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About: Cyclorphan

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

Cyclorphan is an opioid analgesic of the morphinan family that was never marketed. It acts as a μ-opioid receptor (MOR) weak partial agonist or antagonist, κ-opioid receptor (KOR) full agonist, and, to a much lesser extent, δ-opioid receptor (DOR) agonist (75-fold lower affinity relative to the KOR). The drug was first synthesized in 1964 by scientists at Research Corporation. In clinical trials, it had relatively long duration, good absorption, and provided strong pain relief but produced psychotomimetic effects via KOR activation, so its development was not continued.

Property Value
dbo:abstract
  • Cyclorphan is an opioid analgesic of the morphinan family that was never marketed. It acts as a μ-opioid receptor (MOR) weak partial agonist or antagonist, κ-opioid receptor (KOR) full agonist, and, to a much lesser extent, δ-opioid receptor (DOR) agonist (75-fold lower affinity relative to the KOR). The drug was first synthesized in 1964 by scientists at Research Corporation. In clinical trials, it had relatively long duration, good absorption, and provided strong pain relief but produced psychotomimetic effects via KOR activation, so its development was not continued. (en)
dbo:casNumber
  • 4163-15-9
dbo:chEMBL
  • 49269
dbo:fdaUniiCode
  • U6Z73N36V0
dbo:pubchem
  • 5359966
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  • 4163 (xsd:integer)
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  • 49269 (xsd:integer)
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  • 1.190000 (xsd:double)
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  • 27 (xsd:integer)
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  • -3 (xsd:integer)
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  • 1 (xsd:integer)
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  • 5359966 (xsd:integer)
dbp:smiles
  • Oc1ccc4c[C@@]25[C@H]CCCC5 (en)
dbp:unii
  • U6Z73N36V0 (en)
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rdfs:comment
  • Cyclorphan is an opioid analgesic of the morphinan family that was never marketed. It acts as a μ-opioid receptor (MOR) weak partial agonist or antagonist, κ-opioid receptor (KOR) full agonist, and, to a much lesser extent, δ-opioid receptor (DOR) agonist (75-fold lower affinity relative to the KOR). The drug was first synthesized in 1964 by scientists at Research Corporation. In clinical trials, it had relatively long duration, good absorption, and provided strong pain relief but produced psychotomimetic effects via KOR activation, so its development was not continued. (en)
rdfs:label
  • Cyclorphan (en)
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