Absolute stereochemistry of fungal beauveriolide III and ACAT inhibitory activity of four stereoisomers (Q43527333)

24 November 2017

title

Absolute stereochemistry of fungal beauveriolide III and ACAT inhibitory activity of four stereoisomers (English)

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24 November 2017

10

Satoshi Omura

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24 November 2017

Taichi Ohshiro

1

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24 November 2017

Ichiji Namatame

2

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24 November 2017

Kenichiro Nagai

3

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24 November 2017

Takafumi Sekiguchi

4

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24 November 2017

Takayuki Doi

5

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24 November 2017

Takashi Takahashi

6

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24 November 2017

Kazuaki Akasaka

7

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24 November 2017

Lawrence L Rudel

8

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24 November 2017

Hiroshi Tomoda

9

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24 November 2017

language of work or name

English

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publication date

1 September 2006

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Journal of Organic Chemistry

24 November 2017

published in

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24 November 2017

volume

71

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24 November 2017

issue

20

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24 November 2017

page(s)

7643-7649

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Characterization of two human genes encoding acyl coenzyme A:cholesterol acyltransferase-related enzymes

24 November 2017

cites work

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

ACAT-2, a second mammalian acyl-CoA:cholesterol acyltransferase. Its cloning, expression, and characterization

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Antiatherogenic activity of fungal beauveriolides, inhibitors of lipid droplet accumulation in macrophages

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

The Absolute Configuration of Gambieric Acids A–D, Potent Antifungal Polyethers, Isolated from the Marine Dinoflagellate Gambierdiscus toxicus

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Selective ACAT inhibitors as promising antihyperlipidemic, antiathero-sclerotic and anti-Alzheimer drugs.

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Synthesis, absolute stereochemistry and molecular design of the new antifungal and antibacterial antibiotic produced by Streptomyces sp.201.

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

New beauveriolides produced by amino acid-supplemented fermentation of Beauveria sp. FO-6979.

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

ACAT2 is localized to hepatocytes and is the major cholesterol-esterifying enzyme in human liver

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Synthesis and biological evaluation of a beauveriolide analogue library

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Chiral discrimination of branched-chain fatty acids by reversed-phase HPLC after labeling with a chiral fluorescent conversion reagent

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

The Structures of Bioactive Cyclodepsipeptides, Beauveriolides I and II, Metabolites of Entomopathogenic FungiBeauveriasp.

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Synthesis of Four Chiral Isomers of beta-Lactone DU-6622 and Inhibition of HMG-CoA Synthase by the Specific (2R,3R)-Isomer

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Complete inhibition of mouse macrophage-derived foam cell formation by triacsin C

1 reference

12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JO0611667

Beauveriolides, specific inhibitors of lipid droplet formation in mouse macrophages, produced by Beauveria sp. FO-6979.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.52.1

Identifiers

DOI

10.1021/JO0611667

1 reference

release_w62knfdapjcmtd2z7vlpl6smnq

24 November 2017

Fatcat ID

1 reference

https://api.fatcat.wiki/v0/release/w62knfdapjcmtd2z7vlpl6smnq

Fatcat

reference URL

mapped directly with Wikidata item

24 November 2022

based on heuristic

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