Catalog |
name |
Description |
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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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R-R-4943 |
Raluridine CAS No.119644-22-3 |
Raluridine/CAS No.119644-22-3 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. |
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R-R-4944 |
6-O-Methyldeoxyguanosine CAS No.964-21-6 |
O6-Methyldeoxy guanosine/CAS No.964-21-6; DNA adduct 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. |
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R-R-4945 |
6-Mercaptopurine-13C2,15N CAS No.1190008-04-8 |
6-Mercaptopurine-13C2,15N/CAS No.1190008-04-8 is the 13C- and 15N-labeled 6-Mercaptopurine. 6-Mercaptopurine is a purine analogue which acts as an antagonist of the endogenous purines and has been widely used as antileukemic agent and immunosuppressive agent. |
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R-R-4962 |
Tenofovir exalidex CAS No.911208-73-6 |
Tenofovir exalidex (CMX157)/CAS No.911208-73-6 is a lipid conjugate of the acyclic nucleotide analog Tenofovir with activity against both wild-type and antiretroviral drug-resistant HIV strains, including multidrug nucleoside/nucleotide analog-resistant viruses. Tenofovir exalidex is active against all major subtypes of HIV-1 and HIV-2 in fresh human PBMCs and against all HIV-1 strains evaluated in monocyte-derived macrophages, with EC50s ranging between 0.2 and 7.2 nM. CMX157 is orally available and has no apparent toxicity. Tenofovir exalidex also shows antiviral activity against HBV. |
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