N-Methyl-3-piperidyl benzilate

Chemical compound
Identifiers
  • (1-Methylpiperidin-3-yl) 2-hydroxy-2,2-di(phenyl)acetate
CAS Number
  • 3321-80-0 checkY
PubChem CID
  • 62495
ChemSpider
  • 56274 checkY
UNII
  • 3A5HM769QX
ChEMBL
  • ChEMBL139948 checkY
CompTox Dashboard (EPA)
  • DTXSID2046258 Edit this at Wikidata
ECHA InfoCard100.020.031 Edit this at WikidataChemical and physical dataFormulaC20H23NO3Molar mass325.408 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(OC1CCCN(C)C1)C(O)(c2ccccc2)c3ccccc3
InChI
  • InChI=1S/C20H23NO3/c1-21-14-8-13-18(15-21)24-19(22)20(23,16-9-4-2-5-10-16)17-11-6-3-7-12-17/h2-7,9-12,18,23H,8,13-15H2,1H3 checkY
  • Key:ZBEILXWHVSVDBN-UHFFFAOYSA-N checkY
  (verify)

N-Methyl-3-piperidyl benzilate (JB-336 or LBJ) is an anticholinergic drug related to the chemical warfare agent 3-quinuclidinyl benzilate.

N-methyl-3-piperidyl benzilate is less potent and shorter acting than 3-quinuclidyl benzilate, but like 3-QNB its effects on the central nervous system predominate over peripheral effects. It produces deliriant and hallucinogenic effects similar to those of plants such as datura and may be used recreationally at low doses; however, unpleasant side effects such as dysphoria, nausea and vomiting, dizziness and extreme dry mouth tend to make abuse of drugs of this kind uncommon. Both the N-methyl and N-ethyl analogues of 3-piperidyl benzilate are, however, Schedule I controlled drugs.

Radiolabelled versions of this drug are used in scientific research to map the distribution of muscarinic acetylcholine receptors in the brain.[1]

Methylation of JB-336 gives the quat salt, Mepenzolate bromide.

See also

References

  1. ^ Takahashi K, Murakami M, Miura S, Iida H, Kanno I, Uemura K (March 1999). "Synthesis and autoradiographic localization of muscarinic cholinergic antagonist (+)N-[11C]methyl-3-piperidyl benzilate as a potent radioligand for positron emission tomography". Applied Radiation and Isotopes. 50 (3): 521–5. doi:10.1016/S0969-8043(97)10155-5. PMID 10070712.
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