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Cat. No. | Product Name | Target | Signaling Pathways |
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T21370 |
Amiodarone
Nexterone,胺碘酮,Amiodarona,Cordarone,Aratac,Amiodaronum |
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Amiodarone is categorized as a class III antiarrhythmic agent and prolongs phase 3 of the cardiac action potential. It also has numerous other effects, including actions that are similar to those of antiarrhythmic classes Ia, II, and IV. Amiodarone chemic | |||
T1496 |
Amiodarone hydrochloride
盐酸胺碘酮,Amiodar,Amiodarone HCl,Nexterone |
Potassium Channel; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Amiodarone hydrochloride (Amiodarone HCl) 是一种抗心绞痛和 III 类抗心律失常药物,通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间,可导致心率和血管阻力降低。它通过成纤维细胞中的 ERK1/2和 p38 MAPK 信号传导诱导细胞增殖和肌成纤维细胞分化,可研究室上性和室性心律失常。 | |||
T25301 |
Deiodoamiodarone
Amiodarone hydrochloride impurity A,Dideiodo Amiodarone |
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Deiodoamiodarone is an intermediate of amiodarone. Amiodarone is an α/β-adrenergic receptor antagonist and coronary vasodilator. | |||
T20143 |
L-6424
L 6424,Amiodarone related compound G |
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L-6424 is an intermediate of Amiodarone and a non-selective ion channel blocker. It has an antiarrhythmic. | |||
T20141 |
L-6355
L 6355,Amiodarone related compound E,Demonoiodoamiodarone |
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L-6355 is an agent of bioactive chemicals. | |||
T80650 | Di-N-desethyl amiodarone hydrochloride | Autophagy | Autophagy |
Di-N-desethyl Amiodarone hydrochloride为Amiodarone的代谢产物,作为一种强效的呼吸链抑制剂。该 Amiodarone作为抗心律失常剂,其机制涉及抑制ATP敏感性钾通道。 | |||
T20659 |
Desethylamiodarone
N-Deethylamiodarone,DAMI,LB-33020,LB 33020,N-Monodesethylamiodarone,LB33020 |
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Diethylamiodarone is the main metabolite of amiodarone in vivo. | |||
T11002 |
Desethylamiodarone hydrochloride
N-desethylamiodarone hydrochloride,LB 33020 hydrochloride |
Others | Others |
Desethylamiodarone hydrochloride (N-desethylamiodarone hydrochloride) is formed by the CYP3A isozyme. Amiodarone is an antiarrhythmic drug that inhibits ATP-sensitive potassium channels with an IC50 of 19.1 μM. It is the main active metabolite of amiodaro | |||
T1073 |
Dronedarone hydrochloride
Dronedarone HCl,SR33589,决奈达隆盐酸盐,盐酸决奈达隆 |
Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dronedarone hydrochloride (SR33589) 是一种胺碘酮类似物,可抑制 Na+,K+andCa2+的电流,有可能治疗心房颤动。 | |||
T30374 |
Benziodarone
Coronal-crinos,Carofam,Dilacoron,Dila-Vasal,Corofam |
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Benziodarone is a vasodilator that acts as an amiodarone-like action. | |||
T30607 |
Budiodarone
ATI2042,ATI-2042,ATI 2042 |
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Budiodarone(ATI-2042)is a chemical analog of an antiarrhythmic drug and amiodarone. Budedalone is promising as an antiarrhythmic agent for the prevention of atrial fibrillation. | |||
T74678 | Budiodarone tartrate | ||
Budiodarone (ATI-2042) tartrate 是 Amiodarone 的化学类似物,具有平衡的、多种心脏离子通道 (potassium,sodiumandcalcium channels) 抑制活性。Budiodarone tartrate 是一种抗心律失常剂。 | |||
T32030 |
GYKI-16638 HCl
GYKI 16,638,GYKI16,638,GYKI-16638,GYKI-16,638,GYKI16638,GYKI 16638 |
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GYKI-16638 is a novel antiarrhythmic agent that demonstrates combined class IB and class III antiarrhythmic properties in human ventricular muscles, similar to the electrophysiological findings after chronic amiodarone treatment. In addition, GYKI 16638 h | |||
T35712 |
Debutyldronedarone hydrochloride
SR35021 hydrochloride |
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N-Desbutyl dronedarone is an active metabolite of the antiarrhythmic agent dronedarone .1,2,3It is formed from dronedarone by cytochrome P450s (CYPs) and monoamine oxidase (MAO) in human hepatocyte preparations.4N-Desbutyl dronedarone inhibits the binding of 3,3’,5-triiodo-L-thyronine to the thyroid hormone receptors TRα1and TRβ1(IC50s = 59 and 280 μM for the chicken and human receptors, respectively).1It inhibits CYP2J2-mediated formation of 14,15-EET from arachidonic acid and soluble epoxide h... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T7056 |
Dronedarone
决奈达隆,SR 33589 |
P450; Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dronedarone (SR 33589) 是一种胺碘酮类似物,对治疗心房颤动可能有效。它是CYP3A4的底物和中度抑制剂。它是多种离子电流的有效阻滞剂,通过非竞争性结合到肾上腺素能受体显示出抗肾上腺素能的效果。 |