Evidence map›Paper›PMID 42396029›Full record

ArticleACS omega2026

Efficient Synthesis of Novel Propargyl Sulfamate Derivatives and Their Potent Inhibitory Effects on Human Carbonic Anhydrase Isoenzymes.

Ufuk Atmaca, Songül Bayrak, Cetin Bayrak

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Ufuk AtmacaDepartment of Chemistry, Faculty of Science, Atatürk University, Erzurum 25240, Turkey.ORCID https://orcid.org/0000-0002-5598-0443
Songül BayrakDepartment of Chemistry, Faculty of Science, Atatürk University, Erzurum 25240, Turkey.
Cetin BayrakDepartment of Chemistry, Faculty of Science, Atatürk University, Erzurum 25240, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the present study, a total of 21 novel propargyl sulfamate derivatives were designed and synthesized as potential inhibitors of human carbonic anhydrases I and II (hCA I and hCA II). An efficient and practical synthetic protocol was developed based on the reaction of propargyl alcohols with chlorosulfonyl isocyanate (CSI), affording the target sulfamate compounds in good yield. The inhibitory activities of all synthesized compounds against hCA I and hCA II isoenzymes were evaluated in vitro. The compounds exhibited potent inhibition with IC

Identifiers

PMID42396029
PMCPMC13325173

What OpenQuestion holds

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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.