(Q27103090)

Indole-3-carboxylic acid (English)

19 October 2016

chemical formula

C₉H₇NO₂

1 reference

Indole-3-carboxylic acid (English)

19 October 2016

canonical SMILES

C1=CC=C2C(=C1)C(=CN2)C(=O)O

1 reference

Acid constituents from Isatis tinctoria

Indole-3-carboxylic acid (English)

19 October 2016

2 references

Novel indole C-glycosides from Isatis indigotica and their potential cytotoxic activity

Begonia nantoensis

4 references

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis

Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.

Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis

Cucumis sativus

2 references

Two new megastigmanes from the leaves of Cucumis sativus

Two new megastigmanes from the leaves of Cucumis sativus

Haliclona oculata

2 references

Oculatol, oculatolide, and A-nor sterols from the sponge Haliclona oculata

Oculatol, oculatolide, and A-nor sterols from the sponge Haliclona oculata

Pinus sylvestris

2 references

Analysis of 3-indole carboxylic acid in Pinus sylvestris needles

Analysis of 3-indole carboxylic acid in Pinus sylvestris needles

Taraxacum formosanum

3 references

Chemical constituents of Taraxacum formosanum

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Diplodia quercivora

1 reference

Botryorhodines A-D, antifungal and cytotoxic depsidones from Botryosphaeria rhodina, an endophyte of the medicinal plant Bidens pilosa

Aristolochia heterophylla

1 reference

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

Jeotgalibacillus marinus

1 reference

Chemical constituents of halophilic facultatively anaerobic bacteria, 1.

Beta vulgaris

1 reference

5,2′-dihydroxy-6,7-methylenedioxyisoflavone from seed balls of sugar beet

Botryocladia leptopoda

1 reference

Marine Natural Products; II. Chemical Constituents of Red Alga Botryocladia leptopoda

Brassica oleracea

2 references

Indoles in Edible Members of the Cruciferae

Some Indole Constituents of Cabbage

Paraphaeosphaeria minitans

2 references

3(2H)-Benzofuranones and chromanes from liquid cultures of the mycoparasitic fungus Coniothyrium minitans

3(2H)-Benzofuranones and chromanes from liquid cultures of the mycoparasitic fungus Coniothyrium minitans

Dalbergia

1 reference

Detection of abscisic acid, indole-3-acetic acid and indole-3-ethanol in seeds of Dalbergia dolichopetala

Hebeloma hiemale

1 reference

IAA biosynthesis by the ectomycorrhizal fungus Hebeloma hiemale as affected by different precursors

Houttuynia cordata

2 references

The constituents and their bioactivities of Houttuynia cordata

The constituents and their bioactivities of Houttuynia cordata

Penicillium herquei

2 references

Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4.

Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4.

Phyllanthus virgatus

2 references

A New Lignan fromPhyllanthus virgatus

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Prionitis lanceolata

2 references

3-(Hydroxyacetyl)indole, a plant growth regulator from the oregon red alga Prionitis lanceolata

3-(Hydroxyacetyl)indole, a plant growth regulator from the oregon red alga Prionitis lanceolata

Streptomyces abikoensis

1 reference

Elucidation of the structure of olivoretin A and D (teleocidin B).

Bauhinia tarapotensis

2 references

Antioxidant principles from Bauhinia tarapotensis.

Antioxidant principles from Bauhinia tarapotensis.

Streptomyces mutabilis

3 references

Purification and biological evaluation of the metabolites produced by Streptomyces sp. TK-VL_333.

Antimicrobial metabolites from a marine-derived Actinomycete Streptomyces sp. G278.

N-Acetylborrelidin B: a new bioactive metabolite from Streptomyces mutabilis sp. MII.

Streptomyces tendae

2 references

Purification and biological evaluation of the metabolites produced by Streptomyces sp. TK-VL_333.

Antimicrobial metabolites from a marine-derived Actinomycete Streptomyces sp. G278.

Albizia julibrissin

2 references

Flavonol acylglycosides from flower of Albizia julibrissin and their inhibitory effects on lipid accumulation in 3T3-L1 cells

Flavonol acylglycosides from flower of Albizia julibrissin and their inhibitory effects on lipid accumulation in 3T3-L1 cells

Aster indicus

1 reference

Phenolic derivatives from Aster indicus

Paenibacillus polymyxa

1 reference

Production of auxin and other indolic and phenolic compounds by Paenibacillus polymyxa strains isolated from different proximity to plant roots

Vibrio parahaemolyticus

1 reference

New indole alkaloids from the North Sea bacterium Vibrio parahaemolyticus Bio249.

Wallemia sebi

1 reference

Aromatic compounds from the halotolerant fungal strain of Wallemia sebi PXP-89 in a hypersaline medium

Xanthium strumarium

1 reference

(-)-Xanthienopyran, a new inhibitor of superoxide anion generation by activated neutrophils, and further constituents of the seeds of Xanthium strumarium.

Lipschitziella deltoidea

1 reference

Chemical constituents from Saussurea deltoidea

Tarenna attenuata

1 reference

Tarennane and tarennone, two novel chalcone constituents from Tarenna attenuata

Trewia nudiflora

1 reference

New cardenolides from the stem bark of Trewia nudiflora

Perilla frutescens

1 reference

Anti-inflammatory constituents from Perilla frutescens on lipopolysaccharide-stimulated RAW264.7 cells

tomato

2 references

Ultra-high performance liquid chromatography coupled to high resolution Orbitrap mass spectrometry for metabolomic profiling of the endogenous phytohormonal status of the tomato plant.

Metabolism of Some Indole Auxins in Excised Tomato Roots

Aristolochia kaempferi

1 reference

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

Taraxacum mongolicum

2 references

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Brassica rapa

1 reference

Indoles in Edible Members of the Cruciferae

Lasiodiplodia theobromae

1 reference

Botryorhodines A-D, antifungal and cytotoxic depsidones from Botryosphaeria rhodina, an endophyte of the medicinal plant Bidens pilosa

Arabidopsis thaliana

2 references

Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves.

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana

Portulaca oleracea

1 reference

Homoisoflavonoids from the medicinal plant Portulaca oleracea

Commons category

Indole-3-carboxylic acid

0 references

Identifiers

InChI

InChI=1S/C9H7NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-5,10H,(H,11,12)

1 reference

Indole-3-carboxylic acid (English)

KMAKOBLIOCQGJP-UHFFFAOYSA-N

19 October 2016

InChIKey

2 references

Indole-3-carboxylic acid (English)

19 October 2016

ChEBI release 2020-09-01

2 references

indole-3-carboxylic acid (English)

KMAKOBLIOCQGJP-UHFFFAOYSA-N

19 October 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=771-50-6

1 reference

3-Indolecarboxylic acid (English)

19 October 2016

1 reference

Indole-3-carboxylic acid (English)

19 October 2016

Reaxys registry number

129435

1 reference

indole-3-carboxylic acid (English)

19 October 2016

Gmelin number

1875411

0 references

ChEBI ID

24809

mapping relation type

1 reference

indole-3-carboxylic acid (English)

19 October 2016

1 reference

MSBNK-MPI_for_Chemical_Ecology-CE000128

CHEMBL387527 (English)

19 October 2016

1 reference

MassBank accession ID

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000129

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000130

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000131

0 references

MSBNK-MPI_for_Chemical_Ecology-CE000132

0 references

MSBNK-RIKEN-PR100988

0 references

MSBNK-RIKEN-PR101045

0 references

MSBNK-IPB_Halle-PB000615

0 references

MSBNK-IPB_Halle-PB000616

0 references

MSBNK-IPB_Halle-PB000617

0 references

MSBNK-IPB_Halle-PB000618

0 references

MSBNK-IPB_Halle-PB005785

0 references

MSBNK-IPB_Halle-PB005786

0 references

MSBNK-IPB_Halle-PB005787

0 references

SPLASH

splash10-014l-1900000000-1995f9dbe32f987d490a

0 references

splash10-014l-9800000000-670cc23cba665a2c274c

0 references

splash10-00ko-9100000000-933c5733f214b898f898

0 references

splash10-03xu-0900000000-3f9d7c7294f2ea5a6c2c

0 references

splash10-014l-0900000000-a2251627ca78c6acb131

0 references

splash10-014l-0900000000-391c26d59d3501f7004c

0 references

splash10-014i-0900000000-9af372afcef18a3b9f32

0 references

splash10-014i-0900000000-265f90afc22f3879b03e

0 references

splash10-014i-0900000000-3e251a670db5df960fd6

0 references

splash10-014i-0900000000-ff43090393a4f119b73a

0 references

splash10-03di-0900000000-dbf68b6f2a3fd472b3c0

0 references

splash10-014i-0900000000-8c45f845ef01c19b445c

0 references

splash10-014l-1900000000-1c77378b797771275320

0 references

splash10-014l-0900000000-dc9dc68de9496d714346

0 references

splash10-03di-0900000000-13ea7a3c18ebe474dcb1

0 references

splash10-02tc-0900000000-e93fcbd2ca4596b2cafb

0 references

splash10-03di-0900000000-fd710815ad116ba32e46

0 references

splash10-014i-0900000000-d23449ec70813566f98b

0 references

splash10-014i-0900000000-910ac7294776b7eb7ef4

0 references

splash10-014u-9300000000-0af5d90221e77a572181

0 references

splash10-03di-0900000000-104208fcdd8732ebadf0

0 references

splash10-014l-4900000000-6b0c749e944b64d5385c

0 references

RTECS number

NK7882892

0 references

DSSTox substance ID

DTXSID50227886

1 reference

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

DSSTOX compound identifier

DTXCID00150377

0 references

EC number

212-231-6

1 reference

Global Substance Registration System

UNII

59711R38B0

indole-3-carboxylic acid (English)

ECHA Substance Infocard ID

19 October 2016

100.011.119

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.011.119

27 December 2018

Human Metabolome Database ID

Indole-3-carboxylic acid (English)

quotation

CAS no.: 771-50-6 (English)

HMDB0003320

1 reference

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00000113

1 reference

based on heuristic

inferred from InChIKey

UNII

59711R38B0

1 reference

Global Substance Registration System

UNII

59711R38B0

Google Knowledge Graph ID

indole-3-carboxylic acid (English)

19 October 2016

0 references

0 references

0 references

1 reference

4AHU (English)

19 October 2016

1 reference

5CC5 (English)

19 October 2016

1 reference

2PIP (English)