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Bay R 1531

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Bay R 1531
Clinical data
Other namesLY-197206; LY197206
Drug classSerotonin5-HT1A receptoragonist;Simplified/partial LSD analogue
Identifiers
  • 1,3,4,5-tetrahydro-6-methoxy-N,N-dipropyl-benz[cd]indol-4-amine
CAS Number
PubChemCID
PubChem SID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H26N2O
Molar mass286.419 g·mol−1
3D model (JSmol)
  • COc2ccc1[nH]cc3CC(Cc2c13)N(CCC)CCC
  • 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, also known asLY-197206, is atricyclictryptaminederivative. It acts as aselectiveserotonin5-HT1A receptoragonist. It was investigated unsuccessfully for the treatment ofstroke but continues to be used inscientific research.[1][2][3][4] It shows very highaffinity for the serotonin 5-HT1A receptor (Ki = 1.3 nM).[5][6]

See also

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References

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  1. ^Bielenberg GW, Burkhardt M (December 1990). "5-hydroxytryptamine1A agonists. A new therapeutic principle for stroke treatment".Stroke.21 (12 Suppl): IV161-3.PMID 2148035.
  2. ^Critchley MA, Njung'e K, Handley SL (1992). "Actions and some interactions of 5-HT1A ligands in the elevated X-maze and effects of dorsal raphe lesions".Psychopharmacology.106 (4):484–90.doi:10.1007/bf02244819.PMID 1533721.S2CID 8404850.
  3. ^Canto de Souza A, Nunes de Souza RL, Péla IR, Graeff FG (March 1997). "High intensity social conflict in the Swiss albino mouse induces analgesia modulated by 5-HT1A receptors".Pharmacology, Biochemistry, and Behavior.56 (3):481–6.doi:10.1016/s0091-3057(96)00246-8.PMID 9077586.S2CID 20078255.
  4. ^Canto-de-Souza A, Nunes de Souza RL, Pelá IR, Graeff FG (March 1998). "Involvement of the midbrain periaqueductal gray 5-HT1A receptors in social conflict induced analgesia in mice".European Journal of Pharmacology.345 (3):253–6.doi:10.1016/s0014-2999(98)00018-1.PMID 9592023.
  5. ^Nelson DL (December 1991). "Structure-activity relationships at 5-HT1A receptors: binding profiles and intrinsic activity".Pharmacol Biochem Behav.40 (4):1041–1051.doi:10.1016/0091-3057(91)90124-k.PMID 1816558.
  6. ^Taylor EW, Nikam S, Weck B, Martin A, Nelson D (October 1987)."Relative selectivity of some conformationally constrained tryptamine analogs at 5-HT1, 5-HT1A and 5-HT2 recognition sites"(PDF).Life Sci.41 (16):1961–1969.doi:10.1016/0024-3205(87)90749-1.PMID 3657392. Archived from the original on 2019-07-21. Retrieved2025-03-24.{{cite journal}}: CS1 maint: bot: original URL status unknown (link)
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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