Luminacins. A Family of Capillary Tube Formation Inhibitors from Streptomyces sp. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Structure Elucidation. (Q78428512)

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scientific article published on 01 March 2012

Language	Label	Description	Also known as
English	Luminacins. A Family of Capillary Tube Formation Inhibitors from Streptomyces sp. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Structure Elucidation.	scientific article published on 01 March 2012

Statements

scholarly article

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

Luminacins. A Family of Capillary Tube Formation Inhibitors from Streptomyces sp. I. Taxonomy, Fermentation, Isolation, Physico-chemical Properties and Structure Elucidation. (English)

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

1 reference

Streptomyces albidoflavus

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]pentanoyl]-2,6-dihydroxy-5-(2-methylpropyl)benzaldehyde

1 reference

(2S)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]pentan-1-one

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]-4-methylpentanoyl]-2,6-dihydroxy-5-(2-methylpropyl)benzaldehyde

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-4,8-dihydroxy-2-propyl-1,7-dioxaspiro[2.5]octan-6-yl]pentanoyl]-2,6-dihydroxy-5-(2-methylpropyl)benzaldehyde

1 reference

3-[2-(2-Ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl)-4-methylpentanoyl]-2,6-dihydroxy-5-(2-methylpropyl)benzaldehyde

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]hexanoyl]-2,6-dihydroxy-5-(2-methylpropyl)benzaldehyde

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]pentanoyl]-2,6-dihydroxy-5-[(1R)-1-methoxy-2-methylpropyl]benzaldehyde

1 reference

1 reference

3-[(2S)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]pentanoyl]-2,6-dihydroxy-5-[(1S)-1-methoxy-2-methylpropyl]benzaldehyde

1 reference

3-[(2R)-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]-4-methylpentanoyl]-2,6-dihydroxy-5-[(1S)-1-methoxy-2-methylpropyl]benzaldehyde

1 reference

1 reference

(2S)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]-4-methylpentan-1-one

1 reference

3-[2-(2-Ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl)-4-methylpentanoyl]-2,6-dihydroxy-5-(1-methoxy-2-methylpropyl)benzaldehyde

1 reference

1 reference

(2S)-1-[3-acetyl-2,4-dihydroxy-5-(2-methylpropyl)phenyl]-2-[(2S,3S,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,7-dioxaspiro[2.5]octan-6-yl]pentan-1-one

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

Luminacin E1/E2

1 reference

Luminacin A1/A2

1 reference

1 reference

Luminacin C1/C2

1 reference

Luminacin B1/B2

1 reference

author name string

NOBUAKI NARUSE

1

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

RENA KAGEYAMA-KAWASE

2

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

YASUHIRO FUNAHASHI

3

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

TOSHIAKI WAKABAYASHI

4

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

YOSHIO WATANABE

5

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

TOMOHIRO SAMESHIMA

6

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

KAZUYUKI DOBASHI

7

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

publication date

2000

1 reference

16 September 2022

full work available at URL

https://www.jstage.jst.go.jp/article/antibiotics1968/53/6/53_6_579/_pdf

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.7164/antibiotics.53.579?email=unpaywall_01@example.com

The Journal of Antibiotics

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

53

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

6

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

579-590

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

online access status

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.7164/antibiotics.53.579?email=unpaywall_01@example.com

access restriction status

1 reference

based on heuristic

inferred from online access status

Luminacins: a family of capillary tube formation inhibitors from Streptomyces sp. II. Biological activities

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.7164/ANTIBIOTICS.53.579

Borrelidin is an angiogenesis inhibitor; disruption of angiogenic capillary vessels in a rat aorta matrix culture model.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.7164/ANTIBIOTICS.53.579

Identifiers

10.7164/ANTIBIOTICS.53.579

1 reference

10.7164/ANTIBIOTICS.53.579

https://api.crossref.org/v1/works/http://dx.doi.org/10.7164/antibiotics.53.579

14 December 2019

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