Specific, irreversible inactivation of the epidermal growth factor receptor and erbB2, by a new class of tyrosine kinase inhibitor
about
The chemical biology of protein phosphorylationThe Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancyEscape from HER-family tyrosine kinase inhibitor therapy by the kinase-inactive HER3Electrophilic affibodies forming covalent bonds to protein targetsMechanism of carbamate inactivation of FAAH: implications for the design of covalent inhibitors and in vivo functional probes for enzymesErbB receptors: from oncogenes to targeted cancer therapiesDeveloping irreversible inhibitors of the protein kinase cysteinomeIn situ assembly of enzyme inhibitors using extended tetheringStructures of Lung Cancer-Derived EGFR Mutants and Inhibitor Complexes: Mechanism of Activation and Insights into Differential Inhibitor Sensitivity6-Ethynylthieno[3,2-d]- and 6-ethynylthieno[2,3-d]pyrimidin-4-anilines as tunable covalent modifiers of ErbB kinasesTargeted polypharmacology: discovery of dual inhibitors of tyrosine and phosphoinositide kinasesIdentification of Cys255 in HIF-1α as a novel site for development of covalent inhibitors of HIF-1α/ARNT PasB domain protein-protein interactionElectrophilic Fragment-Based Design of Reversible Covalent Kinase InhibitorsReversible targeting of noncatalytic cysteines with chemically tuned electrophilesDiscovery of Novel Irreversible Inhibitors of Interleukin (IL)-2-inducible Tyrosine Kinase (Itk) by Targeting Cysteine 442 in the ATP PocketCEACAM1 modulates epidermal growth factor receptor--mediated cell proliferationFrom oncogene to drug: development of small molecule tyrosine kinase inhibitors as anti-tumor and anti-angiogenic agents.A functional screen for genes inducing epidermal growth factor autonomy of human mammary epithelial cells confirms the role of amphiregulin.Y-box-binding protein 1 confers EGF independence to human mammary epithelial cells.TDAG51 is an ERK signaling target that opposes ERK-mediated HME16C mammary epithelial cell transformation.A liquid chromatography mass spectrometry assay for determination of PD168393, a specific and irreversible inhibitor of erbB membrane tyrosine kinases, in rat serumRoles of specific membrane lipid domains in EGF receptor activation and cell adhesion molecule stabilization in a developing olfactory system.Receptor type protein tyrosine phosphatase-kappa mediates cross-talk between transforming growth factor-beta and epidermal growth factor receptor signaling pathways in human keratinocytesEpidermal growth factor receptor inhibitor ameliorates excessive astrogliosis and improves the regeneration microenvironment and functional recovery in adult rats following spinal cord injuryDetecting intratumoral heterogeneity of EGFR activity by liposome-based in vivo transfection of a fluorescent biosensorAntiviral chemotherapy facilitates control of poxvirus infections through inhibition of cellular signal transduction.Overexpression of ErbB2 in cancer and ErbB2-targeting strategies.A small molecule inhibitor of endoplasmic reticulum oxidation 1 (ERO1) with selectively reversible thiol reactivity.A structure-guided approach to creating covalent FGFR inhibitorsDrug-induced ubiquitylation and degradation of ErbB receptor tyrosine kinases: implications for cancer therapy.Targeting the EGFR signaling pathway in cancer therapy.Cellular signalling pathways: new targets in leukaemia therapy.Targeted covalent inactivation of protein kinases by resorcylic acid lactone polyketides.Phase I dose-escalation study of the pan-HER inhibitor, PF299804, in patients with advanced malignant solid tumors.Anti-epidermal growth factor receptor drugs in cancer therapy.Propagation of human prostate cancer stem-like cells occurs through EGFR-mediated ERK activation.Phosphoproteomic analysis of Her2/neu signaling and inhibition.Developing inhibitors of the epidermal growth factor receptor for cancer treatment.ERBB receptor tyrosine kinases and cellular radiation responses.Oncogenes in thyroid cancer.
P2860
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P2860
Specific, irreversible inactivation of the epidermal growth factor receptor and erbB2, by a new class of tyrosine kinase inhibitor
description
1998 nî lūn-bûn
@nan
1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@ast
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@en
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@nl
type
label
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@ast
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@en
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@nl
prefLabel
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@ast
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@en
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@nl
P2093
P2860
P356
P1476
Specific, irreversible inactiv ...... s of tyrosine kinase inhibitor
@en
P2093
A J Bridges
D J McNamara
E M Dobrusin
J B Smaill
J M Nelson
P2860
P304
P356
10.1073/PNAS.95.20.12022
P407
P577
1998-09-29T00:00:00Z