Hledali jste: 5-Fluoro-5\\\'-deoxyuridine+(Doxifluridine)

Dodavatel: Apollo Scientific

Popis: (+)-5-Fluoro-5'-deoxyuridine

Dodavatel: Thermo Scientific

Popis: 5-Fluoro-5'-deoxyuridine (Doxifluridine)

Dodavatel: Merck

Popis: 5-Fluoro-5'-deoxyuridine (Doxifluridine), Sigma-Aldrich®

Dodavatel: Apollo Scientific

Popis: 5-Fluoro-2'-deoxyuridine (floxuridine) 99%

Dodavatel: Thermo Scientific

Popis: 5-Fluoro-2'-deoxyuridine (floxuridine) ≥98%

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Dodavatel: Thermo Scientific

Popis: 5-Fluoro-2'-deoxyuridine (floxuridine) 99+%

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Dodavatel: Apollo Scientific

Popis: 2'-Deoxy-2'-fluorouridine 98%

Dodavatel: Thermo Scientific

Popis: 2'-Deoxy-2'-fluorouridine 97%

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Dodavatel: Merck

Popis: 5-Fluoro-2'-deoxyuridine (floxuridine), Sigma-Aldrich®

Katalogové číslo: (J64217.06)

Dodavatel: Thermo Scientific

Popis: 5'-O-(4,4'-Dimethoxytrityl)-2'-fluoro-2'-deoxyuridine 98%

Měrná jednotka: 1 * 5 g

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Dodavatel: Cayman Chemical

Popis: 5-Fluoro-2'-deoxyuridine (floxuridine)

Dodavatel: MP Biomedicals

Popis: 5-Fluorodeoxyuridine is an antineoplastic agent, which acts as an anti-metabolite. When administrated by rapid injection it acts as flurouracil, but when infused slowly, usually intra-arterially, it is converted to active F-dUMP, which leads to enhanced inhibition of DNA synthesis. It inhibits DNA synthesis by blocking thymidylic acid synthetase.

Katalogové číslo: (PRSI55-545)

Dodavatel: ProSci Inc.

Popis: Catalyzes the reversible phosphorylytic cleavage of uridine and deoxyuridine to uracil and ribose-or deoxyribose-1-phosphate. The produced molecules are then utilized as carbon and energy sources or in the rescue of pyrimidine bases for nucleotide synthesis. Shows substrate specificity and accept uridine, deoxyuridine, and thymidine as well as the two pyrimidine nucleoside analogs 5-fluorouridine and 5-fluoro-2(')-deoxyuridine as substrates.

Měrná jednotka: 1 * 400 µl

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Dodavatel: Thermo Scientific

Popis: 2'-Deoxy-2'-fluorouridine 97%

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Katalogové číslo: (PRSI30-425)

Dodavatel: ProSci Inc.

Popis: TYMS catalyzes the methylation of deoxyuridylate to deoxythymidylate using 5,10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs.Thymidylate synthase catalyzes the methylation of deoxyuridylate to deoxythymidylate using 5,10-methylenetetrahydrofolate (methylene-THF) as a cofactor. This function maintains the dTMP (thymidine-5-prime monophosphate) pool critical for DNA replication and repair. The enzyme has been of interest as a target for cancer chemotherapeutic agents. It is considered to be the primary site of action for 5-fluorouracil, 5-fluoro-2-prime-deoxyuridine, and some folate analogs. Expression of this gene and that of a naturally occuring antisense transcript rTSalpha (GeneID:55556) vary inversely when cell-growth progresses from late-log to plateau phase. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-47 CR601528.1 1-47 48-1099 X02308.1 14-1065 1100-1603 BC083512.1 1067-1570

Měrná jednotka: 1 * 50 µG

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Dodavatel: Thermo Scientific

Popis: (E)-5-(2-Bromovinyl)-2'-deoxyuridine 98%

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