Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6566 |
Levobupivacaine hydrochloride
Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) 是有效的钠通道阻滞剂。 | |||
T70224 |
Bupivacaine tartrate
|
||
Bupivacaine is a BK/SK, Kv1, Kv3, TASK-2 K Channel and voltage-gated Na channel blocker used as an anesthetic. It maybe neurotoxic at high does, inducing apoptosis in neuroblastoma cells. It acts by binding to the intracellular portion of voltage-gated sodium channels and blocking sodium influx into nerve cells. | |||
T80641 |
Bupivacaine hydrochloride monohydrate
|
Potassium Channel; Calcium Channel; Sodium Channel; NMDAR | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Bupivacaine hydrochloride monohydrate 是一种 NMDA 受体抑制剂,对钠、L-钙和钾通道有抑制作用。Bupivacaine hydrochloride monohydrate 对 SCN5A 通道有抑制作用,常用于研究慢性疼痛。 | |||
T0030 |
Bupivacaine hydrochloride
Vivacaine,Bupivacaine HCl,盐酸布比卡因 |
Sodium Channel | Membrane transporter/Ion channel |
Bupivacaine hydrochloride (Vivacaine) 是NMDA 受体抑制剂,可用于慢性疼痛的研究。它可阻断钠、L-钙和钾通道,还阻断SCN5A 通道,IC50为 69.5 μM。 |