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SDB-005

From Wikipedia, the free encyclopedia
SDB-005
Legal status
Legal status
Identifiers
  • Naphthalen-1-yl 1-pentyl-1H-indazole-3-carboxylate
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC23H22N2O2
Molar mass358.441 g·mol−1
3D model (JSmol)
  • CCCCCN1N=C(C(=O)OC2=CC=CC3=C2C=CC=C3)C2=C1C=CC=C2
  • InChI=1S/C23H22N2O2/c1-2-3-8-16-25-20-14-7-6-13-19(20)22(24-25)23(26)27-21-15-9-11-17-10-4-5-12-18(17)21/h4-7,9-15H,2-3,8,16H2,1H3
  • Key:JBVNFKZVDLFOAY-UHFFFAOYSA-N

SDB-005 (also known as NA-PINAC using systematic EUDA nomenclature)[1] is an indazole-based synthetic cannabinoid that has been sold online as a designer drug.[2] It is presumed to be an agonist of the CB1 and CB2 cannabinoid receptors. SDB-005 is the indazole core analog of PB-22 where the 8-hydroxyquinoline has also been replaced with a naphthalene group.

Structure of Phen-1-yl 1-pentyl-1H-indole-3-carboxamide (PH-PICA)

The code number SDB-005 was originally used by Samuel D. Bannister for a different compound, the N-phenyl instead of N-benzyl analogue of SDB-006, pictured. It is systematically named PH-PICA (Phen-1-yl 1-Pentyl-1H-indazole-3-carboxamide. This compound is a potent agonist of the CB1 receptor (Ki = 21 nM) and CB2 receptor (Ki = 140 nM)[3] but has significant chemical differences; an indazole ring (instead of indole ring), a carboxamide linker (instead of carboxylate ester) and linked phenyl (instead of naphtyl) group).


However, SDB-005 was subsequently used as the name for the indazole-3-napthyl-carboxylate compound when it was sold in Europe as a designer drug. Because of this, it was entered into the EMCDDA synthetic drug database under this name.[4] The UK Forensic Early Warning System reported a detection of SDB-005 in December 2017 as the first occurrence of naphthalen-1-yl-1-pentyl-1H-indazole-3-carboxylate (NA-PINAC) in the UK.[5] Many online sources now list SDB-005 as naphthalen-1-yl 1-pentyl-1H-indazole-3-carboxylate (NA-PINAC).[6][7]

Consequently, there are now two distinct, yet fairly closely related cannabinoid compounds, which may both be referred to under the code SDB-005.

See also

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References

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  1. Pulver B, Fischmann S, Gallegos A, Christie R (March 2023). "EMCDDA framework and practical guidance for naming synthetic cannabinoids". Drug Testing and Analysis. 15 (3): 255–276. doi:10.1002/dta.3403. PMID 36346325.
  2. "SDB-005". Cayman Chemical. Retrieved 27 June 2015.
  3. Banister SD, Wilkinson SM, Longworth M, Stuart J, Apetz N, English K, et al. (July 2013). "The synthesis and pharmacological evaluation of adamantane-derived indoles: cannabimimetic drugs of abuse". ACS Chemical Neuroscience. 4 (7): 1081–92. doi:10.1021/cn400035r. PMC 3715837. PMID 23551277.
  4. EWS_EU: Neue Psychoaktive Substanzen, April 2015
  5. "Annual report on the Home Office forensic early warning system (FEWS), 2017 to 2018". GOV.UK. Retrieved 2026-06-25.
  6. "TRC-S210000-1G". www.lgcstandards.com. Retrieved 2026-06-25. naphthalen-1-yl 1-pentyl-1H-indazole-3-carboxylate
  7. "SDB-005 Monograph" (PDF). DEA SWGDrug Monographs. The Drug Enforcement Administration's Special Testing and Research Laboratory (SWGDrug). 2016-04-04. Retrieved 2026-06-26. naphthalen-1-yl 1-pentyl-1H-indazole-3-carboxylate