起订量:
5-Fluorouracil | 5-氟脲嘧啶 | MedChemExpress (MCE)
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CAS No. : 51-21-8
MCE 国际站:5-Fluorouracil
产品活性:5-Fluorouracil (5-FU) 是一种尿嘧啶的类似物 (nucleoside antimetabolite/analog),是一种有效的抗肿瘤药。5-Fluorouracil 通过抑制胸苷酸合成酶影响嘧啶的合成,从而耗尽细胞内dTTP 池。5-Fluorouracil 诱导细胞凋亡 (apoptosis),可用作化学敏化剂。5-Fluorouracil 还可抑制 HIV 病毒。5-Fluorouracil (5-FU) 可破坏外泌体特异性的 rRNA。
研究领域:Cell Cycle/DNA Damage | Anti-infection | Apoptosis | Metabolic Enzyme/Protease
作用靶点:Nucleoside Antimetabolite/Analog | HIV | Apoptosis | Endogenous Metabolite
In Vitro: 5-Fluorouracil (5-Fu) and NSC 123127 (Dox) show synergistic anticancer efficacy. The IC50 value of 5-Fu/Dox-DNM toward human breast cancer (MDA-MB-231) cells is 0.25 μg/mL, presenting an 11.2-fold and 6.1-fold increase in cytotoxicity compared to Dox-DNM and 5-Fu-DNM, respectively. In 5-fluorouracil (5-FU) and CDDP treated NFBD1-inhibited NPC cells, the NFBD1 expression in NPC CNE1 cell lines is depleted using lentivirus-mediated short hairpin RNA, and the sensitivity of these cells is elevated. NFBD1 knockdown leads to an obvious induction of apoptosis in CDDP- or 5-FU-treated CNE1 cells.
In Vivo: 5-Fluorouracil (23 mg/kg, 3 times/week) for 14 days, induces accelerated gastrointestinal transit associated with acute intestinal inflammation at day 3 after the start of treatment, which may have led to persistent changes in the ENS observed after days 7 and 14 of treatment contributing to delayed gastrointestinal transit and colonic dysmotility.
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CAS | 51-21-8 |
纯度 | 99.86% |
分子量 | 130.08 |
分子式 | C₄H₃FN₂O₂ |
供货周期 | 现货 |
规格 | 10 mM * 1 mL |
货号 | HY-90006 |
应用领域 | 医疗卫生,化工,生物产业,制药 |