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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9530 | W 36017 | Others | |
W36017 is an impurity of lidocaine with a PKA of 7.4 for blocking neurologic activity. | |||
T4S1876 | 3-Deoxyaconitine | Sodium Channel | |
3- Deoxyaconitine is a derivative of Aconitine (A189875), which activates tetrodotoxin-sensitive Na+ channels, inducing presynaptic depolarization, thus blocking the nerve action potential which, in turn, blocks the rele... | |||
T4497 | Amifampridine | 3,4-Pyridinediamine,Pyridine-3,4-Diamine,3,4-Diaminopyridine | Others |
Amifampridine (3,4-Diaminopyridine) is predominantly in the treatment of a number of rare muscle diseases. Amifampridine works by blocking potassium channel efflux in nerve terminals so that action potential duration is ... | |||
T0025 | Haloperidol | Aloperidin,Serenace,Haldol | Dopamine Receptor , 5-HT Receptor |
Haloperidol (Serenace) is a highly potent neuroleptic by relieving nervous through the depression of nerve function. In addition, haloperidol has shown about 50-fold efficacy than chlorpromazine, another antipsychotic dr... | |||
T2S1727 | Lycorenine | Antifection | |
Lycorenine may produce a decrease in blood pressure as the result of alpha-adrenergic blockade in conjunction with the reduction of the spontaneous sympathetic nerve activity, and produce bradycardia by modifying vagal a... | |||
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 intra... | |||
T61475 | Ropivacaine mesylate | ||
Ropivacaine mesylate, a long-acting amide local anaesthetic, is used for spinal block and effectively mitigates neuropathic pain. It achieves analgesia by reversibly inhibiting sodium ion influx in nerve fibers, thus blo... | |||
T81519 | Pentapeptide-3 | ||
Pentapeptide-3, a pentapeptide fragment derived from waglerin-1 neurotoxin, is sourced from Temple Viper venom. This compound serves as a competitive antagonist of nicotinic acetylcholine receptors (nAChRs), blocking ner... |