137138-08-0

Basic information

• Product Name: S-(2-GLYCYLAMIDOETHYL)DITHIO-2-PYRIDINE
• Synonyms: S-(2-GLYCYLAMIDOETHYL)DITHIO-2-PYRIDINE;2-AMino-N-[2-(2-pyridinyldithio)ethyl]acetaMide;2-amino-N-[2-(pyridin-2-yldisulfanyl)ethyl]acetamide
• CAS NO: 137138-08-0
• Molecular Formula: C9H13N3OS2
• Molecular Weight: 243.35
• Product Categories: Nitric Oxide Reagents;Cross Linking Reagents;MTS & Sulfhydryl Active Reagents;Amines;Aromatics
• Mol File: 137138-08-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: S-(2-GLYCYLAMIDOETHYL)DITHIO-2-PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: S-(2-GLYCYLAMIDOETHYL)DITHIO-2-PYRIDINE(137138-08-0)
• EPA Substance Registry System: S-(2-GLYCYLAMIDOETHYL)DITHIO-2-PYRIDINE(137138-08-0)

Safety Data

• Hazardous Substances Data: 137138-08-0(Hazardous Substances Data)

Usage

Description

S-(2-Glycylamidoethyl)dithio-2-pyridine is an organic compound characterized by its unique structure that features a pyridine ring with a dithioether linkage to a glycylethyl side chain. This molecule is known for its reactivity with sulfhydryl groups, making it a versatile tool in the field of biochemistry and molecular biology.

Uses

Used in Biochemistry and Molecular Biology:
S-(2-Glycylamidoethyl)dithio-2-pyridine is used as a sulfhydryl active reagent for the modification of proteins. Its ability to selectively react with cysteine residues in proteins allows for the introduction of various functional groups, enabling the study of protein structure, function, and interactions. This modification can also be used to alter protein stability, solubility, or activity, making it a valuable tool in the development of new therapeutic strategies and the understanding of protein biology.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, S-(2-Glycylamidoethyl)dithio-2-pyridine is used as a sulfhydryl active reagent for the development of novel drug candidates. The compound can be employed to modify proteins or peptides with therapeutic potential, enhancing their pharmacological properties, such as stability, bioavailability, or target specificity. This modification can lead to the development of more effective drugs with improved safety profiles.
Used in Chemical Synthesis:
S-(2-Glycylamidoethyl)dithio-2-pyridine is also used as a building block in the synthesis of complex organic molecules, particularly those with biological activity. Its unique reactivity with sulfhydryl groups makes it a valuable component in the design and synthesis of new molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.