Substance
ID:180941
Names and Identifiers
IUPAC Traditional name
2'-deoxyuridine
IUPAC name
1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione
Synonyms
1-(2-Deoxy-β-D-ribofuranosyl)uracilUracil deoxyriboside2′-Deoxyuridine
Registration numbers
CAS Number
Beilstein Number
PubChem SID
EC Number
MDL Number
Properties
Safety Information
German water hazard class
3
RTECS
YU7490000
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Product Information
Impurities
Thymidine, free
Purity
99-100%
Pharmacology Properties
Gene Information
mouse ... Slc29a1(63959)
Molecule Details
包装
1, 5 g in poly bottle
100, 250 mg in poly bottle
Application
2′-Deoxyuridine (dU) is frequently halogenated to create thymidine analogues useful for studies of DNA synthesis and degradation mechanisms. Derivatized 2′-Deoxyuridines used as labeling substrates include chloro-2′-deoxyuridine (CldU), bromodeoxyuridine (BrdU) and/or iododeoxyuridine (IdU). Other useful analogues of 2′-deoxyuridine include 5-ethynyl-2′-deoxyuridine (DdU) and 5-hydroxymethyl-2′-deoxyuridine (HmdU).
1, 5 g in poly bottle
100, 250 mg in poly bottle
Application
2′-Deoxyuridine (dU) is frequently halogenated to create thymidine analogues useful for studies of DNA synthesis and degradation mechanisms. Derivatized 2′-Deoxyuridines used as labeling substrates include chloro-2′-deoxyuridine (CldU), bromodeoxyuridine (BrdU) and/or iododeoxyuridine (IdU). Other useful analogues of 2′-deoxyuridine include 5-ethynyl-2′-deoxyuridine (DdU) and 5-hydroxymethyl-2′-deoxyuridine (HmdU).
Molecular Spectra
No Data Available
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References
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