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About: MT-45

An Entity of Type: chemical substance, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

MT-45 (IC-6) is an opioid analgesic drug invented in the 1970s by Dainippon Pharmaceutical Co. It is chemically a 1-substituted-4-(1,2-diphenylethyl)piperazine derivative, which is structurally unrelated to most other opioid drugs. Racemic MT-45 has around 80% the potency of morphine, with almost all opioid activity residing in the (S) enantiomer (the opposite stereochemistry from the related drug lefetamine). It has been used as a lead compound from which a large family of potent opioid drugs have been developed, including full agonists, partial agonists, and antagonists at the three main opioid receptor subtypes. Fluorinated derivatives of MT-45 such as 2F-MT-45 are significantly more potent as μ-opioid receptor agonists, and one of its main metabolites 1,2-diphenylethylpiperazine also b

Property Value
dbo:abstract
  • MT-45 (IC-6) is an opioid analgesic drug invented in the 1970s by Dainippon Pharmaceutical Co. It is chemically a 1-substituted-4-(1,2-diphenylethyl)piperazine derivative, which is structurally unrelated to most other opioid drugs. Racemic MT-45 has around 80% the potency of morphine, with almost all opioid activity residing in the (S) enantiomer (the opposite stereochemistry from the related drug lefetamine). It has been used as a lead compound from which a large family of potent opioid drugs have been developed, including full agonists, partial agonists, and antagonists at the three main opioid receptor subtypes. Fluorinated derivatives of MT-45 such as 2F-MT-45 are significantly more potent as μ-opioid receptor agonists, and one of its main metabolites 1,2-diphenylethylpiperazine also blocks NMDA receptors. (en)
dbo:casNumber
  • 52694-52-7 (S) enantiomer
  • 52694-55-0
dbo:fdaUniiCode
  • Q2640DPW33
dbo:pubchem
  • 431865
dbo:thumbnail
dbo:wikiPageExternalLink
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  • 31291294 (xsd:integer)
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  • 11801 (xsd:nonNegativeInteger)
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  • 1086155690 (xsd:integer)
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dbp:atcPrefix
  • None (en)
dbp:c
  • 24 (xsd:integer)
dbp:casNumber
  • 52694 (xsd:integer)
dbp:casSupplemental
  • 52694 (xsd:integer)
dbp:chemspiderid
  • 381935 (xsd:integer)
dbp:h
  • 32 (xsd:integer)
dbp:iupacName
  • 1 (xsd:integer)
dbp:legalDe
  • Anlage II (en)
dbp:legalUk
  • Class A (en)
dbp:legalUs
  • Schedule I (en)
dbp:n
  • 2 (xsd:integer)
dbp:pubchem
  • 431865 (xsd:integer)
dbp:routesOfAdministration
dbp:smiles
  • c3ccccc3CCNCCN1C4CCCCC4 (en)
dbp:stdinchi
  • 1 (xsd:integer)
dbp:stdinchikey
  • IGBRRSIHEGCUEN-UHFFFAOYSA-N (en)
dbp:synonyms
  • MT-45, IC-6 (en)
dbp:unii
  • Q2640DPW33 (en)
dbp:verifiedfields
  • changed (en)
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  • 451607504 (xsd:integer)
dbp:watchedfields
  • changed (en)
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  • 180 (xsd:integer)
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rdfs:comment
  • MT-45 (IC-6) is an opioid analgesic drug invented in the 1970s by Dainippon Pharmaceutical Co. It is chemically a 1-substituted-4-(1,2-diphenylethyl)piperazine derivative, which is structurally unrelated to most other opioid drugs. Racemic MT-45 has around 80% the potency of morphine, with almost all opioid activity residing in the (S) enantiomer (the opposite stereochemistry from the related drug lefetamine). It has been used as a lead compound from which a large family of potent opioid drugs have been developed, including full agonists, partial agonists, and antagonists at the three main opioid receptor subtypes. Fluorinated derivatives of MT-45 such as 2F-MT-45 are significantly more potent as μ-opioid receptor agonists, and one of its main metabolites 1,2-diphenylethylpiperazine also b (en)
rdfs:label
  • MT-45 (en)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
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