Salicylic Acid Based Small Molecule Inhibitor for the Oncogenic Src Homology-2 Domain Containing Protein Tyrosine Phosphatase-2 (SHP2)
about
Protein phosphatases and Alzheimer's diseaseSmall molecule tools for functional interrogation of protein tyrosine phosphatasesRapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling-TMS-deprotection-CuAAC sequenceA Potent and Selective Small-Molecule Inhibitor for the Lymphoid-Specific Tyrosine Phosphatase (LYP), a Target Associated with Autoimmune DiseasesSelective inhibitors of the protein tyrosine phosphatase SHP2 block cellular motility and growth of cancer cells in vitro and in vivoLYP inhibits T-cell activation when dissociated from CSK.Shp2 protein tyrosine phosphatase inhibitor activity of estramustine phosphate and its triterpenoid analogs.Small molecule inhibitors of SHP2 tyrosine phosphatase discovered by virtual screening.Oxime-based click chemistry in the development of 3-isoxazolecarboxylic acid containing inhibitors of Yersinia pestis protein tyrosine phosphatase, YopH.Inhibition of cellular Shp2 activity by a methyl ester analog of SPI-112.Therapeutic potential of targeting the oncogenic SHP2 phosphatase.Identification of cryptotanshinone as an inhibitor of oncogenic protein tyrosine phosphatase SHP2 (PTPN11).Oxime-based linker libraries as a general approach for the rapid generation and screening of multidentate inhibitors.CuAAC click chemistry accelerates the discovery of novel chemical scaffolds as promising protein tyrosine phosphatases inhibitorsProtein tyrosine phosphatases as potential therapeutic targets.A combinatorial strategy for the acquisition of potent and specific protein tyrosine phosphatase inhibitorsInhibition of SHP2-mediated dephosphorylation of Ras suppresses oncogenesisSHP2 is a target of the immunosuppressant tautomycetin.A facile hydroxyindole carboxylic acid based focused library approach for potent and selective inhibitors of Mycobacterium protein tyrosine phosphatase BHydroxyindole carboxylic acid-based inhibitors for receptor-type protein tyrosine protein phosphatase betaDouble click reaction for the acquisition of a highly potent and selective mPTPB inhibitorSHP2 phosphatase promotes mast cell chemotaxis toward stem cell factor via enhancing activation of the Lyn/Vav/Rac signaling axisMolecular targets for the treatment of juvenile myelomonocytic leukemia.A potent and selective inhibitor for the UBLCP1 proteasome phosphatase.Inhibition of Shp2 suppresses mutant EGFR-induced lung tumors in transgenic mouse model of lung adenocarcinoma.Akt2 inhibits the activation of NFAT in lymphocytes by modulating calcium release from intracellular storesBicyclic benzofuran and indole-based salicylic acids as protein tyrosine phosphatase inhibitorsDesign, synthesis and evaluation of novel 19F magnetic resonance sensitive protein tyrosine phosphatase inhibitors.SH2 domain-containing phosphatase 2 is a critical regulator of connective tissue mast cell survival and homeostasis in miceRole of SHP2 phosphatase in KIT-induced transformation: identification of SHP2 as a druggable target in diseases involving oncogenic KIT.Discovery of a Novel Inhibitor of the Protein Tyrosine Phosphatase Shp2.Discovery and evaluation of novel inhibitors of mycobacterium protein tyrosine phosphatase B from the 6-Hydroxy-benzofuran-5-carboxylic acid scaffold.Hematopoietic colony formation from human growth factor-dependent TF1 cells and human cord blood myeloid progenitor cells depends on SHP2 phosphatase functionDesign, synthesis, biological activity and molecular dynamics studies of specific protein tyrosine phosphatase 1B inhibitors over SHP-2Targeting protein tyrosine phosphatase SHP2 for the treatment of PTPN11-associated malignanciesTargeting SHP2 for EGFR inhibitor resistant non-small cell lung carcinoma.Syk kinase and Shp2 phosphatase inhibition cooperate to reduce FLT3-ITD-induced STAT5 activation and proliferation of acute myeloid leukemia.The protein tyrosine phosphatase, Shp2, positively contributes to FLT3-ITD-induced hematopoietic progenitor hyperproliferation and malignant disease in vivo.SHP2 phosphatase as a novel therapeutic target for melanoma treatment.Protein tyrosine phosphatases as drug targets: strategies and challenges of inhibitor development.
P2860
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P2860
Salicylic Acid Based Small Molecule Inhibitor for the Oncogenic Src Homology-2 Domain Containing Protein Tyrosine Phosphatase-2 (SHP2)
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@ast
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@en
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@nl
type
label
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@ast
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@en
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@nl
prefLabel
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@ast
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@en
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@nl
P2093
P2860
P3181
P356
P1476
Salicylic Acid Based Small Mol ...... Tyrosine Phosphatase-2 (SHP2)
@en
P2093
Andrea M Gunawan
Rebecca J Chan
Sarah C Nabinger
Xian Zhang
Yuanshu Dong
Zhenyun Yang
P2860
P304
P3181
P356
10.1021/JM901645U
P407
P577
2010-03-25T00:00:00Z