Chromopyrrolic acid (Q27096807)

lycogalic acid A (English)

19 October 2016

chemical formula

C₂₂H₁₅N₃O₄

1 reference

lycogalic acid A (English)

19 October 2016

canonical SMILES

C1=CC=C2C(=C1)C(=CN2)C3=C(NC(=C3C4=CNC5=CC=CC=C54)C(=O)O)C(=O)O

1 reference

lycogalic acid A (English)

Chromobacterium violaceum

19 October 2016

found in taxon

4 references

A New Metabolite of Tryptophan, Chromopyrrolic Acid, Produced byChromobacterium violaceum

Novel tryptophan metabolites, chromoazepinone A, B and C, produced by a blocked mutant of Chromobacterium violaceum, the biosynthetic implications and the biological activity of chromoazepinone A and B.

Novel tryptophan metabolites, chromoazepinone A, B and C, produced by a blocked mutant of Chromobacterium violaceum, the biosynthetic implications and the biological activity of chromoazepinone A and B.

Novel tryptophan metabolites, chromoazepinone A, B and C, produced by a blocked mutant of Chromobacterium violaceum, the biosynthetic implications and the biological activity of chromoazepinone A and B.

Lycogala epidendrum

5 references

New Bisindole Alkaloids Isolated from Myxomycetes Arcyria cinerea and Lycogala epidendrum.

Isolation and synthesis of 3,4-bis(indol-3-yl)pyrrole-2,5-dicarboxylic acid derivatives from the slime mould Lycogala epidendrum

Isolation and synthesis of 3,4-bis(indol-3-yl)pyrrole-2,5-dicarboxylic acid derivatives from the slime mould Lycogala epidendrum

New cytotoxic bisindole alkaloids with protein tyrosine kinase inhibitory activity from a myxomycete Lycogala epidendrum

New bisindole alkaloids isolated from Myxomycetes Arcyria cinerea and Lycogala epidendrum

Streptomyces albus

1 reference

Production of chromopyrrolic acid by coexpression of inkOD in a heterologous host Streptomyces albus

Identifiers

InChI

InChI=1S/C22H15N3O4/c26-21(27)19-17(13-9-23-15-7-3-1-5-11(13)15)18(20(25-19)22(28)29)14-10-24-16-8-4-2-6-12(14)16/h1-10,23-25H,(H,26,27)(H,28,29)

1 reference

lycogalic acid A (English)

19 October 2016

2 references

lycogalic acid A (English)

19 October 2016

ChEBI release 2020-09-01

0 references

1 reference

3,4-Di(1H-indol-3-yl)-1H-pyrrole-2,5-dicarboxylic acid (English)

19 October 2016

2 references

lycogalic acid A (English)

19 October 2016

ChEBI ID

41625

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C22H15N3O4/c26-21(27)19-17(13-9-23-15-7-3-1-5-11(13)15)18(20(25-19)22(28)29)14-10-24-16-8-4-2-6-12(14)16/h1-10,23-25H,(H,26,27)(H,28,29)

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

LYCOGALIC ACID A (English)

19 October 2016

1 reference

2 references

DSSTOX compound identifier

DTXCID20413315

0 references

DrugBank ID

DB07588

1 reference

KNApSAcK ID

C00028500

2 references

based on heuristic

inferred from InChIKey

Natural Product Atlas ID

NPA005234

2 references

based on heuristic

inferred from InChIKey

0 references

0 references

1 reference

2Z3U (English)