Category: 5330-79-0

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 5330-79-0, Name is 4-(o-Tolyl)thiazol-2-amine, Recommanded Product: 4-(o-Tolyl)thiazol-2-amine.

The reaction of methyl N-(4-aryl-2-thiazolyl)dithiocarbamates (2) with potassium anthranilate (1) in dimethylformamide below room temperature yields benzoxazines (6) whereas in refluxing dimethylformamide affords the isomeric tetrahydroquinazolines (5).The antifungal and antibacterial activities of these compounds have also been evaluated.

The reaction of methyl N-(4-aryl-2-thiazolyl)dithiocarbamates (2) with potassium anthranilate (1) in dimethylformamide below room temperature yields benzoxazines (6) whereas in refluxing dimethylformamide affords the isomeric tetrahydroquinazolines (5).The antifungal and antibacterial activities of these compounds have also been evaluated.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 4-(o-Tolyl)thiazol-2-amine. In my other articles, you can also check out more blogs about 5330-79-0

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Thiazole | C3H4805NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 5330-79-0. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 5330-79-0, Name is 4-(o-Tolyl)thiazol-2-amine

Apical membrane antigen 1 (AMA1) is an essential component of the moving junction complex used by Plasmodium falciparum to invade human red blood cells. AMA1 has a conserved hydrophobic cleft that is the site of key interactions with the rhoptry neck protein complex. Our goal is to develop small molecule inhibitors of AMA1 with broad strain specificity, which we are pursuing using a fragment-based approach. In our screening campaign, we identified fragments that bind to the hydrophobic cleft with a hit rate of 5%. The high hit rate observed strongly suggests that a druggable pocket is present within the cleft. CSIRO 2013.

Apical membrane antigen 1 (AMA1) is an essential component of the moving junction complex used by Plasmodium falciparum to invade human red blood cells. AMA1 has a conserved hydrophobic cleft that is the site of key interactions with the rhoptry neck protein complex. Our goal is to develop small molecule inhibitors of AMA1 with broad strain specificity, which we are pursuing using a fragment-based approach. In our screening campaign, we identified fragments that bind to the hydrophobic cleft with a hit rate of 5%. The high hit rate observed strongly suggests that a druggable pocket is present within the cleft. CSIRO 2013.

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Thiazole | C3H4815NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 5330-79-0. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 5330-79-0, Name is 4-(o-Tolyl)thiazol-2-amine

In this study, a series of novel N-(4-phenylthiazol-2-yl)cinnamamide derivatives (7a-8n) were synthesized and evaluated for their anti-proliferative activities in vitro by MTT assay and a possible antitumor mechanism was also explored. SAR analysis showed that steric effects played an important role on the anti-tumor activity. The most potent analogue 8f showed excellent inhibitions on the K562, Bel7402, A549 and Jurkat cells ranging from sub-micromolar to nanomolar concentration. Compound 8f inhibited Jurkat cells with an IC50 value of 0.035 muM with no apparent toxicity in different non-cancerous cells. Furthermore, it was suggested that the possible mechanism of 8f might be associated with inducing cancer cell apoptosis following flow cytometer analysis and Hoechst 33358 staining assays.

In this study, a series of novel N-(4-phenylthiazol-2-yl)cinnamamide derivatives (7a-8n) were synthesized and evaluated for their anti-proliferative activities in vitro by MTT assay and a possible antitumor mechanism was also explored. SAR analysis showed that steric effects played an important role on the anti-tumor activity. The most potent analogue 8f showed excellent inhibitions on the K562, Bel7402, A549 and Jurkat cells ranging from sub-micromolar to nanomolar concentration. Compound 8f inhibited Jurkat cells with an IC50 value of 0.035 muM with no apparent toxicity in different non-cancerous cells. Furthermore, it was suggested that the possible mechanism of 8f might be associated with inducing cancer cell apoptosis following flow cytometer analysis and Hoechst 33358 staining assays.

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Reference£º
Thiazole | C3H4813NS – PubChem,
Thiazole | chemical compound | Britannica