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2-Deoxy-2-Amino Glucitol-6-Phosphate
go.drugbank.com/drugs/DB02445ExperimentalSynonyms: 2-Deoxy-2-Amino Glucitol-6-Phosphate2-deazo-6-thiophosphate guanosine-5'-monophosphate
go.drugbank.com/drugs/DB03146ExperimentalSynonyms: 2-deazo-6-thiophosphate guanosine-5'-monophosphate6-(2-phenoxyethoxy)-1,3,5-triazine-2,4-diamine
go.drugbank.com/drugs/DB08318ExperimentalSynonyms: 6-(2-phenoxyethoxy)-1,3,5-triazine-2,4-diamineAmpicillin
go.drugbank.com/drugs/DB00415ApprovedInvestigationalVet approvedAmpicillin is a semi-synthetic derivative of penicillin that functions as an orally active broad-spectrum antibiotic.
Mixtures: AMPİSİD 500 MG/250 MG IM ENJEKSİYONLUK TOZ, 1 ADET, AMPİSİD 1000 MG/500 MG IM ENJEKSİYONLUK TOZ, 1 ADETCategories: Penicillin G, Heterocyclic Compounds, 2-RingSotalol
go.drugbank.com/drugs/DB00489ApprovedInvestigationalSotalol is a methanesulfonanilide developed in 1960.[A178579] It was the first of the class III anti arrhythmic drugs.[A178579] Sotalol was first approved as an oral tablet on 30 October 1992. … [L6334] A racemic mixture of sotalol is currently formulated as a tablet, oral solution, and intravenous injection indicated for life threatening ventricular arrhythmias and maintaining normal sinus rhythm
Categories: Cytochrome P-450 CYP2D6 Substrates with a Narrow Therapeutic Index, Cytochrome P-450 SubstratesSynonyms: 4'-(1-hydroxy-2-(isopropylamino)ethyl)methane sulfonanilide, β-cardoneDefactinib
go.drugbank.com/drugs/DB12282ApprovedInvestigational[L53208,A273943] Defactinib was approved by the US FDA in May 2025 in a co-package alongside [avutometinib] (called Avmapki Fakzynja) for the treatment of recurrent KRAS-mutated low-grade serous ovarian … Defactinib is a small molecule kinase inhibitor targeted against focal adhesion kinase (FAK) and proline-rich tyrosine kinase-2 (Pyk2), the two members of the FAK family of nonreceptor tyrosine kinases
Synonyms: N-methyl-4-[[4-[[3-[methyl(methylsulfonyl)amino]pyrazin-2-yl]methylamino]-5-(trifluoromethyl)pyrimidin-2-yl]amino]benzamideCategories: MATE 2 Inhibitors, Cytochrome P-450 Substrates(2e)-N-Allyl-4-{[3-(4-Bromophenyl)-5-Fluoro-1-Methyl-1h-Indazol-6-Yl]Oxy}-N-Methyl-2-Buten-1-Amine
go.drugbank.com/drugs/DB02139ExperimentalSynonyms: (2e)-N-Allyl-4-{[3-(4-Bromophenyl)-5-Fluoro-1-Methyl-1h-Indazol-6-Yl]Oxy}-N-Methyl-2-Buten-1-AmineCilastatin
go.drugbank.com/drugs/DB01597ApprovedInvestigational[L7628] A newer triple-drug product was approved in July 2019 under the trade name Recarbrio which also contains [relebactam].[L4894] … Cilastatin is an inhibitor of renal dehydropeptidase, an enzyme responsible for both the metabolism of thienamycin beta-lactam antibiotics as well as conversion of leukotriene D4 to leukotriene E4.
Synonyms: (Z)-(S)-6-carboxy-6-[(S)-2,2-dimethylcyclopropanecarboxamido]hex-5-enyl-L-cysteine, (Z)-7-((R)-2-Amino-2-carboxy-ethylsulfanyl)-2-[((S)-2,2-dimethyl-cyclopropanecarbonyl)-amino]-hept-2-enoic acidMixtures: IMIPENEM E CILASTATINA SUN, IMIPENEM E CILASTATINA SUNBifonazole
go.drugbank.com/drugs/DB04794ApprovedBifonazole is an azole antifungal drug.
Synonyms: 1-(alpha-(4-Biphenylyl)benzyl)imidazole, 1-((4-Biphenylyl)phenylmethyl)-1H-imidazoleMixtures: CANESTEN ULTRA UÑAS 1%N-(4-carbamimidoylbenzyl)-1-(4-methylpentanoyl)-L-prolinamide
go.drugbank.com/drugs/DB06936ExperimentalSynonyms: N-(4-carbamimidoylbenzyl)-1-(4-methylpentanoyl)-L-prolinamide