دورية أكاديمية

Consecutive 5'- and 3'-amide linkages stabilise antisense oligonucleotides and elicit an efficient RNase H response.

التفاصيل البيبلوغرافية
العنوان: Consecutive 5'- and 3'-amide linkages stabilise antisense oligonucleotides and elicit an efficient RNase H response.
المؤلفون: Epple S; Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk., Thorpe C; Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk., Baker YR; Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk., El-Sagheer AH; Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk and Chemistry Branch, Department of Science and Mathematics, Faculty of Petroleum and Mining Engineering, Suez University, Suez 43721, Egypt., Brown T; Chemistry Research Laboratory, University of Oxford, Oxford, OX1 3TA, UK. tom.brown@chem.ox.ac.uk.
المصدر: Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2020 May 21; Vol. 56 (41), pp. 5496-5499.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 9610838 Publication Model: Print Cited Medium: Internet ISSN: 1364-548X (Electronic) Linking ISSN: 13597345 NLM ISO Abbreviation: Chem Commun (Camb) Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Cambridge : Royal Society of Chemistry
مواضيع طبية MeSH: Amides/*chemistry , Oligonucleotides, Antisense/*chemistry , Ribonuclease H/*chemistry, HeLa Cells ; Humans
مستخلص: Antisense oligonucleotides are now entering the clinic for hard-to-treat diseases. New chemical modifications are urgently required to enhance their drug-like properties. We combine amide coupling with standard oligonucleotide synthesis to assemble backbone chimera gapmers that trigger an efficient RNase H response while improving serum life time and cellular uptake.
معلومات مُعتمدة: BB/M011224/1 United Kingdom BB_ Biotechnology and Biological Sciences Research Council
المشرفين على المادة: 0 (Amides)
0 (Oligonucleotides, Antisense)
EC 3.1.26.4 (Ribonuclease H)
تواريخ الأحداث: Date Created: 20200416 Date Completed: 20210105 Latest Revision: 20211129
رمز التحديث: 20221213
DOI: 10.1039/d0cc00444h
PMID: 32292963
قاعدة البيانات: MEDLINE
الوصف
تدمد:1364-548X
DOI:10.1039/d0cc00444h