Exact Mass: 152.9589

Exact Mass Matches: 152.9589

Found 81 metabolites which its exact mass value is equals to given mass value 152.9589, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 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)


   

Europium

Europium

Eu (152.9212)


Europium, also known as 63eu or europio, is a member of the class of compounds known as homogeneous lanthanide compounds. Homogeneous lanthanide compounds are inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom. Europium can be found in a number of food items such as carrot, black-eyed pea, black walnut, and red beetroot, which makes europium a potential biomarker for the consumption of these food products. Europium is a chemical element with symbol Eu and atomic number 63. It was isolated in 1901 and is named after the continent of Europe. It is a moderately hard, silvery metal which readily oxidizes in air and water. Being a typical member of the lanthanide series, europium usually assumes the oxidation state +3, but the oxidation state +2 is also common. All europium compounds with oxidation state +2 are slightly reducing. Europium has no significant biological role and is relatively non-toxic compared to other heavy metals. Most applications of europium exploit the phosphorescence of europium compounds. Europium is one of the least abundant elements in the universe; only about 5√ó10‚àí8\\% of all matter in the universe is europium . Europium, also known as 63eu or europio, is a member of the class of compounds known as homogeneous lanthanide compounds. Homogeneous lanthanide compounds are inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom. Europium can be found in a number of food items such as carrot, black-eyed pea, black walnut, and red beetroot, which makes europium a potential biomarker for the consumption of these food products. Europium is a chemical element with symbol Eu and atomic number 63. It was isolated in 1901 and is named after the continent of Europe. It is a moderately hard, silvery metal which readily oxidizes in air and water. Being a typical member of the lanthanide series, europium usually assumes the oxidation state +3, but the oxidation state +2 is also common. All europium compounds with oxidation state +2 are slightly reducing. Europium has no significant biological role and is relatively non-toxic compared to other heavy metals. Most applications of europium exploit the phosphorescence of europium compounds. Europium is one of the least abundant elements in the universe; only about 5×10−8\\% of all matter in the universe is europium . D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents

   

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)


   

ALUMINUM CHLORIDE HYDRATE

ALUMINUM CHLORIDE HYDRATE

AlCl3H5O (152.9221)


   

2,4-Dichlorothiazole

2,4-Dichlorothiazole

C3HCl2NS (152.9207)


   

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-Cyano-2-thienyl)boronic acid

(5-Cyano-2-thienyl)boronic acid

C5H4BNO2S (153.0056)


   

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)


   

4-(CHLOROMETHYL)OXAZOLE HYDROCHLORIDE

4-(CHLOROMETHYL)OXAZOLE HYDROCHLORIDE

C4H5Cl2NO (152.9748)


   

7-Chlorofuro[3,2-b]pyridine

7-Chlorofuro[3,2-b]pyridine

C7H4ClNO (152.9981)


   

azanylidynelanthanum

azanylidynelanthanum

LaN (152.9094)


   

4-Chloro-2-hydroxybenzonitrile

4-Chloro-2-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2-Cyano-3-thioenylcarboxylic acid

2-Cyano-3-thioenylcarboxylic acid

C6H3NO2S (152.9884)


   

2,2-dichlorocyclopropane-1-carboxamide

2,2-dichlorocyclopropane-1-carboxamide

C4H5Cl2NO (152.9748)


   

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)


   

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)


   

2-Chloro-4-hydroxybenzonitrile

2-Chloro-4-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2-Chloro-6-hydroxybenzonitrile

2-Chloro-6-hydroxybenzonitrile

C7H4ClNO (152.9981)


   

2,5-Dichlorothiazole

2,5-Dichlorothiazole

C3HCl2NS (152.9207)


   

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)


   

POTASSIUM AMMONIUM SULFATE

POTASSIUM AMMONIUM SULFATE

H4KNO4S (152.9498)


   

p-Chlorophenyl isocyanate

p-Chlorophenyl isocyanate

C7H4ClNO (152.9981)


   

5-FLUOROBENZO[D]THIAZOLE

5-FLUOROBENZO[D]THIAZOLE

C7H4FNS (153.0048)


   

2-Phosphoglycolate

2-Phosphoglycolate

C2H2O6P-3 (152.9589)


   

2,5-Cyclohexadiene-1,4-dione, 2-nitro-

2,5-Cyclohexadiene-1,4-dione, 2-nitro-

C6H3NO4 (153.0062)


   

Europium(3+)

Europium(3+)

Eu+3 (152.9212)


   

Europium(2+)

Europium(2+)

Eu+2 (152.9212)


   

Thiosalicylate

Thiosalicylate

C7H5O2S- (153.001)


   

Europium-151

Europium-151

Eu (152.9212)


   

[Methylseleno]acetate

[Methylseleno]acetate

C3H5O2Se- (152.9455)


   

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.

   
   

2-phosphonatoglycolate(3-)

2-phosphonatoglycolate(3-)

C2H2O6P (152.9589)


Trianion of 2-phosphoglycolic acid arising from deprotonation of the carboxy and phosphate groups; major species at pH 7.3.

   

3-disulfanyl-L-alanine zwitterion

3-disulfanyl-L-alanine zwitterion

C3H7NO2S2 (152.9918)


Zwitterionic form of 3-disulfanyl-L-alanine.

   

Europium

Europium

Eu (152.9212)


D019995 - Laboratory Chemicals > D007202 - Indicators and Reagents > D049408 - Luminescent Agents

   

(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)