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Isamide

From Wikipedia, the free encyclopedia
Serotonin antagonist

Pharmaceutical compound
Isamide
Clinical data
Other namesN-(1-Chloroacetyl)-5-methoxytryptamine
Drug classSerotonin receptor antagonist
Identifiers
  • 2-chloro-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H15ClN2O2
Molar mass266.73 g·mol−1
3D model (JSmol)
  • COC1=CC2=C(C=C1)NC=C2CCNC(=O)CCl
  • InChI=1S/C13H15ClN2O2/c1-18-10-2-3-12-11(6-10)9(8-16-12)4-5-15-13(17)7-14/h2-3,6,8,16H,4-5,7H2,1H3,(H,15,17)
  • Key:UCLPNTKRPMTACI-UHFFFAOYSA-N

Isamide, also known asN-chloroacetyl-5-methoxytryptamine, is aserotonin receptor antagonist and theN-chloroacetylderivative of5-methoxytryptamine.[1][2][3] It was first described in thescientific literature by 1969 and was firstpharmacologically characterized by 1979.[4][2]

References

[edit]
  1. ^Frohlich PF, Meston CM (2000). "Evidence that serotonin affects female sexual functioning via peripheral mechanisms".Physiology & Behavior.71 (3–4):383–393.doi:10.1016/s0031-9384(00)00344-9.PMID 11150571.
  2. ^abHuidobro-Toro JP, Huidobro F, Ruiz M (June 1979). "N-Chloroacetyl 5-methoxytryptamine (isamide): a selective antagonist of 5-hydroxytryptamine in the rat uterus".The Journal of Pharmacy and Pharmacology.31 (6):371–374.doi:10.1111/j.2042-7158.1979.tb13525.x.PMID 39134.
  3. ^Huidobro-Toro JP, Foree B (February 1980). "Dual agonist-antagonist effects of 5-hydroxytryptamine (5-HT) in the guinea pig ileum: evidence for a selective receptor desensitization effect".European Journal of Pharmacology.61 (4):335–345.doi:10.1016/0014-2999(80)90072-2.PMID 6102916.
  4. ^Kobayashi T, Spande TF, Aoyagi H, Witkop B (July 1969). "Tricyclic analogs of melatonin".Journal of Medicinal Chemistry.12 (4):636–638.doi:10.1021/jm00304a017.PMID 5793155.
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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