Evidence map›Paper›PMID 36876597›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2023

Synthesis and biological evaluation of new 3-substituted coumarin derivatives as selective inhibitors of human carbonic anhydrase IX and XII.

Shaik Mahammad Ghouse, Kavyaraj Bahatam, Andrea Angeli, Gaurav Pawar, Krishna Kartheek Chinchilli, Venkata Madhavi Yaddanapudi, Arifuddin Mohammed, Claudiu T Supuran, Srinivas Nanduri

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.4field-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

9 citing papers in PubMed, 22 citations in OpenAlex.

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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 2 countries.

Shaik Mahammad GhouseDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Kavyaraj BahatamDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Andrea AngeliNeurofarba Deptartment, Sezione di ScienzeFarmaceutiche e Nutraceutiche, Università Degli Studi di Firenze, Florence, Italy.ORCID 0000-0002-1470-7192
Gaurav PawarDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Krishna Kartheek ChinchilliDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Venkata Madhavi YaddanapudiDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
Arifuddin MohammedDepartment of Chemistry, Directorate of Distance Education, Maulana Azad National Urdu University, Hyderabad, India.
Claudiu T SupuranNeurofarba Deptartment, Sezione di ScienzeFarmaceutiche e Nutraceutiche, Università Degli Studi di Firenze, Florence, Italy.ORCID 0000-0003-4262-0323
Srinivas NanduriDepartment of Chemical Sciences, National Institute of Pharmaceutical Education and Research (NIPER), Hyderabad, India.
National Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad · INIstituto Nazionale di Fisica Nucleare, Sezione di Firenze · ITMaulana Azad National Urdu University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Carbonic anhydrase isoforms IX and XII play a significant role in regulating the intracellular and extracellular pH in hypoxic tumours abetting the metastasis of solid tumours. Selective and potent inhibitors targeting carbonic anhydrase IX and XII reduce the activity of these isoforms in hypoxic tumours, representing an antitumor and antimetastatic mechanism. Coumarin-based derivatives are selective inhibitors of CA isoforms IX and XII. In this study, we report the design and synthesis of new 3-substituted coumarin derivatives with different functional moieties and their inhibitory activity against various carbonic anhydrase isoforms. We found that the tertiary sulphonamide derivative

Indexed as

Carbonic AnhydrasesCarbonic Anhydrase IXCoumarinsEthersHumansHypoxiaMolecular Docking SimulationCarbonic Anhydrase IXCarbonic AnhydrasesCoumarinsEtherscarbonic anhydrasecarbothioamidecoumarinhypoxic tumoursoxime etherssulphonamide

Identifiers

PMID36876597
PMCPMC10013565
OpenAlexW4323294907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.