Name | 1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidin-2-one |
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Synonyms |
5-Iodo-2-pyrimidinone-2'-deoxyribose
Ropidoxuridine (INN/USAN) IPdR Ropidoxuridine UNII-3HX21A3SQF Ropidoxuridine [USAN:INN] 5-Iodo-2-pyrimidinone 2' deoxyribonucleoside |
Description | Ropidoxuridine (IPdR) is a novel orally available, halogenated thymidine analog and is a potential radiosensitizer for use in human tumors. |
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Related Catalog | |
In Vitro | Ropidoxuridine is an orally bioavailable pro-drug of IUdR (5-iodo-2'-deoxyuridine). Ropidoxuridine demonstrates strong synergy effects with Alisertib at clinically relevant concentrations[1]. |
In Vivo | In an orthotopic tumor model, Ropidoxuridine (750 mg/kg/day) and Alisertib (30 mg/kg/day) demonstrate strong synergy effects[1]. |
References |
Density | 2.22g/cm3 |
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Boiling Point | 478.6ºC at 760mmHg |
Molecular Formula | C9H11IN2O4 |
Molecular Weight | 338.09900 |
Flash Point | 243.3ºC |
Exact Mass | 337.97600 |
PSA | 84.58000 |
Index of Refraction | 1.759 |
~45% 93265-81-7 |
Literature: Efange, Simon M. N.; Alessi, Elaine M.; Shih, H. C.; Cheng, Yung-Chi; Bardos, Thomas J. Journal of Medicinal Chemistry, 1985 , vol. 28, # 7 p. 904 - 910 |
Precursor 1 | |
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DownStream 0 |