Evidence map›Paper›PMID 36718988›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2023

Derivatives of 4-methyl-1,2,3-benzoxathiazine 2,2-dioxide as selective inhibitors of human carbonic anhydrases IX and XII over the cytosolic isoforms I and II.

Jekaterīna Ivanova, Morteza Abdoli, Alessio Nocentini, Raivis Žalubovskis, Claudiu T Supuran

Abstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

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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

5 authors.

Jekaterīna IvanovaLatvian Institute of Organic Synthesis, Riga, Latvia.ORCID 0000-0001-8845-0193
Morteza AbdoliInstitute of Technology of Organic Chemistry, Faculty of Materials Science and Applied Chemistry, Riga Technical University, Riga, Latvia.ORCID 0000-0003-1647-4262
Alessio NocentiniNeurofarba Department, Università degli Studi di Firenze, Florence, Italy.ORCID 0000-0003-3342-702X
Raivis ŽalubovskisLatvian Institute of Organic Synthesis, Riga, Latvia.ORCID 0000-0002-9471-1342
Claudiu T SupuranNeurofarba Department, Università degli Studi di Firenze, Florence, Italy.ORCID 0000-0003-4262-0323

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 4-methyl-1,2,3-benzoxathiazine-2,2-dioxides with various substituents in 5, 6 or 7 positions was obtained from corresponding 2'-hydroxyacetophenones in their reaction with sulphamoyl chloride. 6- and 7-aryl substituted 4-methyl-1,2,3-benzoxathiazine-2,2-dioxides were obtained from aryl substituted 2'-hydroxyacetophenonesprepared from 4- or 5-bromo-2'-hydroxyacetophenones via two-step protocol. 4-Methyl-1,2,3-benzoxathiazine-2,2-dioxides were investigated as inhibitors of four human (h) carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, off-target cytosolic hCA I and II, and target transmembrane, tumour-associated hCA IX and XII. Twenty derivatives of 4-methyl-1,2,3-benzoxathiazine 2,2-dioxide were obtained. With one exception (compound

Indexed as

Carbonic AnhydrasesNeoplasmsAntigens, NeoplasmCarbonic Anhydrase InhibitorsCarbonic Anhydrase IXHumansIsoenzymesMolecular StructureStructure-Activity RelationshipAntigens, NeoplasmCarbonic Anhydrase InhibitorsCarbonic Anhydrase IXCarbonic AnhydrasesIsoenzymes123-benzoxathiazine 22-dioxide4-methyl-123-benzoxathiazine 22-dioxideCarbonic anhydraseisoform-selective inhibitor

Identifiers

PMID36718988
PMCPMC9891166

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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.