{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T16:36:43Z","timestamp":1790872603951,"version":"4.1.0"},"reference-count":62,"publisher":"Springer Science and Business Media LLC","issue":"12","license":[{"start":{"date-parts":[[2023,12,1]],"date-time":"2023-12-01T00:00:00Z","timestamp":1701388800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,11,12]],"date-time":"2023-11-12T00:00:00Z","timestamp":1699747200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100002383","name":"King Saud University","doi-asserted-by":"publisher","award":["RSP2023R235"],"award-info":[{"award-number":["RSP2023R235"]}],"id":[{"id":"10.13039\/501100002383","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Saudi Pharmaceutical Journal"],"published-print":{"date-parts":[[2023,12]]},"DOI":"10.1016\/j.jsps.2023.101874","type":"journal-article","created":{"date-parts":[[2023,11,22]],"date-time":"2023-11-22T09:55:14Z","timestamp":1700646914000},"page":"101874","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":43,"title":["Exploring the synthesis, structure, spectroscopy and biological activities of novel 4-benzylidene-1-(2-(2,4-dichloro phenyl)acetyl) thiosemicarbazide derivatives: An integrated experimental and theoretical investigation"],"prefix":"10.1007","volume":"31","author":[{"given":"Mahnoor","family":"Waheed","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sana","family":"Idris","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Faheem","family":"Jan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0475-2376","authenticated-orcid":false,"given":"Aftab","family":"Alam","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aftab","family":"Alam","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Muhammad","family":"Ibrahim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abdullah F.","family":"AlAsmari","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Metab","family":"Alharbi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fawaz","family":"Alasmari","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0936-5025","authenticated-orcid":false,"given":"Momin","family":"Khan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"10.1016\/j.jsps.2023.101874_b0005","doi-asserted-by":"crossref","unstructured":"Abuamer, K.M., Maihub, A.A., El-Ajaily, M.M., Etorki, A.M., Abou-Krisha, M.M., Almagani, M.A., 2014. The role of aromatic Schiff bases in the dyes techniques. Int. J. Org. Chem., 2014.","DOI":"10.4236\/ijoc.2014.41002"},{"key":"10.1016\/j.jsps.2023.101874_b0010","first-page":"1","article-title":"Alpha-amylase inhibition can treat diabetes mellitus","volume":"5","author":"Agarwal","year":"2016","journal-title":"Res. Rev. J. Med. Health Sci."},{"key":"10.1016\/j.jsps.2023.101874_b0015","doi-asserted-by":"crossref","first-page":"6906","DOI":"10.3390\/molecules27206906","article-title":"Design, synthesis, crystal structure, in vitro and in silico evaluation of new N\u2032-benzylidene-4-tert-butylbenzohydrazide derivatives as potent urease inhibitors","volume":"27","author":"Ahmad","year":"2022","journal-title":"Molecules"},{"issue":"49","key":"10.1016\/j.jsps.2023.101874_b0020","doi-asserted-by":"crossref","first-page":"45077","DOI":"10.1021\/acsomega.2c05498","article-title":"Synthetic transformation of 2-{2-fluoro [1, 1\u2032-biphenyl]-4-yl} propanoic acid into hydrazide-hydrazone derivatives. In vitro urease inhibition and in silico study","volume":"7","author":"Ahmad","year":"2022","journal-title":"ACS Omega"},{"key":"10.1016\/j.jsps.2023.101874_b0025","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1016\/j.molstruc.2019.05.065","article-title":"Synthesis, molecular structure, spectroscopic properties and biological evaluation of 4-substituted-N-(1H-tetrazol-5-yl) benzenesulfonamides: combined experimental, DFT and docking study","volume":"1195","author":"Akram","year":"2019","journal-title":"J. Mol. Struct."},{"issue":"6","key":"10.1016\/j.jsps.2023.101874_b0030","doi-asserted-by":"crossref","first-page":"672","DOI":"10.3390\/ph15060672","article-title":"Bio-oriented synthesis of novel (S)-flurbiprofen clubbed hydrazone Schiff\u2019s bases for diabetic management. In vitro and in silico studies","volume":"15","author":"Alam","year":"2022","journal-title":"Pharmaceuticals"},{"key":"10.1016\/j.jsps.2023.101874_b0035","doi-asserted-by":"crossref","first-page":"903","DOI":"10.2174\/1573406416666200611103039","article-title":"Chalcones: as potent \u03b1-amylase enzyme inhibitors; synthesis, in vitro, and in silico studies","volume":"17","author":"Ali","year":"2021","journal-title":"Med. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0040","doi-asserted-by":"crossref","unstructured":"Alt\u0131ntop, M.D., Atl\u0131, \u00d6., Ilg\u0131n, S., Demirel, R., \u00d6zdemir, A., Kaplanc\u0131kl\u0131, Z.A., 2016a. Synthesis and biological evaluation of new naphthalene substituted thiosemicarbazone derivatives as potent antifungal and anticancer agents. Eur. J. Med. Chem. 108, 406\u2013414.","DOI":"10.1016\/j.ejmech.2015.11.041"},{"key":"10.1016\/j.jsps.2023.101874_b0045","doi-asserted-by":"crossref","unstructured":"Alt\u0131ntop, M.D., Temel, H.E., Sever, B., Akal\u0131n \u00c7ift\u00e7i, G., Kaplanc\u0131kl\u0131, Z.A., 2016b. Synthesis and evaluation of new benzodioxole-based thiosemicarbazone derivatives as potential antitumor agents. Molecules, 21, 1598.","DOI":"10.3390\/molecules21111598"},{"key":"10.1016\/j.jsps.2023.101874_b0050","doi-asserted-by":"crossref","first-page":"893","DOI":"10.1021\/cr00005a013","article-title":"A quantum theory of molecular structure and its applications","volume":"91","author":"Bader","year":"1991","journal-title":"Chem. Rev."},{"key":"10.1016\/j.jsps.2023.101874_b0055","first-page":"117","article-title":"An insight of alpha-amylase inhibitors as a valuable tool in the management of type 2 diabetes mellitus","volume":"16","author":"Bashary","year":"2020","journal-title":"Curr. Diabetes Rev."},{"key":"10.1016\/j.jsps.2023.101874_b0060","doi-asserted-by":"crossref","first-page":"5150","DOI":"10.1016\/j.poly.2007.07.014","article-title":"Synthesis, characterization, crystal structure and antiproliferative in vitro activity of long-chain aliphatic thiosemicarbazones and their Ni (II) complexes","volume":"26","author":"Belicchi-Ferrari","year":"2007","journal-title":"Polyhedron"},{"key":"10.1016\/j.jsps.2023.101874_b0065","doi-asserted-by":"crossref","unstructured":"\u00c7avu\u015fo\u011flu, B.K., Sa\u011fl\u0131k, B.N., Osmaniye, D., Levent, S., Acar \u00c7evik, U., Karaduman, A.B., \u00d6zkay, Y., Kaplanc\u0131kl\u0131, Z.A., 2017. Synthesis and biological evaluation of new thiosemicarbazone derivative Schiff bases as monoamine oxidase inhibitory agents. Molecules, 23, 60.","DOI":"10.3390\/molecules23010060"},{"key":"10.1016\/j.jsps.2023.101874_b0070","doi-asserted-by":"crossref","unstructured":"Coates, J., 2000. Interpretation of infrared spectra, a practical approach.","DOI":"10.1002\/9780470027318.a5606"},{"key":"10.1016\/j.jsps.2023.101874_b0075","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1016\/j.carbpol.2013.01.045","article-title":"Synthesis and characterization of Eu (III) complexes of modified cellulose and poly (N-isopropylacrylamide)","volume":"94","author":"Cui","year":"2013","journal-title":"Carbohydr. Polym."},{"key":"10.1016\/j.jsps.2023.101874_b0080","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1016\/j.msec.2017.03.059","article-title":"Synthesis and characterization of Eu (III) complexes of modified D-glucosamine and poly (N-isopropylacrylamide)","volume":"78","author":"Cui","year":"2017","journal-title":"Mater. Sci. Eng. C"},{"key":"10.1016\/j.jsps.2023.101874_b0085","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1080\/14686996.2019.1700394","article-title":"Synthesis and characterization of phenylboronic acid-containing polymer for glucose-triggered drug delivery+","volume":"21","author":"Cui","year":"2020","journal-title":"Sci. Technol. Adv. Mater."},{"key":"10.1016\/j.jsps.2023.101874_b0090","first-page":"734","article-title":"New thiosemicarbazone and Talinum triangulare vegetal extract formulations with potential anti-corrosion activity","volume":"5","author":"de Albuquerque","year":"2013","journal-title":"Revista Virtual De Quimica"},{"key":"10.1016\/j.jsps.2023.101874_b0095","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1016\/j.biopha.2016.03.047","article-title":"Evaluation of anti-inflammatory effect of derivative (E)-N-(4-bromophenyl)-2-(thiophen-2-ylmethylene)-thiosemicarbazone","volume":"80","author":"de Oliveira","year":"2016","journal-title":"Biomed. Pharmacother."},{"key":"10.1016\/j.jsps.2023.101874_b0100","doi-asserted-by":"crossref","DOI":"10.1016\/j.molstruc.2019.127589","article-title":"Synthesis, molecular structure, spectroscopic and theoretical investigation of 5-chlorosalicylaldehyde-2, 4-dinitrophenylhydrazone","volume":"1205","author":"Gil","year":"2020","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.jsps.2023.101874_b0105","doi-asserted-by":"crossref","first-page":"480","DOI":"10.1016\/j.foodchem.2017.08.117","article-title":"Antioxidant properties of catechins: comparison with other antioxidants","volume":"241","author":"Grzesik","year":"2018","journal-title":"Food Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0110","doi-asserted-by":"crossref","first-page":"1420","DOI":"10.1016\/j.ccr.2007.09.005","article-title":"Catalytic activities of Schiff base transition metal complexes","volume":"252","author":"Gupta","year":"2008","journal-title":"Coord. Chem. Rev."},{"key":"10.1016\/j.jsps.2023.101874_b0115","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/j.bioorg.2015.06.004","article-title":"Synthesis, biological evaluation and molecular docking of N-phenyl thiosemicarbazones as urease inhibitors","volume":"61","author":"Hameed","year":"2015","journal-title":"Bioorg. Chem."},{"issue":"38","key":"10.1016\/j.jsps.2023.101874_b0120","doi-asserted-by":"crossref","first-page":"7014","DOI":"10.1021\/acs.orglett.3c02607","article-title":"Organoelectrophotocatalytic generation of acyl radicals from formamides and aldehydes: access to acylated 3-CF3-2-oxindoles","volume":"25","author":"He","year":"2023","journal-title":"Org. Lett."},{"key":"10.1016\/j.jsps.2023.101874_b0125","doi-asserted-by":"crossref","first-page":"370","DOI":"10.1093\/occmed\/kqs085","article-title":"Socrates","volume":"62","author":"Hobson","year":"2012","journal-title":"Occup. Med. (Oxford, Engl.)"},{"key":"10.1016\/j.jsps.2023.101874_b0130","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/0263-7855(96)00018-5","article-title":"VMD: visual molecular dynamics","volume":"14","author":"Humphrey","year":"1996","journal-title":"J. Mol. Graph."},{"key":"10.1016\/j.jsps.2023.101874_b0135","doi-asserted-by":"crossref","first-page":"6498","DOI":"10.1021\/ja100936w","article-title":"Revealing noncovalent interactions","volume":"132","author":"Johnson","year":"2010","journal-title":"J. Am. Chem. Soc."},{"key":"10.1016\/j.jsps.2023.101874_b0140","doi-asserted-by":"crossref","unstructured":"Kaplanc\u0131kl\u0131, Z.A., Alt\u0131ntop, M.D., Sever, B., Cant\u00fcrk, Z., \u00d6zdemir, A., 2016. Synthesis and in vitro evaluation of new thiosemicarbazone derivatives as potential antimicrobial agents. J. Chem. 2016.","DOI":"10.1155\/2016\/1692540"},{"key":"10.1016\/j.jsps.2023.101874_b0145","doi-asserted-by":"crossref","DOI":"10.1016\/j.molstruc.2020.128541","article-title":"Synthesis, X-ray structure, vibrational spectroscopy, DFT, biological evaluation and molecular docking studies of (E)-N\u2019-(4-(dimethylamino) benzylidene)-5-methyl-1H-pyrazole-3-carbohydrazide","volume":"1219","author":"Karrouchi","year":"2020","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.jsps.2023.101874_b0150","doi-asserted-by":"crossref","unstructured":"Katritzky, A.R., 1996. A guide to the complete interpretation of infrared spectra of organic structures by noel PG roeges (Katholieke Industriele Hogeschool O-VI). Wiley, New York. 1994. x+ 340 pp. $69.95. ISBN 0-471-93998-6. ACS Publications.","DOI":"10.1021\/ja945091c"},{"key":"10.1016\/j.jsps.2023.101874_b0155","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1016\/j.molstruc.2015.04.024","article-title":"Structural, spectroscopic and quantum chemical studies of acetyl hydrazone oxime and its palladium (II) and platinum (II) complexes","volume":"1095","author":"Kaya","year":"2015","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.jsps.2023.101874_b0160","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1016\/j.bioorg.2018.07.038","article-title":"Flurbiprofen derivatives as novel \u03b1-amylase inhibitors: biology-oriented drug synthesis (BIODS), in vitro, and in silico evaluation","volume":"81","author":"Khan","year":"2018","journal-title":"Bioorg. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0165","doi-asserted-by":"crossref","first-page":"249","DOI":"10.2174\/1570180815666180531101404","article-title":"Green synthesis, characterization, DPPH and ferrous ion-chelating (FIC) activity of tetrakis-Schiff's bases of terephthalaldehyde","volume":"16","author":"Khan","year":"2019","journal-title":"Lett. Drug Des. Discovery"},{"issue":"5","key":"10.1016\/j.jsps.2023.101874_b0170","doi-asserted-by":"crossref","first-page":"5116","DOI":"10.1021\/acsomega.2c08108","article-title":"Para-substituted thiosemicarbazones as cholinesterase inhibitors: synthesis, in vitro biological evaluation, and in silico study","volume":"8","author":"Khan","year":"2023","journal-title":"ACS Omega"},{"key":"10.1016\/j.jsps.2023.101874_b0175","doi-asserted-by":"crossref","first-page":"1079","DOI":"10.1016\/j.jinorgbio.2010.06.005","article-title":"Synthesis and in vitro evaluation of gold (I) thiosemicarbazone complexes for antimalarial activity","volume":"104","author":"Khanye","year":"2010","journal-title":"J. Inorg. Biochem."},{"key":"10.1016\/j.jsps.2023.101874_b0180","first-page":"349","article-title":"In vitro \u03b1-glucosidase and \u03b1-amylase inhibitory activity of Psidium guajava extracts","volume":"8","author":"Kumari","year":"2014","journal-title":"J. Pharm. Res."},{"key":"10.1016\/j.jsps.2023.101874_b0185","doi-asserted-by":"crossref","first-page":"785","DOI":"10.1103\/PhysRevB.37.785","article-title":"Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density","volume":"37","author":"Lee","year":"1988","journal-title":"Phys. Rev. B"},{"key":"10.1016\/j.jsps.2023.101874_b0190","doi-asserted-by":"crossref","first-page":"580","DOI":"10.1002\/jcc.22885","article-title":"Multiwfn: a multifunctional wavefunction analyzer","volume":"33","author":"Lu","year":"2012","journal-title":"J. Comput. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0195","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1038\/ncomms14599","article-title":"Stabilizing short-lived Schiff base derivatives of 5-aminouracils that activate mucosal-associated invariant T cells","volume":"8","author":"Mak","year":"2017","journal-title":"Nat. Commun."},{"key":"10.1016\/j.jsps.2023.101874_b0200","article-title":"Synthesis, characterization and antioxidant activities of semicarbazide and thiosemicarbazide derivatives","volume":"43","author":"Manaf","year":"2021","journal-title":"J. Chem. Soc. Pak."},{"key":"10.1016\/j.jsps.2023.101874_b0205","doi-asserted-by":"crossref","first-page":"3332","DOI":"10.1021\/bi701652t","article-title":"Alternative catalytic anions differentially modulate human \u03b1-amylase activity and specificity","volume":"47","author":"Maurus","year":"2008","journal-title":"Biochemistry"},{"key":"10.1016\/j.jsps.2023.101874_b0210","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1002\/1521-4184(200205)335:5<183::AID-ARDP183>3.0.CO;2-U","article-title":"Anti-HIV activity of thiosemicarbazone and semicarbazone derivatives of (\u00b1)-3-menthone","volume":"335","author":"Mishra","year":"2002","journal-title":"Archiv Der Pharmazie: Int. J. Pharm. Med. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0215","article-title":"Computational insights of excited state intramolecular proton transfer (ESIPT) based fluorescent detection and imaging of \u03b3-glutamytranspeptidase activity","author":"Nasim","year":"2023","journal-title":"Spectrochim. Acta A: Mol. Biomol. Spectrosc."},{"key":"10.1016\/j.jsps.2023.101874_b0220","doi-asserted-by":"crossref","first-page":"2101","DOI":"10.1007\/s10973-020-10199-8","article-title":"Butylated hydroxy benzylidene ring: an important moiety for antioxidant synergism of semicarbazones","volume":"146","author":"Nath","year":"2021","journal-title":"J. Therm. Anal. Calorim."},{"key":"10.1016\/j.jsps.2023.101874_b0225","doi-asserted-by":"crossref","first-page":"10569","DOI":"10.1039\/C6NJ02642G","article-title":"A novel nano-sized binuclear nickel (II) Schiff base complex as a precursor for NiO nanoparticles: synthesis, characterization, DFT study and antibacterial activity","volume":"40","author":"Parsaee","year":"2016","journal-title":"New J. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0230","doi-asserted-by":"crossref","DOI":"10.1016\/j.molstruc.2020.128922","article-title":"Isatin based thiosemicarbazide derivatives as potential inhibitor of \u03b1-glucosidase, synthesis and their molecular docking study","volume":"1222","author":"Rahim","year":"2020","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.jsps.2023.101874_b0235","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1080\/15685551.2013.840472","article-title":"Metal-based Schiff base polymers: preparation, spectral, thermal and their in vitro biological investigation","volume":"17","author":"Rasool","year":"2014","journal-title":"Des. Monomers Polym."},{"key":"10.1016\/j.jsps.2023.101874_b0240","doi-asserted-by":"crossref","first-page":"1223","DOI":"10.1063\/1.476673","article-title":"6\u201331G* basis set for atoms K through Zn","volume":"109","author":"Rassolov","year":"1998","journal-title":"J. Chem. Phys."},{"key":"10.1016\/j.jsps.2023.101874_b0245","doi-asserted-by":"crossref","first-page":"381","DOI":"10.1016\/j.molstruc.2018.03.120","article-title":"Structure, tautomerism, spectroscopic and DFT study of o-vanillin derived Schiff bases containing thiophene ring","volume":"1165","author":"Rodr\u00edguez","year":"2018","journal-title":"J. Mol. Struct."},{"key":"10.1016\/j.jsps.2023.101874_b0250","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1038\/s41598-017-11716-w","article-title":"Thiosemicarbazone scaffold for the design of antifungal and antiaflatoxigenic agents: evaluation of ligands and related copper complexes","volume":"7","author":"Rogolino","year":"2017","journal-title":"Sci. Rep."},{"key":"10.1016\/j.jsps.2023.101874_b0255","doi-asserted-by":"crossref","first-page":"29276","DOI":"10.1039\/C5RA04207K","article-title":"Significant photocytotoxic effect of an iron (iii) complex of a Schiff base ligand derived from vitamin B 6 and thiosemicarbazide in visible light","volume":"5","author":"Sarkar","year":"2015","journal-title":"RSC Adv."},{"key":"10.1016\/j.jsps.2023.101874_b0260","doi-asserted-by":"crossref","first-page":"16502","DOI":"10.1021\/jp960976r","article-title":"Harmonic vibrational frequencies: an evaluation of Hartree\u2013Fock, M\u00f8ller\u2013Plesset, quadratic configuration interaction, density functional theory, and semiempirical scale factors","volume":"100","author":"Scott","year":"1996","journal-title":"J. Phys. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0265","doi-asserted-by":"crossref","first-page":"689","DOI":"10.22270\/jddt.v9i3.2888","article-title":"Thiosemicarbazone complexes as versatile medicinal chemistry agents: a review","volume":"9","author":"Siddiqui","year":"2019","journal-title":"J. Drug Del. Therap."},{"key":"10.1016\/j.jsps.2023.101874_b0270","doi-asserted-by":"crossref","DOI":"10.3389\/fendo.2022.1085092","article-title":"Review of the correlation between Chinese medicine and intestinal microbiota on the efficacy of diabetes mellitus","volume":"13","author":"Su","year":"2023","journal-title":"Front. Endocrinol."},{"key":"10.1016\/j.jsps.2023.101874_b0275","first-page":"455","article-title":"Software news and update AutoDock Vina: improving the speed and accuracy of docking with a new scoring function","volume":"31","author":"Trott","year":"2009","journal-title":"Effic. Optim. Multithreading"},{"key":"10.1016\/j.jsps.2023.101874_b0280","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1002\/jcc.21334","article-title":"AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading","volume":"31","author":"Trott","year":"2010","journal-title":"J. Comput. Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0285","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.ccr.2014.02.023","article-title":"RETRACTED: DFT flavor of coordination chemistry","volume":"272","author":"Tsipis","year":"2014","journal-title":"Coord. Chem. Rev."},{"key":"10.1016\/j.jsps.2023.101874_b0290","doi-asserted-by":"crossref","first-page":"3585","DOI":"10.1039\/D3QO00728F","article-title":"Organophotoelectrochemical silylation cyclization for the synthesis of silylated 3-CF 3-2-oxindoles","volume":"10","author":"Wan","year":"2023","journal-title":"Org. Chem. Front."},{"key":"10.1016\/j.jsps.2023.101874_b0295","first-page":"1","article-title":"Surface-functionalized design of blood-contacting biomaterials for preventing coagulation and promoting hemostasis","author":"Wang","year":"2023","journal-title":"Friction"},{"issue":"10","key":"10.1016\/j.jsps.2023.101874_b0300","doi-asserted-by":"crossref","first-page":"1952","DOI":"10.1039\/D3JA00128H","article-title":"Measurement of transient temperature using laser-induced breakdown spectroscopy (LIBS) with the surface temperature effect","volume":"38","author":"Yang","year":"2023","journal-title":"J. Anal. Atomic"},{"key":"10.1016\/j.jsps.2023.101874_b0305","doi-asserted-by":"crossref","first-page":"8411","DOI":"10.1021\/jf502667z","article-title":"\u03b1-Amylase inhibitory triterpene from Abrus precatorius leaves","volume":"62","author":"Yonemoto","year":"2014","journal-title":"J. Agric. Food Chem."},{"key":"10.1016\/j.jsps.2023.101874_b0310","doi-asserted-by":"crossref","first-page":"419","DOI":"10.1016\/j.ejmech.2015.06.047","article-title":"Synthesis and evaluation of isatin-\u03b2-thiosemicarbazones as novel agents against antibiotic-resistant Gram-positive bacterial species","volume":"101","author":"Zhang","year":"2015","journal-title":"Eur. J. Med. Chem."}],"container-title":["Saudi Pharmaceutical Journal"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1319016423003699?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1319016423003699?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,1,6]],"date-time":"2025-01-06T17:29:22Z","timestamp":1736184562000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1319016423003699"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,12]]},"references-count":62,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2023,12]]}},"alternative-id":["S1319016423003699"],"URL":"https:\/\/doi.org\/10.1016\/j.jsps.2023.101874","relation":{},"ISSN":["1319-0164"],"issn-type":[{"value":"1319-0164","type":"print"}],"subject":[],"published":{"date-parts":[[2023,12]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Exploring the synthesis, structure, spectroscopy and biological activities of novel 4-benzylidene-1-(2-(2,4-dichloro phenyl)acetyl) thiosemicarbazide derivatives: An integrated experimental and theoretical investigation","name":"articletitle","label":"Article Title"},{"value":"Saudi Pharmaceutical Journal","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jsps.2023.101874","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.","name":"copyright","label":"Copyright"}],"article-number":"101874"}}