Exact Mass: 354.13616920000004

Exact Mass Matches: 354.13616920000004

Found 10 metabolites which its exact mass value is equals to given mass value 354.13616920000004, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Isofezolac

2-(1,3,4-triphenyl-1H-pyrazol-5-yl)acetic acid

C23H18N2O2 (354.13682079999995)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic

   

6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz-[b,e]azepine (PMDAP)

6-(Phthalimidomethyl)-6,11-dihydro-5H-dibenz-[b,e]azepine (PMDAP)

C23H18N2O2 (354.13682079999995)


   

1-Trityl-1H-imidazole-4-carboxylic acid

1-Trityl-1H-imidazole-4-carboxylic acid

C23H18N2O2 (354.13682079999995)


   

N-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-N-(2-ethoxycarbonylsulfanyl-4-hydroxy-1-methyl-but-1-enyl)-formamide

N-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-N-(2-ethoxycarbonylsulfanyl-4-hydroxy-1-methyl-but-1-enyl)-formamide

C15H22N4O4S (354.13616920000004)


   

2-Diphenylacetyl-1,3-indandione-1-hydrazone

2-Diphenylacetyl-1,3-indandione-1-hydrazone

C23H18N2O2 (354.13682079999995)


   

2-[[3-Methyl-7-(3-methylbutyl)-2,6-dioxo-8-purinyl]thio]propanoic acid methyl ester

2-[[3-Methyl-7-(3-methylbutyl)-2,6-dioxo-8-purinyl]thio]propanoic acid methyl ester

C15H22N4O4S (354.13616920000004)


   

Isofezolac

2-(2,4,5-triphenylpyrazol-3-yl)acetic acid

C23H18N2O2 (354.13682079999995)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic

   

ER-000444793

ER-000444793

C23H18N2O2 (354.13682079999995)


ER-000444793 is a potent inhibitor of mitochondrial permeability transition pore (mPTP) opening. ER-000444793 inhibits mPTP with an IC50 of 2.8?μM.

   

KI-7

KI-7

C23H18N2O2 (354.13682079999995)


KI-7 is an A2B adenosine receptor positive allosteric modulator. KI-7 potentiates the cAMP accumulation induced by the non-selective A2B adenosine receptor agonist NECA (EC50=445.8 nM). KI-7 also potentiates the cAMP accumulation induced by the selective A2B adenosine receptor agonist BAY 60-6583 as well as by adenosine with EC50s of 2390 nM and 2550 nM, respectively[1][2].