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Trifluridine (Trifluorothymidine) is an irreversible and orally active thymidylate synthase inhibitor, and thereby suppressing DNA synthesis. Trifluridine is an antiviral molecule used for research of HSV , rhabdovirus and orthopoxvirus infection. Trifluridine induces cell apoptosis and autophagy. Trifluridine is also an anticancer agent used in studies of metastatic colorectal cancer, gastrointestinal tumors [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Trifluorothymidine; 5-Trifluorothymidine; TFT. CAS No. 70-00-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 200 mg. Product ID: HY-A0061.
Trifluridine
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Trifluridine-[13C,15N2]
Labelled Trifluridine. Trifluorothymidine (TFT) is an inhibitor of thymidine phosphorylase. TFT also inhibits thymidylate synthase (TS), a rate-limiting enzyme of DNA biosynthesis, and is incorporated into DNA. Synonyms: 1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione-13C,15N2. Grade: >98%. CAS No. 2086328-10-9. Molecular formula: C9[13C]H11F3[15N]2O5. Mole weight: 299.18.
Trifluridine Related Compound A
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Trifluridine/tipiracil hydrochloride mixture
Trifluridine/tipiracil hydrochloride mixture (TAS-102) is a potent and orally active nucleoside antitumor agent. The composition of Trifluridine/tipiracil hydrochloride mixture (TAS-102) is a 1:0.5 mixture (on a molar basis) of alpha,alpha,alpha-tri-fluorothymidine (FTD) and thymidine phosphorylase inhibitor (TPI). Trifluridine/tipiracil hydrochloride mixture (TAS-102) shows the antitumor activity mainly via the inhibition of thymidylate synthase (TS) and incorporation into DNA[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAS-102; FTD/TPI. CAS No. 733030-01-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16478.
2'-Deoxy-5-trifluoromethyluridine-5'-monophosphate is a vital compound in the biomedical industry. It is used in the development of antiviral drugs, particularly those aimed at treating RNA-based viruses such as HIV and hepatitis C. Synonyms: α,?α,?α-Trifluoro-5'-thymidylic acid; Trifluridine-5-phosphate; 5-Trifluoromethyl-2'-deoxyuridylic acid. CAS No. 345-02-8. Molecular formula: C10H12F3N2O8P. Mole weight: 376.18.
5-Carboxy-2-deoxyuridine
5-Carboxy-2-deoxyuridine is a metabolite of Trifluridine [1]. 5-Carboxy-2-deoxyuridine is a methyl oxidation product of Thymidine that can be formed by menadione-mediated photosensitization of Thymidine [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 14599-46-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W424779.
5-Carboxy-2'-deoxyuridine
5-Carboxy-2'-deoxyuridine, is a derivative of Trifluridine, an anti-herpesvirus antiviral drug, used primarily on the eye. Synonyms: 1-(2-Deoxy-β-D-erythro-pentofuranosyl)-1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinecarboxylic acid; USP Trifluridine Related Compound A; 5-Carboxy-2'-dU; 1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid. Grade: 98%. CAS No. 14599-46-3. Molecular formula: C10H12N2O7. Mole weight: 272.21.
5-Trifluorothymidine
Trifluorothymidine is an inhibitor of TS (thymidylate synthase). It is also a substrate used to study the specificity and kinetics of thymidine kinases. Acts as an anti-herpesvirus drug by blocking viral DNA replication. Decreases CRISPR-mediated HDR (homology-directed repair) efficiency. Group: Biochemicals. Alternative Names: Trifluridine; Trifluorothymine Deoxyriboside; α, α, α-Trifluorothymidine; 2-Deoxy-5- (trifluoromethyl) uridine; 5-(Trifluoromethyl)-2-deoxyuridine; Viroptic. Grades: Highly Purified. CAS No. 70-00-8. Pack Sizes: 100mg, 250mg, 1g. Molecular Formula: C??H??F?N?O?, Molecular Weight: 296.2. US Biological Life Sciences.
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