Evidence map›Paper›PMID 35204665›Full record

ArticleBiomolecules2022

Synthesis and Structure-Activity Relationships of Novel Non-Steroidal CYP17A1 Inhibitors as Potential Prostate Cancer Agents.

Tomasz M Wróbel, Oksana Rogova, Katyayani Sharma, Maria Natalia Rojas Velazquez, Amit V Pandey, Flemming Steen Jørgensen, Frederic S Arendrup, Kasper L Andersen, Fredrik Björkling

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Pyridine indole hybrids as novel potent CYP17A1 inhibitors.Journal of enzyme inhibition and medicinal chemistry · 2025
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  6. Review
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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 3 institutions in 3 countries.

Tomasz M WróbelDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.ORCID 0000-0002-0313-2522
Oksana RogovaDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.ORCID 0000-0002-5104-2943
Katyayani SharmaDivision of Pediatric Endocrinology, Department of Pediatrics, University Children's Hospital Bern, 3010 Bern, Switzerland.ORCID 0000-0001-6818-0931
Maria Natalia Rojas VelazquezDivision of Pediatric Endocrinology, Department of Pediatrics, University Children's Hospital Bern, 3010 Bern, Switzerland.ORCID 0000-0002-9132-681X
Amit V PandeyDivision of Pediatric Endocrinology, Department of Pediatrics, University Children's Hospital Bern, 3010 Bern, Switzerland.ORCID 0000-0001-8331-5902
Flemming Steen JørgensenDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.ORCID 0000-0001-8040-2998
Frederic S ArendrupBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen, Denmark.ORCID 0000-0001-6488-4616
Kasper L AndersenBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5, DK-2200 Copenhagen, Denmark.ORCID 0000-0002-5127-113X
Fredrik BjörklingDepartment of Drug Design and Pharmacology, University of Copenhagen, Universitetsparken 2, DK-2100 Copenhagen, Denmark.ORCID 0000-0001-7018-8334
University of Copenhagen · DKUniversity of Bern · CHMedical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Twenty new compounds, targeting CYP17A1, were synthesized, based on our previous work on a benzimidazole scaffold, and their biological activity evaluated. Inhibition of CYP17A1 is an important modality in the treatment of prostate cancer, which remains the most abundant cancer type in men. The biological assessment included CYP17A1 hydroxylase and lyase inhibition, CYP3A4 and P450 oxidoreductase (POR) inhibition, as well as antiproliferative activity in PC3 prostate cancer cells. The most potent compounds were selected for further analyses including in silico modeling. This combined effort resulted in a compound (comp

Indexed as

Enzyme InhibitorsProstatic NeoplasmsSteroid 17-alpha-HydroxylaseHumansMalePC-3 CellsStructure-Activity RelationshipCYP17A1 protein, humanEnzyme InhibitorsSteroid 17-alpha-HydroxylaseCYP17A1cytochrome P450 17A1enzyme inhibitionprostate cancer

Identifiers

PMID35204665
PMCPMC8961587
OpenAlexW4205486995

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.