World's Best Scientists 2026 revealed!
Hatem A. Abdel-Aziz

Hatem A. Abdel-Aziz

D-Index & Metrics

Chemistry

D-Index
55
Citations
7689
World Ranking
12421
National Ranking
62

Hatem A. Abdel-Aziz publication distribution in Chemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Chemistry in 2026. The highlighted bar marks where Hatem A. Abdel-Aziz sits on this spectrum.

61–80 publications: 66 scientists 81–100 publications: 302 scientists 101–120 publications: 623 scientists 121–140 publications: 918 scientists 141–160 publications: 1,218 scientists 161–180 publications: 1,350 scientists 181–200 publications: 1,344 scientists 201–220 publications: 1,281 scientists 221–240 publications: 1,216 scientists 241–260 publications: 1,100 scientists 261–280 publications: 979 scientists 281–300 publications: 939 scientists 301–320 publications: 764 scientists 321–340 publications: 643 scientists 341–360 publications: 628 scientists 361–380 publications: 522 scientists 381–400 publications: 459 scientists 401–420 publications: 397 scientists 421–440 publications: 327 scientists 441–460 publications: 270 scientists 461–480 publications: 265 scientists 481–500 publications: 252 scientists 501–520 publications: 201 scientists 521–540 publications: 185 scientists 541–560 publications: 148 scientists 561–580 publications: 148 scientists 581–600 publications: 132 scientists 601–620 publications: 114 scientists 621–640 publications: 104 scientists 641–660 publications: 91 scientists 661–680 publications: 92 scientists 681–700 publications: 73 scientists 701–720 publications: 57 scientists 721–740 publications: 54 scientists 741–760 publications: 67 scientists 761–780 publications: 45 scientists 781–800 publications: 46 scientists 801–820 publications: 39 scientists 821–840 publications: 32 scientists 841–860 publications: 36 scientists 861–880 publications: 29 scientists 881–900 publications: 26 scientists 901–920 publications: 24 scientists 921–940 publications: 14 scientists 941–960 publications: 23 scientists 961–980 publications: 28 scientists 981–1,000 publications: 15 scientists 1,001–1,020 publications: 29 scientists 1,021–1,040 publications: 12 scientists 1,041–1,060 publications: 19 scientists 1,061–1,080 publications: 12 scientists 1,081–1,100 publications: 6 scientists 1,101–1,120 publications: 8 scientists 1,121–1,140 publications: 12 scientists 1,141–1,160 publications: 5 scientists 1,161–1,180 publications: 6 scientists 1,181–1,200 publications: 14 scientists 1,201–1,220 publications: 7 scientists 1,221–1,240 publications: 2 scientists 1,241–1,260 publications: 6 scientists 1,261–1,280 publications: 4 scientists 1,281–1,294 publications: 6 scientists 1,295+ publications: 100 scientists
61 publications 1,295+

This scientist: 239 publications — 46th percentile

46% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 1,295 publications or more.

Hatem A. Abdel-Aziz D-index placement in Chemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Chemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Hatem A. Abdel-Aziz sits on this spectrum.

40–41 D-Index: 289 scientists 42–43 D-Index: 612 scientists 44–45 D-Index: 808 scientists 46–47 D-Index: 776 scientists 48–49 D-Index: 835 scientists 50–51 D-Index: 861 scientists 52–53 D-Index: 872 scientists 54–55 D-Index: 933 scientists 56–57 D-Index: 1,051 scientists 58–59 D-Index: 930 scientists 60–61 D-Index: 882 scientists 62–63 D-Index: 834 scientists 64–65 D-Index: 731 scientists 66–67 D-Index: 775 scientists 68–69 D-Index: 683 scientists 70–71 D-Index: 646 scientists 72–73 D-Index: 561 scientists 74–75 D-Index: 501 scientists 76–77 D-Index: 437 scientists 78–79 D-Index: 388 scientists 80–81 D-Index: 354 scientists 82–83 D-Index: 292 scientists 84–85 D-Index: 275 scientists 86–87 D-Index: 254 scientists 88–89 D-Index: 235 scientists 90–91 D-Index: 185 scientists 92–93 D-Index: 192 scientists 94–95 D-Index: 155 scientists 96–97 D-Index: 163 scientists 98–99 D-Index: 125 scientists 100–101 D-Index: 105 scientists 102–103 D-Index: 105 scientists 104–105 D-Index: 112 scientists 106–107 D-Index: 88 scientists 108–109 D-Index: 68 scientists 110–111 D-Index: 69 scientists 112–113 D-Index: 65 scientists 114–115 D-Index: 79 scientists 116–117 D-Index: 61 scientists 118–119 D-Index: 44 scientists 120–121 D-Index: 37 scientists 122–123 D-Index: 40 scientists 124–125 D-Index: 33 scientists 126–127 D-Index: 26 scientists 128–129 D-Index: 34 scientists 130–131 D-Index: 35 scientists 132–133 D-Index: 25 scientists 134–135 D-Index: 27 scientists 136–137 D-Index: 17 scientists 138–139 D-Index: 16 scientists 140–141 D-Index: 20 scientists 142–143 D-Index: 20 scientists 144–145 D-Index: 15 scientists 146–147 D-Index: 9 scientists 148–149 D-Index: 9 scientists 150–151 D-Index: 16 scientists 152–153 D-Index: 11 scientists 154–155 D-Index: 9 scientists 156–157 D-Index: 3 scientists 158 D-Index: 3 scientists 159+ D-Index: 98 scientists
40 D-Index 159+

This scientist: 55 D-Index — 33rd percentile

33% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 159 D-Index or more.

Overview

Hatem A. Abdel-Aziz is affiliated with King Saud University in Saudi Arabia and has a research focus encompassing chemistry, medicine, and biochemistry, genetics, and molecular biology. Their work primarily addresses organic chemistry, molecular biology, pharmacology, pathology and forensic medicine, and oncology.

The scientist's research concentrates on several key topics including synthesis and biological activity, enzyme function and inhibition, synthesis and catalytic reactions, cancer mechanisms and therapy, synthesis and characterization of heterocyclic compounds, cancer therapeutics and mechanisms, and cholinesterase and neurodegenerative diseases.

Among recent publications authored by or involving Hatem A. Abdel-Aziz are:

  • Development of isatin-thiazolo[3,2-a]benzimidazole hybrids as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological and molecular dynamics investigations (2021, Bioorganic Chemistry)
  • Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights (2020, Journal of Enzyme Inhibition and Medicinal Chemistry)
  • 3-Methylthiazolo[3,2-a]benzimidazole-benzenesulfonamide conjugates as novel carbonic anhydrase inhibitors endowed with anticancer activity: Design, synthesis, biological and molecular modeling studies (2020, European Journal of Medicinal Chemistry)
  • Synthesis, Biological Evaluation and In Silico Studies of Certain Oxindole-Indole Conjugates as Anticancer CDK Inhibitors (2020, Molecules)
  • Benzofuran-Based Carboxylic Acids as Carbonic Anhydrase Inhibitors and Antiproliferative Agents against Breast Cancer (2020, ACS Medicinal Chemistry Letters)

Frequent collaborators in research include Wagdy M. Eldehna, Mahmoud S. Elkotamy, Tarfah Al-Warhi, Claudiu T. Supuran, and Alessio Nocentini.

Hatem A. Abdel-Aziz's work has been published predominantly in the following venues:

  • Bioorganic Chemistry (20 publications)
  • European Journal of Medicinal Chemistry (14 publications)
  • Journal of Enzyme Inhibition and Medicinal Chemistry (11 publications)
  • Drug Development Research (7 publications)
  • International Journal of Biological Macromolecules (4 publications)

Best Publications

  • Synthesis and antimicrobial evaluation of 1-(benzofuran-2-yl)-4-nitro-3-arylbutan-1-ones and 3-(benzofuran-2-yl)-4,5-dihydro-5-aryl-1-[4-(aryl)-1,3-thiazol-2-yl]-1H-pyrazoles.

    Bakr F. Abdel-Wahab;Hatem A. Abdel-Aziz;Essam M. Ahmed

  • Novel 4/3-((4-oxo-5-(2-oxoindolin-3-ylidene)thiazolidin-2-ylidene)amino) benzenesulfonamides: Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular modelling studies

    Wagdy M. Eldehna;Mahmoud F. Abo-Ashour;Alessio Nocentini;Paola Gratteri

  • Synthesis and antitumor activity of pyrido [2,3-d]pyrimidine and pyrido[2,3-d] [1,2,4]triazolo[4,3-a]pyrimidine derivatives that induce apoptosis through G1 cell-cycle arrest.

    Mohamed Fares;Sahar Mahmoud Abou-Seri;Hatem A. Abdel-Aziz;Safinaz E.-S. Abbas

  • Nanomolar Detection of Hypochlorite by a Rhodamine-Based Chiral Hydrazide in Absolute Aqueous Media: Application in Tap Water Analysis with Live-Cell Imaging

    Shyamaprosad Goswami;Avijit Kumar Das;Abhishek Manna;Anup Kumar Maity

  • Design, synthesis and QSAR study of certain isatin-pyridine hybrids as potential anti-proliferative agents.

    Wagdy M. Eldehna;Ayman Altoukhy;Hoda Mahrous;Hatem A. Abdel-Aziz

  • Design, synthesis and antitubercular activity of certain nicotinic Acid hydrazides.

    Wagdy M Eldehna;Mohamed Fares;Marwa M Abdel-Aziz;Hatem A Abdel-Aziz;Hatem A Abdel-Aziz

  • Isatin-pyrazole benzenesulfonamide hybrids potently inhibit tumor-associated carbonic anhydrase isoforms IX and XII.

    Hany S. Ibrahim;Sahar M. Abou-Seri;Muhammet Tanc;Mahmoud M. Elaasser

  • Enhancement of the tail hydrophobic interactions within the carbonic anhydrase IX active site via structural extension: Design and synthesis of novel N-substituted isatins-SLC-0111 hybrids as carbonic anhydrase inhibitors and antitumor agents.

    Wagdy M. Eldehna;Mahmoud F. Abo-Ashour;Alessio Nocentini;Radwan S. El-Haggar

  • Improvement of antibacterial activity of some sulfa drugs through linkage to certain phthalazin-1(2H)-one scaffolds.

    Hany S. Ibrahim;Wagdy M. Eldehna;Hatem A. Abdel-Aziz;Mahmoud M. Elaasser

  • Microwave-assisted synthesis and in-vitro anti-tumor activity of 1,3,4-triaryl-5-N-arylpyrazole-carboxamides

    Hatem A. Abdel-Aziz;Heba S.A. El-Zahabi;Kamal M. Dawood

  • Synthesis and in vitro anti-proliferative activity of some novel isatins conjugated with quinazoline/phthalazine hydrazines against triple-negative breast cancer MDA-MB-231 cells as apoptosis-inducing agents

    Wagdy M Eldehna;Hadia Almahli;Ghada H Al-Ansary;Hazem A Ghabbour

  • Stereoselective synthesis and antimicrobial activity of benzofuran-based (1E)-1-(piperidin-1-yl)-N2-arylamidrazones

    Hatem A. Abdel-Aziz;Amal A.I. Mekawey

  • Development of isatin-thiazolo[3,2-a]benzimidazole hybrids as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological and molecular dynamics investigations.

    Wagdy M. Eldehna;Mahmoud A. El Hassab;Mahmoud F. Abo-Ashour;Tarfah Al-Warhi

  • Convenient synthesis and antimicrobial evaluation of some novel 2-substituted-3-methylbenzofuran derivatives

    Hatem A. Abdel-Aziz;Amal A.I. Mekawey;Kamal M. Dawood

  • Synthesis and antimicrobial evaluation of some 1,3-thiazole, 1,3,4-thiadiazole, 1,2,4-triazole, and 1,2,4-triazolo[3,4-b][1,3,4]-thiadiazine derivatives including a 5-(benzofuran-2-yl)-1-phenylpyrazole moiety

    Bakr F. Abdel-Wahab;Hatem A. Abdel-Aziz;Essam M. Ahmed

  • Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII.

    Wagdy M. Eldehna;Mohamed Fares;Mariangela Ceruso;Hazem A. Ghabbour

  • Convenient Synthesis and Antimicrobial Activity of New 3‐Substituted 5‐(Benzofuran‐2‐yl)‐pyrazole Derivatives

    Bakr F. Abdel-Wahab;Hatem A. Abdel-Aziz;Essam M. Ahmed

  • Dual-tail arylsulfone-based benzenesulfonamides differently match the hydrophobic and hydrophilic halves of human carbonic anhydrases active sites: Selective inhibitors for the tumor-associated hCA IX isoform.

    Hany S. Ibrahim;Heba Abdelrasheed Allam;Walaa R. Mahmoud;Alessandro Bonardi

  • Facile Synthesis and In‐Vitro Antitumor Activity of Some Pyrazolo[3,4‐b]pyridines and Pyrazolo[1,5‐a]pyrimidines Linked to a Thiazolo[3,2‐a]benzimidazole Moiety

    Hatem A. Abdel-Aziz;Tamer S. Saleh;Heba S. A. El-Zahabi

  • Synthesis of New Heterocycles Derived from 3-(3-Methyl-1H-indol-2-yl)-3-oxopropanenitrile as Potent Antifungal Agents

    Sobhi M. Gomha;Hatem A. Abdel-Aziz

  • Synthesis and in vitro anticancer activity of certain novel 1-(2-methyl-6-arylpyridin-3-yl)-3-phenylureas as apoptosis-inducing agents

    Wagdy M. Eldehna;Ghada S. Hassan;Sara T. Al-Rashood;Tarfah Al-Warhi

  • Synthesis and antimicrobial evaluation of some 1,2,4-triazole, 1,3,4-oxa(thia)diazole, and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives

    Kamal M. Dawood;Ahmad M. Farag;Hatem A. Abdel-Aziz

Frequent Co-Authors

Wagdy M. Eldehna
Wagdy M. Eldehna Kafrelsheikh University
Hoong-Kun Fun
Hoong-Kun Fun Universiti Sains Malaysia
Claudiu T. Supuran
Claudiu T. Supuran University of Florence
Seik Weng Ng
Seik Weng Ng University of Malaya
Edward R. T. Tiekink
Edward R. T. Tiekink Sunway University
Daniela Vullo
Daniela Vullo University of Florence
Clemente Capasso
Clemente Capasso National Academies of Sciences, Engineering, and Medicine
Fabrizio Carta
Fabrizio Carta University of Florence
Maurizio Botta
Maurizio Botta University of Siena
Robert McKenna
Robert McKenna University of Florida

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