87233-61-2
87233-61-2 結(jié)構(gòu)式
基本信息
依美斯汀
1-(2-乙氧基乙基)-2-(4-甲基-1,4-二氮雜庚烷-1-基)苯并咪唑
1-(2-Ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)benzimidazole
1-(2-Ethoxyethyl)-2-(4-methylhexahydro-1H-1,4-diazepine-1-yl)-1H-benzimidazole
1-(2-Ethoxyethyl)-2-[(hexahydro-4-methyl-1H-1,4-diazepin)-1-yl]-1H-benzimidazole
物理化學(xué)性質(zhì)
常見(jiàn)問(wèn)題列表
依美斯?。‥medastine，商品名稱(chēng)： Emadine）是第二代抗組織胺，可用作眼藥水以減緩過(guò)敏性結(jié)膜炎的癥狀。依美斯汀屬于H1 接收器抑制劑。借由抑制組織胺的作用來(lái)減緩過(guò)敏性結(jié)膜炎的癥狀。當(dāng)依美斯汀用作眼藥水時(shí)，會(huì)以雙延胡索酸鹽（difumarate）的形式存在。
| Target | Value |
|
H1 receptor
(Cell-free assay) | 1.3 nM(Ki) |
Emedastine inhibits histamine H
2
receptor (K
i
=49067 nM) and histamine H
3
receptor (K
i
=12430 nM).
High concentrations of Emedastine (1 and 10 ng/ml) significantly inhibits type 1 collagen production in normal human dermal fibroblasts.
Emedastine (1, 10, 100, 1000 nM) at concentrations of ≥ 10 nM inhibits CC chemokine-elicited eosinophil migration.
Emedastine (0.03, 0.1, 0.3 mg/kg; orally; pretreatment of 30 min) significantly suppresses histamine-induced scratching with 0.1 and 0.3 mg/kg but not 0.03 mg/kg.
Pretreatment with Emedastine (0.03, 0.1, 0.3 mg/kg; orally) significantly inhibits the scratching induced by substance P and leukotriene B.
Emedastine (0.3 mg/kg, p.o.) produces significant inhibition of passive peritoneal anaphylaxis in guinea-pigs.
Emedastine inhibits histamine-induced contractions of isolated ileum (IC
50
=6.1 nM).
| Animal Model: | Male ICR mice 5-6 weeks of age |
| Dosage: | 0.03, 0.1, 0.3 mg/kg |
| Administration: | Orally; 30 min before pruritogen injection |
| Result: | Significantly suppressed histamine-induced scratching with pretreatment of 0.1 and 0.3 mg/kg. |