Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107455
DC FieldValueLanguage
dc.contributor.authorResnik, Karissa-
dc.contributor.authorBrandão, Pedro-
dc.contributor.authorAlves, Emanuele Amorim-
dc.date.accessioned2023-07-13T08:32:33Z-
dc.date.available2023-07-13T08:32:33Z-
dc.date.issued2021-10-06-
dc.identifier.issn1948-7193pt
dc.identifier.issn1948-7193pt
dc.identifier.urihttps://hdl.handle.net/10316/107455-
dc.description.abstractBucinnazine (1-butyryl-4-cinnamylpiperazine) is a synthetic opioid recently discovered in heroin seized samples in the U.S and in Europe. It was first synthesized in the late 1960s and has been used for the treatment of cancer-associated chronic pain in China for many years. Bucinnazine is one of the most potent compounds among the series of piperazines, which also include other relevant compounds, such as MT-45, AD-1211, and 2-methyl-AP-237, a methylated derivative of bucinnazine. Bucinnazine is considered a μ-selective opioid, binding primarily to the μ-opioid receptor. However, bucinnazine also may share several characteristics with other piperazines, which act primarily on dopamine, serotonin, and norepinephrine neurotransmission. At the present, bucinnazine is not scheduled in the U.S., as it is not a therapeutic choice for the treatment of pain. Nevertheless, with the advent of the cryptocurrency and the easy access of substances on the Darknet, bucinnazine is a real threat to the public health. This review discusses the main aspects of bucinnazine's chemistry, pharmacology, and toxicology and brings attention to the risk of the presence of this opioid in seized samples. Further studies on bucinnazine are still required to better evaluate its toxicity mechanisms, potential for drug-drug interactions, and abuse liability. Such information will be of utmost importance to guide future policies concerning the legal status of bucinnazine in the U.S.pt
dc.language.isoengpt
dc.publisherACS American Chemical Societypt
dc.rightsembargoedAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectNew synthetic opioidspt
dc.subjectbucinnazinept
dc.subjectAP-237pt
dc.subjecttoxicologypt
dc.subject.meshDopaminept
dc.subject.meshHumanspt
dc.subject.meshPainpt
dc.subject.meshPublic Healthpt
dc.subject.meshAnalgesics, Opioidpt
dc.subject.meshNeurosciencespt
dc.titleDARK Classics in Chemical Neuroscience: Bucinnazinept
dc.typearticle-
degois.publication.firstPage3527pt
degois.publication.lastPage3534pt
degois.publication.issue19pt
degois.publication.titleChemical Neurosciencept
dc.peerreviewedyespt
dc.identifier.doi10.1021/acschemneuro.1c00522pt
degois.publication.volume12pt
dc.date.embargo2022-10-06*
uc.date.periodoEmbargo365pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-1455-7470-
Appears in Collections:I&D CQC - Artigos em Revistas Internacionais
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