2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships. (Q40183411)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28586174%20AND%20SRC:MED&resulttype=core&format=json

22 March 2020

title

2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships (English)

1 reference

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22 March 2020

0 references

1

Valentina Straniero

2 references

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22 March 2020

18 September 2017

2

Carlo Zanotto

2 references

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22 March 2020

18 September 2017

3

Letizia Straniero

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22 March 2020

18 September 2017

4

Andrea Casiraghi

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22 March 2020

18 September 2017

5

Stefano Duga

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22 March 2020

18 September 2017

6

Antonia Radaelli

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22 March 2020

18 September 2017

Carlo De Giuli Morghen

series ordinal

7

object named as

Carlo De Giuli Morghen

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22 March 2020

18 September 2017

8

Ermanno Valoti

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22 March 2020

18 September 2017

11 July 2017

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22 March 2020

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22 March 2020

volume

12

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22 March 2020

page(s)

1303-1318

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22 March 2020

issue

16

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New antibiotics from Nature's chemical inventory

22 March 2020

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3-(Benzodioxan-2-ylmethoxy)-2,6-difluorobenzamides bearing hydrophobic substituents at the 7-position of the benzodioxane nucleus potently inhibit methicillin-resistant Sa and Mtb cell division.

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6-methoxy-7-benzofuranoxy and 6-methoxy-7-indolyloxy analogues of 2-[2-(2,6-Dimethoxyphenoxy)ethyl]aminomethyl-1,4-benzodioxane (WB4101):1 discovery of a potent and selective α1D-adrenoceptor antagonist.

21 January 2018

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Identifiers

DOI

10.1002/CMDC.201700201

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28586174%20AND%20SRC:MED&resulttype=core&format=json

22 March 2020

1 reference