Biomimetic oxidation of the antimelanoma agent 4-S-cysteaminylphenol and related catechol thioethers: Isolation and reaction behaviour of novel dihydrobenzothiazinequinones
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (29) , 8757-8764
- https://doi.org/10.1016/s0040-4020(01)85349-7
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Exploitation of Pigment Biosynthesis Pathway as a Selective Chemotherapeutic Approach for Malignant MelanomaJournal of Investigative Dermatology, 1993
- Melanogenesis: a realistic target for antimelanoma therapy?European Journal of Cancer and Clinical Oncology, 1991
- Mechanism of the rearrangement of dopachrome to 5,6-dihydroxyindoleTetrahedron Letters, 1991
- Mechanism of growth inhibition of melanoma cells by 4-S-cysteaminylphenol and its analoguesBiochemical Pharmacology, 1990
- Mechanism of selective toxicity of 4-S-cysteinylphenol and 4-S-cysteaminylphenol to melanocytesBiochemical Pharmacology, 1987
- Depigmentation of black Guinea Pig Skin by Topical Application of Cysteaminylphenol, Cysteinylphenol, and Related CompoundsJournal of Investigative Dermatology, 1987
- Non-enzymic oxidation of cysteinyldopa catalyzed by metallic ionsGeneral Pharmacology: The Vascular System, 1983
- Oxydationsprodukte von 6‐Hydroxy‐dopaminHelvetica Chimica Acta, 1972
- Chemistry of Catecholamines: Revised Structures for the IodoaminochromesJournal of the American Chemical Society, 1963
- 16. The oxidation of adrenalineJournal of the Chemical Society, 1943