122320-81-4

Basic information

• Product Name: Ethanol, 2-(methyl-2-thiazolylamino)-
• Synonyms: Ethanol, 2-(methyl-2-thiazolylamino)-
• CAS NO: 122320-81-4
• Molecular Formula: C₆H₁₀N₂OS
• Molecular Weight: 0
• Mol File: 122320-81-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanol, 2-(methyl-2-thiazolylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-(methyl-2-thiazolylamino)-(122320-81-4)
• EPA Substance Registry System: Ethanol, 2-(methyl-2-thiazolylamino)-(122320-81-4)

Safety Data

• Hazardous Substances Data: 122320-81-4(Hazardous Substances Data)

Upstream product

• 3034-53-5 2-bromo-1,3-thiazole 
• 109-83-1 (2-hydroxyethyl)(methyl)amine 
• 3034-52-4 2-chlorothiazole 

Downstream Products

• 122320-88-1 4-[2-(N-Methyl-N-(2-thiazolyl)amino)ethoxy]benzaldehyde 
• 100374-38-7 4-amino-2-hydroxy-benzoic acid-[2-(methyl-thiazol-2-yl-amino)-ethyl ester] 
• 122320-78-9 4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]-benzaldehyde 
• 1111238-48-2 C₁₈H₂₃N₃O₆S 

Relevant articles and documents

Structure-activity relationships of rosiglitazone for peroxisome proliferator-activated receptor gamma transrepression

Anti-inflammatory effects of peroxisome proliferator-activated receptor gamma (PPRAγ) ligands are thought to be largely due to PPARγ-mediated transrepression. Thus, transrepression-selective PPARγ ligands without agonistic activity or with only partial agonistic activity should exhibit anti-inflammatory properties with reduced side effects. Here, we investigated the structure-activity relationships (SARs) of PPARγ agonist rosiglitazone, focusing on transrepression activity. Alkenic analogs showed slightly more potent transrepression with reduced efficacy of transactivating agonistic activity. Removal of the alkyl group on the nitrogen atom improved selectivity for transrepression over transactivation. Among the synthesized compounds, 3l exhibited stronger transrepressional activity (IC50: 14?μM) and weaker agonistic efficacy (11%) than rosiglitazone or pioglitazone.

benzyl>-2,4-thiazolidinediones as Potent Antihyperglycemic Agents

A series of -2,4-thiazolidinediones and benzyl>-2,4-thiazolidinediones was synthesized from the corresponding aldehydes.Compounds from the urea series, exemplified by 16, showed antihyperglycemic potency comparable with known agents of the type such as pioglitazone and troglitazone (CS-045).The benzoxazole 49, a cyclic analogue of 16, was a very potent enhancer of insulin sensitivity, and by modification of the aromatic heterocycle, an aminopyridine, 37, was identified as a lead compound from SAR studies.Evaluation of antihyperglycemic activity together with effects on blood hemoglobin content, to determine the therapeutic index, was performed in 8-day repeat administration studies in genetically obese C57 BI/6 ob/ob mice.From these studies, BRL 49653 (37) has been selected, on the basis of antihyperglycemic potency combined with enhanced selectivity against reductions in blood hemoglobin content, for further evaluation.