Exact Mass: 152.9953

Exact Mass Matches: 152.9953

Found 62 metabolites which its exact mass value is equals to given mass value 152.9953, 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)


   

5-Chlorobenzoxazole

5-Chlorobenzoxazole

C7H4ClNO (152.9981)


   

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

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

C6H3NO2S (152.9884)


   

2-Chlorobenzoxazole

2-Chlorobenzoxazole

C7H4ClNO (152.9981)


   

3-Chloro-1,2-benzoxazole

3-Chloro-1,2-benzoxazole

C7H4ClNO (152.9981)


   

Thiazolo[5,4-d]pyrimidin-2(1H)-one

Thiazolo[5,4-d]pyrimidin-2(1H)-one

C5H3N3OS (152.9997)


   

4-chloro-1,3-benzoxazole

4-chloro-1,3-benzoxazole

C7H4ClNO (152.9981)


   

chlorophenyl isocyanate

chlorophenyl isocyanate

C7H4ClNO (152.9981)


   

2-FUROYL ISOTHIOCYANATE

2-FUROYL ISOTHIOCYANATE

C6H3NO2S (152.9884)


   

3-chloro-4-hydroxybenzonitrile

3-chloro-4-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

5-CHLOROBENZO[C]ISOXAZOLE

5-CHLOROBENZO[C]ISOXAZOLE

C7H4ClNO (152.9981)


   

4-Chlorofuro[3,2-c]pyridine

4-chlorofuro-[3,2-c]-pyridine

C7H4ClNO (152.9981)


   

3-Chlorophenyl isocyanate

3-Chlorophenyl isocyanate

C7H4ClNO (152.9981)


   

5-Chlorofuro[3,2-b]pyridine

5-Chlorofuro[3,2-b]pyridine

C7H4ClNO (152.9981)


   

6-CHLORO-BENZOXAZOLE

6-CHLORO-BENZOXAZOLE

C7H4ClNO (152.9981)


   

5-Chloro-2-hydroxybenzonitrile

5-Chloro-2-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

COPPER(II) ETHOXIDE

COPPER(II) ETHOXIDE

C4H10CuO2 (152.9977)


   

L-Homocysteine thiolactone hydrochloride

L-Homocysteine thiolactone hydrochloride

C4H8ClNOS (153.0015)


   

7-Chlorofuro[3,2-b]pyridine

7-Chlorofuro[3,2-b]pyridine

C7H4ClNO (152.9981)


   

4-Chloro-2-hydroxybenzonitrile

4-Chloro-2-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2-Cyano-3-thioenylcarboxylic acid

2-Cyano-3-thioenylcarboxylic acid

C6H3NO2S (152.9884)


   

5-CHLORO-1,2-BENZISOXAZOLE

5-CHLORO-1,2-BENZISOXAZOLE

C7H4ClNO (152.9981)


   

6-CHLORO-1,2-BENZISOXAZOLE

6-CHLORO-1,2-BENZISOXAZOLE

C7H4ClNO (152.9981)


   

6-FLUOROBENZOTHIAZOLE

6-FLUOROBENZOTHIAZOLE

C7H4FNS (153.0048)


   

thiazolo[5,4-d]pyrimidin-7-ol

thiazolo[5,4-d]pyrimidin-7-ol

C5H3N3OS (152.9997)


   

2-Fluorobenzothiazole

2-Fluorobenzothiazole

C7H4FNS (153.0048)


   

3-Chloro-2-hydroxybenzonitrile

3-Chloro-2-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

7-chlorobenzo[d]oxazole

7-chlorobenzo[d]oxazole

C7H4ClNO (152.9981)


   

3-Chloro-5-hydroxybenzonitrile

3-Chloro-5-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

4-Cyanothiophene-2-carboxylic acid

4-Cyanothiophene-2-carboxylic acid

C6H3NO2S (152.9884)


   

2-Chloro-4-hydroxybenzonitrile

2-Chloro-4-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2-Chloro-6-hydroxybenzonitrile

2-Chloro-6-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2-fluorophenyl isothiocyanate

2-fluorophenyl isothiocyanate

C7H4FNS (153.0048)


   

4-Fluorophenyl isothiocyanate

4-Fluorophenyl isothiocyanate

C7H4FNS (153.0048)


   

m-Fluorophenyl isothiocyanate

m-Fluorophenyl isothiocyanate

C7H4FNS (153.0048)


   

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

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

C3H5Cl2N3 (152.9861)


   

7-Chlorofuro[2,3-c]pyridine

7-Chlorofuro[2,3-c]pyridine

C7H4ClNO (152.9981)


   

2-Chloro-3-hydroxybenzonitrile

2-Chloro-3-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

3-cyanothiophene-2-carboxylic acid

3-cyanothiophene-2-carboxylic acid

C6H3NO2S (152.9884)


   

3-Aminodihydro-2(3H)-thiophenone hydrochloride

3-Aminodihydro-2(3H)-thiophenone hydrochloride

C4H8ClNOS (153.0015)


DL-Homocysteine thiolactone hydrochloride is a cyclic amino acid derivative that exhibits root-growth inhibitory activity.

   

CARBAMYL PHOSPHATE DILITHIUM SALT

CARBAMYL PHOSPHATE DILITHIUM SALT

CH2Li2NO5P (152.9991)


   

6-CHLOROFURO[3,2-B]PYRIDINE

6-CHLOROFURO[3,2-B]PYRIDINE

C7H4ClNO (152.9981)


   

5-Cyano-2-thiophenecarboxylic acid

5-Cyano-2-thiophenecarboxylic acid

C6H3NO2S (152.9884)


   

2-Chloro-5-hydroxybenzonitrile

2-Chloro-5-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

1,1-dimethyl-2-selenourea

1,1-dimethyl-2-selenourea

C3H9N2Se (152.9931)


   

p-Chlorophenyl isocyanate

p-Chlorophenyl isocyanate

C7H4ClNO (152.9981)


   

5-FLUOROBENZO[D]THIAZOLE

5-FLUOROBENZO[D]THIAZOLE

C7H4FNS (153.0048)


   

Thiosalicylate

Thiosalicylate

C7H5O2S- (153.001)


   

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)