4781-83-3
4781-83-3
Chemical Structure
2-Iminothiolane hydrochloride
- CAS No.: 4781-83-3
- Formula:C4H8ClNS
- Molecular Weight:137.63
IUPAC Name: dihydrothiophen-2(3H)-imine hydrochloride
InChIKey: ATGUDZODTABURZ-UHFFFAOYSA-N
SMILES: N=C1CCCS1.Cl
Biological Activity: 2-Iminothiolane hydrochloride is a reagent for the introduction of sulphydryl groups into oligosaccharides derived from asparagine-linked glycan. 2-Iminothiolane hydrochloride can be used to modify proteins and peptides[1][2].
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2-Iminothiolane hydrochloride | 99.92% | 2-Iminothiolane hydrochloride is a reagent for the introduction of sulphydryl groups into oligosaccharides derived from asparagine-linked glycan. 2-Iminothiolane hydrochloride can be used to modify proteins and peptides. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.70
HY-W010594RTetrahydrothiophen-3-one (Standard) -
Similarity Score 0.68
HY-W002007Tetrahydrothiopyran-4-one -
Similarity Score 0.67
HY-W0129882-Methyl-4,5-dihydrothiazole -
Similarity Score 0.67
HY-W001189R1,3-Dithiane (Standard) -
Similarity Score 0.65
HY-W010628Azetidine hydrochloride -
Similarity Score 0.64
HY-W539895Methylenecyclohexane -
Similarity Score 0.64
HY-753551,3-Cyclopentanedione -
Similarity Score 0.63
HY-W007359Thiomorpholine -
Similarity Score 0.63
HY-W777266Cyclohexane-1,3-dione-13C3 -
Explore the MedChemAI to find more analogs
References
- [1]. A L Tarentino, et al. 2-Iminothiolane: a reagent for the introduction of sulphydryl groups into oligosaccharides derived from asparagine-linked glycans. Glycobiology. 1993 Jun;3(3):279-85. [Content Brief]
- [2]. Singh R, et al. Formation of N-substituted 2-iminothiolanes when amino groups in proteins and peptides are modified by 2-iminothiolane. Anal Biochem. 1996 Apr 5;236(1):114-25. [Content Brief]
