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New, tricyclic compounds containing a sulfonyl moiety in their structure, as potential safer COX inhibitors, were designed and synthesized. New derivatives have three conjugated rings and a sulfonyl group. A third ring, i.e., an oxazine, oxazepine or oxazocin, has been added to the 1,2-benzothiazine skeleton. Their anti-COX-1/COX-2 and cytotoxic effects in vitro on NHDF cells, together with the ability to interact with model membranes and the influence on reactive oxygen species and nitric oxide, were studied. Additionally, a molecular docking study was performed to understand the binding interaction of the compounds with the active site of cyclooxygenases. For the abovementioned biological evaluation of new tricyclic 1,2-benzothiazine derivatives, the following techniques and procedures were employed: the differential scanning calorimetry, the COX colorimetric inhibitor screening assay, the MTT, DCF-DA and Griess assays. All of the compounds studied demonstrated preferential inhibition of COX-2 compared to COX-1. Moreover, all the examined tricyclic 1,2-thiazine derivatives interacted with the phospholipid model membranes. Finally, they neither have cytotoxic potency, nor demonstrate significant influence on the level of reactive oxygen species or nitric oxide. Overall, the tricyclic 1,2-thiazine derivatives are good starting points for future pharmacological tests as a group of new anti-inflammatory agents.
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http://dx.doi.org/10.3390/ijms22157818 | DOI Listing |
Org Lett
September 2025
School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand.
Spiroapplanatumine G () is a spiro-meroterpenoid characterized by an unusual 6/5/7 tricyclic spirobenzofuran-3-one core. The first enantioselective total synthesis of spiroapplanatumine G () is reported, featuring a key enantioselective Diels-Alder reaction between an aurone ester and a silyloxydiene to assemble the spirobenzofuranone core. This strategic Diels-Alder transformation advantageously establishes the two contiguous stereogenic centers in a single step.
View Article and Find Full Text PDFJ Org Chem
September 2025
Institute of Integrated Science and Technology, Nagasaki University, 1-14, Bunkyo-machi, Nagasaki 852-8521, Japan.
An efficient method for the enantio- and diastereoselective synthesis of tricyclic γ-butyrolactones bearing three quaternary stereocenters has been developed through transformations of achiral alkenoic acid substrates. The target optically active tricyclic lactones were obtained as single diastereomers with good enantioselectivities through a sequence of catalytic asymmetric bromolactonization, azidation, and subsequent 1,3-dipolar cycloaddition. The origin of the complete diastereoselectivity observed in the formation of the tricyclic γ-butyrolactone products was elucidated in this study.
View Article and Find Full Text PDFChem Sci
August 2025
Department of Chemistry, University of Georgia Athens Georgia 30602 USA
The observation of allylsilane dual reactivity with α,β-unsaturated platinum carbenes is described. The reaction pathways are controlled by the nature of the catalytic conditions. Under nonpolar conditions, a (3 + 2) cycloaddition is favored to provide decorated tricyclic indole and benzofuran products.
View Article and Find Full Text PDFCureus
August 2025
Pulmonary and Critical Care Medicine, HCA Houston Healthcare Kingwood/University of Houston, Kingwood, USA.
Pulmonary toxicity is a serious yet frequently under-recognized complication of antidepressant therapy. With the continued rise in prescriptions, awareness of potential respiratory adverse effects is crucial. This review outlines documented cases of lung injury linked to various antidepressant classes, including selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), atypical antidepressants, serotonin modulators, tricyclic antidepressants (TCAs), and monoamine oxidase inhibitors (MAOIs).
View Article and Find Full Text PDFPhytochemistry
September 2025
HUN-REN-USZ Biologically Active Natural Products Research Group, University of Szeged, Eötvös Str. 6, 6720, Szeged, Hungary; Department of Pharmacognosy, University of Szeged, Eötvös Str. 6, 6720, Szeged, Hungary. Electronic address:
Previously undescribed steroids vernomigeodiins A-D (1-4), were isolated from the African medicinal plant Vernoniastrum migeodii along with known sterols 5-10 and the tripeptide aurantiamide acetate (11). The isolated steroids featured a stigmastane skeleton with a unique conjugated Δ-diene segment and a highly oxidized side chain, occasionally forming a bi- or tricyclic ring system. Sterols 1-3, 5-9 are glucosylated, whereas 4 and 10 are aglycons.
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