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1.
ChemMedChem ; 18(13): e202300127, 2023 07 03.
Artigo em Inglês | MEDLINE | ID: mdl-37276375

RESUMO

The status of industrial Medicinal Chemistry was discussed with European Medicinal Chemistry Leaders from large to mid-sized pharma and CRO companies as well as biotechs. The chemical modality space has expanded recently from small molecules to address new challenging targets. Besides the classical SAR/SPR optimization of drug molecules also their 'greenness' has increasing importance. The entire pharma discovery ecosystem has developed significantly. Beyond pharma and academia new key players such as Biotech and integrated CROs as well as Digital companies have appeared and are now to a large extend fueled by VC money. Digitalization is happening everywhere but surprisingly did not change speed and success rates of projects so far. Future Medicinal Chemists will still have to be excellent synthetic chemists but in addition they must be knowledgeable in new computational areas such as data sciences. Their ability to collaborate and to work in teams is key.


Assuntos
Química Farmacêutica , Indústria Farmacêutica , Ecossistema , Europa (Continente)
2.
Bioorg Med Chem Lett ; 24(3): 845-9, 2014 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-24405707
3.
Bioorg Med Chem Lett ; 19(13): 3586-92, 2009 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-19447622

RESUMO

The identification of a novel series of Aurora kinase inhibitors and exploitation of their SAR is described. Replacement of the initial quinazoline core with a pyrimidine scaffold and modification of substituents led to a series of very potent inhibitors of cellular proliferation. MK-0457 (VX-680) has been assessed in Phase II clinical trials in patients with treatment-refractory chronic myelogenous leukemia (CML) or Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) containing the T315I mutation.


Assuntos
Piperazinas/química , Inibidores de Proteínas Quinases/química , Proteínas Serina-Treonina Quinases/antagonistas & inibidores , Aurora Quinases , Linhagem Celular Tumoral , Simulação por Computador , Cristalografia por Raios X , Desenho de Fármacos , Humanos , Leucemia Mielogênica Crônica BCR-ABL Positiva/tratamento farmacológico , Proteínas Mutantes/antagonistas & inibidores , Proteínas Mutantes/metabolismo , Piperazinas/farmacologia , Inibidores de Proteínas Quinases/síntese química , Inibidores de Proteínas Quinases/farmacologia , Proteínas Serina-Treonina Quinases/metabolismo , Relação Estrutura-Atividade
4.
J Med Chem ; 48(4): 1278-81, 2005 Feb 24.
Artigo em Inglês | MEDLINE | ID: mdl-15715498

RESUMO

Aryl CH hydrogen bonds play an important role in the binding of several analogues of a pyrazol-3-ylquinazolin-4-ylamine inhibitor of glycogen synthase kinase 3 (GSK3). Understanding the importance of these CH...O and CH...N hydrogen bonds allowed the design of a novel quinazolin-4-ylthiazol-2-ylamine inhibitor of GSK3 with a structurally confirmed CH...O hydrogen bond to the protein.


Assuntos
Quinase 3 da Glicogênio Sintase/antagonistas & inibidores , Quinase 3 da Glicogênio Sintase/química , Quinazolinas/síntese química , Tiazóis/síntese química , Desenho de Fármacos , Ligação de Hidrogênio , Isomerismo , Ligantes , Modelos Moleculares , Conformação Molecular , Quinazolinas/química , Relação Estrutura-Atividade , Tiazóis/química
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