(Q61774180)

N-[3-(2-cyanoethylamino)-3-sulfanylidenepropyl]-4-hydroxybenzenecarbothioamide

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Unk-thionobAla-thionobAla-bAla-ol

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3-[3-[3-[(4-Hydroxybenzenecarbothioyl)amino]propanethioylamino]propanethioylamino]propyl acetate

1 reference

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3-[3-[(4-Hydroxybenzenecarbothioyl)amino]propanethioylamino]propanoic acid

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3-[3-[3-[(4-Hydroxybenzenecarbothioyl)amino]propanethioylamino]propanethioylamino]propanoic acid

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Christian Hertweck

3

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author name string

Florian Kloss

series ordinal

1

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Thorger Lincke

series ordinal

2

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publication date

3 February 2011

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published in

European Journal of Organic Chemistry

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volume

2011

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issue

8

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page(s)

1429-1431

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cites work

Antibakterielle Naturstoffe in der medizinischen Chemie – Exodus oder Renaissance?

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Clostridium cellulolyticum: model organism of mesophilic cellulolytic clostridia

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Thioamides in nature: in search of secondary metabolites in anaerobic microorganisms

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Mechanism of thioamide drug action against tuberculosis and leprosy

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Ethionamide activation and sensitivity in multidrug-resistant Mycobacterium tuberculosis

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Synthesis and anthelmintic activity of thioamide analogues of cyclic octadepsipeptides such as PF1022A.

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Dependence of fungistatic activity of 2, 4-dihydroxythiobenzanilideson the structure and lipophilic nature of the compounds

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Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor

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Applications of Lawesson’s Reagent in Organic and Organometallic Syntheses

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β-Thiopeptides: Synthesis, NMR Solution Structure, CD Spectra, and Photochemistry

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Cervimycin A-D: a polyketide glycoside complex from a cave bacterium can defeat vancomycin resistance

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