The first sorbicillinoid alkaloids, the antileukemic sorbicillactones A and B, from a sponge-derived Penicillium chrysogenum strain (Q78296015)

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

title

The first sorbicillinoid alkaloids, the antileukemic sorbicillactones A and B, from a sponge-derived Penicillium chrysogenum strain (English)

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

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Penicillium chrysogenum

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(1R,3R,4S,5Z,7S)-7-ethoxy-3-hydroxy-5-[(2E,4E)-1-hydroxyhexa-2,4-dienylidene]-1,3-dimethylbicyclo[2.2.2]octane-2,6-dione

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(2E)-3-{[(3S,3aR,4Z,7aS)-7-hydroxy-4-[(4E)-1-hydroxyhex-4-en-1-ylidene]-3,6,7a-trimethyl-2,5-dioxo-3aH-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid

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(2E)-3-{[(3S,3aR,4Z,7aS)-7-hydroxy-4-[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-3,6,7a-trimethyl-2,5-dioxo-3aH-1-benzofuran-3-yl]-C-hydroxycarbonimidoyl}prop-2-enoic acid

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(1R,3Z,4S,5R,6S,7S)-7-ethoxy-5,6-dihydroxy-3-[(2E,4E)-1-hydroxyhexa-2,4-dienylidene]-1,5-dimethylbicyclo[2.2.2]octan-2-one

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(1R,2R,4E,6S,7S,9S,13Z)-6,7,10-trihydroxy-4,13-bis[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]tridec-10-ene-3,5,12-trione

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4-[(4-hex-4-enoyl-5,7-dihydroxy-3,6,7a-trimethyl-2-oxo-3aH-1-benzofuran-3-yl)amino]-4-oxobut-2-enoic acid

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(2E,6R)-5,6-dihydroxy-2-[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-4,6-dimethylcyclohex-4-ene-1,3-dione

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1

Gerhard Bringmann

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Sanja Perović-Ottstadt

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object named as

Sanja Perović-Ottstadt

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

3

Tobias A.M. Gulder

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

author name string

Gerhard Lang

2

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Hideyuki Tsuruta

4

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

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Jörg Mühlbacher

5

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Katja Maksimenka

6

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Stefan Steffens

7

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Karsten Schaumann

8

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Rüdiger Stöhr

9

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Jutta Wiese

10

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

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Johannes F. Imhoff

11

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13 December 2019

Olexandra Boreiko

13

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

Werner E.G. Müller

14

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13 December 2019

publication date

July 2005

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16 September 2022

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

volume

61

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

13 December 2019

issue

30

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13 December 2019

page(s)

7252-7265

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026

BMS-182123, a fungal metabolite that inhibits the production of TNF-alpha by macrophages and monocytes

13 December 2019

cites work

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.49.234

Novel fungal metabolites, demethylsorbicillin and oxosorbicillinol, isolated from Trichoderma sp. USF-2690

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB.64.620

Novel DPPH Radical Scavengers, Bisorbicillinol and Demethyltrichodimerol, from a Fungus

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB.62.661

The metabolites of Trichodermalongibrachiatum. Part 1. Isolation of the metabolites and the structure of trichodimerol

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1139/V92-320

Identifiers

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2005.05.026