107401-55-8

Upstream product

• 64817-79-4 1,8,10-Trihydroxy-9-anthron 
• 108-98-5 thiophenol 
• 2891-30-7 10-bromo-1,8-dihydroxy-9(10H)-anthracenone 
• 1143-38-0 1,8-dihydroxy-9(10H)-anthracenone 

Downstream Products

• 1143-38-0 1,8-dihydroxy-9(10H)-anthracenone 
• 31991-54-5 1,8,1',8'-tetrahydroxy-10,10'-bianthrone 
• 108-98-5 thiophenol 
• 882-33-7 diphenyldisulfane 

Relevant academic research and scientific papers

Electron-impact induced and thermal decomposition of dithranol derivatives, I: Thermolysis of 10-phenylthio-dithranol in the mass spectrometer

Dithranol (anthralin; 1,8-dihydroxy-9-anthrone) and its derivatives bearing a variety of substituents in the 10-position are of actual interest in research on psoriasis. In connection herewith 10-alkylthio- and 10-arylthio-1,8-dihydroxy-9(10H)-anthracenones were synthetized and used for antipsoriatic activity.

Antipsoriatic anthrones with modulated redox properties. 3. 10-Thio- substituted 1,8-dihydroxy-9(10H)-anthracenones as inhibitors of keratinocyte growth, 5-lipoxygenase, and the formation of 12(S)-HETE in mouse epidermis

The synthesis of a series of 1,8-dihydroxy-9(10H)-anthracenones bearing sulfur-linked substituents in the 10-position is described. These compounds were evaluated for their ability to inhibit the growth of the human keratinocyte cell line HaCaT and the 5-