ArticleCurrent medicinal chemistry2026
Discovery of New Hydrazonothiazolines as Bovine and Human Carbonic Anhydrase-II Inhibitors:
Article in Current medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
introductionCarbonic Anhydrase II (CA-II) is crucial for several physiopathological processes, including bone calcification, osteoporosis, tumorigenicity, and epilepsy, among others. Usually, the intraocular pressure observed in glaucoma exacerbates the condition, and CA-II inhibitors have the potential to be used for the reduction of this pressure.
methodsMoreover, to search for novel CA-II inhibitors with high potency, a series of hydrazonothiazoline derivatives (5a-q) were synthesized. The inhibitory potency of our synthesized compounds was investigated for human and bovine CA-II through in-vitro and computational methods. The in vitro screening revealed that 5a-5f, 5g, 5h, and 5l have significant inhibitory action for bCA-II (IC
resultsThe molecular dynamics simulation, MMPBSA analysis, revealed that 5a has better stability in 1BN1 than 5h in 1V9E.
conclusionThose identified inhibitors could serve as a skeleton to design more potent CA-II inhibitors in the future.
Indexed as
Identifiers
41837481What OpenQuestion holds
Registered trials
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.