Chemical Formula: C23H18N2O2

Chemical Formula C23H18N2O2

Found 8 metabolite its formula value is C23H18N2O2

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)


   

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

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

C23H18N2O2 (354.13682079999995)


   

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].