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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. price>
R-R-4880 Trimethyl-beta-cyclodextrin CAS No.:55216-11-0 Trimethyl-beta-cyclodextrin/Trimethyl-β-cyclodextrin/CAS No.:55216-11-0, a fascinating chemical compound, exhibits immense potential in scientific research. Its diverse applications range from drug delivery systems to improving solubility and stability of hydrophobic molecules. With its unique structure, this compound opens up a world of possibilities for innovative scientific studies. price>
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. price>
R-R-4881 Adenosine-13C5 CAS No.159496-13-6 Adenosine-13C5/CAS No.159496-13-6 is the 13C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation. price>
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. price>
R-R-4882 Adenosine-1-13C CAS No.201996-55-6 Adenosine-1-13C/CAS No.201996-55-6 is the 13C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiolo. price>
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). price>
R-R-4883 2-Deoxy-N1-methylguanosine CAS No.5132-79-6 2-Deoxy-N1-methylguanosine/CAS No.5132-79-6 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. price>
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. price>
R-R-4884 5-O-TBDMS-dG CAS No.51549-33-8 5-O-TBDMS-dG/CAS No.51549-33-8 is a modified nucleoside. 5-O-DMT-2-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid. price>
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. price>
R-R-4885 Uridine-13C CAS No.201996-62-5 Uridine-13C/CAS No.201996-62-5 is the 13C labeled Uridine. price>
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. price>
R-R-4886 3-Deoxyguanosine CAS No.3608-58-0 3-Deoxyguanosine (Guanosine, 3-deoxy-)/CAS No.3608-58-0 is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. price>
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. price>
R-R-4887 3-Deoxy-3-fluoroadenosine CAS No.75059-22-2 3-Deoxy-3-fluoroadenosine/CAS No.75059-22-2 is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. price>
R-C-3218 T16Ainh-A01 CAS:552309-42-9 T16Ainh-A01 is a selective TMEM16A calcium-activated chloride channel inhibitor that strongly inhibits chloride current in salivary gland cells.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. price>
R-R-4888 5-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite) CAS No.1197033-17-2 5-ODMT cEt N-Bzm5 C Phosphoramidite Amidite/CAS No.1197033-17-2 is a potent nucleic acid analog. 5-ODMT cEt N-Bzm5 C Phosphoramidite Amidite blongs to modified antisense oligonucleotide. price>
R-C-3219 Luseogliflozin CAS:898537-18-3 Luseogliflozin is an orally active second-generation sodium-glucose co-transporter 2 (SGLT2)inhibitor developed by Taisho Pharmaceutical for the treatment of patients with type 2 diabetes mellitus(T2DM).Our products are only suitable for scientific research experiments, not for clinical experiments and human body. price>
R-R-4889 3-Azido-3-deoxy-5-fluorocytidine CAS No.2095417-18-6 3-Azido-3-deoxy-5-fluorocytidine (Compound 12)/CAS No.2095417-18-6 is a cytidine derivative. 3-Azido-3-deoxy-5-fluorocytidine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups. price>