F5013
5-Fluoroorotic acid hydrate
≥98%
동의어(들):
2,6-Dihydroxy-5-fluoropyrimidine-4-carboxylic acid, 5-Fluorouracil-4-carboxylic acid
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모든 사진(4)
About This Item
실험식(Hill 표기법):
C5H3FN2O4 · xH2O
CAS Number:
Molecular Weight:
174.09 (anhydrous basis)
EC Number:
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:
NACRES:
NA.32
추천 제품
생물학적 소스
synthetic
분석
≥98%
양식
powder
기술
cell culture | plant: suitable
mp
278 °C (dec.) (lit.)
solubility
4 M NH4OH: 50 mg/mL, clear, colorless to light yellow
저장 온도
−20°C
SMILES string
OC(C(NC(N1)=O)=C(F)C1=O)=O.[H]O[H]
InChI
1S/C5H3FN2O4.H2O/c6-1-2(4(10)11)7-5(12)8-3(1)9;/h(H,10,11)(H2,7,8,9,12);1H2
InChI key
LODRRYMGPWQCTR-UHFFFAOYSA-N
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애플리케이션
5-Fluoroorotic acid hydrate has also been used as a counter-selection agent to screen L. lactis (multi) peptidase knockout mutants and C. albicans. It has been used in synthesis of 5-fluoroorotidine 5′-monophosphate (FOMP).
Useful in the selection of orotidine-5′-phosphate decarboxylase mutants of Saccharomyces cerevisiae.
생화학적/생리학적 작용
5-Fluoroorotic acid is a selective inhibitor of rRNA synthesis in mammals.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Inhibition of ribosomal ribonucleic acid maturation in rat liver by 5-fluoroorotic acid resulting in the selective labeling of cytoplasmic messenger ribonucleic acid
Wilkinson D S, et al.
The Journal of Biological Chemistry, 246(21), 6418-6427 (1971)
Mechanism of the orotidine 5?-monophosphate decarboxylase-catalyzed reaction: Effect of solvent viscosity on kinetic constants
Wood B M, et al.
Biochemistry, 48(24), 5510-5517 (2009)
Lakshmi Sreekumar et al.
Genetics, 212(4), 1121-1132 (2019-05-31)
The diploid budding yeast Candida albicans harbors unique CENPA-rich 3- to 5-kb regions that form the centromere (CEN) core on each of its eight chromosomes. The epigenetic nature of these CENs does not permit the stabilization of a functional kinetochore
Jiaxin Gao et al.
Nature communications, 9(1), 4495-4495 (2018-10-31)
Fungal infections by drug-resistant Candida albicans pose a global public health threat. However, the pathogen's diploid genome greatly hinders genome-wide investigations of resistance mechanisms. Here, we develop an efficient piggyBac transposon-mediated mutagenesis system using stable haploid C. albicans to conduct
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