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- BDPC abstract "BDPC (systematic name 4-(4-bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol; also known as bromadol) is a potent narcotic analgesic with a distinctive arylcyclohexylamine chemical structure. It was developed by Daniel Lednicer at Upjohn in the 1970s. Initial studies estimated that it was around 10,000 times the strength of morphine in animal models. However, later studies assigned a value of 504 times the potency of morphine for the more active trans-isomer. To date, it is unknown if this drug has been used by humans, however, it was seized along with three kilograms of acetylfentanyl in an April 25, 2013 police action in Montreal, Canada. Despite taking precautions, at least two officers became intoxicated due to handling the drugs.".
- BDPC atcPrefix "None".
- BDPC casNumber "77239-98-6".
- BDPC casSupplemental "70895-01-1 (HCl)".
- BDPC iupacName "4-(4-Bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol".
- BDPC pubchem "9887338".
- BDPC thumbnail Bromadol_Skeletal.png?width=300.
- BDPC wikiPageID "23906575".
- BDPC wikiPageLength "5967".
- BDPC wikiPageOutDegree "27".
- BDPC wikiPageRevisionID "684278114".
- BDPC wikiPageWikiLink Acetylfentanyl.
- BDPC wikiPageWikiLink Analgesic.
- BDPC wikiPageWikiLink André_Dreiding.
- BDPC wikiPageWikiLink Arene_substitution_pattern.
- BDPC wikiPageWikiLink Arylcyclohexylamine.
- BDPC wikiPageWikiLink Bromine.
- BDPC wikiPageWikiLink C-8813.
- BDPC wikiPageWikiLink Category:Amines.
- BDPC wikiPageWikiLink Category:Cyclohexanols.
- BDPC wikiPageWikiLink Category:Mu-opioid_agonists.
- BDPC wikiPageWikiLink Category:Organobromides.
- BDPC wikiPageWikiLink Category:Synthetic_opioids.
- BDPC wikiPageWikiLink Cebranopadol.
- BDPC wikiPageWikiLink Chemical_structure.
- BDPC wikiPageWikiLink Ciramadol.
- BDPC wikiPageWikiLink Faxeladol.
- BDPC wikiPageWikiLink Hydrochloride.
- BDPC wikiPageWikiLink Methyl_group.
- BDPC wikiPageWikiLink Morphine.
- BDPC wikiPageWikiLink Narcotic.
- BDPC wikiPageWikiLink Pethidine.
- BDPC wikiPageWikiLink Profadol.
- BDPC wikiPageWikiLink Structure–activity_relationship.
- BDPC wikiPageWikiLink Tapentadol.
- BDPC wikiPageWikiLink Tramadol.
- BDPC wikiPageWikiLink File:4-(4-bromophenyl)-4-(dimethylamino)cyclohexan-1-one.png.
- BDPC wikiPageWikiLink File:4-(4-methylphenyl)-4-(dimethylamino)cyclohexan-1-one.png.
- BDPC wikiPageWikiLinkText "BDPC".
- BDPC atcPrefix "None".
- BDPC br "1".
- BDPC c "22".
- BDPC casNumber "77239".
- BDPC casSupplemental "70895".
- BDPC chemspiderid "26001358".
- BDPC h "28".
- BDPC iupacName "4".
- BDPC meltingHigh "210".
- BDPC meltingPoint "208".
- BDPC molecularWeight "402.37".
- BDPC n "1".
- BDPC o "1".
- BDPC pubchem "9887338".
- BDPC smiles "BrC1=CC=C[C@]2CC[C@@]CCC3=CC=CC=C3".
- BDPC stdinchi "1".
- BDPC stdinchikey "PRSUTWWKYIVBEU-HZCBDIJESA-N".
- BDPC verifiedrevid "451567905".
- BDPC watchedfields "changed".
- BDPC width "200".
- BDPC wikiPageUsesTemplate Template:Analgesics.
- BDPC wikiPageUsesTemplate Template:Cascite.
- BDPC wikiPageUsesTemplate Template:Chemspidercite.
- BDPC wikiPageUsesTemplate Template:Distinguish.
- BDPC wikiPageUsesTemplate Template:Drugbox.
- BDPC wikiPageUsesTemplate Template:Opioidergics.
- BDPC wikiPageUsesTemplate Template:Reflist.
- BDPC wikiPageUsesTemplate Template:Stdinchicite.
- BDPC subject Category:Amines.
- BDPC subject Category:Cyclohexanols.
- BDPC subject Category:Mu-opioid_agonists.
- BDPC subject Category:Organobromides.
- BDPC subject Category:Synthetic_opioids.
- BDPC type ChemicalSubstance.
- BDPC type Drug.
- BDPC type Agonist.
- BDPC type Alcohol.
- BDPC type Drug.
- BDPC type Opioid.
- BDPC type Organohalide.
- BDPC type Organohalide.
- BDPC type ChemicalObject.
- BDPC type Thing.
- BDPC type Q8386.
- BDPC comment "BDPC (systematic name 4-(4-bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol; also known as bromadol) is a potent narcotic analgesic with a distinctive arylcyclohexylamine chemical structure. It was developed by Daniel Lednicer at Upjohn in the 1970s. Initial studies estimated that it was around 10,000 times the strength of morphine in animal models. However, later studies assigned a value of 504 times the potency of morphine for the more active trans-isomer.".
- BDPC label "BDPC".
- BDPC differentFrom Bromadoline.
- BDPC differentFrom Bromidol.
- BDPC sameAs Q4973576.
- BDPC sameAs m.0411cnw.
- BDPC sameAs Bromadol.
- BDPC sameAs Bromadol.
- BDPC sameAs Q4973576.
- BDPC wasDerivedFrom BDPC?oldid=684278114.
- BDPC depiction Bromadol_Skeletal.png.
- BDPC isPrimaryTopicOf BDPC.