Hydroxyurea
CAS No. 127-07-1
Hydroxyurea( NCI C04831 | NSC 32065 )
Catalog No. M11135 CAS No. 127-07-1
Hydroxyurea is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
500MG | 41 | In Stock |
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1G | 48 | In Stock |
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Biological Information
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Product NameHydroxyurea
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NoteResearch use only, not for human use.
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Brief DescriptionHydroxyurea is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.
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DescriptionHydroxyurea is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.(In Vitro):Hydroxyurea is used in a number of myeloproliferative, neoplastic, HIV, and non-hematological diseases. Treatment of cells in primary culture with 30 μM hydroxyurea for 96 hours significantly increases the fractional HbF content. The?Gγ:?Aγ-globin mRNA is induced 0.30- to 8-fold?in vitro. Hydroxyurea has been shown to block HIV-1 reverse transcription and/or replication in quiescent peripheral blood mononuclear cells and macrophages.(In Vivo):Hydroxyurea therapy producs consistent reductions in WBC and ANC without improvement in anemia over 17 weeks. Hydroxyurea at 50mg/kg produces a reduced white blood cell count, absolute neutrophil count and no improvement in anemia compared to vehicle treated sickle cell mice.
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In Vitro——
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In Vivo——
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SynonymsNCI C04831 | NSC 32065
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PathwayCell Cycle/DNA Damage
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TargetDNA/RNA Synthesis
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Recptorribonucleoside diphosphate reductase
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number127-07-1
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Formula Weight76.06
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Molecular FormulaCH4N2O2
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Purity>98% (HPLC)
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SolubilityWater: 15 mg/mL (197.23 mM); DMSO: 15 mg/mL (197.23 mM)
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SMILESO=C(N)NO
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Chemical Name1-hydroxyurea
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Culligan K, et al. Plant Cell. 2004 May;16(5):1091-104.
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