has_role
chemical entity
5-nonyloxytryptamine oxalate
0
392.23112
392.496
C19H30N2O.C2H2O4
CCCCCCCCCOc1ccc2ncc(CCN)c2c1.O=C(O)C(=O)O
reaxys:7065207
CHEBI:64147
2-[5-(nonyloxy)-1H-indol-3-yl]ethanaminium hydrogen oxalate
JORSCLBFSAAOFR-UHFFFAOYSA-N
chebi_ontology
Reaxys:7065207
2-[5-(nonyloxy)-1H-indol-3-yl]ethanamine ethanedioate
2-[5-(nonyloxy)-1H-indol-3-yl]ethanamine ethanedioate
3-(2-aminoethyl)-5-nonyloxyindole oxalate
O-nonylserotonin oxalate
InChI=1S/C19H30N2O.C2H2O4/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19;3-1(4)2(5)6/h9-10,14-15,21H,2-8,11-13,20H2,1H3;(H,3,4)(H,5,6)
2-[5-(nonyloxy)-1H-indol-3-yl]ethanamine oxalate
An oxalate salt obtained by reaction of 5-nonyloxytryptamine with one equivalent of oxalic acid. 5-HT<small><sub>1B</sub></small> selective agonist, several times more potent than sumatriptan and inactive as a 5-HT<small><sub>1A</sub></small> agonist (Ki at 5-HT<small><sub>1B</sub></small> = 1 nM, selectivity over 5-HT<small><sub>1A</sub></small> > 300-fold).
drug role