59 Results for "

rectifier

" in MedChemExpress (MCE) Product Catalog:
Products (59)

59 Results for "rectifier" in MCE Product Catalog:

Cat. No.: HY-178058A
Target:  

Potassium Channel

Research Areas:  

Others

VU6080824 (hydrochloride), a derivative of ML-133 (HY-100230), is an inward-rectifier potassium channel (Kir2.1) inhibitor with an IC50 of 0.35  μM. VU6080824 (hydrochloride) has superior thallium flux and manual patch clamp (MPC) functional potency .
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Cat. No.: HY-101436A
CAS No.: 101526-62-9
Purity:  99.33%
Synonyms: CK-1752 hydrochloride
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

Sematilide hydrochloride (CK-1752 hydrochloride) is a selective IKr channel blocker. Sematilide causes a concentration-dependent inhibition of the delayed rectifier K + current (IC50=25 μM). Sematilide is a class III antiarrhythmic agent .
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Cat. No.: HY-A0148
CAS No.: 69756-53-2
Synonyms: SKF-102886 free base; WR-171669
Halofantrine (SKF-102886 hydrochloride; WR-171669 hydrochloride) is a blocker that delays the delayed rectifier potassium current by inhibiting human ERG channels, and it is a potent antimalarial agent with oral activity. Halofantrine inhibits the Cap1-dependent oxidative stress response of Candida albicans, suppresses ROS responses, and enhances the antifungal (Fungal) activity of oxidative damage agents. Halofantrine exhibits antifungal activity in the Galleria mellonella model, and shows antimalarial activity against Plasmodium strains both in vitro and in animal models. Halofantrine can be used in studies related to invasive candidiasis, falciparum malaria, and vivax malaria .
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Cat. No.: HY-108585
CAS No.: 1315380-70-1
Purity:  98.02%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

VU591 hydrochloride is a selective inhibitor of the renal outer medullary potassium channel (ROMK, Kir1.1). VU591 hydrochloride inhibits ROMK via binding to the intracellular pore region near residues Val168 and Asn171, with IC50 of 240 nM in Tl + flux assay and 300 nM in whole cell patch clamp electrophysiology, suppresses native ROMK mediated K + secretion in isolated perfused rat collecting ducts, and exerts antidepressive effects in the mouse tail suspension test (TST). VU591 hydrochloride can be used for the study of ROMK channel function, renal potassium handling, antidepressant mechanisms, and diuretic drug discovery .
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Cat. No.: HY-119649S
CAS No.: 2483830-60-8
Purity:  ≥98.0%
Synonyms: IKI220-15N18O
Flonicamid- 15N, 18O (IKI220- 15N, 18O) is the 18O , 15N-labeled Flonicamid (HY-119649). Flonicamid (IKI220) is an antifeedant Insecticide active against Hemiptera, Thysanoptera, and piercing-sucking pests including aphids of all species, developmental stages and morphs. Flonicamid inhibits the inward rectifier potassium channel NlKir1, blocking stylet penetration, salivation, sap feeding, honeydew secretion, and fluid secretion by isolated Malpighian tubules. Flonicamid reduces renal excretory function in female Culex pipiens pallens. Flonicamid rapidly disrupts insect feeding behavior without neurotoxic poisoning symptoms, induces irreversible starvation, and increases the mortality of nymph progeny of adult aphids exposed to this agent .
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Cat. No.: HY-P1427
CAS No.: 1233152-82-3
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Guangxitoxin 1E is a potent and selective blocker of KV2.1 and KV2.2 channels. Guangxitoxin 1E inhibits KV2 with an IC50 of 1-3 nM. KV2 channels underlie delayed-rectifier potassium currents in various neurons .
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Cat. No.: HY-178058
Target:  

Potassium Channel

Research Areas:  

Others

VU6080824 (Compound 5s), a derivative of ML-133 (HY-100230), is an inward-rectifier potassium channel (Kir2.1) inhibitor with an IC50 of 0.35  μM. VU6080824 has superior thallium flux and manual patch clamp (MPC) functional potency .
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Cat. No.: HY-110015
CAS No.: 163163-24-4
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

(-)-Chromanol 293B is a potent and selective inhibitor of the slow component of delayed rectifier K + current (IKs). (-)-Chromanol 293B can be used for the research of antiarrhythmic .
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Cat. No.: HY-P5887
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Tertiapin-RQ is an inward rectifier K + channel blocker peptide with antidepressive effect .
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Cat. No.: HY-117528
CAS No.: 138490-53-6
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

WAY-123398 is a class III antiarrhythmic agent. WAY-123398 is a selective blocker of the delayed rectifier K + current .
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Cat. No.: HY-106855
CAS No.: 123955-10-2
Synonyms: H 234​/09
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

Almokalant is a class III antiarrhythmic agent, acts as a potassium channel blocker, and inhibits a specific component (Ikr) of the time-dependent delayed rectifier K + current.
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Cat. No.: HY-120685
CAS No.: 139047-48-6
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

WAY-125971, a propylamine analogue, is a potent and specific blocker of the rectifier potassium current (IK). WAY-125971 can be used for the study of arrhythmia .
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Cat. No.: HY-101436
CAS No.: 101526-83-4
Synonyms: CK-1752
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

Sematilide (CK-1752) is a selective IKr channel blocker. Sematilide causes a concentration-dependent inhibition of the delayed rectifier K + current (IC50=25 μM). Sematilide is a class III antiarrhythmic agent .
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Cat. No.: HY-108163A
CAS No.: 179258-62-9
Research Areas:  

Neurological Disease

SB-237376 is a blocker of potassium and calcium channels. SB-237376 inhibits the rapidly activating delayed rectifier potassium current I(Kr) (IC50: 0.42 μM) and blocks the L-type calcium current I(Ca,L) at high concentrations .
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Cat. No.: HY-B0387R
CAS No.: 122647-32-9
Synonyms: U70226E (Standard)
Ibutilide (fumarate) (Standard) is the analytical standard of Ibutilide (fumarate). This product is intended for research and analytical applications. Ibutilide (U70226E) fumarate, an action potential-prolonging antiarrhythmic, is a potent blocker of the rapidly activating delayed rectifier K + current (IKr) in AT-1 cells .
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Cat. No.: HY-101436AR
CAS No.: 101526-62-9
Synonyms: CK-1752 hydrochloride (Standard)
Sematilide (hydrochloride) (Standard) is the analytical standard of Sematilide (hydrochloride). This product is intended for research and analytical applications. Sematilide hydrochloride (CK-1752 hydrochloride) is a selective IKr channel blocker. Sematilide causes a concentration-dependent inhibition of the delayed rectifier K+ current (IC50=25 μM). Sematilide is a class III antiarrhythmic agent .
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Cat. No.: HY-P5771
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Jingzhaotoxin-IX, a C-terminally amidated peptide composed of 35 amino acid residues, is a neurotoxin. Jingzhaotoxin-IX inhibits voltage-gated sodium channels (both tetrodotoxin-resistant and tetrodotoxin-sensitive isoforms) and Kv2.1 channel. Jingzhaotoxin-IX has no effect on delayed rectifier potassium channel Kv1.1, 1.2 and 1.3 .
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Cat. No.: HY-118148
CAS No.: 113049-11-9
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

UK-66914, is a class III antiarrhythmic agent that specifically acts on the delayed rectifier potassium current (I_K). UK-66914 is designed to prolong action potential duration (APD) and increase cardiac refractory period, thereby potentially terminating the reentry mechanism in arrhythmias without affecting the serious side effects of antiarrhythmic drugs associated with other ion channels such as Na+ and Ca2+ currents .
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Cat. No.: HY-P2791
CAS No.: 58694-52-3
Tertiapin (reduced) is a kind of synthesis of melittin, its Cys3-Cys14 and Cys5-Cys18 between containing a disulfide bond. Tertiapin (reduced) is a kind of inward rectifier potassium channels blockers, can block the activity of calcium activates large conductance potassium channels. Tertiapin (reduced) can be used for research in diseases such as rheumatoid arthritis and multiple sclerosis .
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Cat. No.: HY-B0432R
CAS No.: 54063-53-5
Synonyms: SA-79 (Standard)
Propafenone (Standard) is the analytical standard of Propafenone. This product is intended for research and analytical applications. Propafenone (SA-79), a sodium-channel blocker, acts an antiarrhythmic agent. Propafenone also has high affinity for the β receptor (IC50=32 nM) . Propafenone blocks the transient outward current (Ito) and the sustained delayed rectifier K current (Isus) with IC50 values of 4.9 μm and 8.6 μm, respectively . Propafenone suppresses esophageal cancer proliferation through inducing mitochondrial dysfunction and induce apoptosis .
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