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5-Hydroxy-2'-deoxyuridine
5-Hydroxy-2'-deoxyuridine
CAS No. 5168-36-5
5-Hydroxy-2'-deoxyuridine( 5-OHdU )
Catalog No. M27060 CAS No. 5168-36-5
5-Hydroxy-2'-deoxyuridine is a major oxidation product of 2'-Deoxycytidine and can be incorporated into DNA in vitro.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 50 | Get Quote |
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| 5MG | 82 | Get Quote |
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| 10MG | 120 | Get Quote |
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| 25MG | 201 | Get Quote |
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| 50MG | 300 | Get Quote |
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| 100MG | 448 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product Name5-Hydroxy-2'-deoxyuridine
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NoteResearch use only, not for human use.
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Brief Description5-Hydroxy-2'-deoxyuridine is a major oxidation product of 2'-Deoxycytidine and can be incorporated into DNA in vitro.
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Description5-Hydroxy-2'-deoxyuridine is a major oxidation product of 2'-Deoxycytidine and can be incorporated into DNA in vitro.(In Vitro):Translesion synthesis past 5-Hydroxy-2'-deoxyuridine in 18- and 45-member oligodeoxyribonucleotides occurred, but pauses both opposite, and one nucleotide prior to, the modified base in the template is observed. The specificity of nucleotide incorporation opposite 5-Hydroxy-2'-deoxyuridine in the template is sequence context-dependent. In one sequence context, dA is the principal nucleotide incorporated opposite 5-Hydroxy-2'-deoxyuridine. However, in a second sequence context, dC is the predominant base incorporated opposite 5-Hydroxy-2'-deoxyuridine. In that same sequence context, dC is also the predominant nucleotide incorporated opposite 5-Hydroxy-2'-deoxyuridine.
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In VitroTo study the specificity of nucleotide incorporation opposite 5-hydroxypyrimidines in template DNA, 18- and 45-member oligodeoxyribonucleotides, containing an internal 2'-deoxy-5-hydroxyuridine (5-OHdU) in two different sequence contexts, were used. Translesion synthesis past 2'-deoxy-5-hydroxyuridine (5-OHdU) in both oligonucleotides occurred, but pauses both opposite, and one nucleotide prior to, the modified base in the template is observed. The specificity of nucleotide incorporation opposite 2'-deoxy-5-hydroxyuridine (5-OHdU) in the template is sequence context dependent. In one sequence context, dA is the principal nucleotide incorporated opposite 2'-deoxy-5-hydroxyuridine (5-OHdU). However in a second sequence context, dC is the predominant base incorporated opposite 2'-deoxy-5-hydroxyuridine (5-OHdU). In that same sequence context, dC is also the predominant nucleotide incorporated opposite 2'-deoxy-5-hydroxyuridine (5-OHdU).
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In Vivo——
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Synonyms5-OHdU
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PathwayCell Cycle/DNA Damage
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TargetNucleoside Antimetabolite/Analog
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RecptorKCNQ1
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Research Area——
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Indication——
Chemical Information
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CAS Number5168-36-5
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Formula Weight244.2
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Molecular FormulaC9H12N2O6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 33.33 mg/mL (136.49 mM)
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SMILESO=C1N([C@@]2(O[C@H](CO)[C@@H](O)C2)[H])C=C(O)C(=O)N1
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Chemical Name——
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.Mattmann ME, et al. Identification of (R)-N-(4-(4-methoxyphenyl)thiazol-2-yl)-1-tosylpiperidine-2-carboxamide, ML277, as a novel, potent and selective K(v)7.1 (KCNQ1) potassium channel activator. Bioorg Med Chem Lett. 2012;22(18):5936-5941.
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