Exact Mass: 233.0371

Exact Mass Matches: 233.0371

Found 87 metabolites which its exact mass value is equals to given mass value 233.0371, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Sulbactam

Sulbactam (sodium salt)

C8H11NO5S (233.0358)


J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01C - Beta-lactam antibacterials, penicillins > J01CG - Beta-lactamase inhibitors D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D065093 - beta-Lactamase Inhibitors D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D010406 - Penicillins D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams C2140 - Adjuvant > C183118 - Beta-lactamase Inhibitor D004791 - Enzyme Inhibitors

   

Dopamine 3-O-sulfate

4-(2-Aminoethyl)-1,2-benzenediol 2-(hydrogen sulphuric acid)

C8H11NO5S (233.0358)


Dopamine 3-O-sulfate is a sulfonated form of dopamine. In human blood circulation endogenous dopamine exists predominantly in the sulfated form and dopamine sulfate accounts for more than 90\\% of all dopamine. Dopamine-3-O-sulfate predominates in human plasma, with concentrations about 10-fold higher than those of the regioisomer dopamine-4-O-sulfate. Sulfonation is the most important metabolic pathway that interferes with the binding of dopamine to its receptors. The origins of this preponderance for Dopamine-3-O-sulfate have not been determined, although there has been speculation about the contribution of the specificity of transport proteins and/or arylsulfatases. It has also been proposed to depend on the regiospecificity of the metabolizing enzyme(s) for the 3-hydroxy group of dopamine. It is believed that the vast majority of circulating dopamine sulfate originates in the upper gastrointestinal tract, and indeed that is the main site of expression of the enzyme responsible for its formation. Aryl sulfotransferase (SULT1A3, EC 2.8.2.1) is an enzyme that catalyzes the sulfonation of many endogenous and exogenous phenols and catechols; the most important endogenous substrate is dopamine. SULT1A3 strongly favors the 3-hydroxy group of dopamine over the 4-hydroxy group and may indeed be primarily responsible for the difference between the circulating levels of dopamine sulfates in human blood. (PMID: 17548063) [HMDB] Dopamine 3-O-sulfate is a sulfonated form of dopamine. In human blood circulation endogenous dopamine exists predominantly in the sulfated form and dopamine sulfate accounts for more than 90\\% of all dopamine. Dopamine-3-O-sulfate predominates in human plasma, with concentrations about 10-fold higher than those of the regioisomer dopamine-4-O-sulfate. Sulfonation is the most important metabolic pathway that interferes with the binding of dopamine to its receptors. The origins of this preponderance for Dopamine-3-O-sulfate have not been determined, although there has been speculation about the contribution of the specificity of transport proteins and/or arylsulfatases. It has also been proposed to depend on the regiospecificity of the metabolizing enzyme(s) for the 3-hydroxy group of dopamine. It is believed that the vast majority of circulating dopamine sulfate originates in the upper gastrointestinal tract, and indeed that is the main site of expression of the enzyme responsible for its formation. Aryl sulfotransferase (SULT1A3, EC 2.8.2.1) is an enzyme that catalyzes the sulfonation of many endogenous and exogenous phenols and catechols; the most important endogenous substrate is dopamine. SULT1A3 strongly favors the 3-hydroxy group of dopamine over the 4-hydroxy group and may indeed be primarily responsible for the difference between the circulating levels of dopamine sulfates in human blood. (PMID: 17548063).

   

Dopamine 4-sulfate

4-(2-Aminoethyl)-1,2-benzenediol 1-(hydrogen sulphuric acid)

C8H11NO5S (233.0358)


Dopamine 4-sulfate is one of the metabolic products of the endogenous catecholamine dopamine which have also been implicated as intermediate in noradrenaline biosynthesis. In human blood circulation endogenous dopamine exists predominantly in the sulfated form and dopamine sulfate accounts for more than 90\\% of all dopamine. Sulfonation is the most important metabolic pathway that interferes with the binding of dopamine to its receptors. Dopamine-4-O-sulfate has concentrations about a 10th of those of the regioisomer dopamine-3-O-sulfate. It is believed that the vast majority of circulating dopamine sulfate originates in the upper gastrointestinal tract, and indeed that is the main site of expression of the enzyme responsible for its formation. Aryl sulfotransferase (SULT1A3, EC 2.8.2.1) is an enzyme that catalyzes the sulfonation of many endogenous and exogenous phenols and catechols; the most important endogenous substrate is dopamine. SULT1A3 strongly favors the 3-hydroxy group of dopamine over the 4-hydroxy group and may indeed be primarily responsible for the difference between the circulating levels of dopamine sulfates in human blood. (PMID: 17548063) [HMDB] Dopamine 4-sulfate is one of the metabolic products of the endogenous catecholamine dopamine which have also been implicated as intermediate in noradrenaline biosynthesis. In human blood circulation endogenous dopamine exists predominantly in the sulfated form and dopamine sulfate accounts for more than 90\\% of all dopamine. Sulfonation is the most important metabolic pathway that interferes with the binding of dopamine to its receptors. Dopamine-4-O-sulfate has concentrations about a 10th of those of the regioisomer dopamine-3-O-sulfate. It is believed that the vast majority of circulating dopamine sulfate originates in the upper gastrointestinal tract, and indeed that is the main site of expression of the enzyme responsible for its formation. Aryl sulfotransferase (SULT1A3, EC 2.8.2.1) is an enzyme that catalyzes the sulfonation of many endogenous and exogenous phenols and catechols; the most important endogenous substrate is dopamine. SULT1A3 strongly favors the 3-hydroxy group of dopamine over the 4-hydroxy group and may indeed be primarily responsible for the difference between the circulating levels of dopamine sulfates in human blood. (PMID: 17548063).

   

Hydroxyaniline mustard

Hydroxyaniline mustard hydrochloride

C10H13Cl2NO (233.0374)


D000970 - Antineoplastic Agents > D018906 - Antineoplastic Agents, Alkylating > D009588 - Nitrogen Mustard Compounds

   

Sulbactam

3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

C8H11NO5S (233.0358)


   

Isobatzelline E

Isobatzelline E

C11H8ClN3O (233.0356)


   
   

5-Benzotriazol-1-ylmethyl-[1,3,4]oxadiazole-2-thiol

5-Benzotriazol-1-ylmethyl-[1,3,4]oxadiazole-2-thiol

C9H7N5OS (233.0371)


   

1-(4-Bromobutyl)-2-piperidinone

1-(4-Bromobutyl)-2-piperidinone

C9H16BrNO (233.0415)


   
   

Adenine phosphate

Adenine phosphate

C5H8N5O4P (233.0314)


   

5-(4-nitrophenyl)-2-furoic acid

5-(4-nitrophenyl)-2-furoic acid

C11H7NO5 (233.0324)


   

Dichlorophenyl amino alcohol

Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

2-(4-aminophenoxy)ethyl hydrogen sulphate

2-(4-aminophenoxy)ethyl hydrogen sulphate

C8H11NO5S (233.0358)


   

Benzoic acid,4-[(2,2,2-trifluoroacetyl)amino]-

Benzoic acid,4-[(2,2,2-trifluoroacetyl)amino]-

C9H6F3NO3 (233.03)


   

n-(2-chlorobenzylidene)-4-fluoroaniline&

n-(2-chlorobenzylidene)-4-fluoroaniline&

C13H9ClFN (233.0408)


   

(2-Bromo-pyridin-4-ylmethyl)-isopropyl-amine

(2-Bromo-pyridin-4-ylmethyl)-isopropyl-amine

C8H12ClN3OS (233.039)


   

4-Hydroxy-6-nitro-2-naphthoic acid

4-Hydroxy-6-nitro-2-naphthoic acid

C11H7NO5 (233.0324)


   

N-(4,5,6,7-tetrahydro-[1,3]thiazolo[5,4-c]pyridin-2-yl)acetamide,hydrochloride

N-(4,5,6,7-tetrahydro-[1,3]thiazolo[5,4-c]pyridin-2-yl)acetamide,hydrochloride

C8H12ClN3OS (233.039)


   

1-METHYL-4-ETHYLFORMATE-5-PYRAZOLE-SULFONAMIDE

1-METHYL-4-ETHYLFORMATE-5-PYRAZOLE-SULFONAMIDE

C7H11N3O4S (233.047)


   

5-(2-Nitrophenyl)-2-furoic acid

5-(2-nitrophenyl)-2-furancarboxylic acid

C11H7NO5 (233.0324)


   

4-(1H-IMIDAZOL-1-YL)-3-NITROBENZOIC ACID

4-(1H-IMIDAZOL-1-YL)-3-NITROBENZOIC ACID

C10H7N3O4 (233.0437)


   

2-AMINO-6-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL HYDROCHLORIDE

2-AMINO-6-CHLORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL HYDROCHLORIDE

C10H13Cl2NO (233.0374)


   

4-Nitro-1-phenyl-1H-pyrazole-3-carboxylic acid

4-Nitro-1-phenyl-1H-pyrazole-3-carboxylic acid

C10H7N3O4 (233.0437)


   

N-(5-BUTYL-[1,3,4]THIADIAZOL-2-YL)-2-CHLORO-ACETAMIDE

N-(5-BUTYL-[1,3,4]THIADIAZOL-2-YL)-2-CHLORO-ACETAMIDE

C8H12ClN3OS (233.039)


   

Benzoic acid,2-[(2-aminoethyl)thio]-, hydrochloride (1:1)

Benzoic acid,2-[(2-aminoethyl)thio]-, hydrochloride (1:1)

C9H12ClNO2S (233.0277)


   

3-[(4-CHLOROPHENYL)METHOXY]-AZETIDINE HYDROCHLORIDE

3-[(4-CHLOROPHENYL)METHOXY]-AZETIDINE HYDROCHLORIDE

C10H13Cl2NO (233.0374)


   

5-(4-Carboxyphenyl)-1,2-oxazole-3-carboxylic acid

5-(4-Carboxyphenyl)-1,2-oxazole-3-carboxylic acid

C11H7NO5 (233.0324)


   

4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-ol,acetate,hydrochloride

4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-ol,acetate,hydrochloride

C9H12ClNO2S (233.0277)


   

2-ACETYL-4-NITROINDAN-1,3-DIONE

2-ACETYL-4-NITROINDAN-1,3-DIONE

C11H7NO5 (233.0324)


   
   

(S)-(-)-Dichlorophenyl amino alcohol

(S)-(-)-Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

1-[2-Nitro-4-(trifluoromethyl)phenyl]ethanone

1-[2-Nitro-4-(trifluoromethyl)phenyl]ethanone

C9H6F3NO3 (233.03)


   

6-methyl-8-nitro-4-oxochromene-3-carbaldehyde

6-methyl-8-nitro-4-oxochromene-3-carbaldehyde

C11H7NO5 (233.0324)


   

2-bromo-N-cyclopentylbutanamide

2-bromo-N-cyclopentylbutanamide

C9H16BrNO (233.0415)


   

5-(4-Nitrophenyl)-1H-pyrazole-3-carboxylic acid

5-(4-Nitrophenyl)-1H-pyrazole-3-carboxylic acid

C10H7N3O4 (233.0437)


   

5-(3-Nitrophenyl)-1H-pyrazole-3-carboxylic acid

5-(3-Nitrophenyl)-1H-pyrazole-3-carboxylic acid

C10H7N3O4 (233.0437)


   

4-Chloro-8-methoxy-5H-pyrimido[5,4-b]indole

4-Chloro-8-methoxy-5H-pyrimido[5,4-b]indole

C11H8ClN3O (233.0356)


   

5-(3-NITRO-PHENYL)-FURAN-2-CARBOXYLIC ACID

5-(3-NITRO-PHENYL)-FURAN-2-CARBOXYLIC ACID

C11H7NO5 (233.0324)


   

3-(4-nitrophenyl)-pyrazole-4-carboxylic acid

3-(4-nitrophenyl)-pyrazole-4-carboxylic acid

C10H7N3O4 (233.0437)


   

2-AMINO-1-(4-CHLORO-PHENYL)-5-OXO-4,5-DIHYDRO-1H-PYRROLE-3-CARBONITRILE

2-AMINO-1-(4-CHLORO-PHENYL)-5-OXO-4,5-DIHYDRO-1H-PYRROLE-3-CARBONITRILE

C11H8ClN3O (233.0356)


   

8-CHLORO-3-METHYL-2H-PYRAZOLO[4,3-C]QUINOLIN-4(5H)-ONE

8-CHLORO-3-METHYL-2H-PYRAZOLO[4,3-C]QUINOLIN-4(5H)-ONE

C11H8ClN3O (233.0356)


   

2-CHLORO-N-(5-ISOBUTYL-[1,3,4]THIADIAZOL-2-YL)-ACETAMIDE

2-CHLORO-N-(5-ISOBUTYL-[1,3,4]THIADIAZOL-2-YL)-ACETAMIDE

C8H12ClN3OS (233.039)


   

1,1-DIOXIDO-3,4-DIHYDRO-2H-THIOCHROMEN-4-YLAMINE HYDROCHLORIDE

1,1-DIOXIDO-3,4-DIHYDRO-2H-THIOCHROMEN-4-YLAMINE HYDROCHLORIDE

C9H12ClNO2S (233.0277)


   

N-Ethyl-3-fluorobenzylamine

N-Ethyl-3-fluorobenzylamine

C10H13Cl2NO (233.0374)


   

2-bromo-N-cyclohexylpropanamide

2-bromo-N-cyclohexylpropanamide

C9H16BrNO (233.0415)


   

2-(4-Chlorophenyl)morpholine hydrochloride (1:1)

2-(4-Chlorophenyl)morpholine hydrochloride (1:1)

C10H13Cl2NO (233.0374)


   

oxolinic acid impurity a

oxolinic acid impurity a

C11H7NO5 (233.0324)


   

4-Maleimidosalicylic acid

4-Maleimidosalicylic acid

C11H7NO5 (233.0324)


   

Morpholinium hexafluorophosphate

Morpholinium hexafluorophosphate

C4H10F6NOP (233.0404)


   

4-Aminoisothiochroman 2,2-dioxide hydrochloride

4-Aminoisothiochroman 2,2-dioxide hydrochloride

C9H12ClNO2S (233.0277)


   

5,6-DIHYDROXY-2-PYRIDIN-2-YL-PYRIMIDINE-4-CARBOXYLIC ACID

5,6-DIHYDROXY-2-PYRIDIN-2-YL-PYRIMIDINE-4-CARBOXYLIC ACID

C10H7N3O4 (233.0437)


   

BETA-NITRO-4-(TRIFLUOROMETHOXY)STYRENE

BETA-NITRO-4-(TRIFLUOROMETHOXY)STYRENE

C9H6F3NO3 (233.03)


   

dopamine β-sulfonate

dopamine β-sulfonate

C8H11NO5S (233.0358)


   

N-cyclopropyl-3,4-difluorobenzenesulfonaMide

N-cyclopropyl-3,4-difluorobenzenesulfonaMide

C9H9F2NO2S (233.0322)


   

5-(2-NITRO-PHENYL)-1H-PYRIMIDINE-2,4-DIONE

5-(2-NITRO-PHENYL)-1H-PYRIMIDINE-2,4-DIONE

C10H7N3O4 (233.0437)


   

tert-Butyl (5-chlorothiophen-2-yl)carbamate

tert-Butyl (5-chlorothiophen-2-yl)carbamate

C9H12ClNO2S (233.0277)


   
   

5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid

5-(dimethylsulfamoyl)-2-methylfuran-3-carboxylic acid

C8H11NO5S (233.0358)


   

2-BENZO[1,3]DIOXOL-5-YL-OXAZOLE-4-CARBOXYLIC ACID

2-BENZO[1,3]DIOXOL-5-YL-OXAZOLE-4-CARBOXYLIC ACID

C11H7NO5 (233.0324)


   

2-Chloro-10-methyl-3,4-diazaphenoxazine

2-Chloro-10-methyl-3,4-diazaphenoxazine

C11H8ClN3O (233.0356)


   

3-Nitro-4-(1H-pyrazol-1-yl)benzoic acid

3-Nitro-4-(1H-pyrazol-1-yl)benzoic acid

C10H7N3O4 (233.0437)


   

3-(2-Chlorophenoxy)pyrrolidine hydrochloride

3-(2-Chlorophenoxy)pyrrolidine hydrochloride

C10H13Cl2NO (233.0374)


   

(R)-(+)-Dichlorophenyl amino alcohol

(R)-(+)-Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

(5-HYDROXY-4,6-DIMETHYLPYRIDIN-3-YL)METHYL DIHYDROGEN PHOSPHATE

(5-HYDROXY-4,6-DIMETHYLPYRIDIN-3-YL)METHYL DIHYDROGEN PHOSPHATE

C8H12NO5P (233.0453)


   

3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide

3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide

C8H11NO5S (233.0358)


   

1-(3-Isocyanatophenyl)-5-(methylsulfanyl)-1H-tetrazole

1-(3-Isocyanatophenyl)-5-(methylsulfanyl)-1H-tetrazole

C9H7N5OS (233.0371)


   

L-Threonohydroxamate 4-phosphate

L-Threonohydroxamate 4-phosphate

C4H12NO8P (233.0301)


   

NSC-29870

5-Hydroxy-4,6-dimethyl-3-pyridinemethanol 3-(dihydrogen phosphate)

C8H12NO5P (233.0453)


   

5-(2-Azaniumylethyl)-2-hydroxyphenyl sulfate

5-(2-Azaniumylethyl)-2-hydroxyphenyl sulfate

C8H11NO5S (233.0358)


   

2-Hydroxybiphenyl-2-sulfinate

2-Hydroxybiphenyl-2-sulfinate

C12H9O3S- (233.0272)


   

Hexaketide pyrone

Hexaketide pyrone

C12H9O5- (233.045)


   

(2Z,4E)-2-hydroxy-6-oxo-6-phenoxyhexa-2,4-dienoate

(2Z,4E)-2-hydroxy-6-oxo-6-phenoxyhexa-2,4-dienoate

C12H9O5- (233.045)


   
   

4-(2-Azaniumylethyl)-2-hydroxyphenyl sulfate

4-(2-Azaniumylethyl)-2-hydroxyphenyl sulfate

C8H11NO5S (233.0358)


   

2-(4-Chlorophenyl)-5-(methylamino)-1,3-oxazole-4-carbonitrile

2-(4-Chlorophenyl)-5-(methylamino)-1,3-oxazole-4-carbonitrile

C11H8ClN3O (233.0356)


   

2-(2-Chlorophenyl)-5-(methylamino)-1,3-oxazole-4-carbonitrile

2-(2-Chlorophenyl)-5-(methylamino)-1,3-oxazole-4-carbonitrile

C11H8ClN3O (233.0356)


   

2-O,3-dimethylflaviolin-7-olate

2-O,3-dimethylflaviolin-7-olate

C12H9O5- (233.045)


An organic anion that is the conjugate base of 2-O,3-dimethylflaviolin, obtained by deprotonation of the 7-hydroxy group. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).

   

(2E,4Z)-2-hydroxy-6-(2-hydroxyphenyl)-6-oxohexa-2,4-dienoate

(2E,4Z)-2-hydroxy-6-(2-hydroxyphenyl)-6-oxohexa-2,4-dienoate

C12H9O5- (233.045)


   

Dopamine 3-sulfate

dopamine 3-O-sulfate

C8H11NO5S (233.0358)


An aryl sulfate that is dopamine in which the phenolic hydrogen at position 3 has been replaced by a sulfo group.

   

dopamine 3-O-sulfate zwitterion

dopamine 3-O-sulfate zwitterion

C8H11NO5S (233.0358)


A zwitterion obtained by transfer of a proton from the sulfonyl to the amino group of dopamine 3-O-sulfate; major species at pH 7.3.

   

dopamine 4-O-sulfate

dopamine 4-O-sulfate

C8H11NO5S (233.0358)


An aryl sulfate that is dopamine in which the phenolic hydrogen at position 4 has been replaced by a sulfo group.

   

dopamine 4-O-sulfate zwitterion

dopamine 4-O-sulfate zwitterion

C8H11NO5S (233.0358)


A zwitterion obtained by transfer of a proton from the sulfonyl to the amino group of dopamine 4-O-sulfate; major species at pH 7.3.

   

4-Deoxypyridoxine 5'-phosphate

4-Deoxypyridoxine 5'-phosphate

C8H12NO5P (233.0453)


   

Deoxy-pyridoxine phosphate

Deoxy-pyridoxine phosphate

C8H12NO5P (233.0453)


   

10-amino-9-chloro-2-methyl-2,7-diazatricyclo[6.3.1.0⁴,¹²]dodeca-1(12),3,5,7,9-pentaen-11-one

10-amino-9-chloro-2-methyl-2,7-diazatricyclo[6.3.1.0⁴,¹²]dodeca-1(12),3,5,7,9-pentaen-11-one

C11H8ClN3O (233.0356)


   

(5-hydroxy-4,6-dimethylpyridin-3-yl)methoxyphosphonic acid

(5-hydroxy-4,6-dimethylpyridin-3-yl)methoxyphosphonic acid

C8H12NO5P (233.0453)