1002334-12-4Relevant articles and documents
Potent and orally bioavailable CDK8 inhibitors: Design, synthesis, structure-activity relationship analysis and biological evaluation
Yu, Mingfeng,Teo, Theodosia,Yang, Yuchao,Li, Manjun,Long, Yi,Philip, Stephen,Noll, Benjamin,Heinemann, Gary K.,Diab, Sarah,Eldi, Preethi,Mekonnen, Laychiluh,Anshabo, Abel T.,Rahaman, Muhammed H.,Milne, Robert,Hayball, John D.,Wang, Shudong
, (2021)
CDK8 regulates transcription either by phosphorylation of transcription factors or, as part of a four-subunit kinase module, through a reversible association of the kinase module with the Mediator complex, a highly conserved transcriptional coactivator. D
HETEROARYL COMPOUNDS AND PHARMACEUTICAL APPLICATIONS THEREOF
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Paragraph 00690, (2016/01/25)
The present invention provides herein is a heteroaryl compound or a stereoisomer, a geometric isomer, a tautomer, a racemate, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, as well as a pharmaceutical composition containing the compound disclosed herein. The present invention also provides herein is use of the compound or the pharmaceutical composition thereof disclosed herein in the manufacture of a medicine for treating autoimmune diseases or proliferative diseases.
Investigation of the scope and regiochemistry of alkynylboronate cycloadditions with sydnones
Browne, Duncan L.,Vivat, Jerome F.,Plant, Andrew,Gomez-Bengoa, Enrique,Harrity, Joseph P. A.
supporting information; experimental part, p. 7762 - 7769 (2009/10/16)
The cycloaddition of alkynylboronates and sydnones provides a convenientand highly regioselective method for the synthesis of a broad range of di-, tri-, and tetrasubstituted pyrazole boronic esters. The origins of an observed regiochemical divergence in the reactions of terminal alkyny lboronates with their more substituted analogues have been studied by DFT methods.