(Q46800231)

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New superacid synthesized (fluorinated) tertiary benzenesulfonamides acting as selective hCA IX inhibitors: toward a new mode of carbonic anhydrase inhibition by sulfonamides

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

New superacid synthesized (fluorinated) tertiary benzenesulfonamides acting as selective hCA IX inhibitors: toward a new mode of carbonic anhydrase inhibition by sulfonamides (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Claudiu T Supuran

4

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Claudiu T Supuran

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

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Benoît Métayer

1

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Agnès Mingot

2

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Daniella Vullo

3

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Sébastien Thibaudeau

5

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

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1 July 2013

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Chemical Communications

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

49

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

54

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

6015-6017

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Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

Carbonic anhydrase as a model for biophysical and physical-organic studies of proteins and protein-ligand binding

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Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX

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Ureido-substituted benzenesulfonamides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis.

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Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms I and II.

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Superacid synthesis of halogen containing N-substituted-4-aminobenzene sulfonamides: new selective tumor-associated carbonic anhydrase inhibitors

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Superelectrophilic activation in superacid HF/SbF(5) and synthesis of benzofused sultams

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Carbonic anhydrase inhibitors. Inhibition of tumor-associated isozyme IX by halogenosulfanilamide and halogenophenylaminobenzolamide derivatives

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Understanding organofluorine chemistry. An introduction to the C-F bond

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Predicting and tuning physicochemical properties in lead optimization: amine basicities

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The many roles for fluorine in medicinal chemistry

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The enantiomers of syn-2,3-difluoro-4-aminobutyric acid elicit opposite responses at the GABA(C) receptor.

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7,8-disubstituted- but not 6,7-disubstituted coumarins selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II in the low nanomolar/subnanomolar range

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Coumarins incorporating hydroxy- and chloro-moieties selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II.

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Carbonic anhydrase inhibitors

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Carbonic Anhydrase Inhibitors: Clash with Ala65 as a Means for Designing Inhibitors with Low Affinity for the Ubiquitous Isozyme II, Exemplified by the Crystal Structure of the Topiramate Sulfamide Analogue†

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Novel coumarins and 2-thioxo-coumarins as inhibitors of the tumor-associated carbonic anhydrases IX and XII

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Identifiers

10.1039/C3CC40858B

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/23503420

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