Ethyl 2-amino-4-thiazoleacetate

CAS : 53266-94-7

Ref. 3D-FE10858

Informations sur le produit

• Nom: Ethyl 2-amino-4-thiazoleacetate
• Synonymes: (2-Amino-4-thiazolyl)acetic acid ethyl ester, (2-Amino-1,3-thiazol-4-yl)acetic acid ethyl ester, (2-Amino-thiazole-4-yl)acetic acid ethyl ester, 2-(2-Aminothiazol-4-yl)acetic acid ethyl ester, 2-Amino-4-(carbethoxymethyl)thiazole, 2-Amino-4-(ethoxycarbonylmethyl)-1,3-thiazole, 2-Amino-4-[(ethoxycarbonyl)methyl]thiazole, 2-Amino-4-thiazoleacetic acid ethyl ester, 4-Thiazoleacetic acid, 2-amino-, ethyl ester, Eata, Ethyl (2-Amino-1,3-Thiazol-4-Yl)Acetate, Ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate, Ethyl 2-(2-aminothiazol-4-yl) acetate, Ethyl 2-aminothiazol-4-yl-acetate, Ethyl 2-aminothiazol-4-ylacetate

Description

Ethyl 2-amino-4-thiazoleacetate is a supramolecular molecule that has the potential to be an anticancer agent. It inhibits the growth of tumor cells by binding to tyrosinase and hydrogen-bonding with chloride ions in solution. Ethyl 2-amino-4-thiazoleacetate also binds to a metal ion, such as zinc, which is important for biological functions. When it binds to these metals, it inhibits the enzyme hepg2 cell, which is involved in the synthesis of protein from RNA. Inhibition of this enzyme leads to decreased production of cytokines, which are molecules that regulate immune responses. This drug also has inhibitory activities against oral cephalosporins when used in combination with other drugs.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 186.23 g/mol
• Formule: C₇H₁₀N₂O₂S
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C7H10N2O2S/c1-2-11-6(10)3-5-4-12-7(8)9-5/h4H,2-3H2,1H3,(H2,8,9)
• Code InChI: InChIKey=SHQNGLYXRFCPGZ-UHFFFAOYSA-N
• SMILES: CCOC(=O)Cc1csc(N)n1