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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10977 | DCEBIO | Potassium Channel | |
DCEBIO stimulates the secretion of Cl- through the activation of the hIK1 K + channel and the activation of the apical Cl- conductance. DCEBIO is a derivative of 1-EBIO and a very strong activator of Cl- secretion by T84... | |||
T20968 | CyPPA | Potassium Channel , Dopamine Receptor | |
CyPPA, a subtype-selective positive modulator of SK channels, decreased spontaneous firing rate, increased the duration of the apamin-sensitive afterhyperpolarization. | |||
T13164 | Tipepidine hydrochloride | Potassium Channel , Dopamine Receptor | |
Tipepidine hydrochloride is a reversible inhibitor of dopamine (DA) D2 receptor-mediated GIRK currents (IDA(GIRK)) (IC50: 7.0 μM), with antidepressant-like effect. | |||
T2604 | 1-EBIO | Calcium Channel | |
1-EBIO (1-EBIO) is a calium channel agonist. | |||
T14982 | Clofilium tosylate | Potassium Channel | |
Clofilium tosylate is a potassium channel blocker. It induces apoptosis of human promyelocytic leukemia (HL-60) cells via Bcl-2-insensitive activation of caspase-3. | |||
TN1092 | O-Nornuciferine | Potassium Channel , HER | |
O-Nornuciferine reveals distinct in vitro hERG blockages measured in HEK293 cells with the IC50 value of 2.89 uM. | |||
T8189 | Dihydroberberine | Potassium Channel , HSP , HER | |
Dihydroberberine has anti-atherosclerotic, anti-inflammatory, hypolipidemic and antitumor activities. It inhibits human ether-a-go-go-related gene (hERG) channels and remarkably reduces Hsp90 expression and its interacti... | |||
T4224 | ML335 | Potassium Channel | |
ML335 is a selective activator of TREK-1 and TREK-2. | |||
T15385 | Glibornuride | Potassium Channel | |
Glibornuride is an ATP-sensitive K+ channels (KATP channel) blocker ( pKi: 5.75). It is an antidiabetic agent. | |||
T7653 | JNJ 303 | Potassium Channel | |
JNJ 303 is a potent blocker of IKs (IC50 : 64 nM). | |||
T10566 | BMS-191095 | Potassium Channel | |
BMS-191095 is mitochondrial ATP-sensitive potassium (mitoKATP) channel activator. | |||
T0690 | Quinine | Potassium Channel , Platelet aggregation , Parasite | |
Quinine is a natural cinchona alkaloid that has been used for centuries in the prevention and therapy of malaria. Quinine is also used for idiopathic muscle cramps. Quinine therapy has been associated with rare instances... | |||
T3959 | ICA-069673 | ICA069673 | Potassium Channel |
ICA-069673 is an activator of KCNQ2/Q3 potassium channel (IC50: 0.69 μM). | |||
T3192 | NS1643 | Potassium Channel , HER , Autophagy | |
NS1643 is a potent human ether-a-go-go related gene (hERG) KV11.1 channel activator with EC50 of 10.5 μM. | |||
T16110 | ML418 | Potassium Channel | |
ML418 is a potent, selective and CNS penetrating Kir7.1 potassium channel blocker (IC50 = 310 nM), and also potently inhibits Kir6.2/SUR1. | |||
T22745 | DPO-1 | Potassium Channel | |
DPO-1 is a blocker of IKur ultrarapid delayed rectifier potassium current and KV1.5 channels | |||
T7612 | ICA 110381 | Potassium Channel | |
ICA 110381 is a KCNQ2/Q3 potassium channel opener for the treatment of epilepsy | |||
T12255 | NS19504 | Potassium Channel | |
NS19504 is an activator of Ca2+-activated K+ channel with EC50 of 11.0 µM. NS19504 shows relaxing effect on bladder smooth muscle spontaneous phasic contractions[1]. | |||
T5444 | CLP290 | CLP-290 | Potassium Channel |
CLP290 is an activator of the neuron-specific K+-Cl cotransporter KCC2 and displays potential for the treatment of a wide range of neurological and psychiatric indications. | |||
T60061 | RU-TRAAK-2 | Potassium Channel | |
RU-TRAAK-2 is a reversible inhibitor of TWIK-related arachidonic acid-stimulated K+ channel with no activity for non-K2P channels including Kv1.2, GIRK2, and Slo1. |