(Q33509846)

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Synthesis of a resorcylic acid lactone (RAL) library using fluorous-mixture synthesis and profile of its selectivity against a panel of kinases

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Europe PubMed Central

PubMed publication ID

27 July 2017

Synthesis of a resorcylic acid lactone (RAL) library using fluorous-mixture synthesis and profile of its selectivity against a panel of kinases (English)

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Europe PubMed Central

PubMed publication ID

27 July 2017

Nicolas Winssinger

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Nicolas Winssinger

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Rajamalleswaramma Jogireddy

1

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Europe PubMed Central

PubMed publication ID

27 July 2017

Pierre-Yves Dakas

2

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Europe PubMed Central

PubMed publication ID

27 July 2017

Gaëlle Valot

3

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Europe PubMed Central

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27 July 2017

Sofia Barluenga

4

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Europe PubMed Central

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27 July 2017

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1 November 2009

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Europe PubMed Central

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27 July 2017

Chemistry—A European Journal

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Europe PubMed Central

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27 July 2017

15

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Europe PubMed Central

PubMed publication ID

27 July 2017

43

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Europe PubMed Central

PubMed publication ID

27 July 2017

11498-11506

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Europe PubMed Central

PubMed publication ID

27 July 2017

The protein kinase complement of the human genome

1 reference

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Inhibitors of protein tyrosine phosphatases: next-generation drugs?

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Targeting cancer with small molecule kinase inhibitors

1 reference

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Chemistry and biology of resorcylic acid lactones

1 reference

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21 January 2018

Role of a cysteine residue in the active site of ERK and the MAPKK family

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A resorcylic acid lactone, 5Z-7-oxozeaenol, prevents inflammation by inhibiting the catalytic activity of TAK1 MAPK kinase kinase

1 reference

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21 January 2018

Targeted covalent inactivation of protein kinases by resorcylic acid lactone polyketides.

1 reference

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21 January 2018

Synthetic applications of fluorous solid-phase extraction (F-SPE)

1 reference

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21 January 2018

Semisynthesis and cytotoxicity of hypothemycin analogues

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Molecular modeling and crystal structure of ERK2-hypothemycin complexes

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A small molecule-kinase interaction map for clinical kinase inhibitors

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21 January 2018

A quantitative analysis of kinase inhibitor selectivity

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Structural bioinformatics-based design of selective, irreversible kinase inhibitors

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Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies

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FLT3 K663Q is a novel AML-associated oncogenic kinase: Determination of biochemical properties and sensitivity to Sunitinib (SU11248).

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Identifying and characterizing a novel activating mutation of the FLT3 tyrosine kinase in AML.

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Detection of c-kit exons 11- and 17-activating mutations in testicular seminomas by high-resolution melting amplicon analysis.

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Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors

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Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases

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The development and application of methods for activity-based protein profiling

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Protein-reactive natural products

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Anti-inflammatory cyclopentenone prostaglandins are direct inhibitors of IkappaB kinase

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Resorcylic acid lactones: naturally occurring potent and selective inhibitors of MEK

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.7164/ANTIBIOTICS.52.1086

Identifiers

10.1002/CHEM.200901375

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

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