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N-Methyl-N-(Methylbenzyl)Formamide
go.drugbank.com/drugs/DB04379ExperimentalCategories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP2E1 SubstratesSynonyms: N-Methyl-N-(Methylbenzyl)FormamideGlyphosate
go.drugbank.com/drugs/DB04539ExperimentalCategories: N-substituted Glycines, Compounds used in a research, industrial, or household settingAllosamidin
go.drugbank.com/drugs/DB04628ExperimentalAllosamidin exhibits extremely potent inhibitory activity against chitinases from a number of sources, particularly from <i>Candida albicans</i>, and can be utilized as potent antifungal agent.
Categories: Compounds used in a research, industrial, or household settingAtpenin A5
go.drugbank.com/drugs/DB04631ExperimentalSynonyms: 3-[(2S,4S,5R)-5,6-dichloro-2,4-dimethyl-1-oxohexyl]-4-hydroxy-5,6-dimethoxy-2(1H)-pyridinoneCategories: Heterocyclic Compounds, 1-RingCyclic 3',5'-thymidine monophosphate
go.drugbank.com/drugs/DB04672ExperimentalCategories: Heterocyclic Compounds, 1-RingSynonyms: 3',5'-Cyclic dTMP, Cyclic 3',5'-thymidine monophosphateMotuporin
go.drugbank.com/drugs/DB04738ExperimentalMotuporin is a toxin isolated from the marine sponge Thenonella swinhoie grey.
Synonyms: Nodularin VMyxothiazol
go.drugbank.com/drugs/DB04741ExperimentalSynonyms: Myxothiazol ACategories: Heterocyclic Compounds, 1-RingTagetitoxin
go.drugbank.com/drugs/DB04788ExperimentalTagetitoxin is a bacterial phytotoxin. It preferentially inhibits eukaryotic RNA polymerase.
Synonyms: (1R,4R,5R,6R,7S,8R)-6-Acetoxy-7-amino-4-carbamoyl-4-hydroxy-8-(phosphonooxy)-9-oxa-3-thiabicyclo[3.3.1]nonane-1-carboxylic acidBifonazole
go.drugbank.com/drugs/DB04794ApprovedBifonazole is an azole antifungal drug.
Mixtures: CANESTEN ULTRA UÑAS 1%Categories: Heterocyclic Compounds, 1-Ring, Cytochrome P-450 CYP2E1 Inhibitors