Discovery of Novel Tricyclic Thiazepine Derivatives as Anti-Drug-Resistant Cancer Agents by Combining Diversity-Oriented Synthesis and Converging Screening Approach.

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Identification of new inhibitors against human Great wall kinase using in silico approaches.

P2860

Q52725387-8A871896-F199-4CAF-B2CF-55B07C3F84F2

P2860

Discovery of Novel Tricyclic Thiazepine Derivatives as Anti-Drug-Resistant Cancer Agents by Combining Diversity-Oriented Synthesis and Converging Screening Approach.

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http://www.wikidata.org/entity/Q38777885

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

Discovery of Novel Tricyclic T ...... Converging Screening Approach.

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type

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Discovery of Novel Tricyclic T ...... Converging Screening Approach.

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Discovery of Novel Tricyclic T ...... Converging Screening Approach.

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P1476

Discovery of Novel Tricyclic T ...... Converging Screening Approach.

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P2093

Bing Yan

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

Daniel P Russo

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

Hao Zhu

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

Jinbao Xiang

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

Sigen Guo

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

Xianxiu Xu

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

Xu Bai

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

Yan Mu

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

Yongjin Liu

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

Zhuoqi Zhang

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

P2860

Cancer statistics, 2010

Cancer statistics, 2013

Multidrug resistance in cancer: role of ATP-dependent transporters

The concept of synthetic lethality in the context of anticancer therapy

Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study

Synthesis of tricyclic 4-chloro-pyrimido[4,5-b][1,4]benzodiazepines.

P-glycoprotein-independent apoptosis induction by a novel synthetic compound, MMPT [5-[(4-methylphenyl)methylene]-2-(phenylamino)-4(5H)-thiazolone].

Synthesis of novel tricyclic pyrimido[4,5-b][1,4]benzothiazepines via Bischler-Napieralski-type reactions.

A new strategy toward fused-pyridine heterocyclic scaffolds: Bischler-Napieralski-type cyclization, followed by sulfoxide extrusion reaction.

Method development for a pyridobenzodiazepine library with multiple diversification points.

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230-235

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scholarly article

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10.1021/ACSCOMBSCI.6B00010

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

P478

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

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2016-04-15T00:00:00Z

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P698

27082930

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P921

drug screening

P932

5592639

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

Discovery of Novel Tricyclic Thiazepine Derivatives as Anti-Drug-Resistant Cancer Agents by Combining Diversity-Oriented Synthesis and Converging Screening Approach.

about

P2860

P2860

Discovery of Novel Tricyclic Thiazepine Derivatives as Anti-Drug-Resistant Cancer Agents by Combining Diversity-Oriented Synthesis and Converging Screening Approach.

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P2860

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P31

P356

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P577

P698

P921

P932