Thiosemicarbazones as inhibitors of tyrosinase enzyme.

[1]  M. Eberlin,et al.  Antioxidative, Antiproliferative and Antimicrobial Activities of Phenolic Compounds from Three Myrcia Species , 2018, Molecules.

[2]  C. M. Sant’Anna,et al.  Biological interactions of fluorinated chalcones: Stimulation of tyrosinase activity and binding to bovine serum albumin , 2017 .

[3]  T. Roșu,et al.  Antibacterial, antifungal and in vitro antileukaemia activity of metal complexes with thiosemicarbazones , 2015, Journal of cellular and molecular medicine.

[4]  L. Kremer,et al.  Synthesis, Antitubercular Activity and Mechanism of Resistance of Highly Effective Thiacetazone Analogues , 2013, PloS one.

[5]  C. M. Sant’Anna,et al.  Dialkylphosphorylhydrazones as potent tyrosinase inhibitors , 2012 .

[6]  Yong-hua Hu,et al.  Synthesis and antityrosinase mechanism of benzaldehyde thiosemicarbazones: novel tyrosinase inhibitors. , 2012, Journal of agricultural and food chemistry.

[7]  B. Dijkstra,et al.  Crystal structure of Agaricus bisporus mushroom tyrosinase: identity of the tetramer subunits and interaction with tropolone. , 2011, Biochemistry.

[8]  R. Cao,et al.  Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors. , 2010, European journal of medicinal chemistry.

[9]  K. Hemminki,et al.  Malignant melanoma--a genetic overview. , 2009, Actas dermo-sifiliograficas.

[10]  R. Cao,et al.  Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted phenylmethylenethiosemicarbazones as tyrosinase inhibitors. , 2009, Chemical & pharmaceutical bulletin.

[11]  Hiromi Oozeki,et al.  Molecular design of potent tyrosinase inhibitors having the bibenzyl skeleton. , 2008, Bioorganic & medicinal chemistry letters.

[12]  A. Krettli,et al.  Synthesis and antimalarial activity of semicarbazone and thiosemicarbazone derivatives. , 2008, European journal of medicinal chemistry.

[13]  C. Hertel,et al.  1-(2,4-dihydroxyphenyl)-3-(2,4-dimethoxy-3-methylphenyl)propane, a novel tyrosinase inhibitor with strong depigmenting effects. , 2008, Chemical & pharmaceutical bulletin.

[14]  J. Choi,et al.  Inhibitory effects of kurarinol, kuraridinol, and trifolirhizin from Sophora flavescens on tyrosinase and melanin synthesis. , 2008, Biological & pharmaceutical bulletin.

[15]  Keyvan Nouri,et al.  The treatment of melasma: a review of clinical trials. , 2006, Journal of the American Academy of Dermatology.

[16]  E. Perrier,et al.  Analogues of N-hydroxycinnamoylphenalkylamides as inhibitors of human melanocyte-tyrosinase. , 2006, Bioorganic & medicinal chemistry letters.

[17]  Jun Wang,et al.  Inhibition of the activity of mushroom tyrosinase by alkylbenzoic acids , 2006 .

[18]  S. Padhye,et al.  Nickel (II) complexes of naphthaquinone thiosemicarbazone and semicarbazone: synthesis, structure, spectroscopy, and biological activity. , 2005, Journal of inorganic biochemistry.

[19]  Kang-Kang Song,et al.  Inhibitory effects on mushroom tyrosinase by p-alkoxybenzoic acids , 2005 .

[20]  D. Gambino,et al.  The wide pharmacological versatility of semicarbazones, thiosemicarba-zones and their metal complexes. , 2003, Mini reviews in medicinal chemistry.

[21]  Hoi-Seon Lee Tyrosinase inhibitors of Pulsatilla cernua root-derived materials. , 2002, Journal of agricultural and food chemistry.

[22]  E. Ibáñez,et al.  Supercritical fluid extraction and fractionation of different preprocessed rosemary plants. , 1999, Journal of agricultural and food chemistry.

[23]  S. Jinap,et al.  Vicilin-class globulins and their degradation during cocoa fermentation , 1997 .

[24]  S. Smith,et al.  Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-acetylisoquinoline, and related compounds as inhibitors of herpes simplex virus in vitro and in a cutaneous herpes guinea pig model. , 1986, Antiviral research.