Exact Mass: 233.0277

Exact Mass Matches: 233.0277

Found 86 metabolites which its exact mass value is equals to given mass value 233.0277, 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).

   

Aminobutane bisphosphonate

(1-amino-1-phosphonobutyl)phosphonic acid

C4H13NO6P2 (233.0218)


D050071 - Bone Density Conservation Agents > D004164 - Diphosphonates

   

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)


   

Adenine phosphate

Adenine phosphate

C5H8N5O4P (233.0314)


   

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

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

C11H7NO5 (233.0324)


   

6-(3-CHLOROPHENYL)PICOLINIC ACID

6-(3-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

4-(3-Chloropyridin-2-yl)benzoic acid

4-(3-Chloropyridin-2-yl)benzoic acid

C12H8ClNO2 (233.0244)


   

2-(2-Chlorophenyl)-isonicotinic acid

2-(2-Chlorophenyl)-isonicotinic acid

C12H8ClNO2 (233.0244)


   

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)


   

6-(3-CHLOROPHENYL)NICOTINIC ACID

6-(3-CHLOROPHENYL)NICOTINIC ACID

C12H8ClNO2 (233.0244)


   

1H-Isoindole-1,3(2H)-dione,2-(4-chloro-2-butyn-1-yl)-

1H-Isoindole-1,3(2H)-dione,2-(4-chloro-2-butyn-1-yl)-

C12H8ClNO2 (233.0244)


   

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

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

C11H7NO5 (233.0324)


   

4-(4-CHLOROPHENYL)PICOLINIC ACID

4-(4-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

6-(2-CHLOROPHENYL)PICOLINIC ACID

6-(2-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

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

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

C11H7NO5 (233.0324)


   

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-(PYRID-2-YLOXY)BENZOYL CHLORIDE

4-(PYRID-2-YLOXY)BENZOYL CHLORIDE

C12H8ClNO2 (233.0244)


   

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)


   

3-(4-CHLOROPHENYL)PICOLINIC ACID

3-(4-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

o-chlorophenolindophenol

o-chlorophenolindophenol

C12H8ClNO2 (233.0244)


   

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

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

C11H7NO5 (233.0324)


   

5-(4-Chlorophenyl)nicotinic acid

5-(4-Chlorophenyl)nicotinic acid

C12H8ClNO2 (233.0244)


   

(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)


   

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)


   

Adenine hemisulfate

Adenine hemisulfate

C5H7N5O4S (233.0219)


   

2-CHLORO-6-PHENYLNICOTINIC ACID

2-CHLORO-6-PHENYLNICOTINIC ACID

C12H8ClNO2 (233.0244)


   

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)


   

6-(4-CHLOROPHENYL)NICOTINIC ACID

6-(4-CHLOROPHENYL)NICOTINIC ACID

C12H8ClNO2 (233.0244)


   

5-(3-CHLOROPHENYL)PICOLINIC ACID

5-(3-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

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)


   

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)


   

1-chloro-4-(2-nitrophenyl)benzene

1-chloro-4-(2-nitrophenyl)benzene

C12H8ClNO2 (233.0244)


   

2-phenoxypyridine-3-carbonyl chloride

2-phenoxypyridine-3-carbonyl chloride

C12H8ClNO2 (233.0244)


   

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

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

C10H13Cl2NO (233.0374)


   

2-(3-chlorophenyl)pyridine-4-carboxylic acid

2-(3-chlorophenyl)pyridine-4-carboxylic acid

C12H8ClNO2 (233.0244)


   

oxolinic acid impurity a

oxolinic acid impurity a

C11H7NO5 (233.0324)


   

4-Maleimidosalicylic acid

4-Maleimidosalicylic acid

C11H7NO5 (233.0324)


   

4-Aminoisothiochroman 2,2-dioxide hydrochloride

4-Aminoisothiochroman 2,2-dioxide hydrochloride

C9H12ClNO2S (233.0277)


   

6-phenoxynicotinoyl chloride

6-phenoxynicotinoyl chloride

C12H8ClNO2 (233.0244)


   

3-(8-chloroquinoline-4-yl)acrylic acid

3-(8-chloroquinoline-4-yl)acrylic acid

C12H8ClNO2 (233.0244)


   

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)


   

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

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

C9H12ClNO2S (233.0277)


   
   

2-phenoxybenzoyl chloride

2-phenoxybenzoyl chloride

C12H8ClNO2 (233.0244)


   

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

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

C8H11NO5S (233.0358)


   

5-(2-CHLOROPHENYL)NICOTINIC ACID

5-(2-CHLOROPHENYL)NICOTINIC ACID

C12H8ClNO2 (233.0244)


   

5-(2-CHLOROPHENYL)PICOLINIC ACID

5-(2-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

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-(2-Chlorophenoxy)pyrrolidine hydrochloride

3-(2-Chlorophenoxy)pyrrolidine hydrochloride

C10H13Cl2NO (233.0374)


   

(R)-(+)-Dichlorophenyl amino alcohol

(R)-(+)-Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

6-(4-CHLOROPHENYL)PICOLINIC ACID

6-(4-CHLOROPHENYL)PICOLINIC ACID

C12H8ClNO2 (233.0244)


   

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)


   

5-Methyl-7-(trifluoromethyl)-[1,3]thiazolo[4,5-b]pyridin-2-amine

5-Methyl-7-(trifluoromethyl)-[1,3]thiazolo[4,5-b]pyridin-2-amine

C8H6F3N3S (233.0235)


   

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)


   

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)


   

Npi-phospho-L-histidine

Npi-phospho-L-histidine

C6H8N3O5P-2 (233.0202)


   

Ntau-phospho-L-histidine

Ntau-phospho-L-histidine

C6H8N3O5P-2 (233.0202)


   

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)


   

Pyridin-3-yl 4-chlorobenzoate

Pyridin-3-yl 4-chlorobenzoate

C12H8ClNO2 (233.0244)


   

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.

   

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)