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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
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 ... | |||
T11990 | Meclofenamic acid | Meclofenamate | Others , Gap Junction Protein |
Meclofenamic acid (Meclofenamate) is a non-selective gap-junction blocker and a selective fat mass and obesity-associated (FTO) enzyme inhibitor. Meclofenamic acid has anti-inflammatory activities. | |||
T23497 | UK 78282 hydrochloride | Potassium Channel | |
UK 78282 hydrochloride, a novel potent and selective Kv1.3 blocker.UK 78282 hydrochloride inhibits Kv1.3 voltage-gated potassium channels and suppresses human T cell activation. | |||
T12786 | RY785 | Potassium Channel | |
RY785 is a potent and selective inhibitor of voltage-gated potassium channel such as KV2.2 (IC50 = 50 nM). RY785 may be used in pain relief studies. | |||
T7502 | PF 05089771 tosylate | Sodium Channel | |
PF-05089771 is a voltage-gated sodium channel 1.7 (Nav1.7) blocker (IC50: 11, 16, 33, and 20 nM for 5N11S, 5A11L, 5A11S, and 5A11L Nav1.7 splice variants, respectively). It is selective for Nav1.7 over Nav1.1-1.6 and 1.8... | |||
T1496 | Amiodarone hydrochloride | Amiodar,Amiodarone HCl,Nexterone | Potassium Channel , Adrenergic Receptor , Autophagy |
Amiodarone hydrochloride (Amiodarone HCl) is an antianginal and class III antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting POTASSIUM CHANNELS and VOLTAGE-GATED SODIUM C... | |||
T22925 | Linopirdine dihydrochloride | Others | |
KV7 (KCNQ) voltage-gated potassium channels blocker | |||
T16815 | RY796 | Others | |
RY796 is an effective and selective inhibitor of voltage-gated potassium channel (IC50s: 0.25 μM and 0.09 μM for KV2.1 and KV2.2). | |||
T11787 | Kv3 modulator 1 | Others | |
Kv3 modulator 1 is a promising compound for the treatment of inflammatory pain. As a modulator of Kv3 voltage-gated potassium channels, Kv3 modulator 1 exhibits potential therapeutic properties in this indication. | |||
T80064 | Dendrotoxin-I | DTX-I | Potassium Channel |
Dendrotoxin-I, a neurotoxin from Dendroaspis snake venom, potently blocks K⁺ channels, specifically targeting voltage-gated potassium channel subunits KV1.1 and KV1.2 [1] [2] [3]. | |||
T63684 | DAD dichloride | ||
DAD dichloride is an ion channel blocker that blocks voltage-gated potassium channels, a third-generation photoelectric switch that responds to visible light, and can be used to study visual function. | |||
T27564 | Hymenidin | 5-HT Receptor | |
Hymenidin, an alkaloid isolated from the Okinawan sponge Hymeniacidon sp. is a 5-hydroxytryptaminergic receptor antagonist and voltage-gated potassium channel inhibitor with potential antiprotozoal effects.It selectively... | |||
T80980 | Tityustoxin-Kα | TsTx-Kα | |
Tityustoxin-Kα (TsTx-Kα) acts as an inhibitor of potassium voltage-gated channels, exhibiting a dose-dependent blockade of the sustained outward current in cultured hippocampal neurons [1]. | |||
T62770 | DAD | ||
DAD is an ion channel blocker (blocks voltage-gated potassium channels) and is a third generation photoelectric switch that responds to visible light. | |||
T80497 | KTX-Sp2 | Potassium Channel | |
KTX-Sp2, a potassium channel toxin, effectively blocks exogenous voltage-gated potassium channels Kv1.1, Kv1.2, and Kv1.3, as well inhibits the endogenous Kv1.3 channel and suppresses Ca2+ signaling in Jurkat T cells. Ad... | |||
T75792 | Huwentoxin XVI TFA | ||
Huwentoxin XVI TFA, a potent analgesic derived from the Chinese tarantula Ornithoctonus huwena, acts as a highly reversible and selective antagonist of mammalian N-type calcium channels (IC 50 of ~60 nM), with no impact ... | |||
T80426 | Jingzhaotoxin-IX | Sodium Channel | |
Jingzhaotoxin-IX is a C-terminally amidated peptide neurotoxin consisting of 35 amino acid residues. It inhibits both tetrodotoxin-resistant and tetrodotoxin-sensitive isoforms of voltage-gated sodium channels, as well a... | |||
T80851 | VSTx-3 | Kappa-TRTX-Gr4a,κ-Theraphotoxin-Gr4a,Voltage sensor toxin 3,Peptide F | |
VSTx-3 is a potassium voltage-gated channel (K_V) blocker, which has also been shown to be a potent tetrodotoxin-sensitive (TTX-sensitive) sodium channel inhibitor, with particular efficacy against NaV1.8 channels, as ev... | |||
T21819 | Psora 4 | ||
Psora-4 is a potent and selective inhibitor of K v 1.3 (voltage-gated potassium channels) with a Hill coefficient of 2 and an EC50 value of 3 nM [1]. Psora-4 has immunosuppressive activity and inhibits proliferation of h... | |||
T80528 | Ssm spooky toxin | SsTx Toxin | Potassium Channel |
Ssm Spooky Toxin, derived from Scolopendra mutilans, exhibits potent lethality affecting both hematological and respiratory systems primarily through the inhibition of KCNQ (voltage-gated potassium channel family 7) chan... |