Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0468 |
Lidocaine
Lignocaine,Alphacaine,Xylocaine,利多卡因 |
Apoptosis; ERK; NF-κB; MEK; Sodium Channel; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Neuroscience; NF-κB |
Lidocaine (Alphacaine) 是一种酰胺衍生物,抑制涉及复杂电压和依赖性的钠通道,可用于研究室性心律失常。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。 | |||
T1144 |
Lidocaine hydrochloride
Lidocaine HCL,盐酸利多卡因,Lignocaine hydrochloride,Xyloneural,Lidothesin |
Apoptosis; ERK; NF-κB; MEK; Sodium Channel | Apoptosis; MAPK; Membrane transporter/Ion channel; NF-κB |
Lidocaine hydrochloride (Lignocaine hydrochloride) 抑制涉及复杂电压和依赖性的钠通道。它通过调节 miR-145 表达和进一步抑制 MEK/ERK 和 NF-κB 信号通路来减少胃癌细胞的生长,迁移和侵袭。Lidocaine 是一种酰胺衍生物,是一种研究室性心律失常的药物和有效的肿瘤抑制剂。 | |||
T1144L |
Lidocaine Hydrochloride hydrate
|
EGFR; Sodium Channel | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Lidocaine Hydrochloride hydrate 是一种酰胺类局部麻醉剂,具有抗炎作用。 | |||
T23213 |
QX-222 chloride
QX 222,Lidocaine N-Methyl Hydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
QX-222 chloride (Lidocaine N-Methyl Hydrochloride) 是 Lignocaine 的一种三甲基类似物,是有效的 Na+通道阻滞剂。 | |||
T25720 |
Lidocaine methiodide
Methyllidocaine iodide,N-Methyllidocaine |
||
Lidocaine methiodide is an antiarrythmic. It is also exhibiting arrythmogenic effects in subjects. | |||
T8341 |
QX 314
QX-314 |
Others | Others |
QX 314 (Lidocaine N-ethyl bromide) 是一种非膜渗透性阻滞剂,可抑制酸诱导的食管伤害性 C 纤维神经元活化。 | |||
T13177L |
Tocainide
|
Sodium Channel | Membrane transporter/Ion channel |
Tocainide 是口服有活性的 sodium channel 阻滞剂,阻断产生疼痛的病灶中(神经膜上)的钠通道。它是利多卡因 (lignocaine) 的伯胺类似物,可用于研究心律不齐。 | |||
T10679 |
Carcainium chloride
卡氯铵,QX 572,Carcainium (chloride),Carcainiumchloride,RSD 931 |
Others | Others |
Carcainium chloride (Carcainium (chloride)) 是利多卡因的衍生物,具有镇咳作用。 | |||
T9530 |
W 36017
|
Others | Others |
W36017 是利多卡因的一种杂质,其阻滞神经活性的pKa 为 7.4。 | |||
T26287 |
Transcainide
R54718,R 54718,R-54718 |
Sodium Channel | Membrane transporter/Ion channel |
Transcainide(R 54718) 是一种新的利多卡因类似物,是具有口服活性的抗心律失常剂。Transcainide 可阻断牛心脏和大鼠骨骼肌中 BTX 激活的钠通道的开放状态。 | |||
T13177 | Taquidil | ||
Tocainide hydrochloride 是一种sodium channel 阻滞剂,它阻断神经膜中产生疼痛的病灶中的钠通道。Tocainide hydrochloride 是利多卡因 (lignocaine) 的一种伯胺类似物,可有效抑制各种情况下的室性心律失常。 | |||
T1098 |
Denatonium benzoate
苯甲地那铵,THS-839 |
Others | Others |
Denatonium benzoate (THS-839) 是一种已知的最苦的化合物,可作为厌恶剂(苦味剂),加入到工业酒精、防冻液、咬指甲癖预防、呼吸器面罩配合测试、动物驱虫剂、液体皂和洗发水中,防止不适当的摄取。 | |||
T34253 |
Rad 242
Rad242,Rad-242 |
||
Rad 242 is a hydrophobic lidocaine derivative. | |||
T30861 |
CH 200
CH-200,CH200,06-14C |
||
CH 200 is a novel antiarrhythmic drug that inhibits arrhythmias in beagles more effectively than procainamide and lidocaine. | |||
T20732 |
Lignocaine N-oxide
|
||
Lignocaine N-oxide is a metabolite of Lidocaine, which is an antiarrhythmic and anesthetic agent. | |||
T80638 |
Glycinexylidide
GX |
MEK | MAPK |
Glycinexylidide (GX) 是一种 Lidocaine 的活性代谢物。作为有效的局部麻醉药,Lidocaine 可以通过阻断复杂电压依赖性的钠通道来发挥作用。此外,它还能抑制胃癌细胞生长、迁移和侵袭。GX 显示出在麻醉、癌症治疗和心血管疾病研究中的应用潜力。 | |||
T37670 |
CAY10568
|
||
Most local anesthetics act by abolishing voltage gated sodium channel currents indiscriminately in all populations of neurons. Selective analgesia through TRPV1-mediated entry of a cationic lidocaine derivative, QX314, was recently reported. CAY10568 is a physically smaller, less hydrophobic version of QX314 designed to be even more permeable to TRPV1 ion channel when activated by agonists such as capsaicin and N-oleoyl dopamine. CAY10568 when given in combination with suitable TRPV1 agonists sh... |