(3Z)-violacein (Q4013798)

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chemical compound
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Language Label Description Also known as
English
(3Z)-violacein
chemical compound

    Statements

    subclass of
    indole alkaloid
    0 references
    (3EZ)-violacein
    0 references
    chemical structure
    Violacein.svg
    198 × 148; 16 KB
    0 references
    mass
    343.095691 dalton
    1 reference
    stated in
    PubChem
    PubChem CID
    5359453
    language of work or name
    English
    title
    BRN 0049923 (English)
    retrieved
    21 September 2016
    chemical formula
    C₂₀H₁₃N₃O₃
    1 reference
    stated in
    PubChem
    PubChem CID
    5359453
    language of work or name
    English
    title
    BRN 0049923 (English)
    retrieved
    21 September 2016
    canonical SMILES
    C1=CC=C2C(=C1)C(=C3C=C(NC3=O)C4=CNC5=C4C=C(C=C5)O)C(=O)N2
    1 reference
    stated in
    PubChem
    PubChem CID
    5359453
    language of work or name
    English
    title
    BRN 0049923 (English)
    retrieved
    21 September 2016
    isomeric SMILES
    C1=CC=C2C(=C1)/C(=C/3\C=C(NC3=O)C4=CNC5=C4C=C(C=C5)O)/C(=O)N2
    1 reference
    stated in
    PubChem
    PubChem CID
    5359453
    language of work or name
    English
    title
    BRN 0049923 (English)
    retrieved
    21 September 2016
    found in taxon
    Chromobacterium violaceum
    13 references
    stated in
    Violacein and related tryptophan metabolites produced by Chromobacterium violaceum: biosynthetic mechanism and pathway for construction of violacein core
    stated in
    Antifungal activity of violacein purified from a novel strain of Chromobacterium sp. NIIST (MTCC 5522).
    stated in
    A New Metabolite of Tryptophan, Chromopyrrolic Acid, Produced byChromobacterium violaceum
    stated in
    Antileishmanial activity of the violacein extracted from Chromobacterium violaceum
    stated in
    Biosynthesis of Violacein: a Novel Rearrangement in Tryptophan Metabolism with a 1,2-Shift of the Indole Ring
    stated in
    Biosynthesis of Violacein: Evidence for the Intermediacy of 5-Hydroxy-l-tryptophan and the Structure of a New Pigment, Oxyviolacein, Produced by the Metabolism of 5-Hydroxytryptophan
    stated in
    Biosynthesis of violacein: oxygenation at the 2-position of the indole ring and structures of proviolacein, prodeoxyviolacein and pseudoviolacein, the plausible biosynthetic intermediates of violacein and deoxyviolacein
    stated in
    Q105164756
    stated in
    In vitro biosynthesis of violacein from L-tryptophan by the enzymes VioA-E from Chromobacterium violaceum.
    stated in
    147. The chemistry of bacteria. Part VII. The structure of violacein
    stated in
    Cytotoxic activity of violacein in human colon cancer cells.
    stated in
    Growth inhibition and pro-apoptotic activity of violacein in Ehrlich ascites tumor
    stated in
    Molecular mechanism of violacein-mediated human leukemia cell death.

    Identifiers

    ChemSpider ID
    4514290
    1 reference
    stated in
    ChemSpider
    ChemSpider ID
    4514290
    language of work or name
    English
    title
    (3Z)-3-[5-(5-Hydroxy-1H-indol-3-yl)-2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene]-1,3-dihydro-2H-indol-2-one (English)
    retrieved
    21 September 2016
     
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