|
ChemicalBook Optimization Suppliers |
|
| 化学名: | メテルゴリン | | 英語化学名: | METERGOLINE | | 别名: | n-cbz-[(8β)-1,6-dimethylergolin-8-yl]methylamine;N-Cbz-[(8β)-1,6-Dimethylergolin-8-yl]methylamine, [(8β)-1,6-Dimethylergolin-8-yl)methyl]carbamic acid phenylmethyl ester;[((8beta)-1,6-Dimethylergoline-8-yl)methyl]carbamic acid phenylmethyl ester;Lyserdol;N-[(1,6-Dimethylergolin-8β-yl)methyl]carbamic acid benzyl ester;[(8β)-1,6-Dimethylergolin-8-yl)methyl]carbamicacidphenylmethylester;D-[(4,6,6a,7,8,9,10,10a-Octahydro-4,7-dimethyl-10aalpha-indolo[4,3-fg]quinolin-9beta-yl)methyl]carbamic acid benzyl ester;liserdol | | CAS番号: | 17692-51-2 | | 分子式: | C25H29N3O2 | | 分子量: | 403.52 | | EINECS: | 241-686-3 | | カテゴリ情報: | Serotonin receptor | | Mol File: | 17692-51-2.mol |  |
| 融点 | 148-150 °C(lit.) | | 比旋光度 | D28 -7 ±2° | | 沸点 | 612.5±55.0 °C(Predicted) | | 比重(密度) | 1.25±0.1 g/cm3(Predicted) | | 貯蔵温度 | −20°C | | 溶解性 | 0.1 M HCl: 1.4 mg/mL | | 酸解離定数(Pka) | 12.45±0.46(Predicted) | | 外見 | solid | | 色 | White | | Merck | 13,5962 | | 安定性： | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethaqnol may be stored at -20°C for up to 2 month. | | InChIKey | WZHJKEUHNJHDLS-QTGUNEKASA-N | | CAS データベース | 17692-51-2(CAS DataBase Reference) |
| 主な危険性 | Xn | | Rフレーズ | 20/21/22 | | Sフレーズ | 36 | | WGK Germany | 3 | | RTECS 番号 | FA1070000 | | 毒性 | LD50 in mice (mg/kg): 85 i.p., 430 orally; in rats (mg/kg): >800 orally (Beretta) |
| | メテルゴリン Usage And Synthesis |
| 効能 | 血管拡張薬 | | 説明 | Metergoline (17692-51-2) is an ergot alkaloid derivative acting as antagonist at serotonin 5HT1 and 5HT2 receptors1,2 and 5HT7 receptors3. A safe and effective agent for management of hyperprolactinemic amenorrhea and anovulation.4 Displays a long-lasting antidepressant effect in seasonal affective disorder.5 | | 化学的特性 | White Solid | | Originator | Liserdol,Farmitalia,Italy,1970 | | 使用 | Metergoline is an antagonist at 5-HT1, 5-HT2, and 5-HT7 serotonin receptors. Metergoline is an analgesic; antipyretic. | | 定義 | ChEBI: Metergoline is an ergoline alkaloid that is the N-benzyloxycarbonyl derivative of lysergamine. A 5-HT2 antagonist. Also 5-HT1 antagonist and 5-HT1D ligand. Has moderate affinity for 5-HT6 and high affinity for 5-HT7. It has a role as a serotonergic antagonist, a dopamine agonist and a geroprotector. It is an ergoline alkaloid and a carbamate ester. | | Manufacturing Process | 16 g of 1-methyl-dihydro-lysergamine (the 10-position hydrogen has the αconfiguration) are dissolved in 80 cc of anhydrous pyridine by mildly heating. To the solution, cooled to -10°C and stirred, 18 cc of 85% carbobenzoxychloride (in toluene) diluted in 36 cc of chloroform are added dropwise, rather rapidly. The mixture is kept at -10°C during the addition, and for 10 minutes afterwards. The cooling means is removed and the temperature is allowed to rise to room level in 10 minutes. The reaction mixture is diluted with 240 cc of chloroform and rapidly washed with 80 cc of 5% aqueous sodium hydroxide solution, with saturated aqueous sodium bicarbonate solution, and finally with water.
The chloroform solution is briefly dried over anhydrous sodium sulfate and evaporated to dryness in vacuo at 40°C. The oily residue is taken up in 160 cc of benzene and passed through a column containing 48 g of alumina. The column is then eluted with further 160 cc of benzene. The collected eluates are evaporated in vacuo at 40°C. The thick oily residue is mixed with a small amount of anhydrous diethyl ether. After some time a crystalline mass is obtained, which is collected and washed with a small amount of benzene and diethyl ether. 12 g of white crystals are obtained, melting at 146° to 148°C. | | Therapeutic Function | Analgesic | | 生物活性 | Antagonist at 5-HT 1 /5-HT 2 with activity at 5-HT 1D . Has moderate affinity for 5-HT 6 and high affinity for 5-HT 7 . | | Biochem/physiol Actions | Antagonist at 5-HT1, 5-HT2, and 5-HT7 serotonin receptors; analgesic; antipyretic. | | 貯蔵 | Room temperature | | 参考文献 | Aulakh et al. (1992), Effects of various serotonin receptor subtype-selective antagonists alone and on m-chlorophenylpiperazine-induced neuroendocrine changes in rats; J. Pharmacol. Exp. Ther., 263 588
Bagdy et al. (1992), Pharmacological characterization of serotonin receptor subtypes involved in vasopressin and plasma renin activity responses to serotonin agonists; Eur. J. Pharmacol., 210 285
Knight et al. (2009), Pharmacological analysis of the novel, rapid, and potent inactivation of the human 5-Hydroxytryptamine7 receptor by risperidone, 9-OH-Risperidone, and other inactivating antagonists; Mol. Pharmacol., 75 374
Falsetti et al. (1982), Metergoline in the management of hyperprolactinemia amenorrhea and anovulation; Gynecol. Obstet. Invest., 13 108
Turner et al. (2002), Double-blind, placebo-controlled study of single-dose metergoline in depressed patients with seasonal affective disorder; J. Clin. Psychopharmacol., 22 216 |
|