3D-QSAR study of 20 (S)-camptothecin analogs

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Advances in computational methods to predict the biological activity of compounds.Design, Synthesis and Cytotoxicity Evaluation of New 2-Aryl-5, 6-Dihydropyrrolo[2, 1-a]Isoquinoline Derivatives as Topoisomerase Inhibitors.

P2860

Q34289760-599E6E8A-1269-475E-B4D0-4CC175CEC3EE Q38627884-F8F63853-65AF-452B-9C4E-E9D4E7B6BE63

P2860

3D-QSAR study of 20 (S)-camptothecin analogs

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http://www.wikidata.org/entity/Q56864508

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im Februar 2007 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

@nl

наукова стаття, опублікована в лютому 2007

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name

3D-QSAR study of 20 (S)-camptothecin analogs

@en

3D-QSAR study of 20

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Item

label

3D-QSAR study of 20 (S)-camptothecin analogs

@en

3D-QSAR study of 20

@nl

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3D-QSAR study of 20 (S)-camptothecin analogs

@en

3D-QSAR study of 20

@nl

P1476

3D-QSAR study of 20 (S)-camptothecin analogs

@en

P2093

Ai-jun LU

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

Han-jun ZOU

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Hua-liang JIANG

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

Ming-yue ZHENG

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

Zhen-shan ZHANG

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P2860

Nonlinear partial differential equations and applications: The mechanism of topoisomerase I poisoning by a camptothecin analog

Camptothecin: current perspectives.

The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity.

Synthesis, topoisomerase I inhibitory activity, and in vivo evaluation of 11-azacamptothecin analogs.

Water soluble inhibitors of topoisomerase I: quaternary salt derivatives of camptothecin.

Comparison of topoisomerase I inhibition, DNA damage, and cytotoxicity of camptothecin derivatives presently in clinical trials.

Synthesis and biological evaluation of novel A-ring modified hexacyclic camptothecin analogues.

Molecular modeling studies of the DNA-topoisomerase I ternary cleavable complex with camptothecin.

P2888

j.1745-7254.2007.00477.x

P304

307-314

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P31

scholarly article

P356

10.1111/J.1745-7254.2007.00477.X

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P433

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

P478

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

P50

Xiaomin Luo

P577

2007-02-01T00:00:00Z

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P6179

1045299038

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P698

17241535

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3D-QSAR study of 20 (S)-camptothecin analogs

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P2860

P2860

3D-QSAR study of 20 (S)-camptothecin analogs

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698