GAT100

GAT100

Identifiers
IUPAC name 3-ethyl-5-isothiocyanato-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamide
CAS Number	1663564-42-8
Chemical and physical data
Formula	C25H28N4OS
Molar mass	432.59 g·mol−1
3D model (Jmol)	Interactive image
SMILES CCc1c([nH]c2ccc(cc12)N=C=S)C(=O)NCCc3ccc(cc3)N4CCCCC4
InChI 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 negative allosteric modulator of the cannabinoid CB₁ receptor.^[1][2]

See also

• Org 27569
• PSNCBAM-1
• ZCZ-011

References

1. ↑ Pushkar M. Kulkarni; Abhijit R. Kulkarni; Anisha Korde; Ritesh B. Tichkule; Robert B. Laprairie; Eileen M. Denovan-Wright; Han Zhou∥; David R. Janero; Nikolai Zvonok; Alexandros Makriyannis; Maria G. Cascio; Roger G. Pertwee; Ganesh A. Thakur (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. ↑ Robert B. Laprairie; Abhijit R. Kulkarni; Pushkar M. Kulkarni; Dow P. Hurst; Diane Lynch; Patricia H. Reggio; David R. Janero; Roger G. Pertwee; Lesley A. Stevenson; Melanie E. M. Kelly; Eileen M. Denovan-Wright; Ganesh A. Thakur (April 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. doi:10.1021/acschemneuro.6b00041. PMID 27046127.