Evidence map›Paper›PMID 29568434›Full record

ArticleChemical science2017

Tuning the stereo-hindrance of a curcumin scaffold for the selective imaging of the soluble forms of amyloid beta species.

Yuyan Li, Jian Yang, Hongwu Liu, Jing Yang, Lei Du, Haiwei Feng, Yanli Tian, Jianqin Cao, Chongzhao Ran

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
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

28 citing papers in PubMed, 100 citations in OpenAlex.

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  7. Near-infrared II theranostic agents for the diagnosis and treatment of Alzheimer's disease.European journal of nuclear medicine and molecular imaging · 2024
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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

9 authors at 2 institutions in 3 countries.

Yuyan LiMolecular Imaging Laboratory , MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging , Department of Radiology , Massachusetts General Hospital/Harvard Medical School , Charlestown , Massachusetts 02129 , USA.
Jian YangMolecular Imaging Laboratory , MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging , Department of Radiology , Massachusetts General Hospital/Harvard Medical School , Charlestown , Massachusetts 02129 , USA.
Hongwu LiuSchool of Pharmacy , China Pharmaceutical University , Nanjing , 210009 , China.
Jing YangMolecular Imaging Laboratory , MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging , Department of Radiology , Massachusetts General Hospital/Harvard Medical School , Charlestown , Massachusetts 02129 , USA.
Lei DuSchool of Pharmacy , China Pharmaceutical University , Nanjing , 210009 , China.
Haiwei FengSchool of Pharmacy , China Pharmaceutical University , Nanjing , 210009 , China.
Yanli TianMolecular Imaging Laboratory , MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging , Department of Radiology , Massachusetts General Hospital/Harvard Medical School , Charlestown , Massachusetts 02129 , USA.
Jianqin CaoSchool of Pharmacy , China Pharmaceutical University , Nanjing , 210009 , China.
Chongzhao RanMolecular Imaging Laboratory , MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging , Department of Radiology , Massachusetts General Hospital/Harvard Medical School , Charlestown , Massachusetts 02129 , USA.ORCID 0000-0002-3892-4108
Harvard University · USChina Pharmaceutical University · CN

Funding

Imaging AD Amyloidosis Pathology by Novel Multi-modal NIR/PET/19F MRI ProbesK25AG036760 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI RAN, CHONGZHAO · 2010 to 2014
$770k
Double-blocking Anti-crosslinking Strategy for AD Drug DevelopmentR21AG050158 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI RAN, CHONGZHAO · 2015 to 2016
$475k
Near-infrared molecular imaging for monitoring therapy in AD mouse modelsR03AG050038 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI RAN, CHONGZHAO · 2015 to 2016
$171k
NIA NIH HHS K25 AG036760NIA NIH HHS R03 AG050038NIA NIH HHS R21 AG050158
6 · The paper itself

Abstract

Amyloid peptides and proteins are associated with the pathologies of numerous diseases. In the progression of a disease, amyloids exist in soluble and insoluble forms, which are the dominant species at different stages of the disease and they have different degrees of toxicity. However, differentiating between the soluble and insoluble forms is very challenging with small molecule probes due to multiple obstacles that need to be overcome. Inspired by the recognition principle of antibodies for sAβ, we hypothesized that the accessibility/tightness of soluble and insoluble amyloids could be utilized to design imaging probes to recognize different amyloid forms and the stereo-hindrance tuning strategy could be used to design imaging probes for selectively detecting the soluble amyloid beta (sAβ) species in Alzheimer's disease (AD). Herein, we demonstrated that tuning the stereo-hindrance of the phenoxy-alkyl chains at the 4-position of a curcumin scaffold could lead to certain selectivity for sAβ over insoluble Aβs (insAβ). Among the designed compounds,

Identifiers

PMID29568434
PMCPMC5851342
OpenAlexW2754648361

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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.