5-(Nonyloxy)tryptamine

5-(Nonyloxy)tryptamine
Clinical data
Other names	5-(Nonyloxy)-1H-indole-3-ethanamine
Identifiers
	IUPAC name 2-(5-Nonyloxy-1H-indol-3-yl)ethanamine;
CAS Number	157798-12-4 ;
PubChem CID	1797;
IUPHAR/BPS	106;
ChemSpider	1731 ;
ChEBI	CHEBI:64149;
ChEMBL	ChEMBL97450;
Chemical and physical data
Formula	C19H30N2O
Molar mass	302.462 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCCCCCCCOC1=CC2=C(C=C1)NC=C2CCN;
	InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3 ; Key:YHSMSRREJYOGQJ-UHFFFAOYSA-N ;
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Short description: Chemical compound

5-(Nonyloxy)tryptamine is a tryptamine derivative which acts as a selective agonist at the 5-HT_1B receptor. Increasing the O-alkoxy chain length in this series gives generally increasing potency and selectivity for 5-HT_1B, with highest activity found for the nonyloxy derivative, having a 5-HT_1B binding affinity of 1.0 nM, and around 300-fold selectivity over the related 5-HT_1A receptor.^[1]^[2]

References

↑ "5-(Nonyloxy)tryptamine: a novel high-affinity 5-HT1D beta serotonin receptor agonist". Journal of Medicinal Chemistry 37 (18): 2828–30. September 1994. doi:10.1021/jm00044a001. PMID 8071931.
↑ "Binding of O-alkyl derivatives of serotonin at human 5-HT1D beta receptors". Journal of Medicinal Chemistry 39 (1): 314–22. January 1996. doi:10.1021/jm950498t. PMID 8568822.

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[pmid8071931-1] "5-(Nonyloxy)tryptamine: a novel high-affinity 5-HT1D beta serotonin receptor agonist". Journal of Medicinal Chemistry 37 (18): 2828–30. September 1994. doi:10.1021/jm00044a001. PMID 8071931.

[pmid8568822-2] "Binding of O-alkyl derivatives of serotonin at human 5-HT1D beta receptors". Journal of Medicinal Chemistry 39 (1): 314–22. January 1996. doi:10.1021/jm950498t. PMID 8568822.

[1]

[2]

5-(Nonyloxy)tryptamine

Topic: Chemistry

See also

References