Preformulation study of NSC-726796

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Preformulation study of NSC-726796

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http://www.wikidata.org/entity/Q35999066

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2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

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2012年论文

@zh

2012年论文

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name

Preformulation study of NSC-726796

@ast

Preformulation study of NSC-726796

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label

Preformulation study of NSC-726796

@ast

Preformulation study of NSC-726796

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prefLabel

Preformulation study of NSC-726796

@ast

Preformulation study of NSC-726796

@en

P1476

Preformulation study of NSC-726796

@en

P2093

Duoli Guo

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Erin R Gardner

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James P Cain

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S Esmail Tabibi

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Samuel H Yalkowsky

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Sean O'Connell

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Steven Pisle

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William D Figg

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P2860

Selective leukemic-cell killing by a novel functional class of thalidomide analogs

Combinatorial antileukemic disruption of oxidative homeostasis and mitochondrial stability by the redox reactive thalidomide 2-(2,4-difluoro-phenyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3(2H)-dione (CPS49) and flavopiridol.

Importance of the stress kinase p38alpha in mediating the direct cytotoxic effects of the thalidomide analogue, CPS49, in cancer cells and endothelial cells.

Antimyeloma activity of two novel N-substituted and tetraflourinated thalidomide analogs.

Antitumor effects of thalidomide analogs in human prostate cancer xenografts implanted in immunodeficient mice.

Antiangiogenic activity of N-substituted and tetrafluorinated thalidomide analogues.

Comparative molecular field analysis and comparative molecular similarity indices analysis of thalidomide analogues as angiogenesis inhibitors.

P2888

s12249-012-9784-5

P304

661-673

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P31

scholarly article

P356

10.1208/S12249-012-9784-5

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P407

English

P433

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

P478

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

P577

2012-05-03T00:00:00Z

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P5875

224888685

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P6179

1031132027

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P698

22552929

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P932

3364376

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