Evidence map›Paper›PMID 38283216›Full record

ArticleRSC medicinal chemistry2024

Scaffold hopping based designing of selective ALDH1A1 inhibitors to overcome cyclophosphamide resistance: synthesis and biological evaluation.

Gera Narendra, Baddipadige Raju, Himanshu Verma, Manoj Kumar, Subheet Kumar Jain, Gurleen Kaur Tung, Shubham Thakur, Rasdeep Kaur, Satwinderjeet Kaur, Bharti Sapra and 1 more

Open access · greenAbstract read
In one paragraph

Article in RSC medicinal chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. The Significance of Aldehyde Dehydrogenase 1 in Cancers.International journal of molecular sciences · 2024
    Review
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

11 authors at 2 institutions in 1 country.

Gera NarendraDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.
Baddipadige RajuDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.
Himanshu VermaDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.
Manoj KumarDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.
Subheet Kumar JainDepartment of Pharmaceutical Sciences, Guru Nanak Dev University Amritsar India.
Gurleen Kaur TungCentre for Basic and Translational Research in Health Sciences, Guru Nanak Dev University Amritsar India.
Shubham ThakurDepartment of Pharmaceutical Sciences, Guru Nanak Dev University Amritsar India.
Rasdeep KaurDepartment of Botany and Environmental Sciences, Guru Nanak Dev University Amritsar India.
Satwinderjeet KaurDepartment of Botany and Environmental Sciences, Guru Nanak Dev University Amritsar India.
Bharti SapraDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.
Om SilakariDepartment of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala Punjab 147002 India mmlpup73@gmail.com +91 17522 83075 +91 95015 42696.ORCID https://orcid.org/0000-0002-1174-1125
Punjabi University · INGuru Nanak Dev University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aldehyde dehydrogenase 1A1 (ALDH1A1) is an isoenzyme that catalyzes the conversion of aldehydes to acids. However, the overexpression of ALDH1A1 in a variety of malignancies is the major cause of resistance to an anti-cancer drug, cyclophosphamide (CP). CP is a prodrug that is initially converted into 4-hydroxycyclophosphamide and its tautomer aldophosphamide, in the liver. These compounds permeate into the cell and are converted as active metabolites,

Identifiers

PMID38283216
PMCPMC10809718
OpenAlexW4389169095

What OpenQuestion holds

Textmetadata
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.