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Nucleoside Antimetabolite/Analog
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Nucleoside Antimetabolite/Analog Related Products (2437)
Related Products (2437)
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2′,3′-Dideoxy-3′-fluoroadenosine
0 ImagesCat. No.: HY-154038CAS No.: 87418-35-72′,3′-Dideoxy-3′-fluoroadenosine 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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5-Fluoro-3’-beta-C-methyluridine
0 ImagesCat. No.: HY-1541365-Fluoro-3’-beta-C-methyluridine 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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2-Amino-6-chloropurine-9-beta-D-(2’-deoxy-3’,5’-di-O-(p-toluoyl))riboside
0 ImagesCat. No.: HY-W551230CAS No.: 35095-93-32-Amino-6-chloropurine-9-beta-D-(2’-deoxy-3’,5’-di-O-(p-toluoyl))riboside 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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2’-Deoxy-2’-fluoro- N3-(2S)-(2-amino-3-carbonyl)-propyluridine
0 ImagesCat. No.: HY-1547262’-Deoxy-2’-fluoro- N3-(2S)-(2-amino-3-carbonyl)-propyluridine 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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3’-beta-C-Methylcytidine
0 ImagesCat. No.: HY-152394CAS No.: 20724-72-5 -
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3’-O-(2-Methoxyethyl)-2-aminoadenosine
0 ImagesCat. No.: HY-152646CAS No.: 256224-02-93’-O-(2-Methoxyethyl)-2-aminoadenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277). -
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2′-Deoxy-2-hydrazinyladenosine
0 ImagesCat. No.: HY-154559CAS No.: 1000296-26-32′-Deoxy-2-hydrazinyladenosine 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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3α,7α-Dihydroxy-5β-cholestan-26-al
0 ImagesCat. No.: HY-180593CAS No.: 1029053-18-63α,7α-Dihydroxy-5β-cholestan-26-al is a nucleoside metabolite. -
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TLR7 agonist 10
0 ImagesCat. No.: HY-149071CAS No.: 2389988-34-3TLR7 agonist 10 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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3'OMe-m7GpppAmpG ammonium solution (100 mM) (GMP Like)
0 ImagesCat. No.: HY-145973AGLSynonyms: m7(3'OMeG)(5')ppp(5')(2'OMeA)pG ammonium solution (100 mM) (GMP Like)3'OMe-m7GpppAmpG ammonium solution (100 mM) (GMP Like) (m7(3'OMeG)(5')ppp(5')(2'OMeA)pG ammonium solution (100 mM) (GMP Like)) is a GMP-like grade of 3’OMe-m7GpppAmpG. 3’OMe-m7GpppAmpG (m7(3'OMeG)(5')ppp(5')(2'OMeA)pG) ammonium solution (100 mM) is a trinucleotide Cap1 analog with the structure m7 (3'OMeG)(5') ppp (5')(2'OMeA) pG, and also functions as a cis-acting ligase ribozyme inhibitor. 3’OMe-m7GpppAmpG ammonium solution (100 mM) effectively reduces free 5'-triphosphate groups on RNA transcripts, thereby enabling efficient co-transcriptional capping of in vitro transcribed mRNA. 3’OMe-m7GpppAmpG ammonium solution (100 mM) is not only widely used in the preparation of modified mRNA including trivalent influenza vaccine candidates, but also applicable to studies related to SARS-CoV-2 infection and other relevant research. -
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3’-Deoxy-O6-methyl inosine
0 ImagesCat. No.: HY-154201CAS No.: 945215-53-23’-Deoxy-O6-methyl inosine 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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3’-Deoxy-3’-fluoro-2-thiouridine
0 ImagesCat. No.: HY-152754CAS No.: 439579-24-53’-Deoxy-3’-fluoro-2-thiouridine 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. -
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6-Chloro-2-iodopurine-9-riboside
0 ImagesCat. No.: HY-21978CAS No.: 313477-85-99H-Purine, 6-chloro-2-iodo-9-β-D-ribofuranosyl- (6-CHLORO-2-IODOPURINE-9-RIBOSIDE) 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. -
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3’-Azido-3’-deoxy-4-deoxyuridine
0 ImagesCat. No.: HY-152985CAS No.: 2095417-07-36-Chloro-N1-(trimethylsilylethoxymethyl)pseudouridine is a uridine analog. 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. 3’-Azido-3’-deoxy-4-deoxyuridine 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. -
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ADP-β-D-ribofuranose-13C15
0 ImagesCat. No.: HY-157906SADP-β-D-ribofuranose-13C15 is the 13C-labeled ADP-β-D-ribofuranose (HY-157906). ADP-β-D-ribofuranose is a nucleotide derivative composed of ADP and a ribose unit. ADP-β-D-ribofuranose can be produced by NAD+ catalysis. -
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2-Amino-3’-deoxy-3’-fluoroadenosine
0 ImagesCat. No.: HY-152487CAS No.: 125391-75-52-Amino-3’-deoxy-3’-fluoroadenosine 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. -
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α-Phocaecholic acid
0 ImagesCat. No.: HY-W1130518CAS No.: 6879-45-4α-Phocaecholic acid is a nucleoside metabolite. -
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2'-O-Methyl-5-iodouridine
0 ImagesSynonyms: 5-Iodo-2'-O-methyluridine2’-O-Methyl-5-iodouridine (5-Iodo-2'-O-methyluridine) 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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3′-Azido-2′,3′-dideoxy-5-hydroxyuridine
0 ImagesCat. No.: HY-149070CAS No.: 111495-90-03′-Azido-2′,3′-dideoxy-5-hydroxyuridine 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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6-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
0 ImagesCat. No.: HY-1540476-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is a pyrimidine nucleoside analog. Pyrimidine nucleoside analogs have a wide range of biochemical and anticancer activities. These include DNA synthesis inhibition, RNA synthesis inhibition, antiviral effects, and immunomodulatory effects. -
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