Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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Item

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

@en

Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling.

@nl

P1476

Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling

@en

P2093

Eva Schütznerová

http://www.w3.org/2001/XMLSchema#string

Filip Hančík

http://www.w3.org/2001/XMLSchema#string

Igor Popa

http://www.w3.org/2001/XMLSchema#string

Martin Pisár

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P2860

Targeting CDK4 and CDK6: From Discovery to Therapy

A novel approach for the development of selective Cdk4 inhibitors: library design based on locations of Cdk4 specific amino acid residues.

Arylazopyrazole AAP1742 inhibits CDKs and induces apoptosis in multiple myeloma cells via Mcl-1 downregulation.

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.

Design and synthesis of substituted N-(1,3-diphenyl-1H-pyrazol-5-yl)benzamides as positive allosteric modulators of the metabotropic glutamate receptor subtype 5.

Identification and further development of potent TBK1 inhibitors.

Discovery of N-[4-(1H-Pyrazolo[3,4-b]pyrazin-6-yl)-phenyl]-sulfonamides as Highly Active and Selective SGK1 Inhibitors

Suzuki-Miyaura cross-coupling of unprotected, nitrogen-rich heterocycles: substrate scope and mechanistic investigation.

Novel arylazopyrazole inhibitors of cyclin-dependent kinases.

Inhibitors of cyclin-dependent kinases as cancer therapeutics.

P31

scholarly article

P356

10.3390/MOLECULES23010149

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Zdeněk Trávníček

Petr Cankař

P577

2018-01-12T00:00:00Z

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P698

29329219

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P932

6017724

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