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GAT100

From Wikipedia, the free encyclopedia
Chemical compound; modulator of the cannabinoid CB1 receptor
Pharmaceutical compound
GAT100
Identifiers
  • 3-ethyl-5-isothiocyanato-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamide
CAS Number
ChemSpider
UNII
Chemical and physical data
FormulaC25H28N4OS
Molar mass432.59 g·mol−1
3D model (JSmol)
  • CCc1c([nH]c2ccc(cc12)N=C=S)C(=O)NCCc3ccc(cc3)N4CCCCC4
  • InChI=1S/C25H28N4OS/c1-2-21-22-16-19(27-17-31)8-11-23(22)28-24(21)25(30)26-13-12-18-6-9-20(10-7-18)29-14-4-3-5-15-29/h6-11,16,28H,2-5,12-15H2,1H3,(H,26,30)
  • Key:YIYLMDVRSNXYOT-UHFFFAOYSA-N

GAT100 is a negativeallosteric modulator of thecannabinoidCB1receptor.[1][2]

See also

[edit]

References

[edit]
  1. ^Kulkarni PM, Kulkarni AR, Korde A, Tichkule RB, Laprairie RB, Denovan-Wright EM, et al. (January 2016)."Novel Electrophilic and Photoaffinity Covalent Probes for Mapping the Cannabinoid 1 Receptor Allosteric Site(s)".Journal of Medicinal Chemistry.59 (1):44–60.doi:10.1021/acs.jmedchem.5b01303.PMC 4716578.PMID 26529344.
  2. ^Laprairie RB, Kulkarni AR, Kulkarni PM, Hurst DP, Lynch D, Reggio PH, et al. (June 2016)."Mapping Cannabinoid 1 Receptor Allosteric Site(s): Critical Molecular Determinant and Signaling Profile of GAT100, a Novel, Potent, and Irreversibly Binding Probe".ACS Chemical Neuroscience.7 (6):776–98.doi:10.1021/acschemneuro.6b00041.PMC 5358098.PMID 27046127.
Phytocannabinoids
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AllostericCBRTooltip Cannabinoid receptorligands
Endocannabinoid
enhancers

(inactivation inhibitors)
Anticannabinoids
(antagonists/inverse
agonists/antibodies)
Receptor
(ligands)
CB1Tooltip Cannabinoid receptor type 1
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CB2Tooltip Cannabinoid receptor type 2
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NAGly
(
GPR18)
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eCBTsTooltip Endocannabinoid transporter
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(modulators)
FAAHTooltip Fatty acid amide hydrolase
MAGL
ABHD6
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  • 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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