Org 28611: Difference between revisions

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Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'ChEMBL').
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{{Short description|Chemical compound}}
{{Drugbox
{{Drugbox
| Verifiedfields = changed
| verifiedrevid = 451603454
| verifiedrevid = 459852163
| IUPAC_name = [1-(cyclohexylmethyl)-7-methoxyindol-3-yl]-[(3S)-3,4-dimethylpiperazin-1-yl]methanone
| IUPAC_name = [1-(cyclohexylmethyl)-7-methoxyindol-3-yl]-[(3S)-3,4-dimethylpiperazin-1-yl]methanone
| image = Org28611_structure.png
| image = Org 28611 Structure.svg
| width = 200
| width = 200


<!--Clinical data-->
<!--Clinical data-->
| tradename =
| tradename =
| legal_CA = Schedule II
| legal_DE = NpSG
| legal_UK = PSA
| legal_status =
| legal_status =
| routes_of_administration =
| routes_of_administration =


<!--Pharmacokinetic data-->
<!--Pharmacokinetic data-->
| metabolism =
| metabolism =
| elimination_half-life =
| elimination_half-life =
| excretion =
| excretion =


<!--Identifiers-->
<!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number_Ref = {{cascite|changed|??}}
| CAS_number =
| CAS_number = 639068-99-8
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 1U7V49NTQG
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1209709
| ChEMBL = 1209709
| PubChem = 10091392
| PubChem = 10091392
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<!--Chemical data-->
<!--Chemical data-->
| C=23 | H=33 | N=3 | O=2
| C=23 | H=33 | N=3 | O=2
| molecular_weight = 383.526 g/mol
| smiles = COc3cccc(c13)c(C(=O)N(CC2C)CCN2C)cn1CC4CCCCC4
| smiles = COc3cccc(c13)c(C(=O)N(CC2C)CCN2C)cn1CC4CCCCC4
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
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}}
}}


'''Org 28611''' ('''SCH-900,111''') is a drug developed by [[Organon International]] which acts as a potent [[cannabinoid]] [[Receptor (biochemistry)|receptor]] [[full agonist]] at both the [[Cannabinoid receptor 1|CB<sub>1</sub>]] and [[Cannabinoid receptor 2|CB<sub>2</sub>]] receptors. It was developed with the aim of finding a [[solubility|water soluble]] cannabinoid agonist suitable for [[intravenous]] use as an [[analgesic]],<ref>{{Cite doi|10.1039/c0md00022a}}</ref> and while it achieved this aim and has progressed as far as Phase II [[clinical trial]]s in humans as both a [[sedative]] and an [[analgesic]], results against the comparison drugs ([[midazolam]] and [[morphine]] respectively) were not particularly favourable in initial testing.<ref name="pmid18635703">{{cite journal |author=Zuurman L, Passier PC, de Kam M, Kleijn HJ, Cohen AF, van Gerven JM |title=Pharmacodynamic and pharmacokinetic effects of the intravenously administered CB1 receptor agonist Org 28611 in healthy male volunteers |journal=Journal of Psychopharmacology (Oxford, England) |volume=23 |issue=6 |pages=633–44 |year=2009 |month=August |pmid=18635703 |doi=10.1177/0269881108091551 |url=}}</ref><ref>[http://clinicaltrials.gov/ct2/show/NCT00782951 A Comparison of Analgesic Efficacy Between a Single Dose of ORG 28611, Morphine, and Placebo After Dental Impaction Surgery]</ref>
'''Org 28611''' ('''SCH-900,111''') is a drug developed by [[Organon International]] which acts as a potent [[cannabinoid]] [[Receptor (biochemistry)|receptor]] [[full agonist]] at both the [[Cannabinoid receptor 1|CB<sub>1</sub>]] and [[Cannabinoid receptor 2|CB<sub>2</sub>]] receptors. It was developed with the aim of finding a [[solubility|water-soluble]] cannabinoid agonist suitable for [[intravenous]] use as an [[analgesic]],<ref>{{Cite journal |author= Adam, J. M.|title= Design, synthesis, and structure–activity relationships of indole-3-carboxamides as novel water soluble cannabinoid CB1 receptor agonists |doi= 10.1039/c0md00022a |journal= [[MedChemComm]]|publisher= [[Royal Society of Chemistry]]|volume= 1 |pages= 54 |year= 2010 |display-authors=etal}}</ref> and while it achieved this aim and has progressed as far as Phase II [[clinical trial]]s in humans as both a [[sedative]] and an [[analgesic]], results against the comparison drugs ([[midazolam]] and [[morphine]] respectively) were not particularly favourable in initial testing.<ref name="pmid18635703">{{cite journal |vauthors=Zuurman L, Passier PC, de Kam M, Kleijn HJ, Cohen AF, van Gerven JM |title=Pharmacodynamic and pharmacokinetic effects of the intravenously administered CB1 receptor agonist Org 28611 in healthy male volunteers |journal=Journal of Psychopharmacology |volume=23 |issue=6 |pages=633–44 |date=August 2009 |pmid=18635703 |doi=10.1177/0269881108091551 |s2cid=43609218 }}</ref><ref>[http://clinicaltrials.gov/ct2/show/NCT00782951 A Comparison of Analgesic Efficacy Between a Single Dose of ORG 28611, Morphine, and Placebo After Dental Impaction Surgery]</ref>


==See also==
==See also==
* [[Org 28312]]
* [[LBP-1 (drug)|LBP-1]]
* [[N-(S)-Fenchyl-1-(2-morpholinoethyl)-7-methoxyindole-3-carboxamide]]
* [[N-(S)-Fenchyl-1-(2-morpholinoethyl)-7-methoxyindole-3-carboxamide]]
* [[Org 28312]]


== References ==
== References ==
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[[Category:Cannabinoids]]
[[Category:Cannabinoids]]
[[Category:Designer drugs]]
[[Category:Indoles]]
[[Category:Piperazines]]



{{cannabinoid-stub}}
{{cannabinoid-stub}}