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Bioactive substances of marine animals: polyoxygenated substances
-
Y. Hirata
Veröffentlicht/Copyright:
1. Januar 2009
Published Online: 2009-01-01
Published in Print: 1989-01-01
© 2013 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Preface
- Slime moulds (Myxomycetes) as a source of new biologically active metabolites
- A proposal for biosynthesis of the Daphniphyllum alkaloids
- Bioactive substances of marine animals: polyoxygenated substances
- Poly-(R)-3-hydroxybutyrate (PHB) biosynthesis: mechanistic studies on the biological Claisen condensation catalyzed by β-ketoacyl thiolase
- Natural products synthesis: palytoxin
- Contribution to the chemistry of β-lactam antibiotics: 1-oxa nuclear analogs of naturally occurring β-lactam antibiotics
- Biosynthetic and synthetic studies on the pigments of life
- The evolution of terpenes to sterols
- Isolation and structures of peptide hormones from the silkworm Bombyx mori: bombyxins - peptides structurally related to insulin
- Guggultetrols: a new class of naturally occurring lipids
- Isolation and structure elucidation of tannins
- Theory of rhodopsin activation: probable charge redistribution of excited state chromophore
- Structural studies of natural products by new NMR techniques
- Studies on algal carotenoids
- Effect of a marine algal constituent on the growth of lettuce and rice seedlings
- Isolation and structure of new toxins from plants
- Stereocontrolled synthesis of dihydroxycholecalciferol precursors
- Synthetic studies on nogalamycin congeners. Total syntheses of (+)-nogarene, (+)-7-con-O-methylnogarol, and their related compounds
- Synthetic studies on pseudolaric acid A
- Total synthesis of glycinoeclepin A
- Synthetic studies on gibberellins and antheridiogens
- Recent developments in natural product synthesis
- Hitachimycin (a.k.a. stubomycin): structural and synthetic studies
- Natural product syntheses based on asymmetric Diels-Alder reactions
- New methodologies for the synthesis of natural products
- New approach for natural product synthesis using main group organometallic reagents
- Synthetic studies on sesbanimides
- Studies directed towards the stereoselective synthesis of polyene macrolide antibiotics
- The synthesis of brassinosteroid
- Design of an efficient strategy for total synthesis of the microbial metabolite (-)-bactobolin
- The stereospecific synthesis of reserpine
- Chemical and pharmacological studies on sedative cyclopeptide alkaloids in some Rhamnaceae plants
- Studies in biotechnology. Important routes to the synthesis and biosynthesis of biologically active natural products
- Isolation and structural studies on new natural products of potential biological importance
- Some bioactive substances from plants of West China
- Synthesis and biological function of bacterial endotoxin
- Endogenous xanthurenic acid as a regulator of the crustacean molt cycle
- Chemistry, computers and carcinogenesis
- Oxidative strand scission of DNA
- Artificially elicited capabilities of enzymes and their application in natural product chemistry
- Active fragments of natural polysaccharides
- Studies on the biosynthesis of antibiotics
- Investigations of polypeptide biosynthesis: formation of peptide amides
- Stereochemical studies of natural products biosynthesis
- Structure-function relationship of polypeptide toxins: modifying gating mechanism of sodium channel
- NMR studies of the enzyme mechanisms of B12
- Interspecies distribution and biogenetic origin of tetrodotoxin and its derivatives
- Sponge secondary metabolites: new results
- Dinoflagellate and other microalgal toxins: chemistry and biochemistry
- Marine natural products: new results from Red Sea invertebrates
- Novel cytotoxins and fungicides from blue-green algae and marine animals possessing algal symbionts
- Biologically active marine natural products
- Biological activity in New Zealand marine organisms
- Amazing new alkaloid skeletons from the marine sponge Reniera sarai
- Terpenoids from bark beetles, solitary bees and danaine butterflies
- Recent results in the synthesis of semiochemicals: synthesis of glycinoeclepin A
- Synthetic and chemical studies on pheromones of some forest pest insects
- Bio-organic studies of insect olfaction
- The aphid sex pheromone
- Insect chemical communication systems
- Targeting DNA sites with chiral metal complexes
- The use of high affinity binding bioligands modified by transition metal carbonyl moieties
- A novel lysine-substituted nucleoside in the first position of the anticodon of minor isoleucine tRNA from Escherichia coli
- Natural products that cleave DNA
- From natural bleomycins to man-designed bleomycins
- Molecular basis of the activity of antibiotics of the vancomycin group
- Systematic synthesis design: the SYNGEN program
- Computer simulation studies of spherands, crowns and porphyrins: application of computer graphics, distance geometry, molecular mechanics and molecular dynamics approaches
- Application of molecular mechanics to natural product chemistry
- Molecular modelling: scientific and technological boundaries
- The description of organic reactions based on imaginary transition structures. A novel approach to the computer-oriented taxonomy of organic reactions
- Application of the automated structure elucidation system (CHEMICS) to the chemistry of natural products
Artikel in diesem Heft
- Preface
- Slime moulds (Myxomycetes) as a source of new biologically active metabolites
- A proposal for biosynthesis of the Daphniphyllum alkaloids
- Bioactive substances of marine animals: polyoxygenated substances
- Poly-(R)-3-hydroxybutyrate (PHB) biosynthesis: mechanistic studies on the biological Claisen condensation catalyzed by β-ketoacyl thiolase
- Natural products synthesis: palytoxin
- Contribution to the chemistry of β-lactam antibiotics: 1-oxa nuclear analogs of naturally occurring β-lactam antibiotics
- Biosynthetic and synthetic studies on the pigments of life
- The evolution of terpenes to sterols
- Isolation and structures of peptide hormones from the silkworm Bombyx mori: bombyxins - peptides structurally related to insulin
- Guggultetrols: a new class of naturally occurring lipids
- Isolation and structure elucidation of tannins
- Theory of rhodopsin activation: probable charge redistribution of excited state chromophore
- Structural studies of natural products by new NMR techniques
- Studies on algal carotenoids
- Effect of a marine algal constituent on the growth of lettuce and rice seedlings
- Isolation and structure of new toxins from plants
- Stereocontrolled synthesis of dihydroxycholecalciferol precursors
- Synthetic studies on nogalamycin congeners. Total syntheses of (+)-nogarene, (+)-7-con-O-methylnogarol, and their related compounds
- Synthetic studies on pseudolaric acid A
- Total synthesis of glycinoeclepin A
- Synthetic studies on gibberellins and antheridiogens
- Recent developments in natural product synthesis
- Hitachimycin (a.k.a. stubomycin): structural and synthetic studies
- Natural product syntheses based on asymmetric Diels-Alder reactions
- New methodologies for the synthesis of natural products
- New approach for natural product synthesis using main group organometallic reagents
- Synthetic studies on sesbanimides
- Studies directed towards the stereoselective synthesis of polyene macrolide antibiotics
- The synthesis of brassinosteroid
- Design of an efficient strategy for total synthesis of the microbial metabolite (-)-bactobolin
- The stereospecific synthesis of reserpine
- Chemical and pharmacological studies on sedative cyclopeptide alkaloids in some Rhamnaceae plants
- Studies in biotechnology. Important routes to the synthesis and biosynthesis of biologically active natural products
- Isolation and structural studies on new natural products of potential biological importance
- Some bioactive substances from plants of West China
- Synthesis and biological function of bacterial endotoxin
- Endogenous xanthurenic acid as a regulator of the crustacean molt cycle
- Chemistry, computers and carcinogenesis
- Oxidative strand scission of DNA
- Artificially elicited capabilities of enzymes and their application in natural product chemistry
- Active fragments of natural polysaccharides
- Studies on the biosynthesis of antibiotics
- Investigations of polypeptide biosynthesis: formation of peptide amides
- Stereochemical studies of natural products biosynthesis
- Structure-function relationship of polypeptide toxins: modifying gating mechanism of sodium channel
- NMR studies of the enzyme mechanisms of B12
- Interspecies distribution and biogenetic origin of tetrodotoxin and its derivatives
- Sponge secondary metabolites: new results
- Dinoflagellate and other microalgal toxins: chemistry and biochemistry
- Marine natural products: new results from Red Sea invertebrates
- Novel cytotoxins and fungicides from blue-green algae and marine animals possessing algal symbionts
- Biologically active marine natural products
- Biological activity in New Zealand marine organisms
- Amazing new alkaloid skeletons from the marine sponge Reniera sarai
- Terpenoids from bark beetles, solitary bees and danaine butterflies
- Recent results in the synthesis of semiochemicals: synthesis of glycinoeclepin A
- Synthetic and chemical studies on pheromones of some forest pest insects
- Bio-organic studies of insect olfaction
- The aphid sex pheromone
- Insect chemical communication systems
- Targeting DNA sites with chiral metal complexes
- The use of high affinity binding bioligands modified by transition metal carbonyl moieties
- A novel lysine-substituted nucleoside in the first position of the anticodon of minor isoleucine tRNA from Escherichia coli
- Natural products that cleave DNA
- From natural bleomycins to man-designed bleomycins
- Molecular basis of the activity of antibiotics of the vancomycin group
- Systematic synthesis design: the SYNGEN program
- Computer simulation studies of spherands, crowns and porphyrins: application of computer graphics, distance geometry, molecular mechanics and molecular dynamics approaches
- Application of molecular mechanics to natural product chemistry
- Molecular modelling: scientific and technological boundaries
- The description of organic reactions based on imaginary transition structures. A novel approach to the computer-oriented taxonomy of organic reactions
- Application of the automated structure elucidation system (CHEMICS) to the chemistry of natural products