Exact Mass: 270.0168

Exact Mass Matches: 270.0168

Found 73 metabolites which its exact mass value is equals to given mass value 270.0168, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Sulfamethizole

4-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzene-1-sulfonamide

C9H10N4O2S2 (270.0245)


Sulfamethizole is only found in individuals that have used or taken this drug. It is a sulfathiazole antibacterial agent. Sulfamethizole is a competitive inhibitor of bacterial enzyme dihydropteroate synthetase. The normal para-aminobenzoic acid (PABA) substrate is prevented from binding. The inhibited reaction is necessary in these organisms for the synthesis of folic acid. D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BA - Sulfonamides J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01E - Sulfonamides and trimethoprim > J01EB - Short-acting sulfonamides B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05C - Irrigating solutions > B05CA - Antiinfectives S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives > S01AB - Sulfonamides C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013432 - Sulfathiazoles D000890 - Anti-Infective Agents > D013424 - Sulfanilamides CONFIDENCE standard compound; INTERNAL_ID 1017

   

3,5-Dinitro-4-hydroxyphenylpyruvate

3,5-dinitro-4-hydroxyphenylpyruvic acid

C9H6N2O8 (270.0124)


   

Selenocystathionine

(2S)-2-amino-4-{[(2R)-2-amino-2-carboxyethyl]selanyl}butanoic acid

C7H14N2O4Se (270.0119)


Selenocystathionine (CAS: 2196-58-9), also known as SeCysta, belongs to the class of organic compounds known as alpha-amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). Selenocystathionine is a very strong basic compound (based on its pKa). Selenocystathionine participates in a number of enzymatic reactions. In particular, selenocystathionine can be converted into selenocysteine and 2-ketobutyric acid through the action of the enzyme cystathionine gamma-lyase. Selenocystathionine is formed from selenohomocysteine by the enzyme cystathionine beta-synthase (EC 4.2.1.22) as a by-product of cystathionine synthesis. Selenocystathionine is consumed in the diet and is one of the main compounds present in plants that tend to hyperaccumulate selenium for use as an elemental plant defence mechanism (PMID: 10026151, 6456763, 16920881). Selenocystathionine is formed from Selenohomocysteine by the enzyme cystathionine beta-synthase (EC 4.2.1.22), as a by-product of cystathionine synthesis. Selenocystathionine is consumed in the diet, and is one of the main compounds present in plants that tend to hyperaccumulate selenium and use it as an elemental plant defense mechanism. (PMID: 10026151, 6456763, 16920881) [HMDB]

   

Nasutin A

6,13-dihydroxy-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione

C14H6O6 (270.0164)


   

NBD-COCl

2-[methyl(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]acetyl chloride

C9H7ClN4O4 (270.0156)


   

Nasutin A

Nasutin A

C14H6O6 (270.0164)


   

itolide B

itolide B

C14H6O6 (270.0164)


   

sulfamethizole

Sulfamethizole (Proklar)

C9H10N4O2S2 (270.0245)


D - Dermatologicals > D06 - Antibiotics and chemotherapeutics for dermatological use > D06B - Chemotherapeutics for topical use > D06BA - Sulfonamides J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01E - Sulfonamides and trimethoprim > J01EB - Short-acting sulfonamides B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05C - Irrigating solutions > B05CA - Antiinfectives A sulfonamide consisting of a 1,3,4-thiadiazole nucleus with a methyl substituent at C-5 and a 4-aminobenzenesulfonamido group at C-2. S - Sensory organs > S01 - Ophthalmologicals > S01A - Antiinfectives > S01AB - Sulfonamides C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013432 - Sulfathiazoles D000890 - Anti-Infective Agents > D013424 - Sulfanilamides

   

tert-Butyl 4-(bromomethyl)benzoate

4-(bromomethyl)-benzoic acid, 1,1-dimethylethyl ester

C12H15BrO2 (270.0255)


   

2-CHLORO-N-(6-ETHOXY-BENZOTHIAZOL-2-YL)-ACETAMIDE

2-CHLORO-N-(6-ETHOXY-BENZOTHIAZOL-2-YL)-ACETAMIDE

C11H11ClN2O2S (270.023)


   

ETHYL 5-HYDROXY-2-METHYLSULFANYL-THIENO[2,3-D]PYRIMIDINE-6-CARBOXYLATE

ETHYL 5-HYDROXY-2-METHYLSULFANYL-THIENO[2,3-D]PYRIMIDINE-6-CARBOXYLATE

C10H10N2O3S2 (270.0133)


   

2-{[(4-Chlorophenyl)sulfanyl]methyl}-1,4-difluorobenzene

2-{[(4-Chlorophenyl)sulfanyl]methyl}-1,4-difluorobenzene

C13H9ClF2S (270.0082)


   

5-Bromo-1-butyl-6-fluoro-1H-benzo[d]imidazole

5-Bromo-1-butyl-6-fluoro-1H-benzo[d]imidazole

C11H12BrFN2 (270.0168)


   

5-Bromo-2-(3-methylbutoxy)benzaldehyde

5-Bromo-2-(3-methylbutoxy)benzaldehyde

C12H15BrO2 (270.0255)


   

tert-butyl 4-bromo-3-methylbenzoate

tert-butyl 4-bromo-3-methylbenzoate

C12H15BrO2 (270.0255)


   

2-hydroxy-6-(2-thienyl)-4-(trifluoromethyl)nicotinonitrile

2-hydroxy-6-(2-thienyl)-4-(trifluoromethyl)nicotinonitrile

C11H5F3N2OS (270.0075)


   

Anthraquinone-2-carbonyl Chloride

Anthraquinone-2-carbonyl Chloride

C15H7ClO3 (270.0084)


   

Ethyl 4-(4-bromophenyl)butanoate

Ethyl 4-(4-bromophenyl)butanoate

C12H15BrO2 (270.0255)


   

TRICHLORO-((E)-3,7-DIMETHYL-OCTA-2,6-DIENYL)-SILANE

TRICHLORO-((E)-3,7-DIMETHYL-OCTA-2,6-DIENYL)-SILANE

C10H17Cl3Si (270.0165)


   

Tert-butyl 3-(bromomethyl)benzoate

Tert-butyl 3-(bromomethyl)benzoate

C12H15BrO2 (270.0255)


   

6-(2,6-Dichlorophenoxy)-pyrimidine-2,4-diamine

6-(2,6-Dichlorophenoxy)-pyrimidine-2,4-diamine

C10H8Cl2N4O (270.0075)


   

Methyl 3-bromo-5-tert-butylbenzoate

Methyl 3-bromo-5-tert-butylbenzoate

C12H15BrO2 (270.0255)


   

4-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)BENZENESULFONYL CHLORIDE

4-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)BENZENESULFONYL CHLORIDE

C11H11ClN2O2S (270.023)


   

2-Phosphonobutane-1,2,4-tricarboxylic acid

2-Phosphonobutane-1,2,4-tricarboxylic acid

C7H11O9P (270.0141)


   

methyl 3-bromo-4-(tert-butyl)benzoate

methyl 3-bromo-4-(tert-butyl)benzoate

C12H15BrO2 (270.0255)


   

4-isocyanato-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole

4-isocyanato-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole

C11H5F3N2OS (270.0075)


   

benzyl 5-bromopentanoate

benzyl 5-bromopentanoate

C12H15BrO2 (270.0255)


   

2,4-Cyclopentadien-1-ylthallium

2,4-Cyclopentadien-1-ylthallium

C5H5Tl (270.0135)


   

4-[4-(bromomethyl)phenoxy]oxane

4-[4-(bromomethyl)phenoxy]oxane

C12H15BrO2 (270.0255)


   

ethyl 4-bromo-4-phenyl-butanoate

ethyl 4-bromo-4-phenyl-butanoate

C12H15BrO2 (270.0255)


   

2-((4-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

2-((4-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

C12H15BrO2 (270.0255)


   

4-((3-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

4-((3-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

C12H15BrO2 (270.0255)


   

4-((4-Bromophenoxy)methyl)tetrahydro-2H-pyran

4-((4-Bromophenoxy)methyl)tetrahydro-2H-pyran

C12H15BrO2 (270.0255)


   

4-BROMO-2-(CYCLOPENTYLOXY)-1-METHOXYBENZENE

4-BROMO-2-(CYCLOPENTYLOXY)-1-METHOXYBENZENE

C12H15BrO2 (270.0255)


   

2-(4-Chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile

2-(4-Chlorophenyl)-5-(trifluoromethyl)-1H-pyrrole-3-carbonitrile

C12H6ClF3N2 (270.0172)


   

3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-SULFONYL CHLORIDE

3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-SULFONYL CHLORIDE

C11H11ClN2O2S (270.023)


   

2-((3-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

2-((3-BROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

C12H15BrO2 (270.0255)


   

methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate

methyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate

C11H11ClN2O2S (270.023)


   

6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole

6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole

C11H12BrFN2 (270.0168)


   

6-(5-amino-2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine

6-(5-amino-2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine

C9H8Cl2N6 (270.0187)


   

4-Ethoxynaphthalene-1-sulfonyl chloride

4-Ethoxynaphthalene-1-sulfonyl chloride

C12H11ClO3S (270.0117)


   

2-BROMO-1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE

2-BROMO-1-(4-HYDROXYMETHYL-PHENYL)-PENTAN-1-ONE

C12H15BrO2 (270.0255)


   

2-BROMO-1-(4-METHOXY-PHENYL)-PENTAN-1-ONE

2-BROMO-1-(4-METHOXY-PHENYL)-PENTAN-1-ONE

C12H15BrO2 (270.0255)


   

methyl (2Z,4Z)-5-chloro-2-(chloromethyl)-5-phenylpenta-2,4-dienoate

methyl (2Z,4Z)-5-chloro-2-(chloromethyl)-5-phenylpenta-2,4-dienoate

C13H12Cl2O2 (270.0214)


   

N-(2-methylbenzothiazol-5-yl)sulfonylacetamide

N-(2-methylbenzothiazol-5-yl)sulfonylacetamide

C10H10N2O3S2 (270.0133)


   

(2Z)-2-dimethoxyphosphinothioyloxyimino-2-phenyl-acetonitrile

(2Z)-2-dimethoxyphosphinothioyloxyimino-2-phenyl-acetonitrile

C10H11N2O3PS (270.0228)


   

Methyl 3-bromo-4-butylbenzoate

Methyl 3-bromo-4-butylbenzoate

C12H15BrO2 (270.0255)


   

ethyl 3-bromo-4-propan-2-ylbenzoate

ethyl 3-bromo-4-propan-2-ylbenzoate

C12H15BrO2 (270.0255)


   

7-chloro-6-fluoro-1-(methylamino)-4-oxoquinoline-3-carboxylic acid

7-chloro-6-fluoro-1-(methylamino)-4-oxoquinoline-3-carboxylic acid

C11H8ClFN2O3 (270.0207)


   

3,4,5-Trimethoxybenzenesulfonic acid sodium salt

3,4,5-Trimethoxybenzenesulfonic acid sodium salt

C9H11NaO6S (270.0174)


   

IMIBENCONAZOLE-DEBENZYL

IMIBENCONAZOLE-DEBENZYL

C10H8Cl2N4O (270.0075)


   

2-(4-(2-broMoethyl)phenyl)-2-Methylpropanoic acid

2-(4-(2-broMoethyl)phenyl)-2-Methylpropanoic acid

C12H15BrO2 (270.0255)


   

5-Bromo-1-(tert-butyl)-6-fluoro-1H-benzo[d]imidazole

5-Bromo-1-(tert-butyl)-6-fluoro-1H-benzo[d]imidazole

C11H12BrFN2 (270.0168)


   

7-ethoxynaphthalene-2-sulfonyl chloride

7-ethoxynaphthalene-2-sulfonyl chloride

C12H11ClO3S (270.0117)


   

(4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE

(4H-BENZO[D][1,3]THIAZIN-2-YL)-PHENYL-AMINE

C10H10N2O3S2 (270.0133)


   

4-[2-(bromomethyl)phenoxy]oxane

4-[2-(bromomethyl)phenoxy]oxane

C12H15BrO2 (270.0255)


   
   

3-Bromo-4-pentylbenzoic acid

3-Bromo-4-pentylbenzoic acid

C12H15BrO2 (270.0255)


   

3-bromo-4-(2-methylbutan-2-yl)benzoic acid

3-bromo-4-(2-methylbutan-2-yl)benzoic acid

C12H15BrO2 (270.0255)


   

5-Thiophen-2-yl-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrimidine

5-Thiophen-2-yl-7-(trifluoromethyl)-[1,2,4]triazolo[1,5-a]pyrimidine

C10H5F3N4S (270.0187)


   

1-Benzenesulfonyl-5-fluorouracil

1-Benzenesulfonyl-5-fluorouracil

C10H7FN2O4S (270.0111)


   

2-[(4-Bromophenyl)methoxy]oxane

2-[(4-Bromophenyl)methoxy]oxane

C12H15BrO2 (270.0255)


   

(2S)-2-ammonio-4-{[(2R)-2-ammonio-2-carboxylatoethyl]selanyl}butanoate

(2S)-2-ammonio-4-{[(2R)-2-ammonio-2-carboxylatoethyl]selanyl}butanoate

C7H14N2O4Se (270.0119)


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5-Epi-valiolone 7-phosphate(2-)

5-Epi-valiolone 7-phosphate(2-)

C7H11O9P-2 (270.0141)


   

2-Epi-5-epi-valiolone 7-phosphate(2-)

2-Epi-5-epi-valiolone 7-phosphate(2-)

C7H11O9P-2 (270.0141)


   

2-(2,4-dichlorophenyl)-3,5-dihydro-1H-pyrazolo[3,4-d]triazol-6-amine

2-(2,4-dichlorophenyl)-3,5-dihydro-1H-pyrazolo[3,4-d]triazol-6-amine

C9H8Cl2N6 (270.0187)


   

L-Selenocystathionine

L-Selenocystathionine

C7H14N2O4Se (270.0119)


An optically active form of selenocystathionine in which both amino acid residues have L-configuration.

   

3,5-dinitro-4-hydroxyphenylpyruvic acid

3,5-dinitro-4-hydroxyphenylpyruvic acid

C9H6N2O8 (270.0124)


   

2-Epi-5-epi-valiolone 7-phosphate(2-)

2-Epi-5-epi-valiolone 7-phosphate(2-)

C7H11O9P (270.0141)


An organophosphate oxoanion obtained by deprotonation of the phosphate OH groups of 2-epi-5-epi-valiolone 7-phosphate; major species at pH 7.3.

   

Selenocystathionine

Selenocystathionine

C7H14N2O4Se (270.0119)


A member of the class of cystathionines derived from homoselenocysteine and serine residues joined by a selenide bond.

   

5-Epi-valiolone 7-phosphate(2-)

5-Epi-valiolone 7-phosphate(2-)

C7H11O9P (270.0141)


An organophosphate oxoanion obtained by deprotonation of the phosphate OH groups of 5-epi-valiolone 7-phosphate; major species at pH 7.3.

   

L-selenocystathionine zwitterion

L-selenocystathionine zwitterion

C7H14N2O4Se (270.0119)


An amino acid zwitterion arising from transfer of two protons from the carboxy to the amino groups of L-selenocystathionine; major species at pH 7.3.

   

Tebanicline (dihydrochloride)

Tebanicline (dihydrochloride)

C9H13Cl3N2O (270.0093)


Tebanicline dihydrochloride (Ebanicline dihydrochloride) is a nAChR modulator with potent, orally effective analgesic activity. It inhibits the binding of cytisine to α4β2 neuronal nAChRs with a Ki of 37 pM[1].