Exact Mass: 233.0453

Exact Mass Matches: 233.0453

Found 114 metabolites which its exact mass value is equals to given mass value 233.0453, 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).

   

Brassicanal B

2,3-dihydro-3-Hydroxy-3-methylthiazolo[3,2-a]indole-9-carboxaldehyde, 9ci

C12H11NO2S (233.051)


Brassicanal B is found in brassicas. Brassicanal B is an alkaloid from Chinese cabbage Brassica campestris ssp. pekinensis inoculated with Pseudomonas cichorii. Alkaloid from Chinese cabbage Brassica campestris sspecies pekinensis inoculated with Pseudomonas cichorii. Brassicanal B is found in brassicas.

   

Hydroxyaniline mustard

Hydroxyaniline mustard hydrochloride

C10H13Cl2NO (233.0374)


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

   

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid

C8H11NO7 (233.0535)


   

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)


   

2-Aminodiphenylsulfone

2-(Phenylsulfonyl)aniline

C12H11NO2S (233.051)


CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7924; ORIGINAL_PRECURSOR_SCAN_NO 7921 CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7962; ORIGINAL_PRECURSOR_SCAN_NO 7959 CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7964; ORIGINAL_PRECURSOR_SCAN_NO 7961 CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8002; ORIGINAL_PRECURSOR_SCAN_NO 7999 CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8006; ORIGINAL_PRECURSOR_SCAN_NO 8003 CONFIDENCE standard compound; INTERNAL_ID 477; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8013; ORIGINAL_PRECURSOR_SCAN_NO 8010

   

Benzenesulfonanilide

N-phenylbenzenesulphonamide

C12H11NO2S (233.051)


CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1060

   

1-(4-Bromobutyl)-2-piperidinone

1-(4-Bromobutyl)-2-piperidinone

C9H16BrNO (233.0415)


   

SCHEMBL17866754

SCHEMBL17866754

C12H11NO2S (233.051)


   

Aminodiphenylsulfone

2-(Phenylsulfonyl)aniline

C12H11NO2S (233.051)


CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1009

   
   

Brassicanal B

2,3-dihydro-3-Hydroxy-3-methylthiazolo[3,2-a]indole-9-carboxaldehyde, 9ci

C12H11NO2S (233.051)


   

2-(3-METHYLPHENYL)-1,3-THIAZOL-4-YL]ACETIC ACID

2-(3-METHYLPHENYL)-1,3-THIAZOL-4-YL]ACETIC ACID

C12H11NO2S (233.051)


   

Dichlorophenyl amino alcohol

Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

2-Thiophenecarboxamide,N-(3-methoxyphenyl)-

2-Thiophenecarboxamide,N-(3-methoxyphenyl)-

C12H11NO2S (233.051)


   

Furalazine

Furalazine

C9H7N5O3 (233.0549)


C254 - Anti-Infective Agent

   

2-Thiophenecarboxamide,N-(4-methoxyphenyl)-

2-Thiophenecarboxamide,N-(4-methoxyphenyl)-

C12H11NO2S (233.051)


   

Methyl 2-amino-5-phenylthiophene-3-carboxylate

Methyl 2-amino-5-phenylthiophene-3-carboxylate

C12H11NO2S (233.051)


   

2-(4-aminophenoxy)ethyl hydrogen sulphate

2-(4-aminophenoxy)ethyl hydrogen sulphate

C8H11NO5S (233.0358)


   

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)


   

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)


   

METHYL (4-PHENYL-1,3-THIAZOL-2-YL)ACETATE

METHYL (4-PHENYL-1,3-THIAZOL-2-YL)ACETATE

C12H11NO2S (233.051)


   

2-Amino-4-(difluoromethoxy)-5-methoxybenzoic acid

2-Amino-4-(difluoromethoxy)-5-methoxybenzoic acid

C9H9F2NO4 (233.05)


   

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

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

C10H7N3O4 (233.0437)


   

(6-methyl-1H-benzimidazol-2-yl)methanamine

(6-methyl-1H-benzimidazol-2-yl)methanamine

C9H13Cl2N3 (233.0486)


   

ETHYL 3-PHENYLISOTHIAZOLE-5-CARBOXYLATE

ETHYL 3-PHENYLISOTHIAZOLE-5-CARBOXYLATE

C12H11NO2S (233.051)


   

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)


   

(5-Methyl-2-phenylthiazole-4-yl)acetic acid

(5-Methyl-2-phenylthiazole-4-yl)acetic acid

C12H11NO2S (233.051)


   

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)


   

3-Pyridinecarboxylic acid, 1-(4-fluorophenyl)-1,2-dihydro-2-oxo-

3-Pyridinecarboxylic acid, 1-(4-fluorophenyl)-1,2-dihydro-2-oxo-

C12H8FNO3 (233.0488)


   

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

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

C10H13Cl2NO (233.0374)


   

acitazanolast

acitazanolast

C9H7N5O3 (233.0549)


C78273 - Agent Affecting Respiratory System > C29712 - Anti-asthmatic Agent

   

2-(4-FLUOROPHENOXY)NICOTINIC ACID

2-(4-FLUOROPHENOXY)NICOTINIC ACID

C12H8FNO3 (233.0488)


   

2-CHLORO-3-NITROTOLUENE

2-CHLORO-3-NITROTOLUENE

C12H11NO2S (233.051)


   
   

1-(4-fluorophenoxy)-2-nitrobenzene

1-(4-fluorophenoxy)-2-nitrobenzene

C12H8FNO3 (233.0488)


   

3-(2-METHYL-THIAZOL-4-YL)-BENZOIC ACID METHYL ESTER

3-(2-METHYL-THIAZOL-4-YL)-BENZOIC ACID METHYL ESTER

C12H11NO2S (233.051)


   

Ethyl 3-(1,3-thiazol-2-yl)benzoate

Ethyl 3-(1,3-thiazol-2-yl)benzoate

C12H11NO2S (233.051)


   

(S)-(-)-Dichlorophenyl amino alcohol

(S)-(-)-Dichlorophenyl amino alcohol

C10H13Cl2NO (233.0374)


   

4-(PHENYLSULFONYL)ANILINE

4-(PHENYLSULFONYL)ANILINE

C12H11NO2S (233.051)


   

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)


   

2-Methyl-4-phenyl-5-thiazoleacetic acid

2-Methyl-4-phenyl-5-thiazoleacetic acid

C12H11NO2S (233.051)


   

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)


   

ETHYL 4-PHENYLTHIAZOLE-2-CARBOXYLATE

ETHYL 4-PHENYLTHIAZOLE-2-CARBOXYLATE

C12H11NO2S (233.051)


   

Methyl 3-amino-5-phenyl-2-thiophenecarboxylate

Methyl 3-amino-5-phenyl-2-thiophenecarboxylate

C12H11NO2S (233.051)


   

N-Ethyl-3-fluorobenzylamine

N-Ethyl-3-fluorobenzylamine

C10H13Cl2NO (233.0374)


   

2-bromo-N-cyclohexylpropanamide

2-bromo-N-cyclohexylpropanamide

C9H16BrNO (233.0415)


   

Methyl 3-amino-4-phenylthiophene-2-carboxylate

Methyl 3-amino-4-phenylthiophene-2-carboxylate

C12H11NO2S (233.051)


   

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

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

C10H13Cl2NO (233.0374)


   

ethyl 3-amino-4,4,5,5,5-pentafluoropent-2-enoate

ethyl 3-amino-4,4,5,5,5-pentafluoropent-2-enoate

C7H8F5NO2 (233.0475)


   

2-fluoro-2-nitrodiphenyl ether

2-fluoro-2-nitrodiphenyl ether

C12H8FNO3 (233.0488)


   

Dimaprit dihydrochloride

Dimaprit dihydrochloride

C6H17Cl2N3S (233.052)


Dimaprit dihydrochloride is a selective histamine H2 receptor agonist, it also inhibits nNOS with an IC50 of 49 μM. Dimaprit dihydrochloride can stimulate gastric acid secretion[1][2].

   

Morpholinium hexafluorophosphate

Morpholinium hexafluorophosphate

C4H10F6NOP (233.0404)


   

4-Methyl-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid

4-Methyl-2-(4-methylphenyl)-1,3-thiazole-5-carboxylic acid

C12H11NO2S (233.051)


   

(3-(2,2,2-TRIFLUOROACETAMIDO)PHENYL)BORONIC ACID

(3-(2,2,2-TRIFLUOROACETAMIDO)PHENYL)BORONIC ACID

C8H7BF3NO3 (233.0471)


   

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)


   

Ethyl 2-phenyl-1,3-thiazole-4-carboxylate

Ethyl 2-phenyl-1,3-thiazole-4-carboxylate

C12H11NO2S (233.051)


   

dopamine β-sulfonate

dopamine β-sulfonate

C8H11NO5S (233.0358)


   

IMIDAZO[1,2-A]PYRIDIN-2-YLMETHYL-METHYL-AMINE DIHYDROCHLORIDE

IMIDAZO[1,2-A]PYRIDIN-2-YLMETHYL-METHYL-AMINE DIHYDROCHLORIDE

C9H13Cl2N3 (233.0486)


   

4-(N-(2-THIENYL)METHYL)AMINOBENZOIC ACID

4-(N-(2-THIENYL)METHYL)AMINOBENZOIC ACID

C12H11NO2S (233.051)


   

4-Methyl-2-phenyl-5-thiazoleacetic acid

4-Methyl-2-phenyl-5-thiazoleacetic acid

C12H11NO2S (233.051)


   

2-Borono-5-trifluoromethylbenzamide

2-Borono-5-trifluoromethylbenzamide

C8H7BF3NO3 (233.0471)


   

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

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

C10H7N3O4 (233.0437)


   

methyl 2-amino-4-phenylthiophene-3-carboxylate

methyl 2-amino-4-phenylthiophene-3-carboxylate

C12H11NO2S (233.051)


   
   

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

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

C8H11NO5S (233.0358)


   

METHYL 4-METHYL-2-PHENYLTHIAZOLE-5-CARBOXYLATE

METHYL 4-METHYL-2-PHENYLTHIAZOLE-5-CARBOXYLATE

C12H11NO2S (233.051)


   

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)


   

Chuangxinmycin

Chuangxinmycin

C12H11NO2S (233.051)


   

2-Acetylamino-4-hydroxy-6-formylpteridine

2-Acetylamino-4-hydroxy-6-formylpteridine

C9H7N5O3 (233.0549)


   

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

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

C9H7N5OS (233.0371)


   

2-[2-(2-Methylphenyl)-2-oxoethylidene]-1,3-thiazolidin-4-one

2-[2-(2-Methylphenyl)-2-oxoethylidene]-1,3-thiazolidin-4-one

C12H11NO2S (233.051)


   

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)


   

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)


   
   

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid

C8H11NO7 (233.0535)


   

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

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

C8H11NO5S (233.0358)


   

8-Prop-2-enylsulfonylquinoline

8-Prop-2-enylsulfonylquinoline

C12H11NO2S (233.051)


   

2-Ethyl-2H-naphtho[1,8-cd]isothiazole 1,1-dioxide

2-Ethyl-2H-naphtho[1,8-cd]isothiazole 1,1-dioxide

C12H11NO2S (233.051)


   

4-nitro-N-(1,2,4-triazol-4-yl)benzamide

4-nitro-N-(1,2,4-triazol-4-yl)benzamide

C9H7N5O3 (233.0549)


   

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.

   

(-)-chuangxinmycin

(-)-chuangxinmycin

C12H11NO2S (233.051)


A thiinoindole that is 3,5-dihydro-2H-thiino[4,3,2-cd]indole which is substituted at positions 2 and 3 by carboxy and methyl groups, respectively (the 2R,3S diastereoisomer).

   

4-Deoxypyridoxine 5'-phosphate

4-Deoxypyridoxine 5'-phosphate

C8H12NO5P (233.0453)


   

Deoxy-pyridoxine phosphate

Deoxy-pyridoxine phosphate

C8H12NO5P (233.0453)


   

(3s)-3-hydroxy-3-methyl-2h-[1,3]thiazolo[3,2-a]indole-9-carbaldehyde

(3s)-3-hydroxy-3-methyl-2h-[1,3]thiazolo[3,2-a]indole-9-carbaldehyde

C12H11NO2S (233.051)


   

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)