Synthesis and biological activities of the respiratory chain inhibitor aurachin D and new ring versus chain analogues - Wikidata - awgldk - TriplyDB

Synthesis and biological activities of the respiratory chain inhibitor aurachin D and new ring versus chain analogues

Synthesis and biological activities of the respiratory chain inhibitor aurachin D and new ring versus chain analogues

http://www.wikidata.org/entity/Q34942406

about

The cytochrome bd-type quinol oxidase is important for survival of Mycobacterium smegmatis under peroxide and antibiotic-induced stress.Antibiotics from myxobacteria.Synthesis of aurachins B and H.Total Syntheses of Aurachins A and B.The anti-mycobacterial activity of the cytochrome bcc inhibitor Q203 can be enhanced by small-molecule inhibition of cytochrome bd.Total synthesis of aurachins C, D, and L, and a structurally simplified analog of aurachin C.Bioenergetics of Mycobacterium: An Emerging Landscape for Drug Discovery.

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P2860

Synthesis and biological activities of the respiratory chain inhibitor aurachin D and new ring versus chain analogues

http://www.wikidata.org/entity/Q34942406

description

2013 nî lūn-bûn

@nan

2013 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հուլիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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name

Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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type

label

Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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prefLabel

Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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Synthesis and biological activ ...... ew ring versus chain analogues

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P1433

Beilstein Journal of Organic Chemistry

P1476

Synthesis and biological activ ...... ew ring versus chain analogues

@en

P2093

Bastien Nay

http://www.w3.org/2001/XMLSchema#string

Jennifer Herrmann

http://www.w3.org/2001/XMLSchema#string

Philippe Grellier

http://www.w3.org/2001/XMLSchema#string

Rolf Müller

http://www.w3.org/2001/XMLSchema#string

Soizic Prado

http://www.w3.org/2001/XMLSchema#string

Xu-Wen Li

http://www.w3.org/2001/XMLSchema#string

Yi Zang

http://www.w3.org/2001/XMLSchema#string

P2860

Privileged scaffolds for library design and drug discovery

Privileged structures: applications in drug discovery.

Completing the puzzle of aurachin biosynthesis in Stigmatella aurantiaca Sg a15.

Privileged structures: a useful concept for the rational design of new lead drug candidates.

Synthesis of intervenolin, an antitumor natural quinolone with unusual substituents.

Acridones and quinolones as inhibitors of ubiquinone functions in the mitochondrial respiratory chain.

Two binding sites for naturally occurring inhibitors in mitochondrial and bacterial NADH:ubiquinone oxidoreductase (complex I).

Terpenes arrest parasite development and inhibit biosynthesis of isoprenoids in Plasmodium falciparum.

A semipinacol rearrangement directed by an enzymatic system featuring dual-function FAD-dependent monooxygenase.

Divergent route to access structurally diverse 4-quinolones via mono or sequential cross-couplings.

P304

1551-1558

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scholarly article

P356

10.3762/BJOC.9.176

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9

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2013-07-31T00:00:00Z

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255956016

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23946854

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3740496

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