Synthesis and melanin biosynthesis inhibitory activity of (+/-)-terrein produced by Penicillium sp. 20135.

[1]  Y. Pyun,et al.  Melanocins A, B and C, new melanin synthesis inhibitors produced by Eupenicillium shearii. I. Taxonomy, fermentation, isolation and biological properties. , 2003, The Journal of antibiotics.

[2]  K. Mitsumori,et al.  Hepatocellular tumor induction in heterozygous p53-deficient CBA mice by a 26-week dietary administration of kojic acid. , 2003, Toxicological sciences : an official journal of the Society of Toxicology.

[3]  G. Pairaudeau,et al.  Studies Toward the Synthesis of Natural and Unnatural Dienediynes. Part 2: A Practical Approach to Functionalised Cyclopentenones , 2000 .

[4]  G. Pairaudeau,et al.  Synthesis of functionalised cyclopentenones via rearrangement of pyranones , 2000 .

[5]  S. Caddick,et al.  STUDIES TOWARD THE SYNTHESIS OF NATURAL AND UNNATURAL DIENEDIYNES. 1. APPROACHES TO A FUNCTIONALISED BICYCLIC RING SYSTEM , 1999 .

[6]  H. Kondoh,et al.  Enhanced melanogenesis induced by tyrosinase gene-transfer increases boron-uptake and killing effect of boron neutron capture therapy for amelanotic melanoma. , 1998, Pigment cell research.

[7]  H. Watanabe,et al.  Induction of thyroid tumours in (C57BL/6N x C3H/N)F1 mice by oral administration of kojic acid. , 1998, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[8]  S. Caddick,et al.  Stereoselective synthesis of a functionalised bicyclic core of Neocarzinostatin and Kedarcidin Chromophores , 1997 .

[9]  F. García-Carmona,et al.  Kojic Acid, a Cosmetic Skin Whitening Agent, is a Slow‐binding Inhibitor of Catecholase Activity of Tyrosinase , 1994, The Journal of pharmacy and pharmacology.

[10]  K. Kilgore,et al.  Development of an in vitro primary screen for skin depigmentation and antimelanoma agents. , 1994, Skin pharmacology : the official journal of the Skin Pharmacology Society.

[11]  H. Kolb,et al.  A total synthesis of racemic and optically active terrein (trans-4,5-dihydroxy-3-[(E)-1-propenyl]-2-cyclopenten-1-one). , 1990 .

[12]  V. Hearing,et al.  Analysis of mammalian pigmentation at the molecular level. , 1989, Pigment cell research.

[13]  A. Hirota,et al.  Isolation of Acetylaranotin, Bisdethiodi(methylthio)-acetylaranotin and Terrein as Plant Growth Inhibitors from a Strain of Aspergillus terreus , 1983 .

[14]  B. Zwanenburg,et al.  AN EFFICIENT STEREOSPECIFIC TOTAL SYNTHESIS OF (.+-.)-TERREIN , 1982 .

[15]  G. Grynkiewicz,et al.  Synthesis of 6-Alkoxy-2,3-dihydro-6H-pyran-3-ones from the 6-Acyloxy Derivatives , 1979 .

[16]  D. Barton,et al.  Photochemical transformations. Part 35. A simple synthesis of racemic terrein , 1977 .

[17]  W. G. Dauben,et al.  Direct oxidation of tertiary allylic alcohols. A simple and effective method for alkylative carbonyl transposition , 1977 .

[18]  S. Weinreb,et al.  Synthesis of terrein, a metabolite of Aspergillus terreus , 1974 .

[19]  O. Achmatowicz,et al.  Synthesis of methyl 2,3-dideoxy-DL-alk-2-enopyranosides from furan compounds , 1971 .

[20]  D. A. Sprott.  THE STABILITY OF A SEX‐LINKED ALLELIC SYSTEM , 1957, Annals of human genetics.

[21]  H. Raistrick,et al.  Studies in the biochemistry of micro-organisms: The metabolic products of Aspergillus terreus Thom. A new mould metabolic product-terrein. , 1935, The Biochemical journal.