Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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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年學術文章

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2018年學術文章

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2018年學術文章

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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Item

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

@en

Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells.

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P1476

Smenamide A Analogues. Synthesis and Biological Activity on Multiple Myeloma Cells

@en

P2093

Germana Esposito

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

Stefania Trino

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P2860

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A Pyrazolo[3,4-d]pyrimidine compound inhibits Fyn phosphorylation and induces apoptosis in natural killer cell leukemia.

Ruthenium tetroxide and perruthenate chemistry. Recent advances and related transformations mediated by other transition metal oxo-species.

Smenamides A and B, chlorinated peptide/polyketide hybrids containing a dolapyrrolidinone unit from the Caribbean sponge Smenospongia aurea. Evaluation of their role as leads in antitumor drug research.

Structure and biosynthesis of the jamaicamides, new mixed polyketide-peptide neurotoxins from the marine cyanobacterium Lyngbya majuscula.

Dolastatin 15, a potent antimitotic depsipeptide derived from Dolabella auricularia. Interaction with tubulin and effects of cellular microtubules.

A Pyrazolo[3,4-d]pyrimidine Compound Reduces Cell Viability and Induces Apoptosis in Different Hematological Malignancies.

Epha3 acts as proangiogenic factor in multiple myeloma.

Damicoside from Axinella damicornis: the influence of a glycosylated galactose 4-OH group on the immunostimulatory activity of alpha-galactoglycosphingolipids.

P31

scholarly article

P356

10.3390/MD16060206

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P433

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P478

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P50

P577

2018-06-13T00:00:00Z

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P698

29899231

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P932

6025564

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