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Cystamine Dihydrochloride - 10mM in DMSO, high purity , CAS No.56-17-7

    Grade & Purity:
  • 10mM in DMSO
  • Cas Number:  56-17-7
  • Molecular Weight:  225.19
  • PubChem CID: 5941
In stock
Item Number
C424758
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C424758-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90

Transglutaminase inhibitor; neuroprotective

Basic Description

Synonyms Cystamine dihydrochloride | 56-17-7 | 2,2'-Disulfanediyldiethanamine dihydrochloride | Ethanamine, 2,2'-dithiobis-, dihydrochloride | Cystamine 2HCL | MFCD00012905 | 2-[(2-aminoethyl)disulfanyl]ethan-1-amine dihydrochloride | Cystamin dihydrochloride | Decarboxycystine d
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Transglutaminase inhibitor. Attenuates cell death induced by3-nitropropionic acid in Huntington's disease (HD) striatal cells. Also decreases aggregated and cross-linked huntingtin in transfected cells, and increases brain levels of BDNF. Shown to extend
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organosulfur compounds
Class Organic disulfides
Subclass Dialkyldisulfides
Intermediate Tree Nodes Not available
Direct Parent Dialkyldisulfides
Alternative Parents Sulfenyl compounds  Organopnictogen compounds  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Dialkyldisulfide - Sulfenyl compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as dialkyldisulfides. These are organic compounds containing a disulfide group R-SS-R' where R and R' are both alkyl groups.
External Descriptors Not available

Associated Targets(Human)

ALDH2 Tclin Aldehyde dehydrogenase (509 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT1 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 5 (407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2-(2-aminoethyldisulfanyl)ethanamine;dihydrochloride
INCHI InChI=1S/C4H12N2S2.2ClH/c5-1-3-7-8-4-2-6;;/h1-6H2;2*1H
InChIKey YUFRRMZSSPQMOS-UHFFFAOYSA-N
Smiles C(CSSCCN)N.Cl.Cl
Isomeric SMILES C(CSSCCN)N.Cl.Cl
WGK Germany 3
RTECS KR7260000
PubChem CID 5941
Molecular Weight 225.19
Reaxy-Rn 3616850

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Sensitivity Moisture sensitive
Melt Point(°C) 218 °C
Molecular Weight 225.200 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 5
Exact Mass 223.998 Da
Monoisotopic Mass 223.998 Da
Topological Polar Surface Area 103.000 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 37.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 3

Citations of This Product

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