50 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Bioactive Constituents of Glycyrrhiza uralensis (Licorice): Discovery of the Effective Components of a Traditional Herbal Medicine.
Peking University
Rhododendrol glycosides as stereospecific tyrosinase inhibitors.
Tokyo University of Agriculture and Technology
Effect of the tyrosinase inhibitor (S)-N-trans-feruloyloctopamine from garlic skin on tyrosinase gene expression and melanine accumulation in melanoma cells.
Gansu College of Traditional Chinese Medicine
Structure-activity relationships of the thujaplicins for inhibition of human tyrosinase.
Institute For Theoretical Medicine
(-)-N-Formylanonaine from Michelia alba as a human tyrosinase inhibitor and antioxidant.
Kaohsiung Medical University
New tyrosinase inhibitors selected by atomic linear indices-based classification models.
Central University of Las Villas
Identification of oxidation product of arbutin in mushroom tyrosinase assay system.
University of California
Synthesis of N-kojic-amino acid and N-kojic-amino acid-kojiate and their tyrosinase inhibitory activity
TBA
New halogenated phenylcoumarins as tyrosinase inhibitors.
Universidad De Santiago De Compostela
Synthesis and evaluation of bibenzyl glycosides as potent tyrosinase inhibitors.
Utsunomiya University
Evaluation of 3,4-dihydroquinazoline-2(1H)-thiones as inhibitors of alpha-MSH-induced melanin production in melanoma B16 cells.
Chungnam National University
Synthesis and biological evaluation of curcumin-like diarylpentanoid analogues for anti-inflammatory, antioxidant and anti-tyrosinase activities.
Universiti Putra Malaysia
Biphenyl glycosides from the fruit of Pyracantha fortuneana.
Shenyang Pharmaceutical University
Constituents from the leaves of Phellodendron amurense var. wilsonii and their bioactivity.
National Cheng Kung University
Catechol-mimicking transition-state analogues as non-oxidizable inhibitors of tyrosinases.
Univ. Grenoble Alpes
Computational methods to analyze and predict the binding mode of inhibitors targeting both human and mushroom tyrosinase.
University of Messina
The recent discovery of a promising pharmacological scaffold derived from carvacrol: A review.
Universiti Kebangsaan Malaysia
Synthesis and evaluation of 3-hydroxyquinolin-2(1H)-one derivatives as inhibitors of tyrosinase.
North-West University
Pyrrole-containing hybrids as potential anticancer agents: An insight into current developments and structure-activity relationships.
Jiangxi Science & Technology Normal University
Artificial Intelligence-Assisted Optimization of Antipigmentation Tyrosinase Inhibitors: De Novo Molecular Generation Based on a Low Activity Lead Compound.
Hangzhou Normal University
Design and synthesis of 4-amino-2',4'-dihydroxyindanone derivatives as potent inhibitors of tyrosinase and melanin biosynthesis in human melanoma cells.
University of Grenoble Alpes
Synthetic tyrosyl gallate derivatives as potent melanin formation inhibitors.
Amorepacific
Resorcinol-based hemiindigoid derivatives as human tyrosinase inhibitors and melanogenesis suppressors in human melanoma cells.
University Grenoble Alpes
Azole inhibitors of mushroom and human tyrosinases: Current advances and prospects of drug development for melanogenic dermatological disorders.
King Saud University
Exploiting HOPNO-dicopper center interaction to development of inhibitors for human tyrosinase.
University of Grenoble Alpes
Recent advances in the design and discovery of synthetic tyrosinase inhibitors.
National Clinical Research Center For Geriatrics
Pyrazolotriazines: Biological activities, synthetic strategies and recent developments.
Mazandaran University of Medical Sciences
Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent.
Chulalongkorn University
Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes.
Umr-Cnrs 5063
Polyphenolic compounds: Synthesis, assessment of antimicrobial effect and enzymes inhibition against important medicinal enzymes with computational details.
Bartin University
Design, synthesis and biological evaluation of tyrosinase-targeting PROTACs.
University of Chinese Academy of Sciences
Solid-phase synthesis of kojic acid-tripeptides and their tyrosinase inhibitory activity, storage stability, and toxicity.
Seoul National University
2-hydroxy-4-isopropylbenzaldehyde, a potent partial tyrosinase inhibitor.
University of California
Kojic acid-natural product conjugates as mushroom tyrosinase inhibitors.
Mazandaran University of Medical Sciences
Advances in the Design of Genuine Human Tyrosinase Inhibitors for Targeting Melanogenesis and Related Pigmentations.
Universite Grenoble Alpes
Xanthones for melanogenesis inhibition: Molecular docking and QSAR studies to understand their anti-tyrosinase activity.
Universidade Dos A£Ores
Recent applications of hydantoin and thiohydantoin in medicinal chemistry.
College of Pharmacy and Gachon Institute of Pharmaceutical Science
Insights into the chemistry and therapeutic potential of furanones: A versatile pharmacophore.
Jamia Hamdard
Isolation of Sesquiterpene-Amino Acid Conjugates, Onopornoids A-D, and a Flavonoid Glucoside from Onopordum alexandrinum.
Hiroshima University
Artocarmins G-M, Prenylated 4-Chromenones from the Stems of Artocarpus rigida and Their Tyrosinase Inhibitory Activities.
Hiroshima University
Glycybridins A-K, Bioactive Phenolic Compounds from Glycyrrhiza glabra.
Peking University
