About: Carbachol     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
http://linked.open...gbank/description
  • A slowly hydrolyzed cholinergic agonist that acts at both muscarinic and nicotinic receptors. [PubChem] (en)
http://linked.open...y/drugbank/dosage
http://linked.open...gy/drugbank/group
  • approved (en)
http://linked.open...ugbank/indication
  • Primarily used in the treatment of glaucoma, but is also used during ophthalmic surgery. (en)
http://linked.open...bank/manufacturer
sameAs
Title
  • Carbachol (en)
adms:identifier
http://linked.open...mechanismOfAction
  • Carbachol is a parasympathomimetic that stimulates both muscarinic and nicotinic receptors. In topical ocular and intraocular administration its principal effects are miosis and increased aqueous humour outflow. (en)
http://linked.open...drugbank/packager
http://linked.open.../drugbank/synonym
  • Carbachol chloride (en)
  • Choline carbamate chloride (en)
  • Choline chlorine carbamate (en)
  • Karbachol (en)
  • Karbamoylcholin chlorid (en)
  • (2-Carbamoyloxyethyl)trimethylammonium chloride (en)
  • (2-Hydroxyethyl)trimethylammonium chloride carbamate (en)
  • Carbacholum (en)
  • Carbacol (en)
  • Carbamylcholine (en)
  • Choline chloride, carbamate (en)
  • 2-((Aminocarbonyl)oxy)-N,N,N-trimethylethanaminum chloride (en)
  • (2-Hydroxyethyl)trimethyl ammonium chloride carbamate (en)
  • 2-((Aminocarbonyl)oxy)-N,N,N-trimethylethanaminium chloride (en)
http://linked.open...drugbank/toxicity
  • Oral, mouse: LD<sub>50</sub> = 15 mg/kg; Oral, rat: LD<sub>50</sub> = 40 mg/kg. (en)
http://linked.open.../drug/hasAHFSCode
http://linked.open...ynthesisReference
  • Major, R.T. and Bonnett, H.T.; U.S. Patent 2,374,367; April 24,1945; assigned to Merck & Co., Inc. (en)
foaf:page
http://linked.open...ugbank/IUPAC-Name
http://linked.open...gy/drugbank/InChI
http://linked.open...Molecular-Formula
http://linked.open.../Molecular-Weight
http://linked.open...noisotopic-Weight
http://linked.open...y/drugbank/SMILES
http://linked.open.../Water-Solubility
http://linked.open...ogy/drugbank/logP
http://linked.open...ogy/drugbank/logS
http://linked.open...l/drug/hasATCCode
http://linked.open...nd-Acceptor-Count
http://linked.open...-Bond-Donor-Count
http://linked.open...drugbank/InChIKey
http://linked.open...urface-Area--PSA-
http://linked.open...nk/Polarizability
http://linked.open...bank/Refractivity
http://linked.open...atable-Bond-Count
http://linked.open...ugbank/absorption
  • Not well absorbed in the gastro-intestinal tract, and does not cross the blood-brain barrier. (en)
http://linked.open.../affectedOrganism
  • Humans and other mammals (en)
http://linked.open...casRegistryNumber
  • 51-83-2 (en)
http://linked.open...drugbank/category
  • (en)
http://linked.open...gbank/containedIn
http://linked.open...k/Bioavailability
http://linked.open...bank/Ghose-Filter
http://linked.open...nk/MDDR-Like-Rule
http://linked.open...ank/Melting-Point
http://linked.open...k/Number-of-Rings
http://linked.open...siological-Charge
http://linked.open...bank/Rule-of-Five
http://linked.open...tional-IUPAC-Name
http://linked.open...strongest-acidic-
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