Pages that link to "Q44448705"

The following pages link to Fragment-based substrate activity screening method for the identification of potent inhibitors of the Mycobacterium tuberculosis phosphatase PtpB. (Q44448705):

Displaying 38 items.

• Small molecule tools for functional interrogation of protein tyrosine phosphatases (Q26852276) (← links)
• Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia pestis Outer Protein H (YopH) Phosphatase (Q27667338) (← links)
• Structure of the Trypanosoma cruzi protein tyrosine phosphatase TcPTP1, a potential therapeutic target for Chagas’ disease (Q27675033) (← links)
• Substrate Deconstruction and the Nonadditivity of Enzyme Recognition (Q27683622) (← links)
• Using specificity to strategically target proteases (Q33330575) (← links)
• Identification of a new class of nonpeptidic inhibitors of cruzain (Q33330700) (← links)
• Inhibition of MptpB phosphatase from Mycobacterium tuberculosis impairs mycobacterial survival in macrophages (Q33412046) (← links)
• Targeting mycobacterium protein tyrosine phosphatase B for antituberculosis agents (Q33532352) (← links)
• Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA. (Q33571121) (← links)
• Identification of novel inhibitors for a low molecular weight protein tyrosine phosphatase via virtual screening (Q33600807) (← links)
• Dynamic active-site protection by the M. tuberculosis protein tyrosine phosphatase PtpB lid domain (Q33806251) (← links)
• Oxime‐Based Click Chemistry in the Development of 3‐Isoxazolecarboxylic Acid Containing Inhibitors of Yersinia pestis Protein Tyrosine Phosphatase, YopH (Q33931893) (← links)
• Ugi reaction-assisted rapid assembly of affinity-based probes against potential protein tyrosine phosphatases. (Q34208560) (← links)
• Identification and characterization of novel inhibitors of mPTPB, an essential virulent phosphatase from Mycobacterium tuberculosis (Q34353151) (← links)
• Substrate-based fragment identification for the development of selective, nonpeptidic inhibitors of striatal-enriched protein tyrosine phosphatase (Q34374573) (← links)
• Design and synthesis of nonpeptidic, small molecule inhibitors for the Mycobacterium tuberculosis protein tyrosine phosphatase PtpB (Q34437023) (← links)
• Mycobacterium tuberculosis Serine/Threonine Protein Kinases (Q34565203) (← links)
• A facile hydroxyindole carboxylic acid based focused library approach for potent and selective inhibitors of Mycobacterium protein tyrosine phosphatase B (Q34660114) (← links)
• Small molecule substrate phosphorylation site inhibitors of protein kinases: approaches and challenges. (Q34992505) (← links)
• Double Click Reaction for the Acquisition of a Highly Potent and Selective mPTPB Inhibitor (Q35052636) (← links)
• Repositioning the substrate activity screening (SAS) approach as a fragment-based method for identification of weak binders (Q35231270) (← links)
• Identification of multiple structurally distinct, nonpeptidic small molecule inhibitors of protein arginine deiminase 3 using a substrate-based fragment method (Q35572208) (← links)
• Cefsulodin Inspired Potent and Selective Inhibitors of mPTPB, a Virulent Phosphatase from Mycobacterium tuberculosis (Q36367311) (← links)
• Discovery and evaluation of novel inhibitors of mycobacterium protein tyrosine phosphatase B from the 6-Hydroxy-benzofuran-5-carboxylic acid scaffold (Q36615919) (← links)
• Dynamic template-assisted strategies in fragment-based drug discovery. (Q37579402) (← links)
• New Strategies in Fighting TB: Targeting Mycobacterium Tuberculosis -Secreted Phosphatases MptpA & MptpB (Q37855839) (← links)
• Tuberculosis drugs: new candidates and how to find more (Q37894691) (← links)
• Elimination of intracellularly residing Mycobacterium tuberculosis through targeting of host and bacterial signaling mechanisms (Q38056148) (← links)
• Substrate Activity Screening (SAS) and Related Approaches in Medicinal Chemistry (Q38722942) (← links)
• Fragment-based approaches to TB drugs (Q38996602) (← links)
• Substrate activity screening with kinases: discovery of small-molecule substrate-competitive c-Src inhibitors (Q38998432) (← links)
• Organocatalytic multicomponent reaction for the acquisition of a selective inhibitor of mPTPB, a virulence factor of tuberculosis (Q41662986) (← links)
• Diversity-Oriented Synthesis for Novel, Selective and Drug-like Inhibitors for a Phosphatase from Mycobacterium Tuberculosis (Q42010235) (← links)
• Discovery of a new class of inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B by biology-oriented synthesis (Q46499033) (← links)
• Dynamic substrate enhancement for the identification of specific, second-site-binding fragments targeting a set of protein tyrosine phosphatases. (Q52891970) (← links)
• MptpB Promotes Mycobacteria Survival by Inhibiting the Expression of Inflammatory Mediators and Cell Apoptosis in Macrophages. (Q55081012) (← links)
• Fluorogenic structure activity library pinpoints molecular variations in substrate specificity of structurally homologous esterases (Q57159623) (← links)
• Theoretical studies on the interaction of biphenyl inhibitors with Mycobacterium tuberculosis protein tyrosine phosphatase MptpB (Q83620297) (← links)