chorismic acid (Q423531)

inferred from InChIKey

chemical structure

Chorisminsäure.svg
329 × 272; 7 KB

1 reference

German Wikipedia

Chorismic acid.svg
512 × 418; 19 KB

0 references

chemical formula

C₁₀H₁₀O₆

1 reference

German Wikipedia

canonical SMILES

C=C(C(=O)O)OC1C=C(C=CC1O)C(=O)O

1 reference

Chorismic acid (English)

26 July 2018

C=C(C(=O)O)O[C@@H]1C=C(C=C[C@H]1O)C(=O)O

1 reference

Elicitor-mediated induction of isochorismate synthase and accumulation of 2,3-dihydroxy benzoic acid in Catharanthus roseus cell suspension and shoot cultures

Chorismic acid (English)

26 July 2018

1 reference

Galium mollugo

1 reference

Isochorismate hydroxymutase from a cell-suspension culture of Galium mollugo L.

Phycomyces blakesleeanus

1 reference

Acidic metabolites from Phycomyces blakesleeanus

Streptomyces griseus

2 references

Characterization and regulation of p-aminobenzoic acid synthase from Streptomyces griseus

Biosynthesis of chloramphenicol in Streptomyces species 3022a: the nature of the arylamine synthetase system

Phaseolus vulgaris

1 reference

Metabolomics and Transcriptomics Identify Multiple Downstream Targets of Paraburkholderia phymatum σ54 During Symbiosis with Phaseolus vulgaris

Escherichia coli

3 references

Binding of p-nitrophenyl alpha-D-galactopyranoside to lac permease of Escherichia coli

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Microbial synthesis of p‐hydroxybenzoic acid from glucose

Saccharomyces cerevisiae

1 reference

Saccharomyces cerevisiae chorismate synthase has a flavin reductase activity.

mass

226.04773804 dalton

1 reference

inferred from isomeric SMILES

1 reference

https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT

0 references

0 references

Chorismic acid

0 references

Identifiers

InChI

InChI=1S/C10H10O6/c1-5(9(12)13)16-8-4-6(10(14)15)2-3-7(8)11/h2-4,7-8,11H,1H2,(H,12,13)(H,14,15)/t7-,8-/m1/s1

1 reference

Chorismic acid (English)

26 July 2018

2 references

Chorismic acid (English)

26 July 2018

ChEBI release 2020-09-01

CAS Registry Number

617-12-9

1 reference

https://commonchemistry.cas.org/detail?cas_rn=617-12-9

9 April 2021

ChemSpider ID

11542

1 reference

2 references

Chorismic acid (English)

26 July 2018

PubChem CID

12039

Reaxys registry number

2217365

0 references

ChEBI ID

17333

mapping relation type

exact match

2 references

English Wikipedia

International Chemical Identifier

InChI

InChI=1S/C10H10O6/c1-5(9(12)13)16-8-4-6(10(14)15)2-3-7(8)11/h2-4,7-8,11H,1H2,(H,12,13)(H,14,15)/t7-,8-/m1/s1

SureChEMBL ID

812019

2 references

inferred from InChIKey

MSBNK-BGC_Munich-RP011401

1 reference

MassBank accession ID

0 references

MSBNK-BGC_Munich-RP011402

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MSBNK-BGC_Munich-RP011403

0 references

DSSTox substance ID

DTXSID50210697

2 references

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

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.204

27 December 2018

ECHA Substance Infocard ID

Chorismic acid free acid fromenterobacter aerogen (English)

quotation

CAS no.: 617-12-9 (English)

100.164.204

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.164.204

27 December 2018

cyclohexanecarboxylic acids

Chorismic acid free acid fromenterobacter aerogen (English)

quotation

CAS no.: 617-12-9 (English)

1 reference

Chorismic Acid

0 references

MeSH tree code

D02.241.223.268.250

broader concept

0 references

D02.455.426.392.368.367.379.374

broader concept

cyclohexenes

0 references

Human Metabolome Database ID

HMDB0012199

2 references

inferred from InChIKey

0 references

1 reference

Great Russian Encyclopedia portal ID

0 references

0 references

1 reference

28 October 2013

khorizmovaia-kislota-559d39

0 references

Microsoft Academic ID (discontinued)

0 references

1 reference

inferred by common MeSH mappings on source and on Wikidata

UMLS 2023