910129-15-6

910129-15-6 structure
910129-15-6 structure
  • Name: 5'-Deoxy-5-fluoro-N-[(2-methylbutoxy)carbonyl]cytidine
  • Chemical Name: 2-methylbutyl N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-2-oxopyrimidin-4-yl]carbamate
  • CAS Number: 910129-15-6
  • Molecular Formula: C15H22FN3O6
  • Molecular Weight: 359.35
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
  • Create Date: 2018-12-15 07:12:11
  • Modify Date: 2024-01-03 10:45:19
  • 5′-Deoxy-5-fluoro-N-[(2-methylbutoxy)carbonyl]cytidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

Name 2-methylbutyl N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-2-oxopyrimidin-4-yl]carbamate
Synonyms 2(1H)-Pyrimidinone, 1-(5-deoxypentofuranosyl)-5-fluoro-4-[[(pentyloxy)carbonyl]amino]-
unii-0jd5qg20w5
1-(5-Deoxypentofuranosyl)-5-fluoro-4-{[(pentyloxy)carbonyl]amino}-2(1H)-pyrimidinone
1-(5-deoxypentofuranosyl)-5-fluoro-4-{[(pentyloxy)carbonyl]amino}pyrimidin-2(1h)-one
5'-Deoxy-5-fluoro-N-[(2-methylbutoxy)carbonyl]cytidine
Capecitabine Impurity 2
Description 5′-Deoxy-5-fluoro-N-[(2-methylbutoxy)carbonyl]cytidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog
References

[1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.  

Density 1.5±0.1 g/cm3
Melting Point 62-64°C
Molecular Formula C15H22FN3O6
Molecular Weight 359.35
Exact Mass 359.149261
PSA 126.40000
LogP 0.97
Index of Refraction 1.600
Storage condition Hygroscopic, -20°C Freezer, Under Inert Atmosphere
Hazard Codes Xn