AMBIENTUM BIOETHICA BIOLOGIA CHEMIA DIGITALIA DRAMATICA EDUCATIO ARTIS GYMNAST. ENGINEERING EPHEMERIDES EUROPAEA GEOGRAPHIA GEOLOGIA HISTORIA HISTORIA ARTIUM INFORMATICA IURISPRUDENTIA MATHEMATICA MUSICA NEGOTIA OECONOMICA PHILOLOGIA PHILOSOPHIA PHYSICA POLITICA PSYCHOLOGIA-PAEDAGOGIA SOCIOLOGIA THEOLOGIA CATHOLICA THEOLOGIA CATHOLICA LATIN THEOLOGIA GR.-CATH. VARAD THEOLOGIA ORTHODOXA THEOLOGIA REF. TRANSYLVAN
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STUDIA CHEMIA - Issue no. 2 / 2023 | |||||||
Article: |
DESIGN, SYNTHESIS, CHARACTERIZATION, BIOACTIVITY AND MOLECULAR DOCKING STUDIES OF NOVEL SULFAMIDES. Authors: ALI NADERI, AKIN AKINCIOĞLU, AHMET ÇAĞAN, SÜLEYMAN GÖKSU, PARHAM TASLIMI, İLHAMI GÜLÇIN. |
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Abstract: DOI: 10.24193/subbchem.2023.2.10 Published Online: 2023-06-30 Published Print: 2023-07-30 pp. 145-168 VIEW PDF FULL PDF Starting from commercially available 4-phenylbutanoic acids, a series of novel sulfamides were synthesized and investigated for their inhibition properties on the human carbonic anhydrase I and II (hCA I and II), acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. SAR was also evaluated with molecular docking study. These new compounds were tested against hCA I and hCA II, BChE, and AChE. The majority of the synthetic compounds were more effective against AChE than tacrine, a common inhibitor. Additionally, tacrine was not the only synthetic substance that was more effective against BChE. The obtained results revealed that N,N-dimethyl-[3-(2,4-dimethoxyphenyl)propyl]sulfamide 25, with Ki of 94.22±42.37 nM against AChE and Ki of 230.91±46.22 nM against BChE, was the most potent compound against cholinesterase enzymes. These recently created substances were tested for their ability to inhibit hCA I and II isoforms. In comparison to the conventional inhibitor acetazolamide, the majority of produced sulfamide derivatives 25–29 also inhibited these investigated isoforms. In particular, sulfamide derivatives 25-29 with substituents N,N-dimethyl-[3-(3,5-dimethoxyphenyl)propyl]sulfamide 26 and N,N-dimethyl-[3-(3,4-dimethoxyphenyl)propyl]sulfamide 27 emerged as the most potent hCA inhibitors. Keywords: Synthesis; 3-phenylbutylamine; sulfamide; biological effects; molecular docking |
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