M. Kodama

Publications230
h-index29
Citations3,111
Highly Influential Citations42
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Antioxidant xanthones from Garcinia subelliptica
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Anti-plasmin inhibitor. VI. Structure of phlorofucofuroeckol A, a novel phlorotannin with both dibenzo-1,4-dioxin and dibenzofuran elements, from Ecklonia kurome Okamura.
TLDR
The structure has been elucidated to be 1,11-di(3,5-dihydroxyphenoxy)- benzofuro[3,2-a]dibenzo[b,e][1,4]dioxin-2,4,8,10,14-pentaol on the basis of the spectral data.
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Neurotrophic sesquiterpene-neolignans from magnolia obovata: structure and neurotrophic activity
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Structures of americanol A and isoamericanol A having a neurotrophic property from the seeds of Phytolacca americana.
TLDR
Isoamericanol A, americanol A, and americanin A have been found to enhance choline acetyltransferase activity at 10(-5) M in a cultured neuronal cell system derived from fetal rat hemisphere.
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Curcumenone, curcumanolide A and curcumanolide B, three sesquiterpenoids from Curcuma zedoaria
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Identification of thioether intermediates in the reductive transformation of gonyautoxins into saxitoxins by thiols.
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Antibacterial Activity of Pisiferic Acid and Its Derivatives against Gram-negative and-positive Bacteria
TLDR
In the mode of action of the pisiferic acid species on the bacterial macromolecule, peptidoglycan synthesis was predominantly inhibited in B. subtilis, while nonspecific inhibition was observed in P. vulgaris.
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Prenylated C6-C3 compounds from Illicium tashiroi
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Structure and synthesis of 11,12,13-trihydroxy-9Z,15Z-octadecadienoic acids from rice plant suffering from rice blast disease.
Structural elucidation including the absolute configuration was carried out on the trihydroxyoctadecadienoic acids isolated from rice plant suffering from rice blast disease.
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Structure of an anti-plasmin inhibitor, eckol, isolated from the brown alga Ecklonia kurome Okamura and inhibitory activities of its derivatives on plasma plasmin inhibitors.
TLDR
The structure of eckol has been elucidated based on the spectral data, in particular, by means of negative nuclear Overhauser effect (NOE), and finally established as 1-(3,5-dihydroxyphenoxy)-2,4,7,9-tetrahydroxydibenzo-1,4-dio xin by X-ray analysis.
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