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23983-07-5

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23983-07-5 Usage

Description

(2E)-2-(4-hydroxybenzylidene)[1,3]thiazolo[3,2-a]benzimidazol-3(2H)-one, also known as Thioflavin T, is a fluorescent dye that is widely used in the study of protein aggregation and amyloid fibril formation. It is particularly effective in detecting and quantifying beta-amyloid aggregates, which are linked to Alzheimer's disease. Thioflavin T can bind to the cross-beta sheet structure of amyloid fibrils, leading to a significant increase in its fluorescence intensity. This characteristic makes it a valuable tool for visualizing and measuring amyloid formation both in vitro and in vivo. Additionally, Thioflavin T has been employed in various biomedical and biochemical applications, such as the study of prion diseases and other protein misfolding pathologies.

Uses

Used in Alzheimer's Disease Research:
Thioflavin T is used as a diagnostic tool for Alzheimer's disease, specifically for the detection and quantification of beta-amyloid aggregates. Its ability to bind to the cross-beta sheet structure of amyloid fibrils and increase in fluorescence intensity allows for the visualization and measurement of amyloid formation, which is crucial for understanding the progression of the disease and evaluating potential treatments.
Used in Protein Misfolding Pathology Studies:
Thioflavin T is employed as a research tool in the study of prion diseases and other protein misfolding pathologies. Its fluorescence properties enable the investigation of protein aggregation and fibril formation, which are key aspects of these diseases. This helps researchers gain insights into the mechanisms underlying these conditions and develop potential therapeutic strategies.
Used in Biomedical and Biochemical Applications:
Thioflavin T is utilized in various biomedical and biochemical applications, including the study of protein-protein interactions, the development of diagnostic assays, and the investigation of the structural properties of amyloid fibrils. Its versatility as a fluorescent dye makes it a valuable asset in these fields, contributing to advancements in our understanding of protein behavior and its implications for human health.

Check Digit Verification of cas no

The CAS Registry Mumber 23983-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,8 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23983-07:
(7*2)+(6*3)+(5*9)+(4*8)+(3*3)+(2*0)+(1*7)=125
125 % 10 = 5
So 23983-07-5 is a valid CAS Registry Number.

23983-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-hydroxybenzylidene)thiazolo<3,2-a>benzimidazol-3(2H)-one

1.2 Other means of identification

Product number -
Other names 2-[1-(4-Hydroxy-phenyl)-meth-(Z)-ylidene]-benzo[4,5]imidazo[2,1-b]thiazol-3-one

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:23983-07-5 SDS

23983-07-5Downstream Products

23983-07-5Relevant articles and documents

Synthesis of New 2-Substituted Benzylidenethiazolobenzimidazol-3(2H)-ones and Their Biological Activity

Soni, Namita,Barthwal, J. P.,Gupta, T. K.,Bhalla, T. N.,Parmar, S. S.,Bhargava, K. P.

, p. 785 - 788 (2007/10/02)

2-Substituted benzylidenethiazolobenzimidazol-3(2H)-ones (I-XIV) have been synthesized and found to possess anticonvulsant activity (0-60percent).These compounds also inhibit rat brain monoamine oxidase (MAO) (33.70-98.30percent) and succinate dehydrogenase (SDH) (25.72-78.95percent) in vitro of concentrations 4E-4 M and 6E-4 M, respectively.Structure-activity relationship has been dicussed.

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