3542-13-0
3542-13-0
Chemical Structure
Selenocystamine dihydrochloride
- CAS No.: 3542-13-0
- Formula:C4H14Cl2N2Se2
- Molecular Weight:318.99
IUPAC Name: 2,2'-diselanediylbis(ethan-1-amine) dihydrochloride
InChIKey: LACKHEAUUXZNBU-UHFFFAOYSA-N
SMILES: NCC[Se][Se]CCN.Cl.Cl
Biological Activity: Selenocystamine dihydrochloride is a selenocysteine derivative that can be used in the synthesis of other active compounds. Selenocystamine dihydrochloride can also induce the aggregation of amphiphilic p-sulfonatocalixarene to form supramolecular nanoparticles[1][2][3].
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Selenocystamine dihydrochloride | 99.63% | Selenocystamine dihydrochloride is a selenocysteine derivative that can be used in the synthesis of other active compounds. Selenocystamine dihydrochloride can also induce the aggregation of amphiphilic p-sulfonatocalixarene to form supramolecular nanoparticles. | ||||||||||||||||||||
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References
- [1]. Zhuang J, et al. Homocysteine-Responsive Covalent Organic Frameworks as Signaling Scaffolds: Modulating Transsulfuration for Depression Treatment. Small. 2025 Jun;21(23):e2501944. [Content Brief]
- [2]. Hu X Y, et al. Redox-responsive supramolecular nanoparticles based on amphiphilic sulfonatocalixarene and selenocystamine dihydrochloride. Chinese Chemical Letters, 2015, 26(7): 862-866.
- [3]. Lu X, et al. Redox-sensitive hydrogel based on hyaluronic acid with selenocystamine cross-linking for the delivery of Limosilactobacillus reuteri in a DSS-induced colitis mouse model. Int J Biol Macromol. 2024 Sep;276(Pt 2):133855. [Content Brief]
Keywords
