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Catalog | name | Description | price |
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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). | 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> |
R-C-3220 | T-1095 CAS: 209746-59-8 | T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4890 | 5-Methoxycarbonylmethyl-2-O-methyluridine CAS No.60197-31-1 | 5-Methoxycarbonylmethyl-2-O-methyluridine/CAS No.60197-31-1 is a thymidine analogue. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis. | price> |
R-C-3221 | SGL5213 CAS:1240305-17-2 | SGL5213 is a potent, oral active and low-absorbable sodium-dependent glucose cotransporter 1(SGLT1)inhibitor,with IC50 values of 29nM and 20nM for hSGLT1 and hSGLT2,respectively.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4891 | 2-Thiocytidine CAS No.13239-97-9 | 2-Thiocytidine/CAS No.13239-97-9 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-3222 | Licogliflozin CAS:1291094-73-9 | Licogliflozin is a sodium glucose cotransporter(SGLT1 and SGLT2)inhibitor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4892 | N-Propargyladenosine CAS No.67005-97-4 | N-Propargyladenosine/CAS No.67005-97-4 is an adenosine analogue. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. The popular products in this series are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277). N-Propargyladenosine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | price> |