Essential structural factors of acetogenins, potent inhibitors of mitochondrial complex I. (Q44071140)

29 November 2017

Essential structural factors of acetogenins, potent inhibitors of mitochondrial complex I. (English)

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29 November 2017

Tomoko Motoyama

1

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29 November 2017

Hiromi Yabunaka

series ordinal

2

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29 November 2017

Hideto Miyoshi

series ordinal

3

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29 November 2017

language of work or name

English

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publication date

1 August 2002

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Bioorganic & Medicinal Chemistry Letters

29 November 2017

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29 November 2017

12

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29 November 2017

16

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29 November 2017

2089-2092

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Recent advances in Annonaceous acetogenins

29 November 2017

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7 January 2021

Annonaceous acetogenins: recent progress

1 reference

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Natural substances (acetogenins) from the family Annonaceae are powerful inhibitors of mitochondrial NADH dehydrogenase (Complex I)

1 reference

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7 January 2021

Two binding sites of inhibitors in NADH: ubiquinone oxidoreductase (complex I). Relationship of one site with the ubiquinone-binding site of bacterial glucose:ubiquinone oxidoreductase.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900374-8

7 January 2021

Three classes of inhibitors share a common binding domain in mitochondrial complex I (NADH:ubiquinone oxidoreductase).

1 reference

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Probing the ubiquinone reduction site in bovine mitochondrial complex I using a series of synthetic ubiquinones and inhibitors

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Structure-activity relationships of some complex I inhibitors

1 reference

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7 January 2021

Essential structural factors of annonaceous acetogenins as potent inhibitors of mitochondrial complex I

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900374-8

7 January 2021

Definition of crucial structural factors of acetogenins, potent inhibitors of mitochondrial complex I.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900374-8

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Design syntheses and mitochondrial complex I inhibitory activity of novel acetogenin mimics

1 reference

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Membrane conformations and their relation to cytotoxicity of asimicin and its analogues

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A rationally designed anticancer drug targeting a unique binding cavity of tubulin

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A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines

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Interpretation of nonelectrolyte partition coefficients between dimyristoyl lecithin and water.

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10.1016/S0960-894X(02)00374-8

Identifiers

DOI

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29 November 2017

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