Bay R 1531

Bay R 1531
Identifiers
	IUPAC name 1,3,4,5-tetrahydro-6-methoxy-N,N-dipropyl-benz[cd]indol-4-amine;
CAS Number	98770-54-8;
PubChem CID	127153;
ChemSpider	112872;
Chemical and physical data
Formula	C18H28N2O
Molar mass	288.427 g/mol
3D model (Jmol)	Interactive image;
	SMILES COc2ccc1[nH3]cc3CC(Cc2c13)N(CCC)CCC ;
	InChI InChI=1S/C18H26N2O/c1-4-8-20(9-5-2)14-10-13-12-19-16-6-7-17(21-3)15(11-14)18(13)16/h6-7,12,14,19H,4-5,8-11H2,1-3H3 ; Key:BMZWFSGTPJUKJR-UHFFFAOYSA-N ;

Bay R 1531 is a tricyclic tryptamine derivative which acts as a selective serotonin receptor 5-HT_1A agonist. It was researched unsuccessfully for the treatment of stroke but remains in use for scientific research.^[1]^[2]^[3]^[4]

References[edit]

^ Bielenberg GW, Burkhardt M. 5-hydroxytryptamine1A agonists. A new therapeutic principle for stroke treatment. Stroke. 1990 Dec;21(12 Suppl):IV161-3. PMID 2148035
^ Critchley MA, Njung'e K, Handley SL. Actions and some interactions of 5-HT1A ligands in the elevated X-maze and effects of dorsal raphe lesions. Psychopharmacology (Berlin). 1992;106(4):484-90. PMID 1533721
^ Canto de Souza A, Nunes de Souza RL, Péla IR, Graeff FG. High intensity social conflict in the Swiss albino mouse induces analgesia modulated by 5-HT1A receptors. Pharmacology, Biochemistry and Behavior. 1997 Mar;56(3):481-6. PMID 9077586
^ Canto-de-Souza A, Nunes de Souza RL, Pelá IR, Graeff FG. Involvement of the midbrain periaqueductal gray 5-HT1A receptors in social conflict induced analgesia in mice. European Journal of Pharmacology. 1998 Mar 26;345(3):253-6. PMID 9592023

[1] Bielenberg GW, Burkhardt M. 5-hydroxytryptamine1A agonists. A new therapeutic principle for stroke treatment. Stroke. 1990 Dec;21(12 Suppl):IV161-3. PMID 2148035

[2] Critchley MA, Njung'e K, Handley SL. Actions and some interactions of 5-HT1A ligands in the elevated X-maze and effects of dorsal raphe lesions. Psychopharmacology (Berlin). 1992;106(4):484-90. PMID 1533721

[3] Canto de Souza A, Nunes de Souza RL, Péla IR, Graeff FG. High intensity social conflict in the Swiss albino mouse induces analgesia modulated by 5-HT1A receptors. Pharmacology, Biochemistry and Behavior. 1997 Mar;56(3):481-6. PMID 9077586

[4] Canto-de-Souza A, Nunes de Souza RL, Pelá IR, Graeff FG. Involvement of the midbrain periaqueductal gray 5-HT1A receptors in social conflict induced analgesia in mice. European Journal of Pharmacology. 1998 Mar 26;345(3):253-6. PMID 9592023

[1]

[2]

[3]

[4]

Bay R 1531

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Identifiers

IUPAC name 1,3,4,5-tetrahydro-6-methoxy-N,N-dipropyl-benz[cd]indol-4-amine
CAS Number	98770-54-8
PubChem CID	127153
ChemSpider	112872
Chemical and physical data
Formula	C₁₈H₂₈N₂O
Molar mass	288.427 g/mol
3D model (Jmol)	Interactive image
SMILES COc2ccc1[nH3]cc3CC(Cc2c13)N(CCC)CCC
InChI InChI=1S/C18H26N2O/c1-4-8-20(9-5-2)14-10-13-12-19-16-6-7-17(21-3)15(11-14)18(13)16/h6-7,12,14,19H,4-5,8-11H2,1-3H3 Key:BMZWFSGTPJUKJR-UHFFFAOYSA-N