Literature DB >> 12529132

(-)-Axinyssene: a novel cytotoxic diterpene from a Japanese marine sponge Axinyssa sp.

Kota Kodama1, Ryuichi Higuchi, Tomofumi Miyamoto, Rob W M Van Soest.   

Abstract

[structure: see text] A novel diterpene, (-)-axinyssene, was isolated from the Japanese marine sponge Axinyssa sp. The structure of (-)-axinyssene was determined on the basis of spectroscopic and synthetic evidence to be 1-methyl-4-[(4E)-5',9'-dimethyl-1'-methylene-4',8'-decadienyl]-(4S)-cyclohexene. (-)- and (+)-axinyssene showed mild cytotoxicity against acute promyelocytic leukemia, HL-60 cells.

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Year:  2003        PMID: 12529132     DOI: 10.1021/ol027202f

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

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Authors:  Jens Emsermann; Ulrich Kauhl; Till Opatz
Journal:  Mar Drugs       Date:  2016-01-14       Impact factor: 5.118

Review 2.  Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases.

Authors:  Jeffrey D Rudolf; Chin-Yuan Chang
Journal:  Nat Prod Rep       Date:  2020-03-25       Impact factor: 13.423

3.  Dactyloditerpenol acetate, a new prenylbisabolane-type diterpene from Aplysia dactylomela with significant in vitro anti-neuroinflammatory activity.

Authors:  Carlos Jiménez-Romero; Alejandro M S Mayer; Abimael D Rodríguez
Journal:  Bioorg Med Chem Lett       Date:  2013-11-14       Impact factor: 2.823

4.  An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids.

Authors:  De-Sen Li; Juan Hua; Shi-Hong Luo; Yan-Chun Liu; Yue-Gui Chen; Yi Ling; Kai Guo; Yan Liu; Sheng-Hong Li
Journal:  Plant Commun       Date:  2021-08-12
  4 in total

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