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131505-02-7

131505-02-7 Structure

131505-02-7 Structure
IdentificationBack Directory
[Name]

PD 130908
[CAS]

131505-02-7
[Synonyms]

PD 130908
[Molecular Formula]

C8H14Br2N4O2
[MOL File]

131505-02-7.mol
[Molecular Weight]

358.03
Chemical PropertiesBack Directory
[Melting point ]

164-168 °C (decomp)
Hazard InformationBack Directory
[Description]

PD 130908 is an analogue of RSU 1069 and is an effective hypoxic cytotoxin, but less potent than the hypoxic cell radiosensitizer RSU 1069. Toxicity toward hypoxic tumor cells in vivo is demonstrated by clamping tumors (for 60 min) following administration of PD 130908. Systemic toxicity is substantially reduced following oral drug administration. Further, doses achievable following fractionated drug treatments are sufficiently high to produce significant levels of radiosensitization.
[Uses]

PD 130908 is an orally active hypoxic cell radiosensitizer with potent radiosensitizing activity. PD 130908 can be utilized in cancer research[1].
[References]

[1] Cole S, et al. Dual function nitroimidazoles less toxic than RSU 1069: selection of candidate drugs for clinical trial (RB 6145 and/or PD 130908. Int J Radiat Oncol Biol Phys. 1992;22(3):545-8. DOI:10.1016/0360-3016(92)90872-f
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