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184302-49-6

184302-49-6 structure
184302-49-6 structure

Name 4-Amino-1-(2-deoxy-2-fluoro-4-thio-β-D-arabinofuranosyl)-2(1H)-pyrimidinone
Synonyms 2(1H)-Pyrimidinone, 4-amino-1-(2-deoxy-2-fluoro-4-thio-β-D-arabinofuranosyl)-
4-Amino-1-(2-deoxy-2-fluoro-4-thio-β-D-arabinofuranosyl)-2(1H)-pyrimidinone
Description
In Vitro FF-10502 (FF-10502-01) is a pyrimidine nucleoside antimetabolite that shows growth inhibition of pancreatic cancer cell lines with IC50 of 60-330 nM; FF-10502 is far more potent than gemcitabine in inhibiting DNA polymerase ��, significantly induces concentration-dependent cell death in accordance with enhanced DNA damage in combination with DNA damage inducers (H2O2, cisplatin, and temozolomide); also demonstrates complete tumor growth suppression in in vivo patient-derived xenograft models with gemcitabine-resistant pancreatic cancer cells.
Density 1.8±0.1 g/cm3
Boiling Point 516.5±60.0 °C at 760 mmHg
Molecular Formula C9H12FN3O3S
Molecular Weight 261.273
Flash Point 266.2±32.9 °C
Exact Mass 261.058350
LogP -1.73
Vapour Pressure 0.0±3.0 mmHg at 25°C
Index of Refraction 1.754
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