164659-62-5 Usage
Structure
Contains an indole ring and a butyric acid chain
Unique properties
Indole ring contributes to unique properties and biological activity
Therapeutic applications
Potential use in activating the aryl hydrocarbon receptor (AhR) and regulating gene expression
Anti-inflammatory properties
Has been studied for its ability to reduce inflammation
Anti-cancer properties
Has been studied for its ability to inhibit cancer cell growth
Immune system modulation
Has the ability to modulate the immune system
Potential use in treatment
May be used in the treatment of various diseases and conditions
Subject of interest
Is a subject of interest for further research and development
Check Digit Verification of cas no
The CAS Registry Mumber 164659-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,6,5 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 164659-62:
(8*1)+(7*6)+(6*4)+(5*6)+(4*5)+(3*9)+(2*6)+(1*2)=165
165 % 10 = 5
So 164659-62-5 is a valid CAS Registry Number.
164659-62-5Relevant academic research and scientific papers
Levkovskaya,Rudyakova,Mirskova
, p. 1641 - 1646 (2002)
A method was developed for preparation of (3-indolylsulfanyl)alkanecarboxylic acids from 1H-, 1-methyl(benzyl)-, 2-methylindoles, thiourea, iodine, and halocarboxylic acids.
Synthesis of heterylthioalkanoic acids and their use for concentration of tungsten-containing ores
Levkovskaya,Mirskova,Bel'kova
, p. 1849 - 1852 (2007/10/03)
Methods for preparing a series of heterylthioalkanoic acids inclulding α-(indol-3-ylthio)propionic, α-(indol-3-ylthio)butyric, and pur-6-ylthioacetic acids were developed, and flotation properties of these compounds in concentration of tungsten-containing ores are studied.
