A.R. Mason, J. Mason, M. Cork, G. Dooley, and G. Edwards Topical treatments for chronic plaque psoriasis Cochrane Database of Syst. Rev. 2009 Article Number: CD005028
Guidelines of care for the management of psoriasis and psoriatic arthritis. Section 3. Guidelines of care for the management and treatment of psoriasis with topical therapies
A. Menter, N.J. Korman, C.A. Elmets, S.R. Feldman, J.M. Gelfand, K.B. Gordon, A. Gottlieb, J.Y.M. Koo, M. Lebwohl, H.W. Lim, A.S. Van Voorhees, K.R. Beutner, and R. Bhushan Guidelines of care for the management of psoriasis and psoriatic arthritis. Section 3. Guidelines of care for the management and treatment of psoriasis with topical therapies J. Am. Acad. Dermatol. 60 2009 643 659
Anthralin: Primary products of its redox reactions
M. Czerwinska, A. Sikora, P. Szajerski, J. Zielonka, J. Adamus, A. Marcinek, K. Piech, P. Bednarek, and T. Bally Anthralin: primary products of its redox reactions J. Org. Chem. 71 2006 5312 5319
Location of anthralin radical generation in mouse skin by UV-A irradiation: An estimation using microscopic EPR spectral-spatial imaging
K. Matsumoto, S. Kawai, C.F. Chignell, and H. Utsumi Location of anthralin radical generation in mouse skin by UV-A irradiation: an estimation using microscopic EPR spectral-spatial imaging Magn. Reson. Med. 55 2006 738 742
Antipsoriatic anthrones with modulated redox properties. 5. Potent inhibition of human keratinocyte growth, induction of keratinocyte differentiation, and reduced membrane damage by novel 10-arylacetyl-1,8- dihydroxy-9(10H)-anthracenones
K. Müller, H. Reindl, and K. Breu Antipsoriatic anthrones with modulated redox properties. 5. Potent inhibition of human keratinocyte growth, induction of keratinocyte differentiation, and reduced membrane damage by novel 10-arylacetyl-1,8-dihydroxy-9(10H)-anthracenones J. Med. Chem. 44 2001 814 821
Hydroxyl radical damage to DNA sugar and model membranes induced by anthralin (dithranol)
K. Müller, and D. Gürster Hydroxyl radical damage to DNA sugar and model membranes induced by anthralin (dithranol) Biochem. Pharmacol. 46 1993 1695 1704
Dithranol: A review of the mechanism of action in the treatment of psoriasis vulgaris
L. Kemény, T. Ruzicka, and O. Braun-Falco Dithranol: a review of the mechanism of action in the treatment of psoriasis vulgaris Skin Pharmacol. 3 1990 1 20
Simple analogues of anthralin: Unusual specificity of structure and antiproliferative activity
K. Müller, H. Prinz, I. Gawlik, K. Ziereis, and H.-S. Huang Simple analogues of anthralin: unusual specificity of structure and antiproliferative activity J. Med. Chem. 40 1997 3773 3780
Synthesis and cytotoxicity of 9-alkoxy-1,5-dichloroanthracene derivatives in murine and human cultured tumor cells
H.-S. Huang, J.-F. Chiou, H.-F. Chiu, R.-F. Chen, and Y.-L. Lai Synthesis and cytotoxicity of 9-alkoxy-1,5-dichloroanthracene derivatives in murine and human cultured tumor cells Arch. Pharm. (Weinheim) 335 2002 33 38
Synthesis, antiproliferative activity and inhibition of tubulin polymerization by 1,5- and 1,8-disubstituted 10H-anthracen-9-ones bearing a 10-benzylidene or 10-(2-oxo-2-phenylethylidene) moiety
H. Nickel, P. Schmidt, K.J. Böhm, S. Baasner, K. Müller, M. Gerlach, E. Unger, E.G. Günther, and H. Prinz Synthesis, antiproliferative activity and inhibition of tubulin polymerization by 1,5- and 1,8-disubstituted 10H-anthracen-9-ones bearing a 10-benzylidene or 10-(2-oxo-2-phenylethylidene) moiety Eur. J. Med. Chem. 45 2010 3420 3438
Physicochemical properties and stability of anthralin in model systems and human skin
T. Sa e Melo, L. Dubertret, P. Prognon, A. Gond, G. Mahuzier, and R. Santus Physicochemical properties and stability of anthralin in model systems and human skin J. Invest. Dermatol. 80 1983 1 6
Synthesis of anthracenones. 1. Sodium dithionite reduction of peri-substituted anthracenediones
H. Prinz, W. Wiegrebe, and K. Müller Synthesis of anthracenones. 1. Sodium dithionite reduction of peri-substituted anthracenediones J. Org. Chem. 61 1996 2853 2856
Comparison of antiproliferative effects of experimental and established antipsoriatic drugs on human keratinocytes, using a simple 96-well-plate assay
A. Pol, M. Bergers, and J. Schalkwijk Comparison of antiproliferative effects of experimental and established antipsoriatic drugs on human keratinocytes, using a simple 96-well-plate assay In Vitro Cell. Dev. Biol. Anim. 39 2003 36 42
Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line
P. Boukamp, R.T. Petrussevska, D. Breitkreutz, J. Hornung, A. Markham, and N.E. Fusenig Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line J. Cell Biol. 106 1988 761 771
Lactate dehydrogenase release as an indicator of dithranol-induced membrane injury in cultured human keratinocytes
B. Bonnekoh, B. Farkas, J. Geisel, and G. Mahrle Lactate dehydrogenase release as an indicator of dithranol-induced membrane injury in cultured human keratinocytes Arch. Dermatol. Res. 282 1990 325 329
9-Benzylidene-naphtho[2,3-b]thiophen-4-ones as novel antimicrotubule agents - Synthesis, antiproliferative activity, and inhibition of tubulin polymerization
A. Zuse, P. Schmidt, S. Baasner, K.J. Böhm, K. Müller, M. Gerlach, E.G. Günther, E. Unger, and H. Prinz 9-Benzylidene-naphtho[2,3-b] thiophen-4-ones as novel antimicrotubule agents - synthesis, antiproliferative activity, and inhibition of tubulin polymerization J. Med. Chem. 49 2006 7816 7825
10-(2-oxo-2-Phenylethylidene)-10H-anthracen-9-ones as highly active antimicrotubule agents: Synthesis, antiproliferative activity, and inhibition of tubulin polymerization
H. Prinz, P. Schmidt, K.J. Böhm, S. Baasner, K. Müller, E. Unger, M. Gerlach, and E.G. Günther 10-(2-oxo-2-Phenylethylidene)-10H- anthracen-9-ones as highly active antimicrotubule agents: synthesis, antiproliferative activity, and inhibition of tubulin polymerization J. Med. Chem. 52 2009 1284 1294
Antipsoriatic anthrones with modulated redox properties. 2. Novel derivatives of chrysarobin and isochrysarobin - Antiproliferative activity and 5-lipoxygenase inhibition
K. Müller, P. Leukel, K. Ziereis, and I. Gawlik Antipsoriatic anthrones with modulated redox properties. 2. Novel derivatives of chrysarobin and isochrysarobin - antiproliferative activity and 5-lipoxygenase inhibition J. Med. Chem. 37 1994 1660 1669
Theoretical study and X-ray determination of bianthrones: Long C-C bond length and preferred gauche conformation
P.-C. Li, T.-S. Wang, G.-H. Lee, Y.-H. Liu, Y. Wang, C.-T. Chen, and I. Chao Theoretical study and X-ray determination of bianthrones: long C-C bond length and preferred gauche conformation J. Org. Chem. 67 2002 8002 8009
Evidence for the formation of nitrenium ions in the acid-catalysed solvolysis of mutagenic N-acetoxy-N-alkoxybenzamides
J.J. Campbell, S.A. Glover, G.P. Hammond, and C.A. Rowbottom Evidence for the formation of nitrenium ions in the acid-catalysed solvolysis of mutagenic N-acetoxy-N-alkoxybenzamides J. Chem. Soc. Perkin Trans. 2 1991 2067 2079
Reciprocal induced polarity effects in cresols and their derivatives. Properties of the isomeric methoxybenzyl bromides
A. Lapworth, and J.B. Shoesmith Reciprocal induced polarity effects in cresols and their derivatives. Properties of the isomeric methoxybenzyl bromides J. Chem. Soc. Trans. 1922 1391 1400
Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol
K. Thakkar, R.L. Geahlen, and M. Cushman Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol J. Med. Chem. 36 1993 2950 2955
Phenol oxidation and bosynthesis. Part XXV. New syntheses of bis-(2-arylethyl)amines of biosynthetic importance
D.H.R. Barton, R.D. Bracho, A.A.L. Gunatilaka, and D.A. Widdowson Phenol oxidation and bosynthesis. Part XXV. New syntheses of bis-(2-arylethyl)amines of biosynthetic importance J. Chem. Soc. Perkin Trans. 1 1975 579 588
Structure-activity relationship studies of acridones as potential antipsoriatic agents. 1. Synthesis and antiproliferative activity of simple N-unsubstituted 10H-acridin-9-ones against human keratinocyte growth
A. Putic, L. Stecher, H. Prinz, and K. Müller Structure-activity relationship studies of acridones as potential antipsoriatic agents. 1. Synthesis and antiproliferative activity of simple N-unsubstituted 10H-acridin-9-ones against human keratinocyte growth Eur. J. Med. Chem. 2010 3299 3310