
Talinolol - Wikipedia
Talinolol is a beta blocker. [1] Talinolol contains a stereocenter and consists of two enantiomers. This is a racemate, i.e. a 1: 1 mixture of (R)- and the (S)-forms: [2] ^ Abmann, I. (1995). "The …
Talinolol: Uses, Interactions, Mechanism of Action - DrugBank …
Talinolol has been investigated for the basic science of Gastrointestinal Motility Disorder. The next evolution of DrugBank is here. Designed for scientists, driven by AI, and powered by real-time …
他林洛尔 - 维基百科,自由的百科全书
他林洛尔 (英语:Talinolol)是一种 β受体阻滞剂 [1] 和 抗高血压药 物。 他林洛尔含有一个 立体中心 并由两种 对映体 组成。 这是一种 外消旋体,即 (R)-和 (S)-形式的1:1混合物: [2] ^ …
talinolol - Drug Central
Talinolol is a beta1-selective adrenoceptor antagonist well known for its cardioprotective and antihypertensive activity. By blocking beta1-adrenergic receptors, talinolol delays the …
TALINOLOL - National Center for Advancing Translational Sciences
Talinolol (brand name Cordanurn) is the cardioselective beta-receptor antagonist which has been used for a long time in the treatment of various cardiovascular diseases and in …
Talinolol | C20H33N3O3 | CID 68770 - PubChem
Talinolol | C20H33N3O3 | CID 68770 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity …
Talinolol | Drug Information, Uses, Side Effects, Chemistry ...
Technical details about Talinolol, learn more about the structure, uses, toxicity, action, side effects and more
他林洛尔(Talinolol) - 药物靶点:β-adrenoceptors_在研适应症:高 …
Efflux ratios (ERs) of talinolol and rosuvastatin by P-gp and BCRP, respectively, were higher in enteroid monolayers compared to Ussing chamber, likely caused by experimental differences …
Talinolol - an overview | ScienceDirect Topics
Talinolol (TAL), a poorly water-soluble, long-acting beta-blocker, suffers from a fluctuating bioavailability most likely due to precipitation in the GIT, inchoate and irregular absorption as …
Dose-effect and kinetic-dynamic relationships of the beta ... - PubMed
Talinolol was confirmed to bind to beta-adrenoceptors with moderate affinity but to act as a highly selective and efficient beta 1-adrenoceptor antagonist in terms of the relative degree and …