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Fidarestat
go.drugbank.com/drugs/DB02021ExperimentalSynonyms: (S,S)-fidarestatCategories: Heterocyclic Compounds, 1-Ring4-Hydroxy-1,2,5-oxadiazole-3-carboxylic acid
go.drugbank.com/drugs/DB02401ExperimentalCategories: Heterocyclic Compounds, 1-RingSynonyms: 4-Hydroxy-1,2,5-oxadiazole-3-carboxylic acidMethoxy arachidonyl fluorophosphonate
go.drugbank.com/drugs/DB02465ExperimentalMethoxy arachidonyl fluorophosphonate, commonly referred as MAFP, is an irreversible active site-directed enzyme inhibitor that inhibits nearly all serine hydrolases and serine proteases. It inhibits phospholipase A2 and fatty acid amide...
Categories: Phospholipases A, antagonists & inhibitors9-Methylguanine
go.drugbank.com/drugs/DB02489ExperimentalCategories: Cytochrome P-450 Substrates, Heterocyclic Compounds, 2-RingSynonyms: 9-MethylguanineMesoheme
go.drugbank.com/drugs/DB02577ExperimentalThe color-furnishing portion of hemoglobin. It is found free in tissues and as the prosthetic group in many hemeproteins.
Categories: Heterocyclic Compounds, 1-Ring, Heterocyclic Compounds with 4 or More RingsResveratrol
go.drugbank.com/drugs/DB02709InvestigationalResveratrol (3,5,4'-trihydroxystilbene) is a polyphenolic phytoalexin. It is a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. … It exists as cis-(Z) and trans-(E) isomers. The trans- form can undergo isomerisation to the cis- form when heated or exposed to ultraviolet irradiation. In a 2004 issue of Science, Dr.
Categories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP1A2 InducersSynonyms: (E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol, 5-[(E)-2-(4-hydroxyphenyl)vinyl]benzene-1,3-diolKabiramide C
go.drugbank.com/drugs/DB03616ExperimentalCategories: Heterocyclic Compounds, 1-RingSynonyms: Kabiramide CDibenzofuran-4,6-Dicarboxylic Acid
go.drugbank.com/drugs/DB03682ExperimentalCategories: Heterocyclic Compounds, 2-RingN-Ethyl-5'-Carboxamido Adenosine
go.drugbank.com/drugs/DB03719ExperimentalA stable adenosine A1 and A2 receptor agonist. Experimentally, it inhibits cAMP and cGMP phosphodiesterase activity. [PubChem]
Synonyms: N-Ethyl-5'-Carboxamido Adenosine