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Structure-guided optimization of 3-hydroxybenzoisoxazole derivatives as inhibitors of Aldo-keto reductase 1C3 (AKR1C3) to target prostate cancer 3-羟基苯并异恶唑衍生物作为醛酮还原酶1C3 (AKR1C3) 抑制剂靶向前列腺癌的结构指导优化 Pippione, Agnese Chiara; Kovachka, Sandra; Vigato, Chiara; Bertarini, Laura; Mannella, Iole; Sainas, Stefano; Rolando, Barbara; Denasio, Enrica; Piercy-Mycock, Helen; Romalho, Linda; Salladini, Edoardo; Adinolfi, Salvatore; Zonari, Daniele; Peraldo-Neia, Caterina; Chiorino, Giovanna; Passoni, Alice; Mirza, Osman Asghar; Frydenvang, Karla; Pors, Klaus; Lolli, Marco Lucio; Spyrakis, Francesca; Oliaro-Bosso, Simonetta; Boschi, Donatella 分享 收藏
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New aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the hydroxytriazole scaffold Pippione, Agnese Chiara; Kilic-Kurt, Zuhal; Kovachka, Sandra; Sainas, Stefano; Rolando, Barbara; Denasio, Enrica; Pors, Klaus; Adinolfi, Salvatore; Zonari, Daniele; Bagnati, Renzo; Lolli, Marco Lucio; Spyrakis, Francesca; Oliaro-Bosso, Simonetta; Boschi, Donatella 分享 收藏
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Expansion of the 4-(Diethylamino)benzaldehyde Scaffold to Explore the Impact on Aldehyde Dehydrogenase Activity and Antiproliferative Activity in Prostate Cancer Ibrahim, Ali I. M.; Batlle, Elisabet; Sneha, Smarakan; Jimenez, Rafael; Pequerul, Raquel; Pares, Xavier; Rungeler, Till; Jha, Vibhu; Tuccinardi, Tiziano; Sadiq, Maria; Frame, Fiona; Maitland, Norman J.; Farres, Jaume; Pors, Klaus 分享 收藏
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Cytochrome P450 isoforms 1A1, 1B1 AND 2W1 as targets for therapeutic intervention in head and neck cancer Presa, Daniela; Khurram, Syed A.; Zubir, Amir Z. A.; Smarakan, Sneha; Cooper, Patricia A.; Morais, Goreti R.; Sadiq, Maria; Sutherland, Mark; Loadman, Paul M.; McCaul, James; Shnyder, Steven D.; Patterson, Laurence H.; Pors, Klaus 分享 收藏
Design, Synthesis, Biological Evaluation and In Silico Study of Benzyloxybenzaldehyde Derivatives as Selective ALDH1A3 Inhibitors Ibrahim, Ali I. M.; Ikhmais, Balqis; Batlle, Elisabet; AbuHarb, Waed K.; Jha, Vibhu; Jaradat, Khaled T.; Jimenez, Rafael; Pequerul, Raquel; Pares, Xavier; Farres, Jaume; Pors, Klaus 分享 收藏
Probing cytochrome P450 (CYP) bioactivation with chloromethylindoline bioprecursors derived from the duocarmycin family of compounds Ortuzar, Natalia; Karu, Kersti; Presa, Daniela; Morais, Goreti R.; Sheldrake, Helen M.; Shnyder, Steve D.; Barnieh, Francis M.; Loadman, Paul M.; Patterson, Laurence H.; Pors, Klaus; Searcey, Mark 分享 收藏
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Synthesis and biologic evaluation of diethylbenzaldehyde analogues to probe functional activity of aldehyde dehydrogenase activity in cancer Ibrahim, Ali; Sadiq, Maria; Presa, Daniela; Ntafoulis, Ioannis; Alkawi, Ahmad; Frame, Fiona; Maitland, Norman J.; Cournia, Zoe; Loadman, Paul M.; Moreb, Jan; Pors, Klaus 分享 收藏
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid 基于苯并异恶唑部分的有效和选择性的醛酮还原酶1C3 (AKR1C3) 抑制剂: 生物等排支架跳跃方法在氟芬那酸中的应用 Pippione, Agnese Chiara; Carnovale, Irene Maria; Bonanni, Davide; Sini, Marcella; Goyal, Parveen; Marini, Elisabetta; Pors, Klaus; Adinolfi, Salvatore; Zonari, Daniele; Festuccia, Claudio; Wahlgren, Weixiao Yuan; Friemann, Rosmarie; Bagnati, Renzo; Boschi, Donatella; Oliaro-Bosso, Simonetta; Lolli, Marco Lucio 分享 收藏