About: Levomethadyl Acetate Hydrochloride     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Levomethadyl Acetate Hydrochloride
rdfs:subClassOf
Has_Free_Acid_Or_Base_Form
Concept_In_Subset
Semantic_Type
  • Pharmacologic Substance
Preferred_Name
  • Levomethadyl Acetate Hydrochloride
UMLS_CUI
  • C0722317
CAS_Registry
  • 38821-43-1
  • 43033-72-3
FDA_UNII_Code
  • B54CW5KG52
Contributing_Source
  • FDA
Chemical_Formula
  • C23H31NO2.HCl
Legacy_Concept_Name
  • Levomethadyl_Acetate_Hydrochloride
FULL_SYN
  • Benzeneethanol, beta-(2-(dimethylamino)propyl)-alpha-ethyl-beta-phenyl-, Acetate(Ester)SNNCI
  • Levomethadyl Acetate HydrochloridePTNCI
  • 3-Heptanol, 6-(dimethylamino)-4,4-diphenyl-, Acetate (Ester), (3S,6S)-(-)-SNNCI
  • OrlaamBRNCI
  • l-Acetylmethadol HydrochlorideSYNCI
  • LEVOMETHADYL ACETATE HYDROCHLORIDEPTFDAB54CW5KG52
DEFINITION
  • The hydrochloride salt form of levomethadyl acetate, a synthetic mu-receptor agonist with analgesic activity. Levomethadyl acetate hydrochloride mimics the actions of endogenous peptides at CNS opioid receptors, including analgesia, euphoria, sedation, respiratory depression, miosis, bradycardia and physical dependence. Levomethadyl acetate hydrochloride has less severe withdrawal symptoms compared to the morphine-like agents. In addition, with chronic use, levomethadyl acetate hydrochloride produces cross-tolerance to the effects of other mu-receptor agonists, thereby decreasing the physical dependence.NCI
code
  • C47583
http://linked.open...y/mesh/hasConcept
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