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Masaaki Kurabayashi

Bio: Masaaki Kurabayashi is an academic researcher. The author has contributed to research in topics: Diterpene & Beta (finance). The author has an hindex of 10, co-authored 16 publications receiving 272 citations.

Papers
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Journal ArticleDOI
TL;DR: A potent antipeptic ulcer substance, acyclic diterpene alcohol, was isolated from a Thai medicinal plant identified with Croton sublyratus KURZ and the structure was determined by the spectral data and stereospecific synthesis.
Abstract: A potent antipeptic ulcer substance, acyclic diterpene alcohol, was isolated from a Thai medicinal plant identified with Croton sublyratus KURZ. The structure was determined by the spectral data and stereospecific synthesis to be (E, Z, E)-7-hydroxymethyl-3, 11, 15-trimethyl-2, 6, 10, 14-hexadecatetraen-1-ol.

81 citations


Cited by
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Journal ArticleDOI
TL;DR: The secondary metabolites isolated from Piper species for the period 1907 to June 1996 have been reviewed in this paper, where nearly six hundred chemical constituents belonging to different classes of bioactive compounds are listed together with their source(s) and references.

849 citations

BookDOI
01 Jan 1989
TL;DR: This comprehensive monograph satisfies the need for a review and synthesis of current knowledge about the use of ivermectin and abamectin in crop protection as well as in cattle, sheep, swine, horses, dogs, cats, birds, fish, reptiles, and in man.
Abstract: Ivermectin and abamectin, members of the avermectin family of compounds, were introduced to the market in the 1980's as a veterinary antiparasitic drug and agricultural pesticide, respectively. Their acceptance and commercial success have been remarkable; both are highly effective and in worldwide use. The efficacy of ivermectin in river blindness has expanded the interest in its use in human medicine. In response to the intense scientific and industrial interest in ivermectin and abamectin and the likelihood that they will be forerunners of an expanding family of drugs, this comprehensive monograph satisfies the need for a review and synthesis of current knowledge about the use of these substances in crop protection as well as in cattle, sheep, swine, horses, dogs, cats, birds, fish, reptiles, and in man. This overview presents chemical, biochemical, and microbiological data, as well as pharmacological, safety, and environmental aspects and covers practical use of the compounds as antiparasitic and pesticide agents, as well as the available safety data that have emerged from the clinical experience with human applications.

645 citations

Journal ArticleDOI
TL;DR: Taxus suspension cells (induced for taxoid biosynthesis by methyl jasmonate) were used for feeding studies, as the foundation for cell-free enzymology and as the source of transcripts for cDNA library construction and a variety of cloning strategies.
Abstract: Biosynthesis of the anticancer drug Taxol in Taxus (yew) species involves 19 steps from the universal diterpenoid progenitor geranylgeranyl diphosphate derived by the plastidial methyl erythritol phosphate pathway for isoprenoid precursor supply. Following the committed cyclization to the taxane skeleton, eight cytochrome P450-mediated oxygenations, three CoA-dependent acyl/aroyl transfers, an oxidation at C9, and oxetane (D-ring) formation yield the intermediate baccatin III, to which the functionally important C13-side chain is appended in five additional steps. To gain further insight about Taxol biosynthesis relevant to the improved production of this drug, and to draw inferences about the organization, regulation, and origins of this complex natural product pathway, Taxus suspension cells (induced for taxoid biosynthesis by methyl jasmonate) were used for feeding studies, as the foundation for cell-free enzymology and as the source of transcripts for cDNA library construction and a variety of cloning strategies. This approach has led to the elucidation of early and late pathway segments, the isolation and characterization of over half of the pathway enzymes and their corresponding genes, and the identification of candidate cDNAs for the remaining pathway steps, and it has provided many promising targets for genetically engineering more efficient biosynthetic production of Taxol and its precursors.

394 citations

Book ChapterDOI
TL;DR: In the twelve years since the first review article dealing with chemical constituents of the Hepaticae appeared in this series as Volume 42 (19), several short reviews concerned withchemical constituents of bryophytes have been published.
Abstract: In the twelve years since the first review article dealing with chemical constituents of the Hepaticae appeared in this series as Volume 42 (19), several short reviews concerned with chemical constituents of bryophytes have been published (22, 96, 144, 265, 271, 647, 649, 650) In 1988, a Symposium on Chemistry and Chemical Taxonomy of Bryophytes was organised on the behalf of the Phytochemical Society of Europe; the proceedings of this meeting appeared as a book entitled Bryophytes: Their Chemistry and Chemical Taxonomy (651) The symposium concerned itself with phytochemical, biochemical, botanical, chemotaxonomical, pharmaceutical, biotechnological and environmental aspects of bryophytes as well as with the synthesis of the terpenoids and aromatic compounds bryophytes elaborate The physiological and biochemical aspects of bryophytes have also been described in a recent book Bryophytes Development: Physiology and Biochemistry (139)

291 citations

Journal ArticleDOI
TL;DR: The status of acaricide resistance in cattle ticks from different parts of the world is summarized and modes of action of currently used acaricides, mechanism of resistance development, contributory factors for the development and spread of resistance, management of resistant strains and strategies to prolong the effect of the available acar pesticides are reviewed.

291 citations