Exact Mass: 347.9837

Exact Mass Matches: 347.9837

Found 83 metabolites which its exact mass value is equals to given mass value 347.9837, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Pyrithiobac sodium

pyrithiobac-sodium

C13H10ClN2NaO4S (347.9947)

Formononetin 7-sulfate

[3-(4-Methoxyphenyl)-4-oxo-4H-chromen-7-yl]oxidanesulphonic acid

C16H12O7S (348.0304)

Daidzein sulfate

7-hydroxy-12-(4-hydroxyphenyl)-2,4,13-trioxa-3lambda6-thiatricyclo[7.3.1.0^{5,10}]trideca-1(12),5,7,9-tetraene-3,3,11-trione

C15H8O8S (347.994)

7-Methoxy-2-phenyl-3-sulfooxy-chromen-4-on|7-methoxy-2-phenyl-3-sulfooxy-chromen-4-one|rhamnocitrin 3-sulphate

C16H12O7S (348.0304)

4-Bromophenol glucuronide|4-bromophenyl beta-D-glucopyranosiduronic acid|O1-(4-Brom-phenyl)-beta-D-glucopyranuronsaeure|O1-(4-bromo-phenyl)-beta-D-glucopyranuronic acid

C12H13BrO7 (347.9845)

Dehydro-L-(+)-ascorbic acid dimer

C12H12O12 (348.0329)

Fenazepam

7-bromo-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

C15H10BrClN2O (347.9665)

Halocarban

Cloflucarban

C14H9Cl2F3N2O (348.0044)

C254 - Anti-Infective Agent > C28394 - Topical Anti-Infective Agent

2-(4-Bromophenyl)-3-phenylimidazo[1,2-a]pyridine

C19H13BrN2 (348.0262)

hexyl 2-hydroxy-5-iodobenzoate

C13H17IO3 (348.0222)

2-(4-Bromophenyl)-1-phenyl-1H-benzimidazole

C19H13BrN2 (348.0262)

2-(2-Fluoro-4-iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

C12H15BFIO2 (348.0194)

1-(2-bromonaphthalen-1-yl)naphthalen-2-ol

C20H13BrO (348.015)

Azumolene

C13H9BrN4O3 (347.9858)

C78281 - Agent Affecting Musculoskeletal System > C29696 - Muscle Relaxant

3-Amino-7-nitronaphthalene-1,5-disulfonic acid

C10H8N2O8S2 (347.9722)

Disodium 3-hydroxy-2,6-naphthalenedisulfonate

C10H6Na2O7S2 (347.935)

Methanone,(7-bromo-2,3-dihydro-1,4-benzodioxin-6-yl)(2-methoxyphenyl)-

C16H13BrO4 (347.9997)

1-Naphthol-3,6-disulfonic acid disodium salt

C10H6Na2O7S2 (347.935)

2,2,3,3,5,5,6,6-OCTAFLUORO-4,4-BIPHENYLDICARBONITRILE

C14F8N2 (347.9934)

1-(4-chloro-3-isocyanatobenzenesulfonyl)-1,2,3,4-tetrahydroquinoline

C16H13ClN2O3S (348.0335)

1,3-DIAMINO-4-(HEPTAFLUOROISOPROPYL)BENZENE DIHYDROCHLORIDE

C9H9Cl2F7N2 (348.0031)

2-((2,4-DIBROMOPHENOXY)METHYL)TETRAHYDRO-2H-PYRAN

C12H14Br2O2 (347.936)

4-Iodo-1-tosyl-1H-imidazole

C10H9IN2O2S (347.9429)

Dinatrium-8-hydroxynaphthalen-1,6-disulfonat

C10H6Na2O7S2 (347.935)

4,4-DIHYDROXYOCTAFLUORODIPHENYL MONOHYDRATE

C12H4F8O3 (348.0033)

3-O-Decyclopropyl Roflumilast

C13H8Cl2F2N2O3 (347.988)

dichlorobis(indenyl)titanium(iv)

C18H14Cl2Ti (347.9952)

Sorivudine

C11H13BrN2O6 (347.9957)

C471 - Enzyme Inhibitor > C2019 - Dihydropyrimidine Dehydrogenase Inhibitor D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C254 - Anti-Infective Agent > C281 - Antiviral Agent D004791 - Enzyme Inhibitors Sorivudine (BV-araU) is an orally active synthetic pyrimidine nucleoside antimetabolite agent. Sorivudine derives its antiviral activity from selective conversion by a specific thymidine kinase present in certain DNA viruses to nucleotides, which can in turn interfere with viral DNA synthesis[1].

Disodium 3-hydroxy-2,7-naphthalenedisulfonate

C10H6Na2O7S2 (347.935)

2-(3-Bromophenyl)-1-phenyl-1H-benzimidazole

C19H13BrN2 (348.0262)

4,6-Dichloro-5-(2-methoxyphenoxy)-2,2-bipyrimidine

C15H10Cl2N4O2 (348.0181)

1,2,3,4,5,6-Cyclohexanehexacarboxylic acid

C12H12O12 (348.0329)

Pifithrin-β (hydrobromide)

C16H17BrN2S (348.0296)

Pifithrin-β hydrobromide (PFT β hydrobromide) is a potent p53 inhibitor with an IC50 of 23 μM.

MMV665852

C13H8Cl4N2O (347.9391)

1-(4-Bromophenyl)-2-phenyl-1H-benzimidazole

C19H13BrN2 (348.0262)

2-[[(4-amino-2,5-dichlorophenyl)sulphonyl]amino]ethanesulphonic acid

C8H10Cl2N2O5S2 (347.9408)

6-bromo-4-chloro-2-(4-methoxyphenyl)quinazoline

C15H10BrClN2O (347.9665)

2-(N-Boc-methylamino)-5-iodo-3-methylpyridine

C12H17IN2O2 (348.0335)

Ethyl 4-(3-bromo-4-formylphenoxy)benzoate

C16H13BrO4 (347.9997)

3-iodo-2-phenylchromen-4-one

C15H9IO2 (347.9647)

4-AMINO-5-(4-CHLOROPHENYLSULFONYL)-2-(PROPYLTHIO)THIAZOLE

C12H13ClN2O2S3 (347.9828)

(1S,4S)-(+)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide

C12H18Br2N2 (347.9837)

Ethyl 4-butoxy-3-iodobenzoate

C13H17IO3 (348.0222)

disodium 7-hydroxynaphthalene-1,3-disulphonate

C10H6Na2O7S2 (347.935)

1-5-diamino-2-bromo-4,8-dihydroxyanthraquinone

C14H9BrN2O4 (347.9746)

3,6-Dichloro-2-hydroxybenzoic acid-13C6

C 13C6H2Cl2O3 (347.9381)

N-([3,5-BIS(TRIFLUOROMETHYL)BENZOYL]OXY)-2-CHLOROETHANIMIDAMIDE

C11H7ClF6N2O2 (348.01)

Palladium(II) benzoate

C14H10O4Pd (347.9614)

Disperse Blue 81

C14H9BrN2O4 (347.9746)

1-Piperazineethanol, 4-[(3-bromophenyl)sulfonyl]-

C12H17BrN2O3S (348.0143)

1-(phenylethynyl)-1l3-benzo[d][1,2]iodaoxol-3(1H)-one

C15H9IO2 (347.9647)

(Acetylacetonato)dicarbonyliridium (I)

C7H7IrO4 (347.9974)

Diethyl2,6-bis(methylthio)-4-oxo-4H-thiopyran-3,5-dicarboxylate

C13H16O5S3 (348.016)

1-Bromo-6-ferrocenylhexane 6-Ferrocenylhexyl bromide

C16H21BrFe (348.0176)

3-iodo-4-(oxan-4-yloxy)benzoic acid

C12H13IO4 (347.9859)

4-hexoxy-3-iodobenzoic acid

C13H17IO3 (348.0222)

Acetylcysteine magnesium

C10H16MgN2O6S2 (348.03)

Florpyrauxifen

C13H8Cl2F2N2O3 (347.988)

Nomega-phospho-D-lombricine

C6H14N4O9P2-2 (348.0236)

Formononetin 7-sulfate

C16H12O7S (348.0304)

(2,5-dichlorothiophen-3-yl)methyl N-(pyridin-3-ylmethyl)carbamodithioate

C12H10Cl2N2S3 (347.9383)

4-Chloro-6-[5-(4-ethoxyphenyl)-1,2,3-thiadiazol-4-yl]benzene-1,3-diol

C16H13ClN2O3S (348.0335)

5-[(3-chlorophenoxy)methyl]-N-(4-methyl-2-thiazolyl)-2-furancarboxamide

C16H13ClN2O3S (348.0335)

({6-[4-(Methylsulfanyl)phenyl]thieno[3,2-d]pyrimidin-4-yl}sulfanyl)acetic acid

C15H12N2O2S3 (348.0061)

3-(4-Bromoanilino)-1-(3-nitrophenyl)-1-propanone

C15H13BrN2O3 (348.0109)

N-phosphonato-L-lombricine(2-)

C6H14N4O9P2-2 (348.0236)

4,5-Dichloro-3-isothiazolecarboxylic acid [1-(2-furanylmethylamino)-1-oxopropan-2-yl] ester

C12H10Cl2N2O4S (347.9738)

pyrithiobac-sodium

C13H10ClN2NaO4S (347.9947)

COH-SR4

C13H8Cl4N2O (347.9391)

COH-SR4 is an AMPK activator. COH-SR4 shows potent anti-proliferative activities against leukemia, melanoma, breast and lung cancers. COH-SR4 inhibits adipocyte differentiation via AMPK activation. COH-SR4 can be used for the research of obesity and related metabolic disorders[1].