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LY-215840

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
LY-215840
Clinical data
Drug classSerotonin receptor antagonist;Serotonin5-HT2 receptorantagonist;Serotonin5-HT7 receptorantagonist
Identifiers
  • (6aR,9R,10aR)-N-((1S,2R)-2-hydroxycyclopentyl)-4-isopropyl-7-methyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxamide
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC24H33N3O2
Molar mass395.547 g·mol−1
3D model (JSmol)
  • CN1[C@]([C@]2([H])C[C@@H](C(N[C@@H]3[C@H](O)CCC3)=O)C1)([H])CC4=CN(C(C)C)C5=CC=CC2=C54
  • InChI=1S/C24H33N3O2/c1-14(2)27-13-15-11-21-18(17-6-4-8-20(27)23(15)17)10-16(12-26(21)3)24(29)25-19-7-5-9-22(19)28/h4,6,8,13-14,16,18-19,21-22,28H,5,7,9-12H2,1-3H3,(H,25,29)/t16-,18-,19+,21-,22-/m1/s1
  • Key:IMSDOBUYDTVEHN-ILMFXRJHSA-N

LY-215,840 is anergoline andlysergamide derivative drug developed byEli Lilly, which acts as a potent and selectiveantagonist at theserotonin5-HT2 and5-HT7receptors. It has anti-hypertensive andmuscle relaxant effects in animal studies.[1][2][3][4][5][6][7][8]

See also

[edit]

References

[edit]
  1. ^Cohen ML, Robertson DW, Bloomquist WE, Wilson HC (April 1992). "LY215840, a potent 5-hydroxytryptamine (5-HT)2 receptor antagonist, blocks vascular and platelet 5-HT2 receptors and delays occlusion in a rabbit model of thrombosis".The Journal of Pharmacology and Experimental Therapeutics.261 (1):202–8.PMID 1560366.
  2. ^Cushing DJ, Zgombick JM, Nelson DL, Cohen ML (June 1996). "LY215840, a high-affinity 5-HT7 receptor ligand, blocks serotonin-induced relaxation in canine coronary artery".The Journal of Pharmacology and Experimental Therapeutics.277 (3):1560–6.PMID 8667223.
  3. ^Terrón JA, Falcón-Neri A (June 1999)."Pharmacological evidence for the 5-HT7 receptor mediating smooth muscle relaxation in canine cerebral arteries".British Journal of Pharmacology.127 (3):609–16.doi:10.1038/sj.bjp.0702580.PMC 1566051.PMID 10401550.
  4. ^Meneses A, Terrón JA (June 2001). "Role of 5-HT(1A) and 5-HT(7) receptors in the facilitatory response induced by 8-OH-DPAT on learning consolidation".Behavioural Brain Research.121 (1–2):21–8.doi:10.1016/S0166-4328(00)00378-8.PMID 11275281.S2CID 26090343.
  5. ^Watts SW, Yang P, Banes AK, Baez M (October 2001)."Activation of Erk mitogen-activated protein kinase proteins by vascular serotonin receptors".Journal of Cardiovascular Pharmacology.38 (4):539–51.doi:10.1097/00005344-200110000-00006.PMID 11588524.S2CID 43167169.
  6. ^Lenglet S, Louiset E, Delarue C, Vaudry H, Contesse V (May 2002)."Activation of 5-HT(7) receptor in rat glomerulosa cells is associated with an increase in adenylyl cyclase activity and calcium influx through T-type calcium channels".Endocrinology.143 (5):1748–60.doi:10.1210/endo.143.5.8817.PMID 11956157.
  7. ^Meneses A (December 2002)."Involvement of 5-HT(2A/2B/2C) receptors on memory formation: simple agonism, antagonism, or inverse agonism?".Cellular and Molecular Neurobiology.22 (5–6):675–88.doi:10.1023/A:1021800822997.PMC 11533738.PMID 12585687.S2CID 25703079.
  8. ^Sánchez-Lopez A, Centurión D, Vázquez E, Arulmani U, Saxena PR, Villalón CM (October 2003)."Pharmacological profile of the 5-HT-induced inhibition of cardioaccelerator sympathetic outflow in pithed rats: correlation with 5-HT1 and putative 5-ht5A/5B receptors".British Journal of Pharmacology.140 (4):725–35.doi:10.1038/sj.bjp.0705489.PMC 1574076.PMID 14504136.
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
Ergolines
(incl.lysergines)
Clavines
(6,8-dimethylergolines)
Lysergamides
(lysergic acid amides)
Ergopeptines
(peptide ergolines)
Partial ergolines
Related compounds
Natural sources
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