86427-43-2 Usage
Chemical Family
Thiazolidin-4-one
Core Structure
Thiazolidine derivative with a thiazolidin-4-one core
Side Chains
Indole and methoxyphenyl side chains
Pharmaceutical Applications
Potential anti-cancer and anti-inflammatory properties
Biological Interactions
May interact with enzymes and receptors
Lead Compound Potential
May be a useful lead compound for the development of new drugs
Further Research Needed
To fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 86427-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,2 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86427-43:
(7*8)+(6*6)+(5*4)+(4*2)+(3*7)+(2*4)+(1*3)=152
152 % 10 = 2
So 86427-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H18N2O2S/c1-23-14-8-6-13(7-9-14)11-21-18(22)12-24-19(21)16-10-20-17-5-3-2-4-15(16)17/h2-10,19-20H,11-12H2,1H3
86427-43-2Relevant academic research and scientific papers
Substituted Azitidinonylindoles and Thiazolidinonylindoles as Antiparkinsonian Agents
Kumar, P.,Nath, C.,Bhargava, K.P.,Shanker, K.
, p. 1128 - 1129 (2007/10/02)
3-(1-Arylalkyl-3-chloro-2-oxo-4azetidinyl)indoles (IIa-h) and 3-(3-arylalkyl-4-oxo-2-thiazolinyl)indoles (IIi-n) have been synthesized by the cyclocondensation of 3-(N-arylalkyliminomethyl)indoles (Ia-h) with chloroacetyl and thioglycolic acid respectivel
