Chemical Formula: C3H7NO2S2

Chemical Formula C3H7NO2S2

Found 10 metabolite its formula value is C3H7NO2S2

Thiocysteine

(2S)-2-amino-3-disulfanyl-propanoic acid

C3H7NO2S2 (152.9918)


The reactive species in the phosphofructokinase modulation system could be considered thiocysteine (R-S-S-) or cystine trisulfide (R-S-S-S-R) produced from cystine in the presence of gamma-Cystathionase (CST, EC 4.4.1.1). The desulfuration reaction of cystine in vivo produces thiocysteine containing a bound sulfur atom. Persulfide generated from L-cysteine inactivates tyrosine aminotransferase. Thiocysteine is the reactive (unstable) intermediate of thiocystine which functions as a persulfide in transferring its sulfane sulfur to thiophilic acceptors. Thiocystine conversion to unstable thiocysteine is accelerated by sulfhydryl compounds, or reagents that cleave sulfur-sulfur bonds to yield sulfhydryl groups. Thiocystine is proposed as the storage form of sulfane sulfur in biological systems. Liver cytosols contain factors that produce an inhibitor of tyrosine aminotransferase in 3 steps: initial oxidation of cysteine to form cystine; desulfurization of cystine catalyzed by cystathionase to form the persulfide, thiocysteine; and reaction of thiocysteine (or products of its decomposition) with proteins to form protein-bound sulfane. (PMID: 2903161, 454618, 7287665) [HMDB] The reactive species in the phosphofructokinase modulation system could be considered thiocysteine (R-S-S-) or cystine trisulfide (R-S-S-S-R) produced from cystine in the presence of gamma-Cystathionase (CST, EC 4.4.1.1). The desulfuration reaction of cystine in vivo produces thiocysteine containing a bound sulfur atom. Persulfide generated from L-cysteine inactivates tyrosine aminotransferase. Thiocysteine is the reactive (unstable) intermediate of thiocystine which functions as a persulfide in transferring its sulfane sulfur to thiophilic acceptors. Thiocystine conversion to unstable thiocysteine is accelerated by sulfhydryl compounds, or reagents that cleave sulfur-sulfur bonds to yield sulfhydryl groups. Thiocystine is proposed as the storage form of sulfane sulfur in biological systems. Liver cytosols contain factors that produce an inhibitor of tyrosine aminotransferase in 3 steps: initial oxidation of cysteine to form cystine; desulfurization of cystine catalyzed by cystathionase to form the persulfide, thiocysteine; and reaction of thiocysteine (or products of its decomposition) with proteins to form protein-bound sulfane. (PMID: 2903161, 454618, 7287665).

   

Cysteine thiol

2-Amino-3-sulphanylpropane(thioperoxoic) os-acid

C3H7NO2S2 (152.9918)


   

Sulfhydryl cysteine

3-Sulphanyl-2-(sulphanylamino)propanoic acid

C3H7NO2S2 (152.9918)


   

Sulfhydryl cysteine

3-Sulphanyl-2-(sulphanylamino)propanoic acid

C3H7NO2S2 (152.9918)


   

S-sulfanyl-L-cysteine

S-sulfanyl-L-cysteine

C3H7NO2S2 (152.9918)


   
   

3-disulfanyl-L-alanine zwitterion

3-disulfanyl-L-alanine zwitterion

C3H7NO2S2 (152.9918)


Zwitterionic form of 3-disulfanyl-L-alanine.

   

(2S)-2-amino-3-disulfanyl-propanoic acid

(2S)-2-amino-3-disulfanyl-propanoic acid

C3H7NO2S2 (152.9918)


   

3-Disulfanyl-L-alanine

3-Disulfanyl-L-alanine

C3H7NO2S2 (152.9918)


An S-substituted L-cysteine where the S-substituent is specified as sulfanyl.

   

s-mercaptocysteine

s-mercaptocysteine

C3H7NO2S2 (152.9918)