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JZL195

From Wikipedia, the free encyclopedia
JZL195
Names
Preferred IUPAC name
4-Nitrophenyl 4-[(3-phenoxyphenyl)methyl]piperazine-1-carboxylate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C24H23N3O5/c28-24(32-22-11-9-20(10-12-22)27(29)30)26-15-13-25(14-16-26)18-19-5-4-8-23(17-19)31-21-6-2-1-3-7-21/h1-12,17H,13-16,18H2
    Key: QNYRAEKLMNDRFY-UHFFFAOYSA-N
  • c1ccc(cc1)Oc2cccc(c2)CN3CCN(CC3)C(=O)Oc4ccc(cc4)[N+](=O)[O-]
Properties
C24H23N3O5
Molar mass433.464 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

JZL195 is a potent inhibitor of bothfatty acid amide hydrolase (FAAH) andmonoacylglycerol lipase (MAGL), the primaryenzymes responsible for degrading theendocannabinoidsanandamide (AEA) and2-arachidonoylglycerol (2-AG), respectively.[1]

See also

[edit]

References

[edit]
  1. ^Long JZ, Nomura DK, Vann RE, Walentiny DM, Booker L, Jin X, Burston JJ, Sim-Selley LJ, Lichtman AH, Wiley JL, Cravatt BF (December 2009)."Dual blockade of FAAH and MAGL identifies behavioral processes regulated by endocannabinoid crosstalk in vivo".Proceedings of the National Academy of Sciences of the United States of America.106 (48):20270–5.Bibcode:2009PNAS..10620270L.doi:10.1073/pnas.0909411106.PMC 2787168.PMID 19918051.
Phytocannabinoids
(comparison)
Cannabibutols
Cannabichromenes
Cannabicyclols
Cannabidiols
Cannabielsoins
Cannabigerols
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Cannabinols
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Cannabivarins
Delta-3-tetrahydrocannabinols
Delta-4-tetrahydrocannabinols
Delta-7-tetrahydrocannabinols
Delta-8-tetrahydrocannabinols
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Delta-10-Tetrahydrocannabinols
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Miscellaneous cannabinoids
Active metabolites
Endocannabinoids
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cannabinoid
receptor
agonists /
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AllostericCBRTooltip Cannabinoid receptorligands
Endocannabinoid
enhancers

(inactivation inhibitors)
Anticannabinoids
(antagonists/inverse
agonists/antibodies)
Receptor
(ligands)
CB1Tooltip Cannabinoid receptor type 1
Agonists
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CB2Tooltip Cannabinoid receptor type 2
Agonists
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NAGly
(
GPR18)
Agonists
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Agonists
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Agonists
Transporter
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eCBTsTooltip Endocannabinoid transporter
Enzyme
(modulators)
FAAHTooltip Fatty acid amide hydrolase
MAGL
ABHD6
ABHD12
Others
  • Others:2-PG(directly potentiates activity of 2-AG at CB1 receptor)
  • ARN-272(FAAH-like anandamide transporter inhibitor)
See also
Receptor/signaling modulators
Cannabinoids (cannabinoids by structure)
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