The chemical substance known as 2-[[4-Ethyl-5-(1-methylethyl)-4H-1,2,4-triazol-3-yl]thio]-N-[5-[4-(1-methylethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide, with the CAS number 2140901-88-6, is a complex organic compound characterized by its multi-functional groups and heterocyclic structures. It features a triazole ring and a thiadiazole moiety, which contribute to its potential biological activity. The presence of ethyl and isopropyl groups suggests lipophilicity, which may influence its solubility and permeability in biological systems. The compound's thioether linkage indicates potential reactivity and stability under various conditions. Its structural complexity may allow for interactions with specific biological targets, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or therapeutic agents. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, including spectroscopic methods for confirmation of its structure and purity. Overall, this substance exemplifies the intricate design often seen in modern chemical compounds aimed at specific applications.

2-[[4-Ethyl-5-(1-methylethyl)-4H-1,2,4-triazol-3-yl]thio]-N-[5-[4-(1-methylethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide

2140901-88-6: The chemical substance known as 2-[[4-Ethyl-5-(1-methylethyl)-4H-1,2,4-triazol-3-yl]thio]-N-[5-[4-(1-methylethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide, with the CAS number 2140901-88-6, is a complex organic compound characterized by its multi-functional groups and heterocyclic structures. It features a triazole ring and a thiadiazole moiety, which contribute to its potential biological activity. The presence of ethyl and isopropyl groups suggests lipophilicity, which may influence its solubility and permeability in biological systems. The compound's thioether linkage indicates potential reactivity and stability under various conditions. Its structural complexity may allow for interactions with specific biological targets, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or therapeutic agents. The compound's synthesis and characterization would typically involve standard organic chemistry techniques, including spectroscopic methods for confirmation of its structure and purity. Overall, this substance exemplifies the intricate design often seen in modern chemical compounds aimed at specific applications.

<p>RG100204 is an orally active AQP9 inhibitor with anti-inflammatory properties. It alleviates cardiac dysfunction (systolic and diastolic) induced by sepsis, improves renal dysfunction, and reduces the elevation of the cellular damage marker LDH.</p>

CAS 2140901-88-6

2-[[4-Ethyl-5-(1-methylethyl)-4H-1,2,4-triazol-3-yl]thio]-N-[5-[4-(1-methylethoxy)phenyl]-1,3,4-thiadiazol-2-yl]acetamide

RG100204

Ref: TM-T88698