Search
Degenerative Joint Disease
go.drugbank.com/conditions/DBCOND0039319Drugs: MethylprednisoloneSynonyms: O/ASezary Syndrome
go.drugbank.com/conditions/DBCOND0001518Synonyms: Cutaneous T-cell lymphoma, no ICD-O subtypeSquamous Cell Carcinoma (SCC)
go.drugbank.com/conditions/DBCOND0043488Drugs: BleomycinSynonyms: Squamous cell carcinoma, no ICD-O subtypeSplinter
go.drugbank.com/conditions/DBCOND0015551Drugs: IchthammolSynonyms: Splinter in skin (disorder)Cytoplasmic tyrosine-protein kinase BMX
go.drugbank.com/bio_entities/BE0009416TargetHumansMay also play a role in the growth and differentiation of hematopoietic cells; as well as in signal transduction in endocardial and arterial endothelial cells … Plays a critical role in TNF-induced angiogenesis, and implicated in the signaling of TEK and FLT1 receptors, 2 important receptor families essential for angiogenesis.
Synonyms: Bone marrow tyrosine kinase gene in chromosome X proteinNepidermin
go.drugbank.com/drugs/DB14145InvestigationalMixtures: EASYDEW DW EGF Derma Oneshot AmpouleCategories: EGF Family of ProteinsGlutamic acid
go.drugbank.com/drugs/DB00142ApprovedInvestigationalNutraceuticalA peptide that is a homopolymer of glutamic acid.
Mixtures: Aminosyn II 7% M In 10% Dextrose(dual Chamber), Aminosyn II in DextroseSynonyms: (S)-2-Aminopentanedioic acid, L-GlutamateCobimetinib
go.drugbank.com/drugs/DB05239ApprovedInvestigationalIt has been approved in Switzerland and the US, in combination with vemurafenib for the treatment of patients with unresectable or metastatic BRAF V600 mutation-positive melanoma. … Cobimetinib is an orally active, potent and highly selective small molecule inhibiting mitogen-activated protein kinase kinase 1 (MAP2K1 or MEK1), and central components of the RAS/RAF/MEK/ERK signal transduction
Categories: P-glycoprotein substrates with a Narrow Therapeutic Index, Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic IndexProducts: COTELLIC® (COBIMETINIB) 20 MG TABLETAS RECUBIERTASTicagrelor
go.drugbank.com/drugs/DB08816ApprovedInvestigational[A2903] Unlike [clopidogrel], ticagrelor is not a prodrug.[A2903] It is marketed by Astra Zeneca as Brilinta in the US[L14201] and Brilique or Possia in the EU,[L14207]. … Ticagrelor, or AZD6140, was first described in the literature in 2003.[A204170,A2903] Ticagrelor is an ADP derivative developed for its P2Y<sub>12</sub> receptor antagonism.
Categories: P-glycoprotein inhibitors, P-glycoprotein substratesSynonyms: (1S,2S,3R,5S)-3-(7-((1R,2S)-2-(3,4-Difluorophenyl)cyclopropylamino)-5-(propylthio)-3H-(1,2,3)triazolo(4,5-d)pyrimidin-3-yl)-5-(2-hydroxyethoxy)cyclopentane-1,2-diolLysocardiolipin acyltransferase 1
go.drugbank.com/bio_entities/BE0015711EnzymeHumansExhibits acyl-CoA:lysocardiolipin acyltransferase (ALCAT) activity; catalyzes the reacylation of lyso-cardiolipin to cardiolipin (CL), a key step in CL remodeling (By similarity).
Synonyms: 1-acylglycerol-3-phosphate O-acyltransferase 8Function: 1-acylglycerol-3-phosphate O-acyltransferase activity