2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine

Catalog No.: A56359
Uridine Analog
2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine is a uridine analog that serves as a valuable tool in the study of anticonvulsant and anxiolytic properties, with potential applications in developing antihypertensive agents. This compound features an azide group, enabling it to function as a click chemistry reagent through copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized compounds, facilitating bioconjugation and tracer development in chemical biology.
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5mg
10mg
50mg
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Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
Description2’,3’-Di-O-isopropylidene-4’-alpha-C-azidouridine is a uridine analog that serves as a valuable tool in the study of anticonvulsant and anxiolytic properties, with potential applications in developing antihypertensive agents. This compound features an azide group, enabling it to function as a click chemistry reagent through copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized compounds, facilitating bioconjugation and tracer development in chemical biology.
Product Information
Catalog NumA56359
FormulaC12H15N5O6
Molecular Weight325.28
CAS Number690271-27-3
SMILESO=C(NC1=O)C=CN1[C@H](O2)[C@H]3[C@H](OC(C)(C)O3)[C@]2(CO)N=[N+]=[N-]
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