Details

Autor(en) / Beteiligte

• Charalambous, Anna
• Koyioni, Maria
• Antoniades, Ioanna
• Pegeioti, Despoina
• Eleftheriou, Iro
• Michaelidou, Sophia S
• Amelichev, Stanislav A
• Konstantinova, Lidia S
• Rakitin, Oleg A
• Koutentis, Panayiotis A
• Skourides, Paris A

Titel

1,2,3-Dithiazoles - new reversible melanin synthesis inhibitors: a chemical genomics study

Ist Teil von

• MedChemComm, 2015-05, Vol.6 (5), p.935-946

Erscheinungsjahr

2015

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• A chemical genomic screen of an in-house library of small molecule heterocycles was carried out using Xenopus laevis embryos. This led to the identification of N -(4-chloro-5 H -1,2,3-dithiazol-5-ylidene)-4-methoxyaniline ( 1c ), which elicits loss of pigmentation in melanophores and the retinal pigment epithelium (RPE) of developing embryos, independent of the developmental stage of initial exposure. The phenotype was reversible, since pigmentation returned upon compound removal while analysis of neural crest cell markers (Pax7) and melanophore markers (Dct/Xtrp2) revealed that both neural crest precursors and fully differentiated melanophores were present in the dithiazole 1c treated embryos. A subsequent focused structure-activity relationship (SAR) study identified the more active dithiazole 4-benzyloxy- N -(4-chloro-5 H -1,2,3-dithiazol-5-ylidene)-aniline ( 1l ) and the need for a chlorine substituent at the dithiazole C-4 position. Both the initial chemical genomic screen and the focused SAR study highlighted the toxicity of (dithiazolylidene)aminoazines, and also of methoxyaniline (anisidine) analogues that hosted strong electron-withdrawing or electronegative substituents or acidic hydroxyl groups on the anisidine moiety. This study suggests that 1,2,3-dithiazoles can act as reversible melanin synthesis inhibitors, revealing a new biological activity for this class of compounds. The inhibition of melanin synthesis is medically relevant as a potential treatment for pigmentation disorders such as melasma. 1,2,3-Dithiazolimines show potent and reversible inhibition of melanin synthesis in Xenopus laevis embryos.