Alfuzosin hydrochloride/SL 77499-10;盐酸阿夫唑嗪

Alfuzosin hydrochloride/SL 77499-10;盐酸阿夫唑嗪

货号:
IA1910

品牌:
Jinpan

Alfuzosin hydrochloride/SL 77499-10;盐酸阿夫唑嗪

暂无详情
产品简介
MDL MFCD00879135
EC EINECS 620-512-3
别名 阿夫唑嗪盐酸盐;AlfuzosinHCl
英文名称 Alfuzosin hydrochloride/SL 77499-10
CAS 81403-68-1
分子式 C19H27N5O4·HCl
分子量 425.91
纯度 HPLC≥98%
单位
生物活性 Alfuzosin, a new quinazoline derivative, acts as a selective and competitive antagonist of alpha 1-adrenoceptor-mediated contraction of prostatic, prostatic capsule, bladder base and proximal urethral smooth muscle, thereby reducing the tone of these structures. [1]Alfuzosin is a potent selective alpha1-adrenoceptor antagonist in tissues of the lower urinary tract including the human prostate. This provides a pharmacological basis for its use in the treatment of benign prostatic hypertrophy.[2]
In Vitro Phenylephrine-induced contractions of rabbit isolated trigone and urethra were antagonized in a competitive manner by alfuzosin (pA2 7.44 and 7.30, respectively) and prazosin. [2]
In Vivo In the pithed rat, alfuzosin (0.03-0.3 mg kg-1, i.v.) markedly inhibited pressor responses produced by the alpha 1-selective agonist, cirazoline but inhibited only slightly responses to the alpha 2-selective agonist, UK 14,304. Alfuzosin (1 mg kg-1, i.v.) had minimal effects against responses mediated by stimulation of prejunctional alpha 2-receptors (UK 14,304-induced inhibition of sympathetic tachycardia).[2] In the anaesthetized cat, alfuzosin (0.001-1 mg kg-1, i.v.) and prazosin (0.001-0.3 mg kg-1, i.v.) produced dose-related inhibition of the increases in urethral pressure caused by stimulation of sympathetic hypogastric nerves. [2]
SMILES O=C(C1OCCC1)NCCCN(C2=NC(N)=C3C=C(OC)C(OC)=CC3=N2)C.Cl
靶点 Adrenergic Receptor
数据来源文献 [1]. Wilde MI, et al. Alfuzosin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in benign prostatic hyperplasia. Drugs. 1993 Mar;45(3):410-29.
[2]. Lefèvre-Borg F, O’Connor SE, Schoemaker H, Hicks PE, Lechaire J, Gautier E, Pierre F, Pimoule C, Manoury P, Langer SZ. Alfuzosin, a selective alpha 1-adrenoceptor antagonist in the lower urinary tract. Br J Pharmacol. 1993 Aug;109(4):1282-9.
规格 10mg 50mg 100mg

是α1肾上腺素受体拮抗剂

未甲基帽 G(5′)ppp(5′)A #S1406L 5 μmol-NEB酶试剂 New England Biolabs

上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。

产品资料 – RNA 试剂 – RNA 合成

未甲基帽 G(5′)ppp(5′)A                              收藏

货 号
规 格
价 格(元)
北京库存
上海库存
广州库存
成都库存
苏州库存
武汉库存

#S1406L
5 μmol
8,019.00

#S1406S
1 μmol
1,999.00

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  • isoschizomers     |
  • compatible ends     | 
  • single letter code

概述

体外实验的初始阶段,绝大多数真核生物 mRNA 5´ 端 m7G 帽结构可促进翻译。对于绝大多数
RNA,帽结构都可提高 RNA 的稳定性,降低其对核酸外切酶降解的敏感性,并促进 mRNA 起始复合体的形成。在真核生物无细胞蛋白合成系统的情况下,5´ 端帽结构甚至可使原核 mRNA 的翻译效率与真核 mRNA 一样高。另外,还发现在真核生物靶 RNA 的剪切过程同样需要帽结构。

应用

• 使用 T7 RNA 聚合酶从 phi2.5 启动子共转录加帽,启动子在转录起始点包含一个 A
• 合成未甲基化 G 加帽的 RNA
• 合成 A 加帽的 RNA