Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

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Synthesis of kinase inhibitors containing a pentafluorosulfanyl moiety.

P2860

Q47116598-4AFDCF48-EA2A-4BF9-A430-3F5DDB41DE81

P2860

Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

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http://www.wikidata.org/entity/Q38637720

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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name

Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

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Item

label

Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

@en

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Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

@en

P1476

Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

@en

P2093

David A Colby

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

Munia F Sowaileh

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

Robert Alan Hazlitt

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P2860

Structure-Guided Lead Optimization of Triazolopyrimidine-Ring Substituents Identifies Potent Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitors with Clinical Candidate Potential

p97-containing complexes in proliferation control and cancer: emerging culprits or guilt by association?

Identification of orally-bioavailable antagonists of the TRPV4 ion-channel.

The synthesis and biological activity of pentafluorosulfanyl analogs of fluoxetine, fenfluramine, and norfenfluramine.

Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice

Synthesis of α-halo-α,α-difluoromethyl ketones by a trifluoroacetate release/halogenation protocol.

Development of potent and selective inhibitors of aldo-keto reductase 1C3 (type 5 17β-hydroxysteroid dehydrogenase) based on N-phenyl-aminobenzoates and their structure-activity relationships.

Pentafluorosulfanyl-containing flufenamic acid analogs: Syntheses, properties and biological activities

Structure-Activity Study of Bioisosteric Trifluoromethyl and Pentafluorosulfanyl Indole Inhibitors of the AAA ATPase p97.

Novel cis-selective and non-epimerisable C3 hydroxy azapodophyllotoxins targeting microtubules in cancer cells

P31

scholarly article

P356

10.1002/CMDC.201700356

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

P577

2017-08-07T00:00:00Z

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

P698

28782186

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Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

about

P2860

P2860

Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P577

P698

P356

P1433

P1476

P2093

P2860

P31

P356

P577

P698