Merck
CN

F7129

Sigma-Aldrich

5-氟胞嘧啶

nucleoside analog

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别名:
4-氨基-5-氟-2(1H)-嘧啶酮, 氟胞嘧啶
经验公式(希尔记法):
C4H4FN3O
CAS号:
分子量:
129.09
Beilstein:
127285
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.32

检测方案

≥99% (TLC)

mp

298-300 °C (dec.) (lit.)

抗生素抗菌谱

fungi

作用机制

DNA synthesis | interferes
protein synthesis | interferes

储存温度

2-8°C

SMILES string

NC1=NC(=O)NC=C1F

InChI

1S/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)

InChI key

XRECTZIEBJDKEO-UHFFFAOYSA-N

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相关类别

一般描述

化学结构:核苷

应用

用于 TMP 生物合成研究。

生化/生理作用

具有抗真菌活性的核苷类似物。 5-FC由胞嘧啶脱氨基酶脱氨,可产生5-氟尿嘧啶,导致RNA密码错编。 5-氟尿嘧啶可抑制DNA和RNA的合成,干扰核糖体蛋白质合成。

象形图

Health hazard

警示用语:

Warning

危险声明

预防措施声明

危险分类

Repr. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Annemarie E Brouwer et al.
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In a randomized controlled trial of amphotericin B-based therapy for human immunodeficiency virus (HIV)-associated cryptococcal meningitis in Thailand, we also compared the mycological efficacy, toxicity, and pharmacokinetics of oral versus intravenous flucytosine at 100 mg/kg of body weight/day for the
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Although antibiotic resistance represents a public health emergency, the pipeline of new antibiotics is running dry. Repurposing of old drugs for new clinical applications is an attractive strategy for drug development. We used the bacterial pathogen Pseudomonas aeruginosa as a
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