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AM-1714

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
AM-1714
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1,9-dihydroxy-3-(2-methyloctan-2-yl)-6H-benzo[c]chromen-6-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H26O4
Molar mass354.446 g·mol−1
3D model (JSmol)
  • O=C(O1)C2=C(C=C(O)C=C2)C3=C1C=C(C(C)(C)CCCCCC)C=C3O
  • InChI=1S/C22H26O4/c1-4-5-6-7-10-22(2,3)14-11-18(24)20-17-13-15(23)8-9-16(17)21(25)26-19(20)12-14/h8-9,11-13,23-24H,4-7,10H2,1-3H3
  • Key:BWKBVEVEQOCSCF-UHFFFAOYSA-N

AM-1714 (part of theAM cannabinoid series) is a drug that acts as a reasonably selectiveagonist of the peripheralcannabinoid receptorCB2, with sub-nanomolar affinity and 490x selectivity over the relatedCB1 receptor. In animal studies it has bothanalgesic and anti-allodynia effects. The 9-methoxy derivative AM-1710 has similar CB2 affinity but only 54x selectivity over CB1.[1][2]

See also

[edit]

References

[edit]
  1. ^Khanolkar AD, Lu D, Ibrahim M, Duclos RI, Thakur GA, Malan TP, et al. (December 2007). "Cannabilactones: a novel class of CB2 selective agonists with peripheral analgesic activity".Journal of Medicinal Chemistry.50 (26):6493–500.doi:10.1021/jm070441u.PMID 18038967.
  2. ^Rahn EJ, Zvonok AM, Thakur GA, Khanolkar AD, Makriyannis A, Hohmann AG (November 2008)."Selective activation of cannabinoid CB2 receptors suppresses neuropathic nociception induced by treatment with the chemotherapeutic agent paclitaxel in rats".The Journal of Pharmacology and Experimental Therapeutics.327 (2):584–91.doi:10.1124/jpet.108.141994.PMC 2682949.PMID 18664590.
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