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JAK・STATシグナル
| Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
|---|---|---|---|---|
| T2806 | Lappaconitine | 32854-75-4 | 98% |
|
| Lappaconitine, isolated from Aconitum sinomontanum Nakai, was characterized as an analgesic. | ||||
| T31716 | Etidocaine Hydrochloride | 36637-19-1 | 98% |
|
| Etidocaine Hydrochloride (Duranest, W-19053) is a voltage-gated sodium channel blocker used as an anesthetic with extended action. | ||||
| T27205 | DPI 201-106 | 97730-95-5 | 98% |
|
| DPI-201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel inactivation. DPI-201-106 inhibits the L-type calcium current, and inward and delay... | ||||
| T1144 | Lidocaine hydrochloride | 73-78-9 | 98% |
|
| Lidocaine hydrochloride is a local anesthetic and cardiac depressant used as an antiarrhythmic agent. Its actions are more intense and its effects more prolonged... | ||||
| T0440 | Oxcarbazepine | 28721-07-5 | 98% |
|
| Oxcarbazepine is an Anti-epileptic Agent. The physiologic effect of oxcarbazepine is by means of Decreased Central Nervous System Disorganized Electrical Activit... | ||||
| T9685 | DS-1971a | 1450595-86-4 | 98% |
|
| DS-1971a is a highly potent and selective NaV1.7 inhibitor. DS-1971a exhibits a favorable toxicological profile and analgesic effects. | ||||
| T6782L | Benzocaine xHCl(94-09-7(free base)) | T6782L | 98% |
|
| Benzocaine shares a common receptor with all othe rLAs in the voltage-gated Na+ channel(IC50 of 0.8 mM tested with a potential of +30 mV). | ||||
| T1320 | Disopyramide | 3737-09-5 | 98% |
|
| A class I anti-arrhythmic agent (one that interferes directly with the depolarization of the cardiac membrane and thus serves as a membrane-stabilizing agent) wi... | ||||
| T69552 | Suzetrigine | 2649467-58-1 | 98% |
|
| Suzetrigine（VX-548） is an orally active and specific NaV1.8 inhibitor. Suzetrigine has analgesic activity and can be used to study acute pain and neurotransmissi... | ||||
| T0806 | Flunarizine dihydrochloride | 30484-77-6 | 98% |
|
| Flunarizine is a selective calcium entry blocker with calmodulin binding properties and histamine H1 blocking activity. Flunarizine hydrochloride is effective in... | ||||
| T6566 | Levobupivacaine hydrochloride | 27262-48-2 | 98% |
|
| Levobupivacaine HCl is a reversible neuronal sodium channel inhibitor, which is the pure S(-)-enantiomer of bupivacaine. It was utilized as a long-acting local a... | ||||
| T34081 | Piromelatine | 946846-83-9 | 98% |
|
| Piromelatine is an agonist of melatonin MT1/MT2 receptors, 5-HT1A and 5-HT1D, and an antagonist of 5-HT2B.Piromelatine has antinociceptive activity with inhibito... | ||||
| T37688 | Cyfluthrin | 68359-37-5 | 98% |
|
| Cyfluthrin is a pyrethroid insecticide and a modulator of voltage-gated sodium channels (Nav).1,2It slowly activates rat recombinant Nav1.8 channels, delays inac... | ||||
| T1389 | Dyclonine hydrochloride | 536-43-6 | 98% |
|
| Dyclonine, an over the counter throat lozenge, is found in Sucretswith local anesthetic effect . | ||||
| T19554 | L-Aspartic aicd sodium | 3792-50-5 | 98% |
|
| L-Aspartic aicd sodium is an amino acid, a precursor active molecule for colon-specific active molecule delivery, that promotes Na+ efflux from rat forebrain mem... | ||||
| T0916 | Butamben | 94-25-7 | 98% |
|
| Butamben is a long-duration local anesthetic used for the treatment of chronic pain. | ||||
| T1332 | Permethrin | 52645-53-1 | 98% |
|
| Permethrin is a pyrethroid insecticide commonly used in the treatment of LICE INFESTATIONS and SCABIES. | ||||
| T6541 | Ibutilide Fumarate | 122647-32-9 | 98% |
|
| Ibutilide Fumarate is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominat... | ||||
| T0030 | Bupivacaine hydrochloride | 18010-40-7 | 98% |
|
| Bupivacaine Hydrochloride is a long-acting, amide-type local anesthetic. Bupivacaine reversibly binds to specific sodium ion channels in the neuronal membrane, r... | ||||
| T6645 | Ropivacaine hydrochloride monohydrate | 132112-35-7 | 98% |
|
| Ropivacaine HCl is an anaesthetic agent and blocks impulse conduction in nerve fibres through inhibiting sodium ion influx reversibly. | ||||
