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Quinfamide
go.drugbank.com/drugs/DB12780InvestigationalQuinfamide has been used in trials studying the treatment of Amoebiasis and Helminthiasis.
Mixtures: L-OMBRIX-DUET, L-OMBRIX-DUETCategories: Heterocyclic Compounds, 2-RingAcetyldigitoxin
go.drugbank.com/drugs/DB00511ApprovedCardioactive derivative of lanatoside A or of digitoxin used for fast digitalization in congestive heart failure.
Synonyms: Desglucolanatoside A, Digitoxin 3'''-acetateCategories: Compounds used in a research, industrial, or household settingPrasugrel
go.drugbank.com/drugs/DB06209ApprovedInvestigationalPrasugrel, a thienopyridine derivative, is a platelet activation and aggregation inhibitor structurally and pharmacologically related to clopidogrel and ticlopidine. … As a result, inhibition of ADP-mediated platelet activation and aggregation occurs.
Categories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP2B6 SubstratesProducts: PRASUGREL AL 5MG HBR FTA, PRASUGREL AL 10MG HBR FTALithium cation
go.drugbank.com/drugs/DB01356ApprovedInvestigationalWithdrawnThe active principle in these salts is the lithium ion Li+, which having a smaller diameter, can easily displace K+ and Na+ and even Ca+2, in spite of its greater charge, occupying their sites in several … Lithium can also be used to augment other antidepressant drugs. It is also sometimes prescribed as a preventive treatment for migraine disease and cluster headaches.
Synonyms: LI, Li(+)Carbinoxamine
go.drugbank.com/drugs/DB00748ApprovedCarbinoxamine is a first generation antihistamine that competes with free histamine for binding at HA-receptor sites. … This antagonizes the effects of histamine on HA-receptors, leading to a reduction of the negative symptoms brought on by histamine HA-receptor binding.
Synonyms: 2-(p-chloro-α-(2-(dimethylamino)ethoxy)benzyl)pyridine, {2-[(4-Chloro-phenyl)-pyridin-2-yl-methoxy]-ethyl}-dimethyl-amineMixtures: PHILDEX 2Cannabidivarin
go.drugbank.com/drugs/DB14050Investigational, which is a member of a large family of ion channels that are involved in the onset and progression of several types of epilepsy. … Desensitization of these ion channels is a potential mechanism by which these molecules cause a reduction of neuronal hyperexcitability that contributes to epileptic activity and seizures.
Synonyms: 2-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-5-propylbenzene-1,3-diol, CBD-VTrimoprostil
go.drugbank.com/drugs/DB19935ExperimentalTrimoprostil has a monoisotopic molecular weight of 378.28 Da. … Trimoprostil is a small molecule drug. The usage of the INN stem '-prostil' in the name indicates that Trimoprostil is a anti-ulcer prostaglandin.
Categories: Prostaglandins EMarine collagen, soluble
go.drugbank.com/drugs/DB14246InvestigationalMarine collagen, soluble is an animal extract used in some OTC (over-the-counter) products. It is not an approved drug.
Mixtures: NutraVita MARINE COLLAGEN + ALA CapsuleDoxepin
go.drugbank.com/drugs/DB01142ApprovedInvestigational[T559] It is a tertiary amine that can be presented as (E) and (Z) stereoisomers with the (Z) stereoisomer corresponding to [cidoxepin]. Doxepin commonly produces a 5:1 (E):(Z) racemic mixture. … [T83] In a strict sense, doxepin is not a tricyclic antidepressant but it is commonly associated with the class since it shares a lot of properties with members of the drug family including [amitriptyline
Categories: P-glycoprotein substrates, Cytochrome P-450 SubstratesProducts: PURDOX %5 KREM, 30 G, EXPAN® 50 MGMeteneprost
go.drugbank.com/drugs/DB19692ExperimentalMeteneprost is a small molecule drug. Meteneprost has a monoisotopic molecular weight of 378.28 Da.
Categories: Prostaglandins E, Synthetic