CB-13

Chemical compound
Identifiers
  • Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone
CAS Number
  • 432047-72-8 checkY
PubChem CID
  • 9799417
ChemSpider
  • 7975182
UNII
  • 9XRJ6055XT
ChEMBL
  • ChEMBL244403
CompTox Dashboard (EPA)
  • DTXSID60430920 Edit this at Wikidata
Chemical and physical dataFormulaC26H24O2Molar mass368.476 g·mol−13D model (JSmol)
  • Interactive image
  • c13ccccc1cccc3C(=O)c4ccc(OCCCCC)c2ccccc24
InChI
  • InChI=1S/C26H24O2/c1-2-3-8-18-28-25-17-16-24(21-13-6-7-14-22(21)25)26(27)23-15-9-11-19-10-4-5-12-20(19)23/h4-7,9-17H,2-3,8,18H2,1H3
  • Key:RSUMDJRTAFBISX-UHFFFAOYSA-N
  (verify)

CB-13 (CRA13, SAB-378)[1] is a cannabinoid drug, which acts as a potent agonist at both the CB1 and CB2 receptors, but has poor blood–brain barrier penetration, and so produces only peripheral effects at low doses, with symptoms of central effects such as catalepsy only appearing at much higher dose ranges. It has antihyperalgesic properties in animal studies,[2] and has progressed to preliminary human trials.[3]

Legal Status

As of October 2015 CB-13 is a controlled substance in China.[4]

CB-13 is a Schedule I controlled substance in North Dakota.[5]

See also

References

  1. ^ Cluny NL, Keenan CM, Duncan M, Fox A, Lutz B, Sharkey KA (September 2010). "Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone (SAB378), a peripherally restricted cannabinoid CB1/CB2 receptor agonist, inhibits gastrointestinal motility but has no effect on experimental colitis in mice". The Journal of Pharmacology and Experimental Therapeutics. 334 (3): 973–980. doi:10.1124/jpet.110.169946. PMID 20571060. S2CID 9198992.
  2. ^ Dziadulewicz EK, Bevan SJ, Brain CT, Coote PR, Culshaw AJ, Davis AJ, et al. (August 2007). "Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone: a potent, orally bioavailable human CB1/CB2 dual agonist with antihyperalgesic properties and restricted central nervous system penetration". Journal of Medicinal Chemistry. 50 (16): 3851–3856. doi:10.1021/jm070317a. PMID 17630726.
  3. ^ Gardin A, Kucher K, Kiese B, Appel-Dingemanse S (April 2009). "Cannabinoid receptor agonist 13, a novel cannabinoid agonist: first in human pharmacokinetics and safety". Drug Metabolism and Disposition. 37 (4): 827–833. doi:10.1124/dmd.108.024000. PMID 19144772. S2CID 15150118.
  4. ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" [Notice on Printing and Distributing the "Measures for the Scheduling of Non-Pharmaceutical Narcotic Drugs and Psychotropic Substances"] (in Chinese). China Food and Drug Administration. 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
  5. ^ "Schedule 1" (PDF). Sixty-eighth Legislative Assembly of North Dakota. 3 January 2023.
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