Synthesis of Methyl Epijasmonate(Organic Chemistry)
- Trial of intraventricular ribavirin therapy for subacute sclerosing panencephalitis in Japan
- Neuronal protein NP25 interacts with F-actin
- Neuronal protein25は神経細胞の分化により増加する
- Pathophysiology of the transient temporal lobe lesion in a patient with Menkes disease
- Serial brain imaging analysis of stroke-like episodes in MELAS
- Favorable response of ADHD with giant SEP to extended-release valproate
- Administration of secretin for autism alters dopamine metabolism in the central nervous system
- Synthesis of 4-Hydroxy-3(2H)-furanone Acyl Derivatives and Their Anti-cataract Effect on Spontaneous Cataract Rats (ICR/f)
- Antioxidative Activities of 4-Hydroxy-3 (2H)-furanones and Their Anti-cataract Effect on Spontaneous Cataract Rat (ICR/f)
- Synthesis of Methyl (5Z, 9Z, 17R)-17-Methylnonadeca-5, 9-dienoate, the (R)-Enantiomer of the Structure Proposed for a Metabolite of the Philippine Sponge Plakinastrella sp.(Organic Chemistry)
- MK800-62F1, a New Inhibitor of Apoptotic Cell Death, from Streptomyces diastatochromogenes MK800-62F1 : II. Structure Elucidation
- Patients with West syndrome whose ictal SPECT showed focal cortical hyperperfusion
- A case of acute encephalitis with refractory, repetitive partial seizures, presenting autoantibody to glutamate receptor Gluε2
- Successful Management of Intractable Epilepsy with Lidocaine Tapes and Continuous Subcutaneous Lidocaine Infusion
- A case of idiopathic portal hypertension associated with rheumatoid arthritis
- Improved Conditions for the Production and Characterization of 1-Arylpropane-1,2-diols and Related Compounds
- Improved Enzymatic Procedure for a Preparative-Scale Synthesis of Sialic Acid and KDN
- Synthesis of Both the Enantiomers of trans-Chrysanthenol and trans-Chrysanthenyl Acetate as the Characteristic Major Constituents of Kougiku
- Synthesis of All Four Possible Stereoisomers of 1-Phenyl-2,3-butanediol and Both Enantiomers of 3-Hydroxy-4-phenyl-2-butanone to Determine the Absolute Configuration of the Natural Constituents
- Simple Synthesis of Dehydrololiolide
- Synthesis of (±)-Methyl Epijasmonate and (±)-Methyl Cucurbate(Organic Chemistry)
- A Simple and Efficient Synthesis of (±)-Methyl Dihydroepijasmonate(Organic Chemistry)
- Stereoselective Synthesis of erythro-Serricornin, (4R, 6R, 7S)-, and (4596R, 75)-4?6-Dimethyl-7-hydroxynonan-3-one9 Stereoisomers of the Sex Pheromone of Cigarette Beetle
- Molecular Action Mode of Hippospongic Acid A, an Inhibitor of Gastrulation of Starfish Embryos
- Access to Enantiomerically Pure Intermediates for (-) -Geosmin Synthesis Starting from (4aS, 5S) -4, 4a, 5, 6, 7, 8-Hexahydro-5-hydroxy-4a-methyl-naphthalen-2 (3H) -one(Organic Chemistry)
- Preparation of Optically Active α-Hydroxy Acid Derivatives by Microbial Hydrolysis of Cyanohydrins and Its Application to the Synthesis of (R)-4-Dodecanolide(Organic Chemistry)
- Biochemical Preparation of Optically Active 4-Hydroxy-β-ionone and Its Transformation to (S)-6-Hydroxy-α-ionone(Organic Chemistry)
- Synthesis of Regioselectively Protected Forms of Cytidine Based on Enzyme-catalyzed Deacetylation as the Key Step
- Degradation of Derivatives of N-Acetyl-D-glucosamine by Rhodococcus rhodochrous IFO 15564 : Substrate Specificity and Its Application to the Synthesis of Allyl α-N-Acetyl-D-glucosaminide
- A Chemo-Enzymatic Synthesis of _D-Allosamine Derivatives from Tri-O-acetyl-_D-glucal
- Efficient Route to (S)-Azetidine-2-carboxylic Acid
- Preparation of Methyl Ursodeoxycholate in an Interface Bioreactor : Use of a Mixed Solvent System to Increase the Solubilities of Substrate and Product
- Synthesis of Citronellyl Acetate via a Transacetylation to Citronellol from Acetyl Coenzyme A Produced from Glucose and Acetate in Growing Yeasts
- Preparation of Methyl Ursodeoxycholate via Microbial Reduction of Methyl 7-Ketolithocholate in an Anaerobic Interface Bioreactor
- Synthesis of Methyl Ursodeoxycholate via Microbial Reduction of Methyl 7-Ketolithocholate with Eubacterium aerofaciens JCM 7790 Grown on Two Kinds of Carbon and Hydride Sources, Glucose and Mannitol
- Syntheses of Optically Active Citronellol, Citronellal, and Citronellic Acid by Microbial Oxidation and Double Coupling System in an Interface Bioreactor
- Synthesis of (Rc,Ss)-1,1,1-Trifluoro-3-(p-tolylsulfinyl)-2-propanol by an Asymmaaaaetric Reduction with a Test, Yamadazyma farinosa, as a Key-step
- Preparative-scale Enzyme-catalyzed Synthesis of (R)-α-Fluorophenylacetic Acid
- Biocatalysis in Organic Synthesis : The Use of Nitrile- and Amide-hydrolyzing Microorganisms
- Pivotal Role of (E)-3-Carbamoyl-1-propenylboronic Acid in the Combination of Suzuki-Miyaura Coupling and Enzyme Reactions : Synthesis of (3E, 5E)- and (3E, 5Z)-6-Phenyl-3, 5-hexadienoic Acid
- Preparation of Sulfur-Containing Optically Active Secondary Alcohols Based on Pichia farinosa-Catalyzed anti-Prelog-Rule Reduction
- Efficient Lipase-catalyzed Preparation of Long-chain Fatty Acid Esters of Bile Acids: Biological Activity and Synthetic Application of the products
- Action of Nitrile Hydratase from Rhodococcus rhodochrous IFO 15564 on Derivatives of 2,5-Anhydro-D-allononitrile
- Enantioselective Oxidation of Sulfinic Acid Esters with the Aid of a Microorganism
- Enzymatic Preparation of Glycerol-related Chiral Pool Possessing tert-Alkoxy Group
- Biological activity of pestalotins on the elongation growth of rice seedlings
- Subtilisin-Like Proprotein Convertases, PACE4 and PC8, as Well as Furin, are Endogenous Proalbumin Convertases in HepG2 Cells
- Biological Activities of YTIT/YTIY Analogous Sequences Present in Fibronectin-Like Type III Repeats
- A remarkable large hamartoma around the knee in a patient with tuberous sclerosis
- Long-term follow-up of a patient with subacute sclerosing panencephalitis successfully treated with intrathecal interferon alpha
- Adrenocorticotropic hormone therapy for infantile spasms alters pyruvate metabolism in the central nervous system
- Behavioral and Electroantennogram Responses of Male American Cockroaches to Periplanones and Their Analogs(Organic Chemistry)
- Pb7 HAUPTMANN'S PERIPLANONE-A : CHARACTERIZATION AND ELUCIDATION OF THE FORMATION
- Syntheses of Four Methyl-branched Secondary Acetates and a Methyl-branched Ketone as Possible Candidates for the Female Pheromone of the Screwworm Fly, Cochliomyia hominivorax(Organic Chemistry)
- Syntheses of Racemic and Diastereomeric Mixtures of 3,7,11,15-Tetramethylhentriacontane and 4,8,12,16-Tetramethyldotriacontane, the Cuticular Tetramethylalkanes of the Tsetse Fly, Glossina brevipalpis(Organic Chemistry)
- Concise Synthesis of a Racemic and Diastereomeric Mixture of the Sex Pheromones of Matsucoccus Pine Scales
- Determination of the (2E, 4E)-Geometry of the 3,5-Dimethyl-2,4-diene System of Antibiotic 1233A by NMR Comparison with the Four Geometrical Isomers of Methyl 3,5-Dimethyl-2,4-heptadienoate
- Percutaneous hot water injection and microwave coagulation therapy for small hepatocellular carcinoma
- Genomic Organization and Alternative Splicing of Human PACE4 (SPC4), Kexin-Like Processing Endoprotease
- Syntheses of Highly Oxygen-functionalized Derivatives of Dihydrodihydroxyphthalic Acid in Enantiomerically Enriched Forms
- Synthesis of (+)-Turmeronol A, an Inhibitor of Soybean Lipoxygenase, and (+)-ar-Turmerone
- Human Subtilisin-Like Proprotein Convertase, PACE4 (SPC4) Gene Expression Is Highly Regulated through E-Box Elements in HepG2 and GH4C1 Cells
- Synthesis of the Enantiomers of 7-Methyl-1,6-dioxaspiro[4.5]decane, Pheromone of the Common Wasp and the Pine Beetle
- Biocatalytic Preparation of (R) - (-) -4- (Phenylthio) -2-butanol and (R) - (-) -4- (Phenylsulfonyl) -2-butanol by the Sequential Use of Pichia farinosa and Rhodococcus rhodochrous
- Synthesis of (4aR, 10aS)-(-)-8-Methoxy-1, 1, 4a-trimethyl-2-oxo-1, 2, 3, 4, 4a, 9, 10, 10a-octahydrophenanthrene, an Optically Active Intermediate for the Synthesis of Diterpenes(Organic Chemistry)
- Synthesis of (±)-Hiburipyranone, a Cytotoxic Metabolite of Marine Sponge Mycale adhaerens
- Synthesis of the Esterified Cerebroside in the Epidermis of Guinea Pigs
- Reinvestigation of the Structure of the Esterified Cerebroside in the Epidermis of Guinea pigs
- Synthesis of (-)-Allosamizoline, the Pseudoaminosugar Moiety of Allosamidin, a Chitinase Inhibitor
- Brassinolide and Homobrassinolide Promotion of Lamina Inclination of Rice Seedlings
- Synthesis of (R)-Callosobruchusic Acid from Methyl (R)-3-Carboxybutanoate
- Compounds with Juvenile Hormone Activity. I. Inhibitory Effects of the Synthetic Juvenile Hormone and Its Analogues on the Metamorphosis of Several Insects
- New Optically Active 4,4-Dialky1-γ-lactones as Chiral Dopants for Ferroelectric Liquid Crystals
- Mechanistic Studies on Nitrosation-Deaminocyclization of Mono-Carbamoylated Vicinal Amino Alcohols and Diols : A New Preparative In Situ Formation of Ethanediazo Hydroxide for the Ethylation of Carboxylates under Mild Conditions
- Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate, the Sex Pheromone of the Hessian Fly, Mayetiola destructor
- Enzymatic Preparation of Ethyl (S)-3-Hydroxybutanoate with a High Enantiomeric Excess(Organic Chemistry)
- Synthesis of the (4R, 5R)-Isomer of 5-Hydroxy-6-phenyl-4-hexanolide, a Lateral Root-inducing Substance Isolated from Erwinia quercina
- Biochemical Preparation of (R)-Sulcatol(Organic Chemistry)
- Short-Step and Scalable Synthesis of (±)-Cytoxazone
- Lipase-Catalyzed Kinetic Resolution of 2-Hydroxyhexadecanoic Acid and Its Esters(Organic Chemistry)
- A Simple Preparation of (R)-2-Hydroxy-4-phenyl-butanoic Acid(Organic Chemistry)
- B-10-5 Synthesis of Substances related to Gibberellins(Terpenoids)
- Sex Pheromone of the Comstock Mealybug, Pseudococcus comstocki KUWANA : Isolation and Identification
- Synthesis of Brassinolide Analogs with a Modified Ring B and Their Plant Growth-promoting Activity(Organic Chemistry)
- Biochemical Reduction of 3-Oxoalkanoic Esters by a Bottom-fermentation Yeast, Saccharomyces cerevisiae IFO 0565
- Reduction of Acyl Enolates of α-Substituted β-Keto Esters by Bakers' Yeast(Organic Chemistry)
- Both Enantiomers of N-Boc-indoline-2-carboxylic Esters
- An Expeditious Route to N-Acetyl-D-galactosamine from N-Acetyl-D-glucosamine Based on the Selective Protection of Hydroxy Groups
- A Chemo-Enzymatic Expeditious Route to Racemic Dihexanoyl (2R*,3R*,4R*)-Dehydroxymethylepoxyquinomycin (DHMEQ), the Precursor for Lipase-Catalyzed Synthesis of the Potent Nuclear Factor-κB Inhibitor, (2S,3S,4S)-DHMEQ
- Synthesis of (S)-2-Hydroxy-β-ionone, Employing (S)-3-Hydroxy-2, 2-dimethylcyclohexanone as the Chiral Starting Material
- Preparation of Optically Active Secondary Alcohols Related to Synthetic Pyrethroids by Microbial Asymmetric Hydrolysis of the Corresponding Acetates
- Synthesis of Both the Enantiomers of 4-Dodecanolide, a Defensive Secretion of Rove Beetles
- Both Enantiomers of 8-Hydroxyhexadecanoic Acid Inhibit the Spore Germination of Lygodium japonicum
- Synthesis of Okicamelliaside, a Glucoside of Ellagic Acid with Potent Anti-Degranulation Activity