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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T0984 | 5-Fluorouracil | 5-FU,Fluorouracil,NSC 19893,5-Fluoracil | Apoptosis , Nucleoside Antimetabolite/Analog , HIV Protease , DNA/RNA Synthesis , Endogenous Metabolite |
5-Fluorouracil (5-FU) is a uracil analog, an inhibitor of DNA synthesis. 5-Fluorouracil has antitumor activity and affects pyrimidine synthesis through inhibition of thymidylate synthase. 5-Fluorouracil causes apoptosis ... | |||
T36895 | 5-Fluorouracil-13C,15N2 | 5-Fluorouracil-13C,15N2 | |
5-Fluorouracil-13C,15N2 is intended for use as an internal standard for the quantification of 5-flurouracil by GC- or LC-MS. 5-Fluorouracil is a pyrimidine analog that irreversibly inhibits thymidylate synthase, blocking... | |||
T36870 | 5,6-dihydro-5-Fluorouracil | 5-fluorodihydrouracil,5-Fluoro-dihydro-pyrimidine-2,4-dione | Others |
5,6-dihydro-5-Fluorouracil (5-FUH2) is an inactive metabolite of 5-FU and can be used for the study of organismal metabolism. | |||
T7614 | Eniluracil | GW776C85,5-Ethynyluracil | Others |
Eniluracil (GW776C85) is an orally activedihydropyrimidine dehydrogenase (DPD) inhibitor,increases the oral bioavailability of 5-FU to 100%, facilitating uniform absorption and predictable toxicity. | |||
T0964 | Floxuridine | 5-Fluorouracil 2'-deoxyriboside,FUDR,Deoxyfluorouridine,NSC 27640 | Apoptosis , Nucleoside Antimetabolite/Analog , Others , DNA/RNA Synthesis , Antibacterial , HSV |
Floxuridine (FUDR) is an antimetabolite, floxuridine inhibits thymidylate synthase, resulting in disruption of DNA synthesis and cytotoxicity. | |||
T10013 | 1-Acetyl-3-o-toluyl-5-fluorouracil | A-OT-Fu | Others |
1-Acetyl-3-o-toluyl-5-fluorouracil is a potent antineoplastic agent. | |||
T33762 | Fosifloxuridine nafalbenamide | NUC-3373,NUC3373,NUC 3373 | DNA/RNA Synthesis |
Fosifloxuridine nafalbenamide (NUC 3373), a pyrimidine nucleotide analogue, is a Thymidylate synthase inhibitor. NUC-3373 has anticancer activity. NUC-3373 is a ProTide transformation of 5-FU that generates much higher c... | |||
T1307 | Carmofur | HCFU | Nucleoside Antimetabolite/Analog , Virus Protease , SARS-CoV , DNA/RNA Synthesis |
Carmofur (HCFU) is a highly potent acid ceramidase inhibitor, used in the treatment of breast and colorectal cancer. Carmofur has been known to induce leukoencephalopathy. | |||
TNU1053 | 5-Fluorouracil-1-yl acetic acid | ||
5-Fluorouracil-1-yl acetic acid is a PNA-related derivative. | |||
TNU1481 | 1-(b-D-Xylofuranosyl)-5-fluorouracil | ||
1-(b-D-Xylofuranosyl)-5-fluorouracil is a nucleoside derivative-xylo-nucleoside, fluoro-modified nucleoside, 5-modified pyrimidine nucleoside. | |||
TNU1052 | 5-Fluorouracil-1-yl acetic acid methyl ester | ||
5-Fluorouracil-1-yl acetic acid methyl ester is a PNA-related derivative. | |||
T1349 | 5-Fluorouridine | Others , DNA/RNA Synthesis | |
5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine. 5-fluorouridine is a solid. This compound belongs to the pyrimidine nucleosides and analogues. These are compound... | |||
T27259 | Emitefur | BOFA2,BOF A2,BOF-A2 | Others |
Emitefur (BOF-A 2) is an orally active and potent 5-fluorouracil derivative with anticancer and antitumor activity.Emitefur is used in advanced gastric cancer, breast cancer and metabolism-related diseases. | |||
T4720 | 6-Hydroxypyridin-2(1H)-one hydrochloride | 2,6-Dihydroxypyridine hydrochloride | Others , Endogenous Metabolite |
6-Hydroxypyridin-2(1H)-one hydrochloride (2,6-Dihydroxypyridine hydrochloride) is used as a reagent to synthesize uridine phosphorylase inhibitors that increase Uridine (Urd) (U829910) levels. Uridine is a promising bioc... | |||
T1600 | Doxifluridine | Ro 21-9738,AMC 0101,5'-DFUR,5-Fluoro-5'-deoxyuridine | Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis |
Doxifluridine (AMC 0101) is a fluoropyrimidine derivative and oral prodrug of the antineoplastic agent 5-fluorouracil (5-FU) with antitumor activity. Doxifluridine, designed to circumvent the rapid degradation of 5-FU by... | |||
T1408 | Capecitabine | Xeloda,Capecitibine,Capiibine,RO 09-1978 | Apoptosis , Nucleoside Antimetabolite/Analog , DNA/RNA Synthesis |
Capecitabine (Capecitibine) is a fluoropyrimidine carbamate belonging to the class of antineoplastic agents called antimetabolites. As a prodrug, capecitabine is selectively activated by tumor cells to its cytotoxic moie... | |||
T9936 | ZX-J-19J | N-(2,3-Diphenyl-6-quinoxalinyl)octanamide | Others |
ZX-J-19J (N-(2,3-Diphenyl-6-quinoxalinyl)octanamide), an inhibitor of Cyclophilin J (CyPJ), demonstrates remarkable inhibition of tumor cell growth, comparable to cyclosporine A but much stronger than 5-fluorouracil. | |||
T4374 | Edoxudine | Aedurid,EUDR,Epoxudine | Antiviral , Antibacterial |
Edoxudine (Epoxudine), an antiviral drug, is an analogue of thymidine and shows effectiveness against the herpes simplex virus. Edoxudine is used as a 5-fluorouracil (FU) modulator. Edoxudine may be used to enhance the t... | |||
T21327 | Uridine triacetate | RG 2133 triacetate,PN-401,Tri-O-acetyluridine,PN401,RG 2133,RG-2133,PN 401,RG2133,RG2133 triacetate | Others |
Uridine triacetate (RG 2133 triacetate) (Tri-O-acetyl uridine), an orally active prodrug of uridine, is efficiently absorbed in the gut and swiftly deacetylated in the circulation to release free uridine. It is utilized ... | |||
T4919 | Ureidopropionic acid | Carbamoyl-b-alanine,3-Ureidopropionic acid | Endogenous Metabolite |
Ureidopropionic acid (3-Ureidopropionic acid) is an intermediate in the metabolism of uracil. More specifically it is a breakdown product of dihydrouracil and is produced by the enzyme dihydropyrimidase. It is further de... |