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Cystamine

Cystamine structure

Cystamine 

structure
  • CAS No:

    51-85-4

  • Formula:

    C4H12N2S2

  • Chemical Name:

    Cystamine

  • Synonyms:

    Ethanamine,2,2′-dithiobis-;Ethylamine,2,2′-dithiobis-;Ethylamine,β,β′-dithiobis-;2,2′-Dithiobis[ethanamine];Bis(β-aminoethyl) disulfide;Cystamine;Cysteinamine disulfide;Cystineamine;Decarboxycystine;β,β′-Diaminodiethyl disulfide;Mercamine disulfide;β-Mercaptoethylamine disulfide;Merkamine disulfide;Bis(2-aminoethyl) disulfide;2,2′-Dithiobis[ethylamine];2-Aminoethane disulfide;L 1591;1,6-Diamino-3,4-dithiahexane;2,2′-Dithiodiethylamine;2-Aminoethyl disulfide;3,4-Dithiahexane-1,6-diamine;2,2′-Disulfanediyldiethanamine;2-(2-Amino-ethyldisulfanyl)-ethylamine;2-[(2-Aminoethyl)disulfanyl]ethan-1-amine;2-(2-Aminoethyldisulfanyl)ethanamine;2087491-48-1

  • Categories:

    Organic Chemistry  >  Amides

Description

Cystamine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1].


Cystamine is an organic disulfide obtgained by oxidative dimerisation of cysteamine. It has a role as an EC 2.3.2.13 (protein-glutamine gamma-glutamyltransferase) inhibitor. It is an organic disulfide and a primary amino compound. It derives from a cysteamine.|A radiation-protective agent that interferes with sulfhydryl enzymes. It may also protect against carbon tetrachloride liver damage.

Cystamine Basic Attributes

152.28100

152.28

200-129-4

R110LV8L02

DTXSID60199005

2930909090

Characteristics

102.64000

1.68580

1.1559 g/cm3 @ Temp: 20 °C

135-136 °C

106-108 °C @ Press: 5 Torr

114ºC

1.587

Drug Information

Drugs used to protect against ionizing radiation. They are usually of interest for use in radiation therapy but have been considered for other purposes, e.g. military. (See all compounds classified as Radiation-Protective Agents.)|Chemical agents that react with SH groups. This is a chemically diverse group that is used for a variety of purposes. Among these are enzyme inhibition, enzyme reactivation or protection, and labelling. (See all compounds classified as Sulfhydryl Reagents.)|Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)

2,2' Dithiobisethanamine

Computed Properties

Molecular Weight:152.3
XLogP3:-1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:152.04419074
Monoisotopic Mass:152.04419074
Topological Polar Surface Area:103
Heavy Atom Count:8
Complexity:37
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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