Exact Mass: 152.9858

Exact Mass Matches: 152.9858

Found 24 metabolites which its exact mass value is equals to given mass value 152.9858, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

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)


   

Thieno[3,2-c]isoxazole-3-carboxaldehyde (9CI)

Thieno[3,2-c]isoxazole-3-carboxaldehyde (9CI)

C6H3NO2S (152.9884)


   

2-FUROYL ISOTHIOCYANATE

2-FUROYL ISOTHIOCYANATE

C6H3NO2S (152.9884)


   

2-Cyano-3-thioenylcarboxylic acid

2-Cyano-3-thioenylcarboxylic acid

C6H3NO2S (152.9884)


   

5-(CHLORO-DIFLUORO-METHYL)-ISOXAZOLE

5-(CHLORO-DIFLUORO-METHYL)-ISOXAZOLE

C4H2ClF2NO (152.9793)


   

4-Cyanothiophene-2-carboxylic acid

4-Cyanothiophene-2-carboxylic acid

C6H3NO2S (152.9884)


   

3-Chloro-1H-pyrazol-4-amine hydrochloride (1:1)

3-Chloro-1H-pyrazol-4-amine hydrochloride (1:1)

C3H5Cl2N3 (152.9861)


   

3-cyanothiophene-2-carboxylic acid

3-cyanothiophene-2-carboxylic acid

C6H3NO2S (152.9884)


   

5-Cyano-2-thiophenecarboxylic acid

5-Cyano-2-thiophenecarboxylic acid

C6H3NO2S (152.9884)


   

1,1-dimethyl-2-selenourea

1,1-dimethyl-2-selenourea

C3H9N2Se (152.9931)


   

Sulfhydryl cysteine

3-Sulphanyl-2-(sulphanylamino)propanoic acid

C3H7NO2S2 (152.9918)


   

S-sulfanyl-L-cysteine

S-sulfanyl-L-cysteine

C3H7NO2S2 (152.9918)


   

Glycerol 1,2-cyclic phosphate(1-)

Glycerol 1,2-cyclic phosphate(1-)

C3H6O5P- (152.9953)


   

3-Sulfolactaldehyde(1-)

3-Sulfolactaldehyde(1-)

C3H5O5S- (152.9858)


   

(2S)-3-sulfolactaldehyde

(2S)-3-sulfolactaldehyde

C3H5O5S- (152.9858)


   

1-Hydroxy-2-oxo-3-sulfopropane

1-Hydroxy-2-oxo-3-sulfopropane

C3H5O5S- (152.9858)


   

D-3-sulfolactaldehyde(1-)

D-3-sulfolactaldehyde(1-)

C3H5O5S- (152.9858)


A 3-sulfolactaldehyde(1-) in which the stereocentre at position 3 has R-configuration.

   
   

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)