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Featured researches published by Shinichi Sakemi.


Tetrahedron Letters | 1986

Venustatriol. A new, anti-viral, triterpene tetracyclic ether from Laurencia venusta

Shinichi Sakemi; Tatsuo Higa; Charles W. Jefford; Gérald Bernardinelli

Abstract Venustatriol, a new tetracyclic ether derived from squalene, which has anti-viral activity, has been isolated from the red alga Laurencia venusta . Its structure and absolute configuration were determined by X-ray using the absolute structure parameter x. By comparison of their spectral properties, the absolute configuration of its congener, thyrsiferol, was deduced.


Tetrahedron Letters | 1989

Batzellines A, B, and C. Novel pyrroloquinoline alkaloids from the sponge Batzella Sp.

Shinichi Sakemi; Hao H. Sun; Charles W. Jefford; Gérald Bernardinelli

Three highly functionalized pyrroloquinoline alkaloids, batzelline A ( 1 ), B ( 2 ), and C ( 3 ) were isolated from the deep water Bahamas sponge Batzella sp. The structure of 1 was determined by X-ray and those of 2 and 3 deduced by comparison of their spectral data with that of 1 and by chemical transformations.


Tetrahedron | 1987

Antitumor cyclic peroxides from the sponge plakortis lita

Shinichi Sakemi; Tatsuo Higa; Uffe Anthoni; Carsten Christophersen

Abstract Four new cyclic peroxides (5–8) along with known chondrillin (4) have been isolated as antitumor constituents of the sponge Plakortis lita. These are methyl-(3S*, 6S*)-3, 6-epidioxy- 6-methoxyoctadec-4-enoate (5), methyl( 3S*, 6S*, 16E)-3, 6-epidoxy- 6-methoxyoctadeca-4,16-dienoate (6), methyl( 3S*, 6S*, 14E, 16E)- 3, 6-epidioxy-6-methoxyoctadeca-4, 14, 16-trienoate (7), and methyl-( 3S*, 6S*, 16E, 18E)-3, 6-epidioxy-6-methoxyeicosa-4 ,16 ,18- trinoate (8). All of them are epimeric to 4 and exhibit higher antitumor potency than 4.


Journal of Chemical Ecology | 1983

Environmental studies on natural halogen compounds. I Estimation of biomass of the acorn wormPtychodera flava Eschscholtz (Hemichordata: Enteropneusta) and excretion rate of metabolites at Kattore Bay, Kohama Island, Okinawa

Tatsuo Higa; Shinichi Sakemi

In order to study the environmental significance of the acorn wormPtychodera flava, which excretes a copious amount of halogenated metabolites, the biomass and the excretion rate were estimated at Kattore Bay, Kohama Island, Okinawa. The habitat, which extends over 1 km2, could be divided into two areas: zone A, 3.0 × 105m2, density 95.6/m2; and zone B, 7.2 × 105 m2, density 48.8/m2, according to the densities. The total population was estimated to be 6.4 × 107 ± 2.0 × 107 individuals or 93.0 ± 28.9 tons. These worms daily excrete about 480 tons of fecal sand which was estimated to contain 43 kg of the material extractable with organic solvents. The material contained halogenated metabolites which showed antimicrobial activity.


Comparative Biochemistry and Physiology B | 1985

Isolation of free deoxyribonucleosides and their bases from the acorn worm Ptychodera flava

Shinichi Sakemi; Tatsuo Higa

Abstract 1. 1. An aqueous extract of the acorn worm Ptychodera flava was investigated for hydrophilic constituents. 2. 2. Isolated from the extract were four deoxyribonucleasides (deoxyguanosine, deoxyinosine, deoxyuridine, and deoxythymidine) and three bases (hypoxanthine, uracil, and thymine). 3. 3. Free deoxyribonucleosides, especially deoxyinosine and deoxyuridine have rarely been isolated from marine invertebrates.


Journal of the American Chemical Society | 1988

Isolation and structure elucidation of onnamide A, a new bioactive metabolite of a marine sponge, Theonella sp

Shinichi Sakemi; Toshio Ichiba; Shigeo Kohmoto; Gabriel Saucy; Tatsuo Higa


Archive | 1988

Antiviral, antitumor and antifungal compositions and their methods of use

Tatsuo Higa; Shinichi Sakemi; Sue Shipley Cross


Archive | 1987

Guaiazulenes derivatives and their methods of use

Tatsuo Higa; Shinichi Sakemi


Archive | 1988

Antiviral, antitumor and antifungal compositions

Tatsuo Higa; Shinichi Sakemi; Sue Shipley Cross


Archive | 1988

Antivirale, antitumoraktive und fungizide zusammensetzungen. Antiviral, antitumor and antifungal compositions.

Tatsuo Higa; Shinichi Sakemi; Sue Shipley Cross

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Tatsuo Higa

Harbor Branch Oceanographic Institute

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Tatsuo Higa

Harbor Branch Oceanographic Institute

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Toshio Ichiba

University of Hawaii at Manoa

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Uffe Anthoni

University of Copenhagen

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