Chemistry & Biodiversity

Papers
(The H4-Index of Chemistry & Biodiversity is 32. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-06-01 to 2026-06-01.)
ArticleCitations
70
Chemical and Antioxidant Profiles of Aerial Parts and Leaf Morpho‐anatomy of 13 Selected Genotypes of Salimenaea integrifolia (Verbenaceae)68
Synthesis and Evaluating the Anticandidal Activities of Triazino[4,3‐a]Quinolinecarboxylate Derivatives: A Promising Approach to Combat Candida Infections64
63
The Phytochemical Tactics for Battling Antibiotic Resistance in Microbes: Secondary Metabolites and Nano Antibiotics Methods58
Four New Polyhydroxysteroids From the South China Sea Cryptomonad Rhodomonas sp.53
Design, Synthesis and Antibacterial Assessment of Active (4‐Arylazo‐3‐Methyl‐2‐Thienyl) 4‐Antipyrine Ketones53
Phyllofolactones V–X, Bishomoscalaranes With Proangiogenic and Hypolipidemic Activities From Sponge Phyllospongia foliascens52
Design, Synthesis and Bioassay of 2‐Phenylglycine Derivatives as Potential Pesticide Candidates50
Soluble Protein Content, Bioactive Compounds and the Antioxidant Activity in Seeds of Ten Rheum tanguticum Lines from Qinghai‐Tibet Plateau50
Two New Alkaloids from Roots of Zea mays and Their Cytotoxic Activity against Hep3B and SW480 Cells47
A New Monoterpene Alkaloid from Incarvillea sinensis with Migration Inhibitory Activity on Cancer Cell46
New Glycerolipids from the Traditional Chinese Medicine of Syngnathus acus (Hai‐Long)46
Seasonal Variation in the Essential Oil Yield and Composition of Cinnamomum parthenoxylon (Jack) Meisner41
Antifungal Azole Derivatives Featuring Naphthalene Prove Potent and Competitive Cholinesterase Inhibitors with Potential CNS Penetration According to the in Vitro and in Silico Studies40
Phytochemical Characterization and Assessment of Antioxidant and Anti‐Alzheimer Effects of Algerian Seseli Tortuosum40
Ephedra intermedia Schrenk & C. A. Mey Methanol Extract: Nanoencapsulation by Mini‐Emulsion Polymerization and its Release Trend under Simulated Conditions of the Human Body39
Five New C21‐Steroidal Sapogenins from the Acid Hydrolysate of Cynanchum otophyllum Roots39
Naringen's Effects on Diuresis and Prevention of Urolithiasis in Hypertensive Rats38
Unveiling the Chemical Constituents and Inhibitory Roles of Extracts from Pinus Pinea L. Nut and Nutshell: A Novel Source for Pharmaceutical Antimicrobials38
In Vitro Assessment of Immunobiological Effectivity of Synthetic Non‐Ionic Glycolipids37
Synthesis of Cytotoxic Benzofurans and Ethers Derivatives of Paeonol37
Cu‐Catalyzed Chan–Evans–Lam Coupling Reactions of 2‐Nitroimidazole with Aryl Boronic Acids: An Effort toward New Bioactive Agents against S. pneumoniae37
Five New Phenylpropanoyl Phloroglucinol Derivatives from Leptospermum scoparium36
Design, Synthesis and Cytotoxic Evaluation of N‐Acylhydrazone‐Incorporated Isoxazolo[4,5‐d]pyridazin‐4(5H)‐one Derivatives36
GC‐MS/HPLC Profiling and Sono‐Maceration Mediated Extraction of Osbeckia Parvifolia Polyphenols: In Silico and In Vitro Analysis on Anti‐Proliferative Activity in Ovarian Cancer Cell Lin34
Parietin, the Vibrant Natural Dye in Xanthoria parietina34
Isolation, Purification, and Characterization of Lentinus edodes Polysaccharides Extracted With Subcritical Water Enhanced With Deep Eutectic Solvent34
Diversity of Endophytic Fungi Isolated From Huperzia serrata and Research on the Secondary Metabolites of Penicillium panissanguineum SZSS 4‐2‐234
ent‐Kaurane‐Type Diterpenes Induce ROS‐Mediated Mitochondrial Dysfunction and Apoptosis by Suppress the Homologous Recombination DNA Repair in Triple‐Negative Breast Cancer Cells33
3‐Hydroxy‐3‐Methylglutaryl Coenzyme‐A Inhibitory Activity of Padina pavonia Terpenoids: An Integrated In Vitro and In Silico Exploration33
Phytochemical Characterization, Prooxidant, Antiproliferative and Anti‐Inflammatory Potential of Meyna spinosa Roxb. Ex Link Ripe Fruit32
Comprehensive Review—Chemistry and Bioactivities of Secondary Metabolites From Chaetomium globosum32
0.1188690662384