| Name | eletriptan |
|---|---|
| Synonyms |
3-benzyl-5-(1-(2-(pyrrolidin-1-yl)ethyl)-1H-indol-3-yl)-1,2,4-oxadiazole
1H-Indole, 3-(((2R)-1-methyl-2-pyrrolidinyl)methyl)-5-(2-(phenylsulfonyl)ethyl)ethyl) Tianfu Chem Eletriptan ELETRIPTAN EletriptanHydrobromide(ForR&DOnly) 3-{[(2R)-1-Methylpyrrolidin-2-yl]methyl}-5-[2-(phenylsulfonyl)ethyl]-1H-indole 5-[2-(benzenesulfonyl)ethyl]-3-[(1-methyl-2-pyrrolidinyl)methyl]-1H-indole 3-[[(R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]indolemonohydrobromide 5-[2-(benzenesulfonyl)ethyl]-3-[(1-Methylpyrrolidin-2-yl)Methyl]-1H-indole (R)-5-[2-(Benzenesulfonyl)ethyl]-3-[(N-methylpyrrolidin-2-yl)methyl]-1H-indole Eletriptan Also see: R143400 1H-Indole,3-[[(2R)-1-Methyl-2-pyrrolidinyl]Methyl]-5-[2-(phenylsulfonyl)ethyl] Unii-22qoo9B8ki UK-116044,Relpax,3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole Relpax UK-116044 3-{[(2R)-1-Methyl-2-pyrrolidinyl]methyl}-5-[2-(phenylsulfonyl)ethyl]-1H-indole (R)-3-[(1-Methyl-2-pyrrolidinyl)methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-Indole MFCD00943792 5-(2-(Benzenesulfoyl)vinyl)-3-(1-Methylpyrrolidin-2(R)-ylmethyl)-1H-Indole Eletriptan Impurity 6 Eletriptan //BP 3-[[(2R)-1-Methyl-2-pyrrolidinyl]methyl]-5-[2-(phenylsulfonyl)ethyl]-1H-indole 5-[2-(benzenesulfonyl)ethyl]-3-{[(2R)-1-Methylpyrrolidin-2-yl]Methyl}-1H-indole UK-116,[as hydrobromide] Eletriptan Free Base (R)-Eletriptan According to triptans 5-[2-(benzenesulfonyl)ethyl]-3-[1-methylpyrrolidin-2(R)-ylmethy] -1H-indole 3-[(1-methylpyrrolidin-2-yl)methyl]-5-(2-phenylsulfonylethyl)-1h-indole 5-(2-(BENZENESULFONYL)VINYL)-3-(1-METHYLPYRROLIDIN-2(R)-YLMETHYL)-1H-INDOLE Relpax free aMine (R)-3-((1-methylpyrrolidin-2-yl)methyl)-5-(2-(phenylsulfonyl)ethyl)-1H-indole 5-[2-(benzenesulfonyl)ethyl]-3-[[(2R)-1-methylpyrrolidin-2-yl]methyl]-1H-indole |
| Description | Eletriptan (UK-116044) is a highly selective and orally active serotonin 5-HT1B and 5-HT1D receptor agonist, with pKi values of 8.0 and 8.9, respectively. Eletriptan has inhibitory effects on markers of neurogenic inflammation in rats. Eletriptan can be used for researching migraine[1]. |
|---|---|
| Related Catalog | |
| Target |
5-HT1B Receptor:8.0 (pKi) 5-HT1D Receptor:8.9 (pKi) |
| In Vivo | Eletriptan (10, 30, 100, 300 and 1000 µg/kg; i.v.) reduces total carotid blood flow in anaesthetised pigs by selectively reducing carotid arteriovenous anastomotic blood flow and increasing nutrient blood flow within the carotid vascular bed[2]. |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 613.4±55.0 °C at 760 mmHg |
| Molecular Formula | C22H26N2O2S |
| Molecular Weight | 382.519 |
| Flash Point | 324.8±31.5 °C |
| Exact Mass | 382.171509 |
| PSA | 61.55000 |
| LogP | 3.08 |
| Vapour Pressure | 0.0±1.8 mmHg at 25°C |
| Index of Refraction | 1.634 |
| Storage condition | Hygroscopic, Refrigerator, Under Inert Atmosphere |
| Precursor 8 | |
|---|---|
| DownStream 1 | |