Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors. (Q40815863)

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17 February 2020

title

Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors (English)

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17 February 2020

11

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17 February 2020

Alessandro Vergara

2

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17 February 2020

Marco Caterino

3

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17 February 2020

Vincenzo Alterio

4

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17 February 2020

Simona Maria Monti

5

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17 February 2020

Pascal Dumy

7

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17 February 2020

Jean-Yves Winum

10

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17 February 2020

9

Claudiu T Supuran

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17 February 2020

Daniela Vullo

8

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author name string

Anna Di Fiore

1

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17 February 2020

Joanna Ombouma

6

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17 February 2020

language of work or name

English

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publication date

1 July 2015

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17 February 2020

published in

Chemical Communications

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17 February 2020

volume

51

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17 February 2020

issue

57

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17 February 2020

page(s)

11519-11522

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Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?

17 February 2020

cites work

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Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

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The zinc coordination pattern in the η-carbonic anhydrase from Plasmodium falciparum is different from all other carbonic anhydrase genetic families

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Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII.

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Human carbonic anhydrase VII protects cells from oxidative damage.

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Which carbonic anhydrases are targeted by the antiepileptic sulfonamides and sulfamates?

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Recent advances in the discovery of zinc-binding motifs for the development of carbonic anhydrase inhibitors.

21 January 2018

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Out of the active site binding pocket for carbonic anhydrase inhibitors

21 January 2018

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Transition metal coordination chemistry ofN,N-bis(2-{pyrid-2-ylethyl})hydroxylamine

21 January 2018

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Hydroxamate represents a versatile zinc binding group for the development of new carbonic anhydrase inhibitors

21 January 2018

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High-resolution structure of human carbonic anhydrase II complexed with acetazolamide reveals insights into inhibitor drug design

21 January 2018

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A structure-based analysis of the vibrational spectra of nitrosyl ligands in transition-metal coordination complexes and clusters

21 January 2018

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Mononuclear metal-O2 complexes bearing macrocyclic N-tetramethylated cyclam ligands

21 January 2018

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Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors

21 January 2018

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Thermodynamic optimisation in drug discovery: a case study using carbonic anhydrase inhibitors

21 January 2018

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Non-zinc mediated inhibition of carbonic anhydrases: coumarins are a new class of suicide inhibitors

21 January 2018

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Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule

21 January 2018

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Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations

21 January 2018

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Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo.

21 January 2018

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Sulfocoumarins (1,2-benzoxathiine-2,2-dioxides): a class of potent and isoform-selective inhibitors of tumor-associated carbonic anhydrases

21 January 2018

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Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors

21 January 2018

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Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins

21 January 2018

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Interaction of anticancer ruthenium compounds with proteins: high-resolution X-ray structures and raman microscopy studies of the adduct between hen egg white lysozyme and AziRu

21 January 2018

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An Order-Disorder Transition Plays a Role in Switching Off the Root Effect in Fish Hemoglobins

21 January 2018

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21 January 2018

Identifiers

DOI

10.1039/C5CC03711E

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26094945%20AND%20SRC:MED&resulttype=core&format=json

release_sojjtb5yzfcbnbszstovoowy3m

17 February 2020

Fatcat ID

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Fatcat

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mapped directly with Wikidata item

24 November 2022

based on heuristic

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