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1H-Indole-3,5,6-triol is a naturally occurring organic compound that belongs to the indole family. It is a tricyclic molecule with three hydroxyl groups attached to the indole ring structure. 1H-Indole-3,5,6-triol is known for its presence in various biological systems, including the human body, where it plays a role in the metabolism of tryptophan, an essential amino acid. 1H-Indole-3,5,6-triol has been studied for its potential antioxidant properties and its involvement in the immune response. It is also found in certain foods and has been identified as a metabolite in the gut microbiome, suggesting it may have implications for health and disease. The compound's chemical structure and biological activity make it a subject of interest in the fields of chemistry, biochemistry, and pharmacology.

3569-19-5

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3569-19-5 Usage

Derivative of

Indole (a heterocyclic aromatic organic compound)

Occurrence

Naturally occurring compound found in certain plants and fungi

Potential properties

Antioxidant, anti-inflammatory

Use in research

Precursor for the synthesis of other biologically active compounds

Potential effects

Neuroprotective, ability to inhibit certain enzymes involved in inflammatory processes

Potential use

Therapeutic agent for various health conditions

Check Digit Verification of cas no

The CAS Registry Mumber 3569-19-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3569-19:
(6*3)+(5*5)+(4*6)+(3*9)+(2*1)+(1*9)=105
105 % 10 = 5
So 3569-19-5 is a valid CAS Registry Number.

3569-19-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,3-trihydroxyindole

1.2 Other means of identification

Product number -
Other names Indol-3,5,6-triol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3569-19-5 SDS

3569-19-5Downstream Products

3569-19-5Relevant academic research and scientific papers

The participation of Singlet Oxygen in Dye-Sensitized Photooxidation Reaction of Catecholamines

Kruk, I.

, p. 607 - 613 (2007/10/02)

The photooxidation of catecholamines (adrenaline, noradrenaline and dopamine) sensitized by methylene blue (MB), rose bengal (RB) and fluoresceine (FL) proceed via aminochromes and an indolic pathway.In D2O rate constants of sensitized photooxidation are increased for about 2,7 times over rates in water. 1,3-diphenylisobenzofuran (DPBF), 1,4-diazobicyclooctane (DABCO) and azide anion were more effective inhibitors of the reaction in D2O than in H2O.Superoxide dismutase markedly decreases the rates of photooxidation in H2O and in D2O.Isotope effects and 1O2-quenchers sensitivities indicate that singlet oxygen participates on photooxidation processes of catecholamines.

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