Catalog |
name |
Description |
price |
R-C-3208 |
NS1619 CAS:153587-01-0 |
NS1619 is a Bkca opener or large-conductance Ca2+-activated potassium(BKCa, KCa1.1)channel activator.Our products are only suitable for scientific research experiments,not for clinical experiments and human body. |
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R-C-3209 |
NS-1643 CAS:448895-37-2 |
NS1643 is one of the small molecule HERG (Kv11.1)channel activators and has also been found to increase erg2(Kv11.2)currents.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. |
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R-C-3210 |
SKA-31 CAS:40172-65-4 |
SKA-31(Naphtho[1,2-d]thiazol-2-ylamine)is a potent activator of potassium channel with EC50 of 260nM,1.9μM,2.9μM,and 2.9μM for KCa3.1,KCa2.2,KCa2.1 and KCa2.3,respectively. |
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R-C-3211 |
ML418 CAS:1928763-08-9 |
ML418 is a potent, selective and CNS penetrating blocker of Kir7.1 potassium channel with IC50 of 310 nM.ML418 also potently inhibits Kir6.2/SUR1,and exhibits superior selectivity over other Kir channels. |
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R-C-3212 |
Y-26763 CAS:127408-31-5 |
Y-26763 is a K+ channel opener and active metabolite of Y-27152.Y-26763 is an ATP-sensitive K+(KATP)channel activator. |
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R-C-3213 |
JNJ 303 CAS:878489-28-2 |
JNJ 303 is a potent blocker of the voltage dependent IKs-channel encoded by KCNQ1/KCNE1 with IC50 of 64 nM. JNJ 303 induces QT-prolongations and causes unprovoked torsades de pointes (TdP). |
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R-C-3214 |
RPR-260243 CAS:668463-35-2 |
RPR-260243 is a novel activator of HERG;modifies HERG currents inhibited by dofetilide (IC50=58nM);little effect on HERG current amplitude and no significant effects on steady-state activation parameters or on channel inactivation processes.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. |
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R-C-3215 |
MK-7145 CAS:1255204-84-2 |
MK-7145 is a ROMK inhibitor, with an IC50 of 0.045μM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. |
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R-C-3216 |
Talniflumate CAS: 66898-62-2 |
Talniflumate is a calcium-activated chloride channel(CaCC)(hCLCA1/mCLCA3)blocker; reduces mucin synthesis and release in cell culture and animal models.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. |
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R-C-3217 |
CaCCinh-A01 CAS: 407587-33-1 |
CaCCinh-A01(TMEM16 Blocker I)is a TMEM16 Blocker. CaCCinh-A01 is a non-selective inhibitor of calcium-activated chloride channels (CaCCs) that blocks ATP-stimulated chloride conductance in human salivary gland, intestinal, and bronchial epithelium (mean IC50=10µM)Our products are only suitable for scientific research experiments, not for clinical experiments and human body. |
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