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| Catalog | name | Description | 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> |
| R-C-3223 | AR-C155858 CAS:496791-37-8 | AR-C155858 is a potent inhibitor of monocarboxylate transporters MCT1 and MCT2 that binds to an intracellular site involving transmembrane helices 7-10.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
| R-R-4893 | Bredinin aglycone CAS No.56973-26-3 | Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide)/CAS No.56973-26-3 is a purine nucleotide analogue. Bredinin aglycone can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogues. | price> |
| R-C-3224 | AR-C117977 CAS:216685-07-3 | AR-C117977 is a potent MCT1 inhibitor,which can reduce vimmune responses both in vitro and in vivo,maintains long-term graft survival,and induces operational tolerance.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
| R-R-4894 | 4-C-Azidouridine CAS No.139442-01-6 | 4-C-azidouridine (4-Azidouridine)/CAS No.139442-01-6 is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents. 4-C-Azidouridine 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-3225 | UK 5099 CAS:56396-35-1 | UK 5099 is a potent inhibitor of plasma membrane monocarboxylate transporters(MCTs) and the mitochondrial pyruvate carrier(MPC);inhibits pyruvate-dependent O2 consumption with an IC50 of 50nM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |

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