(Q27103575)

INDOLE-3-CARBOXALDEHYDE (English)

19 October 2016

chemical formula

C₉H₇NO

1 reference

INDOLE-3-CARBOXALDEHYDE (English)

20 November 2016

canonical SMILES

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

1 reference

INDOLE-3-CARBOXALDEHYDE (English)

20 November 2016

melting point

197.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Pinus sylvestris

1 reference

Identification of 4-chloroindole-3-acetic acid and indole-3-aldehyde in seeds of Pinus sylvestris

Cucumis sativus

3 references

Two new megastigmanes from the leaves of Cucumis sativus

Inhibitory effect of Cucumis sativus on melanin production in melanoma B16 cells by downregulation of tyrosinase expression

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

Phalaris aquatica

1 reference

Separation of tryptophan derivatives inPhalaris aquatica by thin-layer chromatography

Taraxacum formosanum

4 references

Chemical constituents from roots of Taraxacum formosanum

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Chemical constituents from roots of Taraxacum formosanum

Penicillium vinaceum

1 reference

Penicillivinacine, antimigratory diketopiperazine alkaloid from the marine-derived fungus Penicillium vinaceum

Acinetobacter

1 reference

6-Bromoindole-3-Carbaldehyde, from an Acinetobacter Sp. Bacterium Associated with the Ascidian Stomozoa murrayi

Arthrographis

1 reference

Taxonomy and chemistry of a new fungus from bark beetle infested Pinus contorta var. latifolia. Part 2. Arthrographol, the metabolite inhibitory to Ophiostoma clavigerum

Jeotgalibacillus marinus

1 reference

Chemical constituents of halophilic facultatively anaerobic bacteria, 1.

Begonia nantoensis

2 references

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

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

Boltonia asteroides

1 reference

Acetylenic and terpenoid constituents of Boltonia asteroides

Botryocladia leptopoda

1 reference

Marine Natural Products: 3-Formylindole from the Red Algae Botryocladia leptopoda

Brassica oleracea

3 references

Indoles in Edible Members of the Cruciferae

Indole-3-carboxaldehyde in the cabbage Brassica oleracea: A systematic determination

High-performance liquid chromatographic analysis of anticarcinogenic indoles in Brassica oleracea

Chondria

1 reference

Chondriamides A and B, new indolic metabolites from the red alga Chondria sp.

Dendrophyllia

1 reference

Aplysinopsin-type alkaloids fromDendrophyllia sp., a scleractinian coral of the family dendrophylliidae of the philippines, facile photochemical (Z/E) photoisomerization and thermal reversal

Dysidea etheria

1 reference

Plant Growth Regulatory Indoles from the Sponges Dysidea etheria and Ulosa ruetzleri

Euphorbia hirsuta

1 reference

Three new jatrophane-type diterpenes from Euphorbia pubescens.

Gossypium hirsutum

2 references

Isolation of Indole-3 Carboxaldehyde from Cotton Plant Parts

Quantitative Determination of Indole-3 Carboxyaldehyde in Aqueous Extracts of Cotton Bracts by HPLC

Haraldiophyllum

1 reference

Almazole C, a New Indole Alkaloid Bearing an Unusually 2,5-Disubstituted Oxazole Moiety, and its putative biogenetic peptidic precursors, from a senegalese delesseriacean seaweed

Hebeloma hiemale

1 reference

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

Lactarius deliciosus

1 reference

Aromatic Compounds from Liquid Cultures of Lactarius deliciosus

Lactarius subplinthogalus

1 reference

Alkaloids from the fungus Lactarius subplinthogalus

Monodora brevipes

2 references

Terpenoid and alkaloid compounds from the seeds of Monodora brevipes

Terpenoid and alkaloid compounds from the seeds of Monodora brevipes

Monodora undulata

2 references

Terpenoid and alkaloid compounds from the seeds of Monodora brevipes

Terpenoid and alkaloid compounds from the seeds of Monodora brevipes

Mycale tenuispiculata

2 references

New 5-alkylpyrrole-2-carboxaldehyde derivatives from the sponge Mycale tenuispiculata

New 5-alkylpyrrole-2-carboxaldehyde derivatives from the sponge Mycale tenuispiculata

Ophryosporus lorentzii

2 references

Chromanones, benzofurans and other constituents from Ophryosporus lorentzii

Chromanones, benzofurans and other constituents from Ophryosporus lorentzii

Phyllanthus virgatus

2 references

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Piptostigma fugax

2 references

Aporphinoid alkaloids and terpenoids from Piptostigma fugax

Aporphinoid alkaloids and terpenoids from Piptostigma fugax

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

Pseudomonas syringae

1 reference

Isolation of Indole-3-Aldehyde from Psuedomonas syringae pv. savastanoi

radish

1 reference

Three sulphur-containing stress metabolites from Japanese radish

Stenochlaena palustris

2 references

Glycosides from Stenochlaena palustris

Glycosides from Stenochlaena palustris

Streptomyces abikoensis

1 reference

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

Aquilaria sinensis

1 reference

Five 2-(2-Phenylethyl)chromones from Sodium Chloride-Elicited Aquilaria sinensis Cell Suspension Cultures.

Capparis spinosa

1 reference

Nematicidal activity of 2-thiophenecarboxaldehyde and methylisothiocyanate from caper (Capparis spinosa) against Meloidogyne incognita

Enterobacter cloacae

1 reference

A new oxathiolane from Enterobacter cloacae

sweet potato

1 reference

Antioxidants and α-glucosidase inhibitors from Ipomoea batatas leaves identified by bioassay-guided approach and structure-activity relationships.

Isatis tinctoria

4 references

Alkaloids from the root of Isatis indigotica

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts

Indole alkaloids from the roots of Isatis ingigotica and their antiherpes simplex virus type 2 (HSV-2) activity in vitro

A new ceramide from the root of Isatis Indigotica and its cytotoxic activity

Marinomonas

1 reference

An in silico, in vitro and in vivo investigation of indole-3-carboxaldehyde identified from the seawater bacterium Marinomonas sp. as an anti-biofilm agent against Vibrio cholerae O1.

Patrinia villosa

1 reference

A New Biphenyl Neolignan from Leaves of Patrinia villosa (Thunb.) Juss

Streptomyces antibioticus

3 references

A new secondary metabolite from the fermented mycelia of Streptomyces antibiotic H41-55.

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

Chemical constituents of Streptomyces sp. strain Al-Dhabi-97 isolated from the marine region of Saudi Arabia with antibacterial and anticancer properties

Amorphophallus konjac

1 reference

Peroxynitrite scavenging activities of aromatic compounds isolated from Konnyaku, Amorphophallus konjac K.Koch

Aster indicus

1 reference

Phenolic derivatives from Aster indicus

Commelina communis

1 reference

A new C-glucoside from Commelina communis

Derris ovalifolia

1 reference

A chromanone alkaloid from Derris ovalifolia stem

Equisetum telmateia

1 reference

The isolation of indole-3-carboxaldehyde from Equisetum telmateia

Escherichia coli

1 reference

A novel indole alkaloid from deep-sea sediment metagenomic clone-derived Escherichia coli fermentation broth.

Euphorbia lagascae

1 reference

Lagaspholones A and B: two new jatropholane-type diterpenes from Euphorbia lagascae

Meehania urticifolia

1 reference

New phenolic compounds from Meehania urticifolia

Murraya exotica

1 reference

3-formylindole from Murraya exotica

Murraya paniculata

1 reference

3-formylindole from Murraya exotica

Mycale tenuis

1 reference

New 5-alkylpyrrole-2-carboxaldehyde derivatives from the sponge Mycale tenuispiculata

Paenibacillus polymyxa

1 reference

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

Pseudomonas cichorii

1 reference

Antifungal compounds from Dioscorea batatas inoculated with Pseudomonas cichorii

Vibrio parahaemolyticus

1 reference

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

Xanthium strumarium

1 reference

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

Zanthoxylum nitidum

1 reference

New benzenoids and anti-inflammatory constituents from Zanthoxylum nitidum

Stomozoa roseola

1 reference

6-Bromoindole-3-Carbaldehyde, from an Acinetobacter Sp. Bacterium Associated with the Ascidian Stomozoa murrayi

pea

1 reference

Isolation of a plant growth inhibitory substance from garden peas (Pisum sativum L.) and its identification with (+)-abscisin-II

Stomozoa murrayi

1 reference

6-Bromoindole-3-Carbaldehyde, from an Acinetobacter Sp. Bacterium Associated with the Ascidian Stomozoa murrayi

Streptomyces

3 references

Amorphane sesquiterpenes from a marine Streptomyces sp.

Amorphane Sesquiterpenes from a Marine Streptomyces sp.1

Metabolism studies of indole derivatives using a staurosporine producer, Streptomyces staurosporeus

Brassica rapa

2 references

Indoles in Edible Members of the Cruciferae

Brassicanals A and B, Novel Sulfur-Containing Phytoalexins from the Chinese CabbageBrassica campestrisL. ssp.pekinensis

Perilla frutescens

1 reference

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

Caenorhabditis elegans

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

tomato

1 reference

Biosynthesis and Metabolism of Indol-3yl-acetic Acid

Taraxacum mongolicum

3 references

Chemical constituents from roots of Taraxacum formosanum

Chemical Constituents of Taraxacum formosanum.

Chemical constituents of Taraxacum formosanum

Arabidopsis thaliana

1 reference

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

Phellodendron chinense var. glabriusculum

3 references

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Constituents of leaves of Phellodendron japonicum MAXIM. and their antioxidant activity

Phellodendron amurense var. wilsonii

3 references

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity

Constituents of leaves of Phellodendron japonicum MAXIM. and their antioxidant activity

Commons category

Indole-3-carbaldehyde

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Identifiers

InChI

InChI=1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H

1 reference

INDOLE-3-CARBOXALDEHYDE (English)

OLNJUISKUQQNIM-UHFFFAOYSA-N

20 November 2016

InChIKey

2 references

INDOLE-3-CARBOXALDEHYDE (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

487-89-8

2 references

Global Substance Registration System

indole-3-carboxaldehyde (English)

OLNJUISKUQQNIM-UHFFFAOYSA-N

20 November 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=487-89-8

1 reference

3-Formylindole (English)

20 November 2016

1 reference

INDOLE-3-CARBOXALDEHYDE (English)

20 November 2016

Reaxys registry number

114117

1 reference

indole-3-carbaldehyde (English)

19 October 2016

ChEBI ID

28238

mapping relation type

1 reference

indole-3-carbaldehyde (English)

19 October 2016

1 reference

MSBNK-Fac_Eng_Univ_Tokyo-JP000428

3-FORMYLINDOLE (English)

20 November 2016

1 reference

MassBank accession ID

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MSBNK-Fac_Eng_Univ_Tokyo-JP002872

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MSBNK-Fac_Eng_Univ_Tokyo-JP010547

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MSBNK-IPB_Halle-PB000506

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MSBNK-IPB_Halle-PB000507

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MSBNK-IPB_Halle-PB000508

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MSBNK-IPB_Halle-PB000509

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MSBNK-Fac_Eng_Univ_Tokyo-JP008303

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MSBNK-Kazusa-KZ000216

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MSBNK-Kazusa-KZ000217

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SPLASH

splash10-0007-2900000000-90cfb2317bcbb908e2e8

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splash10-0007-2900000000-c43b940db5ef735c79d6

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splash10-00kb-0900000000-597c804d77e9a7930c9e

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splash10-014i-2900000000-878ab4a0cfc6d8f0e9d0

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splash10-00kf-9400000000-74dbc81ab5e686655977

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splash10-00kf-9100000000-22b52274e9bec85c9488

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splash10-00kk-2950000000-8901bc9a710fac996fbc

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splash10-00kb-2960000000-0b154d6ce8924292e9ed

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splash10-00di-9430000000-252f37d7921252e01ac0

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splash10-00di-9430000000-868873ec5dc494bef752

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splash10-014i-3900000000-b8cbcf3139ea5a313666

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splash10-0006-0900000000-39d11dbd7bebe565fa94

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splash10-014l-0900000000-c9a64e9031a8d467a02b

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splash10-0006-0900000000-b7ccb1c640ee7aaf06b4

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splash10-014l-0900000000-d434c2e937c83d1ffd7c

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splash10-014i-2900000000-94ec8ba0db56440ffc3f

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splash10-0002-0900000000-e92b5164439869cd1624

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splash10-014i-0900000000-b36198290d6046d6c51e

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splash10-014l-5900000000-464872f8d6794f010301

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splash10-0006-9400000000-82e9b3517f83d75f9cc2

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splash10-0006-9200000000-b6707237a4a55ce1d4d1

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splash10-0002-0900000000-955d0907f52618b8a316

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splash10-014j-0900000000-5f046d55bd55e3afdbeb

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splash10-014l-5900000000-65ad84959224b888a37c

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splash10-0006-9400000000-a444a09a239215390fdd

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splash10-0006-9200000000-9c22387ac3b43f107c88

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splash10-014i-1900000000-d6d5e0fb4f754504b9a8

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splash10-0007-2900000000-fcb37c6394c016a4e2d0

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DSSTox substance ID

DTXSID5060069

1 reference

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

DSSTOX compound identifier

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207-665-8

1 reference

Global Substance Registration System

indole-3-carboxaldehyde (English)

ECHA Substance Infocard ID

20 November 2016

100.006.969

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.969

27 December 2018

Human Metabolome Database ID

Indole-3-carbaldehyde (English)

quotation

CAS no.: 487-89-8 (English)

1 reference

HMDB0029737

1 reference

based on heuristic

inferred from InChIKey

2 references

indole-3-carbaldehyde (English)

19 October 2016

based on heuristic

inferred from InChIKey

1 reference

Global Substance Registration System

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

indole-3-carboxaldehyde (English)

20 November 2016

0 references

1 reference

PDB ligand ID

I3A

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Google Knowledge Graph ID

/g/11f2m04x5s

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/g/12vzprdgk

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Microsoft Academic ID

0 references

1 reference

3BWL (English)

19 October 2016

1 reference

5A4U (English)

19 October 2016

1 reference

3NVZ (English)

19 October 2016

1 reference

2OU3 (English)