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Catalog | name | Description | price |
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R-C-3263 | GZ-793A CAS:1356447-90-9 | GZ-793A is a selective inhibitor of vesicular monoamine transporter 2(VMAT2),which transports the monoamine neurotransmitters from cellular cytosol into synaptic vesicles.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4933 | Nucleoside-Analog-1 CAS No.876707-99-2 | Nucleoside-Analog-1/CAS No.876707-99-2 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-3264 | NBI-98782 CAS:85081-18-1 | NBI-98782(alpha-dihydrotetrabenazine)is a vesicular monoamine transporter(VMAT2) inhibtior with an Ki value of 0.97nM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4934 | AzddMeC CAS No.87190-79-2 | AzddMeC (CS-92)/CAS No.87190-79-2 is an antiviral nucleoside analogue and a potent potent, selective and orally active HIV-1 reverse transcriptase and HIV-1 replication inhibitor. In HIV-1-infected human PBM cells and HIV-1-infected human macrophages, the EC50 values of AzddMeC are 9 nM and 6 nM, respectively. AzddMeC 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-3265 | U18666A CAS:3039-71-2 | U18666A, an intra-cellular cholesterol transport inhibitor, inhibits replication of Ebola virus, dengue virus, and human hepatitis C virus.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4935 | 3-Deoxycytidine CAS No.7057-33-2 | 3-Deoxycytidine/4-Amino-1-((2R,3R,5S)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one/CAS No.7057-33-2 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-3166 | TUG-770 CAS:1402601-82-4 | TUG-770 is a Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatment of Type 2 Diabetes.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-C-3266 | TAK-441 CAS:1186231-83-3 | TAK-441 is a pyrrolo[3,2-c]pyridine derivative,as a highly potent and orally active hedgehog signaling inhibitor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4936 | Peldesine CAS No.133432-71-0 | Peldesine (BCX 34)/CAS No.133432-71-0 is a potent, competitive, reversible and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50s of 36 nM, 5 nM, and 32 nM for human, rat, and mouse red blood cell (RBC) PNP, respectively. Peldesine is also a T-cell proliferation inhibitor with an IC50 of 800 nM. Peldesine has the potential for cutaneous T-cell lymphoma, psoriasis and HIV infection research.At equivalent molar concentrations, both the salt and free forms of a compound exhibit comparable biological activity. Nevertheless, the salt form (Peldesine dihydrochloride) usually boasts enhanced water solubility and stability. | price> |
R-C-3267 | GANT61 CAS:500579-04-4 | GANT61 is an inhibitor for GLI1 as well as GLI2-induced transcription,inhibits hedgehog with IC50 of 5μM,displays selectivity over other pathways,such as TNF and glucocorticoid receptor gene transactivation.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4937 | 2-Deoxy-N3-methylcytidine hydriodide CAS No.79043-77-9 | 2-Deoxy-N3-methylcytidine hydriodide/CAS No.79043-77-9 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-3268 | RU-SKI 43 CAS:1043797-53-0 | RU-SKI 43 is a small molecule inhibitor of Hhat(Hedgehog acyltransferase), the enzyme responsible for the attachment of palmitate onto Shh.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4938 | Alpha-Adenosine CAS No.5682-25-7 | Alpha-Adenosine/CAS No.5682-25-7 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-3269 | ETC-159 CAS:1638250-96-0 | ETC-159 is a potent and specific inhibitor of Wnt secretion.ETC-159 inhibits beta-catenin reporter activity in a dose-dependent manner with an IC50 of 2.9nM.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4939 | Nucleoside-Analog-2 CAS No.876708-01-9 | Nucleoside-Analog-2/CAS No.876708-01-9 is a 4-Azidocytidine analogue against Hepatitis C virus (HCV) replication. Nucleoside-Analog-2 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-3270 | WAY-262611 CAS:1123231-07-1 | WAY-262611 is a wingless β-Catenin agonist that increases bone formation rate with an EC50 of 0.63 μM in TCF-Luciferase assay,WAY-262611 is also a Dkk1 inhibitor.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4940 | N-6-Methyl-2-deoxyadenosine-d3 CAS No.1354782-02-7 | N-6-Methyl-2-deoxyadenosine-d3/CAS No.1354782-02-7 is the deuterium labeled N-6-Methyl-2-deoxyadenosine (HY-W011725). N-6-Methyl-2-deoxyadenosine is an adenine nucleoside analogue. | price> |
R-C-3271 | CCT251545 CAS:1661839-45-7 | CCT251545 is an orally bioavailable and potent inhibitor of WNT signaling with an IC50 of 5 nM in 7dF3 cells.CCT251545 is a selective chemical probe for exploring the role of CDK8 and CDK19 in human disease.Our products are only suitable for scientific research experiments, not for clinical experiments and human body. | price> |
R-R-4941 | KIN59 CAS No.4152-77-6 | KIN59 (5-O-Tritylinosine)/CAS No.4152-77-6 is a potent thymidine phosphorylase allosteric inhibitor. KIN59 inhibits FGF2-stimulated cell growth. KIN59 inhibits the expression of p-FGFR1, P-Akt in FGF2 (10 ng/mL) stimulated cells. KIN59 shows anti-tumor activity. | price> |
R-R-4942 | 2-Deoxy-N4-methylcytidine CAS No.22882-02-6 | 2-Deoxy-N4-methylcytidine/CAS No.22882-02-6 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> |