Travoprost (Synonyms: 曲伏前列素; Fluprostenol isopropyl ester; AL6221; Flu-Ipr)
目录号: PL10119 纯度: ≥99%
CAS No. :157283-68-6
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中文名称
Travoprost
中文别名
曲沃前列素;(E)-7-[(1R,2S,3R,5S)-3,5-二羟基-2-[(E)-3-羟基-4-[3-(三氟甲基)苯氧基]丁-1-烯基]环戊基]庚-5-烯酸异丙醚;曲伏前列素;曲伏前列素 Travoprost;曲伏前列素乙腈水溶液;曲伏前列腺素;曲沃前列素 API;曲沃前列素 USP标准品;曲伏前列素 曲沃前列腺素;曲沃前列素(曲伏前列素);曲伏前列腺素 10G;曲伏前列素/曲沃前列素;曲沃前列素157283-68-6,工厂零售157283-68-6;欺负前列腺素杂质
英文名称
Travoprost
英文别名
Travoprost;Propan-2-yl (E)-7-[(1R,2S,3R,5S)-3,5-dihydroxy-2-[(E)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-enyl]cyclopentyl]hept-5-enoate;Fluprostenol isopropyl ester;Travaprost; AL 6221;FLU-IPR;Travatan;15(S)-FLU-IPR;cGMP Travoprost;Travoprost (AL-6221);Travoprostintermediates;Travoprost, >=99%;(Z)-isopropyl 7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((R,E)-3-hydroxy-4-(3-(trifluoromethyl)phenoxy)but-1-enyl)cyclopentyl)hept-5-enoate;Propan-2-yl 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-e;Propan-2-yl 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(E,3R)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-enyl]cyclopentyl]hept-5-enoate
Cas No.
157283-68-6
分子式
C26H35F3O6
分子量
500.55
包装储存
Pure form -20°C 3 years;In solvent -80°C 6 months
产品详情
Travoprost (Fluprostenol isopropyl ester) 是一种异丙基酯前药,是一种高亲和力的,选择性的 FP 前列腺素全受体激动剂。Travoprost 有降眼压功效,有潜力应用于青光眼和眼高压。
生物活性
Travoprost (Fluprostenol isopropyl ester), an isopropyl ester prodrug, is a high affinity, selective FP prostaglandin full receptor agonist. Travoprost has the ocular hypotensive efficacy and has the potential for glaucoma and ocular hypertension.
性状
Liquid
IC50 & Target[1][2]
FP
体外研究(In Vitro)
Travoprost has sub-micromolar affinity for the DP, EP1, EP3, EP4, IP, and TP receptors. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Travoprost produces a lower incidence of ocular irritation than PGF20 isopropyl ester at a dose of 1 μg in the New Zealand albino (NZA) rabbit. Topical ocular application of Travoprost produces a marked miotic effect in cats following doses of 0.01, 0.03 and 0.1 μg. In the ocular hypertensive monkey, b.i.d. application of 0.1 and 0.3 μg of travoprost afforded peak reduction in intraocular pressure (IOP) of 22.7% and 28.6%, respectively. Topical application of travoprost was well tolerated in rabbits, cats and monkeys, causing no ocular irritation or discomfort at doses up to 1 μg. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Pure form -20°C 3 years;In solvent -80°C 6 months
ClinicalTrial
参考文献
[1]. M R Hellberg, et al. Preclinical efficacy of travoprost, a potent and selective FP prostaglandin receptor agonist. J Ocul Pharmacol Ther. 2001 Oct;17(5):421-32.
溶解度数据
In Vitro: Ethanol : 60 mg/mL (119.87 mM; Need ultrasonic)DMSO : ≥ 41.67 mg/mL (83.25 mM)
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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