Chemistry:5F-CUMYL-P7AICA
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Short description: Chemical compound
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| Formula | C22H26FN3O |
| Molar mass | 367.468 g·mol−1 |
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5F-CUMYL-P7AICA (also known as CUMYL-5F-P7AICA or SGT-263) is a pyrrolo[2,3-b]pyridine-3-carboxamide based synthetic cannabinoid that has been sold as a designer drug.[1][2][3][4][5][6] It was first identified by the EMCDDA in February 2015.[7]
See also
- 5F-A-P7AICA[8]
- 5F-AB-P7AICA[8]
- 5F-CUMYL-PINACA
- 5F-MDMB-P7AICA[8]
- 5F-PCN
- 5F-SDB-006
- ADB-P7AICA
References
- ↑ "Identification and quantification of synthetic cannabinoids in 'spice-like' herbal mixtures: Update of the German situation in early 2017". Forensic Science International 277: 51–58. August 2017. doi:10.1016/j.forsciint.2017.05.019. PMID 28601726.
- ↑ "In vitro metabolism of the synthetic cannabinoids CUMYL-PINACA, 5F-CUMYL-PINACA, CUMYL-4CN-BINACA, 5F-CUMYL-P7AICA and CUMYL-4CN-B7AICA". Drug Testing and Analysis 10 (1): 148–157. January 2018. doi:10.1002/dta.2298. PMID 28885775.
- ↑ "Structural characterization of the new synthetic cannabinoids CUMYL-PINACA, 5F-CUMYL-PINACA, CUMYL-4CN-BINACA, 5F-CUMYL-P7AICA and CUMYL-4CN-B7AICA". Forensic Science International 281: 98–105. December 2017. doi:10.1016/j.forsciint.2017.10.020. PMID 29125990.
- ↑ "Synthesis and pharmacology of new psychoactive substance 5F-CUMYL-P7AICA, a scaffold-hopping analog of synthetic cannabinoid receptor agonists 5F-CUMYL-PICA and 5F-CUMYL-PINACA". Drug Testing and Analysis 11 (2): 279–291. August 2018. doi:10.1002/dta.2491. PMID 30151911. https://researchrepository.rmit.edu.au/view/delivery/61RMIT_INST/12247438080001341/13257312090001341.
- ↑ "Comparison of in vitro and in vivo models for the elucidation of metabolic patterns of 7-azaindole-derived synthetic cannabinoids exemplified using cumyl-5F-P7AICA". Drug Testing and Analysis 13 (1): 74–90. July 2020. doi:10.1002/dta.2899. PMID 32678962.
- ↑ "Behavioral pharmacology of five novel synthetic cannabinoids". Behavioural Pharmacology 33 (2&3): 175–183. February 2021. doi:10.1097/FBP.0000000000000618. PMID 33595956.
- ↑ "Annual Report on the implementation of Council Decision 2005/387/JHA". Europol. 2015. http://www.emcdda.europa.eu/system/files/publications/2880/TDAS16001ENN.pdf.
- ↑ 8.0 8.1 8.2 "Synthesis and in Vitro Cannabinoid Receptor 1 Activity of Recently Detected Synthetic Cannabinoids 4F-MDMB-BICA, 5F-MPP-PICA, MMB-4en-PICA, CUMYL-CBMICA, ADB-BINACA, APP-BINACA, 4F-MDMB-BINACA, MDMB-4en-PINACA, A-CHMINACA, 5F-AB-P7AICA, 5F-MDMB-P7AICA, and 5F-AP7AICA". ACS Chemical Neuroscience 11 (24): 4434–4446. 2020. doi:10.1021/acschemneuro.0c00644. PMID 33253529.
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