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191421-10-0

191421-10-0 Structure

191421-10-0 Structure
IdentificationBack Directory
[Name]

1-(BETA-D-2-DEOXYRIBOFURANOSYL)-5-NITROINDOLE
[CAS]

191421-10-0
[Synonyms]

5-NIdR
2'-DEOXY-NITRO INDOLE NUCLEOSIDE
5-Nitroindole 2'-deoxyribonucleoside
1-(b-D-2-Deoxyribofuranosyl)-5-nitroindole
1-(β-D-2-Deoxyribofuranosyl)-5-nitroindole
1-(β-D-2-Deoxyribofuranosyl)-5-nitroindole
1-(2-Deoxy-b-D-ribofuranosyl)-5-nitroindole
1-(BETA-D-2-DEOXYRIBOFURANOSYL)-5-NITROINDOLE
1H-Indole, 1-(2-deoxy-β-D-erythro-pentofuranosyl)-5-nitro-
1-(2-Deoxy-β-D-erythro -pentofuranosyl)-5- nitro-1H -indole
1-(2-Deoxy-beta-D-erythro-pentofuranosyl)-5-nitro-1H-indole
[Molecular Formula]

C13H14N2O5
[MDL Number]

MFCD01631019
[MOL File]

191421-10-0.mol
[Molecular Weight]

278.26
Chemical PropertiesBack Directory
[Boiling point ]

572.5±50.0 °C(Predicted)
[density ]

1.60±0.1 g/cm3(Predicted)
[storage temp. ]

-10 to -25°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

14.01±0.60(Predicted)
[color ]

Light yellow to yellow
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

5-NIdR (1-(β-D-2-Deoxyribofuranosyl)-5-nitroindole), an artificial nucleoside, exhibits the ability to inhibit the replication of DNA lesions generated by Temozolomide (HY-17364). 5-NIdR induces cancer cells apoptosis and arrests cell cycle at G0 phase. 5-NIdR enhances Temozolomide anti-tumor efficacy in murine glioblastoma model[1].
[in vivo]

5-NIdR (100 mg/kg; ip; for 5 consecutive days), together with Temozolomide (40 mg/kg), results complete tumor regression in a murine xenograft model of glioblastoma. Temozolomide alone only delayed tumor growth[1].

[References]

[1] Choi JS, et al. Inhibition of Translesion DNA Synthesis as a Novel Therapeutic Strategy to Treat Brain Cancer. Cancer Res. 2018 Feb 15;78(4):1083-1096. DOI:10.1158/0008-5472.CAN-17-2464
Spectrum DetailBack Directory
[Spectrum Detail]

1-(BETA-D-2-DEOXYRIBOFURANOSYL)-5-NITROINDOLE(191421-10-0)1HNMR
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