17
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T7938 | Quinidine | Parasite | |
Quinidine is a stereoisomer of the antimalarial agent quinine and a class Ia antiarrhythmic agent. for the treatment of abnormal heart rhythms and also malaria. | |||
T0266 | Quinidine hydrochloride monohydrate | Quinidine hydrochloride | Potassium Channel , Sodium Channel , Parasite |
Quinidine hydrochloride monohydrate is an optical isomer of quinine, extracted from the bark of the Cinchona tree and similar plant species. It prolongs cellular action potential and decreases automaticity. This alkaloid... | |||
T8125 | Quinidine sulfate dihydrate | Chinidin Sodium,β-quinine Sodium,Pitayine Sodium,Quinidine sulfate | P450 |
Quinidine sulfate dihydrate (Pitayine Sodium) is a potent and selective cytochrome P450db inhibitor | |||
T77550 | O-Desmethyl Quinidine | Others | |
O-Desmethyl Quinidine is a novel quinidine analog with significant antiarrhythmic activity and low acute toxicity that may be useful in the treatment of cardiac arrhythmias. | |||
T1317 | Cinchonidine | α-Quinidine,L-Cinchonidine | 5-HT Receptor , Serotonin Transporter , Parasite |
Cinchonidine (L-Cinchonidine) is an alkaloid extracted from Cinchona officinalis. It is a pseudo-enantiomer and stereoisomer of cinchonine. | |||
T36561 | (3S)-hydroxy Quinidine | ||
(3S)-hydroxy Quinidine is an active quinidine metabolite. Quinidine, an antiarrhythmic agent, undergoes rapid first-pass metabolism by the cytochrome P450 (CYP) isoforms CYP3A4, CYP2C9, CYP2E1, and CYP3A5, with CYP3A4 be... | |||
T64286 | Quinidine polygalacturonate | ||
Quinidine polygalacturonate is a potent, selective, orally active inhibitor of cytochrome P450db (cytochrome P450db) and a potent K+channel blocker with an IC50 value of 19.9 μM, which also induces apoptosis. Quinidine p... | |||
T61517 | Quinidine Monosulfate | ||
Quinidine Monosulfate is an antiarrhythmic agent. Quinidine Monosulfate is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine Monosulfate is also a K + channel blocker with an IC 50 of 19.9 μM. Qui... | |||
T124756 | Quinidine sulfate | ||
Quinidine sulfate is a useful organic compound for research related to life sciences and the catalog number is T124756. | |||
T60893 | Ep vinyl quinidine | ||
Ep vinyl quinidine (3-Epiquinine) is an epi-vinyl stereoisomer of Quinidine. Quinidine can be used in malaria research which is also an antiarrhythmic agent. Quinidine is a potent, orally active, selective inhibitor of c... | |||
T1334 | Hydroquinidine | Hydroconchinine,Dihydroquinidine,Hydroconquinine,(+)-Hydroquinidine,Dihydroquinine | Potassium Channel , Sodium Channel |
Hydroquinidine ((+)-Hydroquinidine) is an organic compound, used as an antiarrhythmic agent. | |||
T40657 | Epiquinidine | ||
Epiquinidine, an analogue of quinine, serves as an agonist for ggTas2r1, exhibiting activation at concentrations of 10 μM or higher. | |||
T13302 | Viquidil hydrochloride | Quinotoxine hydrochloride | Others |
Viquidil hydrochloride (Quinotoxine hydrochloride) is an isomer of Quinidine. Viquidil hydrochloride is an agent of cerebral vasodilator with antithrombotic activity. | |||
T1012 | Acebutolol hydrochloride | Acebutolol HCl | Adrenergic Receptor |
Acebutolol hydrochloride (Acebutolol HCl) acts as a cardioselective beta-adrenergic antagonist with little effect on bronchial receptors and has intrinsic sympathomimetic properties. Acebutolol hydrochloride is the hydro... | |||
T21266 | Quinine sulfate | ||
Quinidine is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a blocker of K + channel with an IC 50 of 19.9 μM. Quinidine has potential to be used ... | |||
T61999 | Quinine hydrobromide | ||
Quinidine is a potent, orally active, selective inhibitor of cytochrome P450db. Quinidine hydrobromide is a K + channel blocker (IC 50= 19.9 μM). Quinidine hydrobromide shows antiarrhythmic activity. Quinidine hydrobromi... | |||
T23940 | DA 1686 | BRN 1029299,DA-1686,DA1686 | |
DA 1686 is a therapeutic antiarrhythmic compound.DA 1686 reduces the tachycardic effects of aconitine. It also reduces the effects of increased frequency of electrical stimulation and is 1.8 times more active than quinid... |