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Revision as of 16:43, 10 August 2011 editBeetstra (talk | contribs)Edit filter managers, Administrators172,031 edits Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'DrugBank', 'ChEBI').← Previous edit Latest revision as of 02:41, 19 October 2023 edit undoPashihiko (talk | contribs)Extended confirmed users3,559 editsNo edit summary 
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{{Short description|Chemical compound}}
{{drugbox
{{Distinguish|α-PCyP}}
| Verifiedfields = changed
{{Drugbox
| UNII_Ref = {{fdacite|changed|FDA}}
| verifiedrevid = 444089733
| UNII = 183O9O9JE3
| IUPAC_name = 1-(1-phenylcyclohexyl)pyrrolidine
| verifiedrevid = 401043924
|IUPAC_name = 1-(1-phenylcyclohexyl)pyrrolidine
| image = Rolicyclidine.svg | image = Rolicyclidine.svg
| width= 125px | width = 125px

<!--Clinical data-->
| tradename =
| legal_AU = S9
| legal_BR = F2
| legal_BR_comment = <ref>{{Cite web |author=Anvisa |author-link=Brazilian Health Regulatory Agency |date=2023-07-24 |title=RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial |trans-title=Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control|url=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451 |url-status=live |archive-url=https://web.archive.org/web/20230827163149/https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451 |archive-date=2023-08-27 |access-date=2023-08-27 |publisher=] |language=pt-BR |publication-date=2023-07-25}}</ref>
| legal_CA = Schedule III
| legal_UK = Class A
| legal_US = Schedule I
| legal_DE = Anlage I
| legal_UN = P I

<!--Identifiers-->
| CAS_number = 2201-39-0
| ATC_prefix = none
| PubChem = 62436
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB01549
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 56218 | ChemSpiderID = 56218
| UNII_Ref = {{fdacite|correct|FDA}}
| InChI = 1/C16H23N/c1-3-9-15(10-4-1)16(11-5-2-6-12-16)17-13-7-8-14-17/h1,3-4,9-10H,2,5-8,11-14H2
| UNII = 183O9O9JE3
| InChIKey = FYOWWXMGDATDQY-UHFFFAOYAQ
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 60805
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D12706

<!--Chemical data-->
| C=16 | H=23 | N=1
| smiles = c1ccccc1C3(N2CCCC2)CCCCC3 | smiles = c1ccccc1C3(N2CCCC2)CCCCC3
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = FYOWWXMGDATDQY-UHFFFAOYSA-N | StdInChIKey = FYOWWXMGDATDQY-UHFFFAOYSA-N
| CAS_number= 2201-39-0
| ATC_prefix= none
| ATC_suffix=
| ChEBI = 60805
| PubChem= 62436
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB01549
| C=16 | H=23 | N=1
| molecular_weight = 229.361 g/mol
| bioavailability=
| metabolism =
| elimination_half-life=
| excretion =
| pregnancy_category =
| legal_status = Schedule I / Class A
| routes_of_administration=
}} }}


'''Rolicyclidine''' ('''PCPy''') is a ] ] drug with ]ic and ] effects. It is similar in effects to ] but is slightly less potent and has less stimulant effects <ref> Kalir A, Edery H, Pelah Z, Balderman D, Porath G. 1-Phenylcycloalkylamine derivatives. II. Synthesis and pharmacological activity. Journal of Medicinal Chemistry. 1969. 12(3):473-477</ref> instead producing a sedative effect described as being somewhat similar to a ], but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects.<ref> DEA Microgram Bulletin, 8, 143, 1975</ref> Due to its similarity in effects to PCP, PCPy was placed into the Schedule I list of illegal drugs in the 1970s, although it has never been widely abused and is now little known. '''Rolicyclidine''' ('''PCPy''') is a ] ] that is similar in effects to ], but is slightly less potent and has fewer stimulant effects.<ref>{{cite journal | vauthors = Kalir A, Edery H, Pelah Z, Balderman D, Porath G | title = 1-Phenycycloalkylamine derivatives. II. Synthesis and pharmacological activity | journal = Journal of Medicinal Chemistry | volume = 12 | issue = 3 | pages = 473–7 | date = May 1969 | pmid = 4977945 | doi = 10.1021/jm00303a030 }}</ref> It instead produces a sedative effect described as being somewhat similar to a ], but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects.<ref>DEA Microgram Bulletin, 8, 143, 1975</ref> Due to its similarity in effects to PCP, PCPy was placed into the Schedule I list of illegal drugs in the 1970s, although it has never been widely abused and is now little known.


==See also== ==See also==
* ]
* ] * ]
* ]
* ]


==References== ==References==
{{Reflist|2}} {{Reflist}}


{{General_anesthetics}} {{General_anesthetics}}
{{Depressants}}
{{Hallucinogens}} {{Hallucinogens}}
{{Dopamine receptor modulators}}
{{Dopaminergics}}
{{Ionotropic glutamate receptor modulators}}
{{Glutamatergics}}


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] ]
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{{nervous-system-drug-stub}} {{nervous-system-drug-stub}}

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