1314020-68-2Relevant articles and documents
Potent "clicked" MMP2 inhibitors: Synthesis, molecular modeling and biological exploration
Zapico, Jose Maria,Serra, Pilar,Garcia-Sanmartin, Josune,Filipiak, Kamila,Carbajo, Rodrigo J.,Schott, Anne K.,Pineda-Lucena, Antonio,Martinez, Alfredo,Martin-Santamaria, Sonsoles,De Pascual-Teresa, Beatriz,Ramos, Ana
, p. 4587 - 4599 (2011/07/29)
A new series of MMP2 inhibitors is described, following a fragment-based drug design approach. One fragment containing an azide group and a well known hydroxamate Zinc Binding Group in a α-sulfone, α-tetrahydropyrane scaffold, has been synthesized. Water-