Evidence map›Paper›PMID 35897862›Full record

ArticleMolecules (Basel, Switzerland)2022

Fluorescence, Absorption, Chromatography and Structural Transformation of Chelerythrine and Ethoxychelerythrine in Protic Solvents: A Comparative Study.

Jinjin Cao, Yanhui Zheng, Ting Liu, Jiamiao Liu, Jinze Liu, Jing Wang, Qirui Sun, Wenhong Li, Yongju Wei

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 1 institution in 1 country.

Jinjin CaoDepartment of Environmental and Chemical Engineering, Hebei College of Industry and Technology, Shijiazhuang 050091, China.
Yanhui ZhengDepartment of Preschool and Arts Education, Shijiazhuang Vocational College of Finance & Economics, Shijiazhuang 050061, China.ORCID 0000-0001-9770-0545
Ting LiuDepartment of Environmental and Chemical Engineering, Hebei College of Industry and Technology, Shijiazhuang 050091, China.
Jiamiao LiuDepartment of Environmental and Chemical Engineering, Hebei College of Industry and Technology, Shijiazhuang 050091, China.
Jinze LiuDepartment of Environmental and Chemical Engineering, Hebei College of Industry and Technology, Shijiazhuang 050091, China.
Jing WangCollege of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024, China.
Qirui SunCollege of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024, China.
Wenhong LiDepartment of Environmental and Chemical Engineering, Hebei College of Industry and Technology, Shijiazhuang 050091, China.
Yongju WeiCollege of Chemistry and Material Science, Hebei Normal University, Shijiazhuang 050024, China.
Hebei Normal University · CN

Funding

Doctoral fund of Hebei College of Industry and Technology Nos: BZ201701, BZ2020004Hebei Province "333 Talents Project" Funded project No. A202101097National Natural Science Foundation of China No. 81173496Natural Science Foundation of Hebei Province No. 17273003Science and Technology Research Project of Hebei Province Nos: ZD2019033, Z2020138
6 · The paper itself

Abstract

Chelerythrine (CH) and ethoxychelerythrine (ECH) are chemical reference substances for quality control of Chinese herbal medicines, and ECH is the dihydrogen derivative of CH. In this study, their fluorescence and absorption spectra, as well as their structural changes in different protic solvents were compared. It was observed that their emission fluorescence spectra in methanol were almost the same (both emitted at 400 nm), which may be attributed to the nucleophilic and exchange reactions of CH and ECH with methanol molecules with the common product of 6-methoxy-5,6-dihydrochelerythrine (MCH). When diluted with water, MCH was converted into CH, which mainly existed in the form of positively charged CH

Indexed as

MethanolWaterBenzophenanthridinesChromatography, High Pressure LiquidSolventsSpectrometry, FluorescenceBenzophenanthridineschelerythrineMethanolSolventsWaterabsorbancechelerythrineethoxychelerythrinefluorescencestructural transformation

Identifiers

PMID35897862
PMCPMC9331999
OpenAlexW4287149227

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.