Structure-Based Design and Synthesis of New Estrane-Pyridine Derivatives as Cytochrome P450 (CYP) 1B1 Inhibitors.

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Structure-Based Design and Synthesis of New Estrane-Pyridine Derivatives as Cytochrome P450 (CYP) 1B1 Inhibitors.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Structure-Based Design and Syn ...... ome P450 (CYP) 1B1 Inhibitors.

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Structure-Based Design and Syn ...... Derivatives as Cytochrome P450

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label

Structure-Based Design and Syn ...... ome P450 (CYP) 1B1 Inhibitors.

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Structure-Based Design and Syn ...... Derivatives as Cytochrome P450

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prefLabel

Structure-Based Design and Syn ...... ome P450 (CYP) 1B1 Inhibitors.

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Structure-Based Design and Syn ...... Derivatives as Cytochrome P450

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P1476

Structure-Based Design and Syn ...... ome P450 (CYP) 1B1 Inhibitors.

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P2093

Donald Poirier

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Jenny Roy

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Raphaël Dutour

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P2860

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Identification of fused 16β,17β-oxazinone-estradiol derivatives as a new family of non-estrogenic 17β-hydroxysteroid dehydrogenase type 1 inhibitors.

Human CYP1B1 and anticancer agent metabolism: mechanism for tumor-specific drug inactivation?

Cytochrome P450 CYP1A1: wider roles in cancer progression and prevention.

Inhibition of carcinogen-activating enzymes by 16alpha-fluoro-5-androsten-17-one.

P304

1159-1164

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P31

scholarly article

P356

10.1021/ACSMEDCHEMLETT.7B00265

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P433

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

P478

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P50

Francisco Cortés-Benítez

P577

2017-10-11T00:00:00Z

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P698

29152048

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P932

5683706

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