PMID
Data
Article Title
Organization
Chemical and bioactivity of flavanones obtained from roots of Dalea pazensis Rusby.

Universidad Nacional De C£Rdoba
2-Hydroxypyridine-

Univ. Grenoble-Alpes/Cnrs
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
Tyrosinase inhibitory activity of a glucosylated hydroxystilbene in mouse melan-a melanocytes.

The Chinese University of Hong Kong
(-)-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 anti-melanogenic activity of hydroxyphenyl benzyl ether analogues.

Catholic University of Daegu
Synthesis and evaluation of bibenzyl glycosides as potent tyrosinase inhibitors.

Utsunomiya University
Natural ortho-dihydroxyisoflavone derivatives from aged Korean fermented soybean paste as potent tyrosinase and melanin formation inhibitors.

Amorepacific
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
N-[(Dihydroxyphenyl)acyl]serotonins as potent inhibitors of tyrosinase from mouse and human melanoma cells.

National Institute of Advanced Industrial Science and Technology
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
Acetophenone derivatives from Acronychia pedunculata.

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
Recent advances in triazoles as tyrosinase inhibitors.

University of Health Sciences
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
Tyrosinase inhibitors as potential antibacterial agents.

The University of Queensland
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
Aurone: A biologically attractive scaffold as anticancer agent.

King Khalid University
Recent applications of hydantoin and thiohydantoin in medicinal chemistry.

College of Pharmacy and Gachon Institute of Pharmaceutical Science
Inhibitors of Melanogenesis: An Updated Review.

University of Bonn
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
Melanogenic inhibitory effects of Triangularin in B16F0 melanoma cells, in vitro and molecular docking studies.

Universidad Nacional De C£Rdoba
Dimeric cinnamoylamide analogues for regulation of tyrosinase activity in melanoma cells: A role of diamide-link chain length.

Seoul National University of Science and Technology
Resorcinol alkyl glucosides as potent tyrosinase inhibitors.

Utsunomiya University
Refinement of the pharmacophore of 3,4-dihydroquinazoline-2(1H)-thiones for their anti-melanogenesis activity.

Chungnam National University
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine Fragments.

Universit�
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
Pyridone derivative, pharmaceutical containing the same and methods of use thereof

Kaken Pharmaceutical
Benzolamide is not a membrane-impermeant carbonic anhydrase inhibitor.

UniversitÀ Degli Studi Di Firenze