(Q5479351)

Gene Ontology release 2020-05-02

Rhea release 113

indole-3-acetaldehyde reductase (NADPH) activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Tryptophol.svg
512 × 509; 9 KB

0 references

mass

161.084064 dalton

1 reference

Tryptophol (English)

5 October 2016

C₁₀H₁₁NO

1 reference

Tryptophol (English)

5 October 2016

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

1 reference

Tryptophol (English)

5 October 2016

58.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Curvularia nodulosa

1 reference

Tryptophola phytotoxin produced by Drechslera nodulosum

Pichia membranaefaciens

1 reference

Indole derivatives from a marine sponge-derived yeast as DPPH radical scavengers

Paraphaeosphaeria minitans

1 reference

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

Balansia epichloe

1 reference

In vitro auxin production by Balansia epichloë

Mucor moelleri

1 reference

Indole-3-ethanol produced by Zygorrhynchus moelleri, an indole-3-acetic acid analogue with antifungal activity

Streptomyces mutabilis

3 references

Bioactive secondary metabolites from a new terrestrial Streptomyces sp. TN262

Chromophenazines from the Terrestrial Streptomyces sp. Ank 315

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

Pinus sylvestris

3 references

Biosynthesis and metabolism of indole-3-ethanol and indole-3-acetic acid by Pinus sylvestris L. needles

Dynamics of indole-3-acetic acid and indole-3-ethanol during development and germination of Pinus sylvestris seeds

Identification of oxindole-3-acetic acid, and metabolic conversion of indole-3-acetic acid to oxindole-3-acetic acid in Pinus sylvestris seeds

Streptomyces atroolivaceus

3 references

Bioactive secondary metabolites from a new terrestrial Streptomyces sp. TN262

Chromophenazines from the Terrestrial Streptomyces sp. Ank 315

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

Dalbergia

1 reference

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

Candida albicans

1 reference

Phenethyl Alcohol and Tryptophol: Autoantibiotics Produced by the Fungus Candida albicans

Desmanthus illinoensis

1 reference

Indolealkylamines of Desmanthus illinoensis and their growth inhibition activity

common sunflower

1 reference

Occurrence of Indoleacetaldehyde and Tryptophol in the Extracts of Etiolated Shoots of Pisum and Helianthus Seedlings

Luffariella geometrica

1 reference

A new cytotoxic calyculinamide derivative, geometricin A, from the Australian sponge Luffariella geometrica

Picea abies

1 reference

Dynamics of indole-3-acetic acid during germination of Picea abies seeds

Grosmannia crassivaginata

1 reference

Phenolic and polyketide metabolites of the aspen blue stain fungus Ophiostoma crassivaginata

Grosmannia clavigera

1 reference

The chemistry of the blue stain fungi. Part 1. Some metabolites of Ceratocystis species associated with mountain pine beetle infected lodgepole pine

Paenibacillus polymyxa

1 reference

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

Phycomyces blakesleeanus

1 reference

Indole-3-ethanol oxidase in Phycomyces blakesleeanus. Is indole-3-ethanol a "storage pool" for IAA?

Pisum sativum

3 references

Occurrence of Indoleacetaldehyde and Tryptophol in the Extracts of Etiolated Shoots of Pisum and Helianthus Seedlings

Indole-3-acetic acid and indole-3-ethanol in light-grown Pisum sativum seedlings and their localization in chloroplast fractions

Auxin biosynthesis in pea: characterization of the tryptamine pathway.

potato

1 reference

l-Tryptophan metabolism in wound-activated and Agrobacterium tumefaciens-transformed potato tuber 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

Biosynthesis and Metabolism of Indol-3yl-acetic Acid

Saccharomyces cerevisiae

1 reference

The catabolism of amino acids to long chain and complex alcohols in Saccharomyces cerevisiae

1 reference

Tryptophol

0 references

Identifiers

InChI

InChI=1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2

1 reference

Tryptophol (English)

5 October 2016

2 references

Tryptophol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

tryptophol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=526-55-6

9 April 2021

1 reference

Tryptophol (English)

5 October 2016

2 references

Tryptophol (English)

5 October 2016

Reaxys registry number

125553

1 reference

tryptophol (English)

5 October 2016

142970

0 references

ChEBI ID

17890

mapping relation type

2 references

tryptophol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2

1 reference

TRYPTOPHOL (English)

5 October 2016

2 references

Biological Magnetic Resonance Data Bank

1 reference

1 reference

BMRB ID

bmse000473

splash10-03e9-0900000000-54f7b6548b8a00c91c3f

MassBank accession ID

MSBNK-Keio_Univ-KO001201

0 references

MSBNK-Keio_Univ-KO001202

0 references

MSBNK-Keio_Univ-KO001203

0 references

MSBNK-Keio_Univ-KO001204

0 references

MSBNK-Keio_Univ-KO001205

0 references

SPLASH

0 references

splash10-003u-0900000000-fb2793cd76eefaaf45c5

0 references

splash10-016r-0900000000-78c3b34c10c43b6a9317

0 references

splash10-014i-0900000000-d00c24bc728f46156c60

0 references

splash10-03di-0900000000-d41cd8e81a55b3e00538

0 references

splash10-0udi-0490000000-15708d306e1f75b1e76f

0 references

splash10-00kf-0900000000-44158c348db109504af4

0 references

splash10-014l-6900000000-48b709f034a27e74e73f

0 references

splash10-01ox-0900000000-5fb5f5b5efe809cbe9ad

0 references

splash10-001i-2900000000-20fec68981d54c2e7002

0 references

splash10-0udi-1591000000-5b173cc0ac0dc2b874a9

0 references

NMRShiftDB structure ID

20191947

1 reference

DSSTox substance ID

DTXSID2060173

2 references

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

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

UNII

5809LZ7G1U

TRYPTOPHOL (English)

ECHA Substance Infocard ID

5 October 2016

100.007.632

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.632

27 December 2018

Human Metabolome Database ID

β-indol-3-ylethanol (English)

quotation

CAS no.: 526-55-6 (English)

HMDB0003447

2 references

based on heuristic

3 references

tryptophol (English)

5 October 2016

UNII

5809LZ7G1U

2 references

Global Substance Registration System

UNII

5809LZ7G1U

TRYPTOPHOL (English)

5 October 2016

Natural Product Atlas ID

NPA006412

2 references

based on heuristic