Two theonellapeptolide congeners from marine sponge Theonella sp.

Masashi Tsuda; Kazutaka Shimbo; Takaaki Kubota; Yuzuru Mikami; Jun'ichi Kobayashi

doi:10.1016/S0040-4020(99)00586-4

Two theonellapeptolide congeners from marine sponge Theonella sp.

Masashi Tsuda, Kazutaka Shimbo, Takaaki Kubota, Yuzuru Mikami, Jun'ichi Kobayashi

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

Abstract

Two new theonellapeptolide-related cyclic depsipeptides (1 and 2) have been isolated from an Okinawan marine sponge Theonella sp. and the structures were elucidated on the basis of the 2D NMR data, PSD analysis of MALDI- TOFMS, and chemical means. Compound 1 was a theonellapeptolide congener possessing a methylsulfinylacetyl group at the N-terminus, while 2 was another theonellapeptolide congener having an acetyl group at the N-terminus. Compounds 1 and 2 exhibited antimicrobial activity.

Original language	English
Pages (from-to)	10305-10314
Number of pages	10
Journal	Tetrahedron
Volume	55
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4020(99)00586-4
Publication status	Published - Aug 20 1999
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1016/S0040-4020(99)00586-4

Cite this

@article{39f80f50971b40fc8f941309da9f3d56,

title = "Two theonellapeptolide congeners from marine sponge Theonella sp.",

abstract = "Two new theonellapeptolide-related cyclic depsipeptides (1 and 2) have been isolated from an Okinawan marine sponge Theonella sp. and the structures were elucidated on the basis of the 2D NMR data, PSD analysis of MALDI- TOFMS, and chemical means. Compound 1 was a theonellapeptolide congener possessing a methylsulfinylacetyl group at the N-terminus, while 2 was another theonellapeptolide congener having an acetyl group at the N-terminus. Compounds 1 and 2 exhibited antimicrobial activity.",

author = "Masashi Tsuda and Kazutaka Shimbo and Takaaki Kubota and Yuzuru Mikami and Jun'ichi Kobayashi",

year = "1999",

month = aug,

day = "20",

doi = "10.1016/S0040-4020(99)00586-4",

language = "English",

volume = "55",

pages = "10305--10314",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Limited",

number = "34",

}

TY - JOUR

T1 - Two theonellapeptolide congeners from marine sponge Theonella sp.

AU - Tsuda, Masashi

AU - Shimbo, Kazutaka

AU - Kubota, Takaaki

AU - Mikami, Yuzuru

AU - Kobayashi, Jun'ichi

PY - 1999/8/20

Y1 - 1999/8/20

N2 - Two new theonellapeptolide-related cyclic depsipeptides (1 and 2) have been isolated from an Okinawan marine sponge Theonella sp. and the structures were elucidated on the basis of the 2D NMR data, PSD analysis of MALDI- TOFMS, and chemical means. Compound 1 was a theonellapeptolide congener possessing a methylsulfinylacetyl group at the N-terminus, while 2 was another theonellapeptolide congener having an acetyl group at the N-terminus. Compounds 1 and 2 exhibited antimicrobial activity.

AB - Two new theonellapeptolide-related cyclic depsipeptides (1 and 2) have been isolated from an Okinawan marine sponge Theonella sp. and the structures were elucidated on the basis of the 2D NMR data, PSD analysis of MALDI- TOFMS, and chemical means. Compound 1 was a theonellapeptolide congener possessing a methylsulfinylacetyl group at the N-terminus, while 2 was another theonellapeptolide congener having an acetyl group at the N-terminus. Compounds 1 and 2 exhibited antimicrobial activity.

UR - http://www.scopus.com/inward/record.url?scp=0033588213&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033588213&partnerID=8YFLogxK

U2 - 10.1016/S0040-4020(99)00586-4

DO - 10.1016/S0040-4020(99)00586-4

M3 - Article

AN - SCOPUS:0033588213

SN - 0040-4020

VL - 55

SP - 10305

EP - 10314

JO - Tetrahedron

JF - Tetrahedron

IS - 34

ER -

Two theonellapeptolide congeners from marine sponge Theonella sp.

Abstract

ASJC Scopus subject areas

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this