Ethylene glycol bisthioglycolate

CAS: 123-81-9

Ref. 3D-FE32808

Product Information

• Name: Ethylene glycol bisthioglycolate
• Synonyms: 2-[(2-Sulfanylacetyl)oxy]ethyl 2-sulfanylacetate, Acetic acid, 2-mercapto-, 1,1′-(1,2-ethanediyl) ester, Acetic acid, mercapto-, 1,2-ethanediyl ester, Acetic acid, mercapto-, ethylene ester, EGTG (polythiol), Ethane-1,2-Diyl Bis(Sulfanylacetate), Ethylene Bis(thioglycolate), Ethylene bis(mercaptoacetate), Ethylene glycol bis(2-mercaptoacetate), Ethylene glycol bis(thioglycolate), Ethylene glycol bis(thioglycolic ester), Ethylene glycol dimercaptoacetate, Ethylene glycol, bis(mercaptoacetate), Ethylene mercaptoacetate, Ethylenebis(thioglycolate), Gdma, Glycol bis(mercaptoacetate), Glycol(bis thioglycolate), NSC 30032, S,S'-ethane-1,2-diyl diethanethioate, Thiocure GDMA, ethylene di(S-thioacetate)

Description

Ethylene glycol bisthioglycolate is a water-soluble compound that is composed of two hydroxyl groups and one bisthioglycolate anion. It has been shown to be highly permeable in water, and can be used as a growth factor for hematopoietic cells. Ethylene glycol bisthioglycolate has been shown to inhibit the G1/S phase cell cycle transition by suppressing the expression of protein kinase C δ (PKCδ) and CDK2. This compound also inhibits the production of inflammatory mediators such as prostaglandin E2 (PGE2) and nitric oxide (NO). The metabolic disorder associated with ethylene glycol bisthioglycolate is sodium citrate deficiency, which can result in a decrease in blood acidity due to reduced citrate levels. The compound also inhibits the activity of glycolysis enzymes such as phosphofructokinase,

• Brand: Biosynth

Chemical properties

• Molecular weight: 210.27 g/mol
• Formula: C₆H₁₀O₄S₂
• Purity: Min. 95%
• InChI: InChI=1S/C6H10O4S2/c7-5(3-11)9-1-2-10-6(8)4-12/h11-12H,1-4H2
• InChI key: InChIKey=PSYGHMBJXWRQFD-UHFFFAOYSA-N
• SMILES: O=C(CS)OCCOC(=O)CS