
CAS 147366-41-4
:1-Ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]pyridinium chloride (1:1)
Description:
1-Ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]pyridinium chloride (1:1), with CAS number 147366-41-4, is a complex organic compound characterized by its unique structural features, which include a pyridinium ring and thiazolidine moieties. This substance exhibits properties typical of quaternary ammonium compounds, such as solubility in polar solvents and potential antimicrobial activity. The presence of the benzothiazole group suggests possible applications in pharmaceuticals or as a dye, given its conjugated system that may exhibit fluorescence. The compound's chloride salt form indicates it is likely to be stable and soluble in aqueous environments. Its intricate structure may also contribute to specific biological activities, making it of interest in medicinal chemistry. However, detailed studies on its toxicity, stability, and reactivity would be necessary to fully understand its potential applications and safety profile. As with many synthetic organic compounds, proper handling and storage conditions should be observed to ensure safety and integrity.
Formula:C21H22ClN3OS2
InChI:InChI=1/C21H22N3OS2.ClH/c1-4-23-13-9-8-10-15(23)14-18-24(5-2)20(25)19(27-18)21-22(3)16-11-6-7-12-17(16)26-21;/h6-14H,4-5H2,1-3H3;1H/q+1;/p-1/b21-19+;
InChI key:InChIKey=VSKYOTRJSLYFHX-UHFFFAOYSA-M
SMILES:O=C1C(SC(=CC=2[N+](CC)=CC=CC2)N1CC)=C3N(C)C=4C(S3)=CC=CC4.[Cl-]
Synonyms:- 1-Ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]pyridinium chloride (1:1)
- 1-ethyl-2-{(Z)-[(5E)-3-ethyl-5-(3-methyl-1,3-benzothiazol-2(3H)-ylidene)-4-oxo-1,3-thiazolidin-2-ylidene]methyl}pyridinium chloride
- FJ-776(formerly)
- Fj 776
- Mkt-077
- Pyridinium, 1-ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]-, chloride
- Pyridinium, 1-ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]-, chloride (1:1)
- Sdz-Mkt-077
- 1-Ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]-pyridinium chloride
- MKT077;MKT-077;FJ-776
- MKT-077 >=98% (HPLC), powder
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 8 products.
Pyridinium, 1-ethyl-2-[[3-ethyl-5-(3-methyl-2(3H)-benzothiazolylidene)-4-oxo-2-thiazolidinylidene]methyl]-, chloride (1:1)
CAS:Formula:C21H22ClN3OS2Purity:95%Color and Shape:SolidMolecular weight:432.00191-Ethyl-2-((Z)-((Z)-3-Ethyl-5-(3-mEthylbenzo[d]Thiazol-2(3H)-Ylidene)-4-oxoThiazolidin-2-Ylidene)mEthyl)Pyridin-1-Ium Chloride
CAS:1-Ethyl-2-((Z)-((Z)-3-Ethyl-5-(3-mEthylbenzo[d]Thiazol-2(3H)-Ylidene)-4-oxoThiazolidin-2-Ylidene)mEthyl)Pyridin-1-Ium ChloridePurity:95%Molecular weight:432.00g/molMKT-077
CAS:Formula:C21H22N3OS2ClPurity:(HPLC) ≥ 98.0%Color and Shape:Orange-red crystalline powder or solidMolecular weight:432.00MKT-077
CAS:<p>MKT-077 (FJ-776) is a cationic rhodacyanine dye that demonstrates antiproliferative activity against cancer cell lines.</p>Formula:C21H22ClN3OS2Purity:98.2%Color and Shape:SolidMolecular weight:4321-Ethyl-2-((Z)-((Z)-3-ethyl-5-(3-methylbenzo[d]thiazol-2(3H)-ylidene)-4-oxothiazolidin-2-ylidene)methyl)pyridin-1-ium chloride
CAS:Purity:95.0%Molecular weight:432.0MKT-077
CAS:Controlled Product<p>Applications MKT-077 is used in the treatment of Alzheimer’s diseases and other tauopathie’s. Also, is a rhodacyanine derivative that selectively targets cancer cells and overcomes tamoxifen resistance<br>References Jinwal, U. K., et al.: Pharm. Nanotechnol., 2, 217, (2014); Koren, J., et al. : PLoS One, 7, 35566 (2012)<br></p>Formula:C21H22N3OS2·CiColor and Shape:NeatMolecular weight:432.0MKT-077
CAS:<p>MKT-077 is a rhodacyanine dye analogue, which is a compound derived from the class of compounds known as rhodacyanines. This particular analogue is synthesized for its biochemical properties, specifically targeting mitochondrial functions. The mode of action of MKT-077 involves the selective accumulation within the mitochondria of cancer cells, where it induces mitochondrial stress and disrupts mitochondrial membrane potential. This disruption leads to apoptotic cell death, making it a potential agent in cancer treatment research.</p>Formula:C21H22ClN3OS2Purity:Min. 95%Molecular weight:432 g/mol






