Evidence map›Paper›PMID 41646886›Full record

ArticleMolecular therapy. Nucleic acids2026

2'-Ribose-modified nucleotides: A strategy for reducing off-target effects of oligonucleotide drugs.

Honglei Zhang, Yangjian Liu, Jingxuan Ma, Huajie Huang, Wannian Zhang, Donghui Xiu, Teng Ma, Man Zhang, Fei Yu, Gengshen Song

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Honglei ZhangBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.
Yangjian LiuHangzhou Tianlong Pharmaceutical Co., Ltd., Hangzhou 310020, P.R. China.
Jingxuan MaBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.
Huajie HuangHangzhou Tianlong Pharmaceutical Co., Ltd., Hangzhou 310020, P.R. China.
Wannian ZhangHangzhou Tianlong Pharmaceutical Co., Ltd., Hangzhou 310020, P.R. China.
Donghui XiuHangzhou Tianlong Pharmaceutical Co., Ltd., Hangzhou 310020, P.R. China.
Teng MaBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.
Man ZhangBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.
Fei YuBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.
Gengshen SongBeijing Youcare Kechuang Pharmaceutical Technology Co., Ltd., Beijing 100176, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necessary chemical modifications can enhance the metabolic stability and therapeutic efficacy of oligonucleotide-based drugs. Herein, a series of mononucleotides with different functional group modifications at the ribose 2'-position were designed and synthesized for reducing off-target effects of oligonucleotide drugs. After incorporating them into the antisense strand of small interfering RNAs (siRNAs), we assessed their biophysical and biological properties. The results revealed that, following the substitution of the conventional 2'-O-methyl or 2'-O-fluoro ribose modifications with our newly designed functional groups, although the thermal stability of the duplexes decreased, the

Indexed as

2′-ribose-modified nucleotidesmononucleotide synthesisMT: Oligonucleotides: Therapies and ApplicationsPCSK9 suppressionreducing off-target effectssiRNA

Identifiers

PMID41646886
PMCPMC12870468

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.