Synthesis of sulfonamide conjugates of Cu(II), Ga(III), In(III), Re(V) and Zn(II) complexes: carbonic anhydrase inhibition studies and cellular imaging investigations.

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Easy access to heterobimetallic complexes for medical imaging applications via microwave-enhanced cycloaddition.Advances in structure-based drug discovery of carbonic anhydrase inhibitors.

P2860

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P2860

Synthesis of sulfonamide conjugates of Cu(II), Ga(III), In(III), Re(V) and Zn(II) complexes: carbonic anhydrase inhibition studies and cellular imaging investigations.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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Synthesis of sulfonamide conju ...... llular imaging investigations.

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P1476

Synthesis of sulfonamide conju ...... ellular imaging investigations

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P2093

Claudiu T Supuran

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Daniela Vullo

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Jonathan R Dilworth

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Martin Christlieb

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Philip A Waghorn

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Simon R Bayly

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

Xin Sun

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P2860

Human carbonic anhydrase XII: cDNA cloning, expression, and chromosomal localization of a carbonic anhydrase gene that is overexpressed in some renal cell cancers

[(Cp-R)M(CO)3] (M=Re or 99mTc) Arylsulfonamide, arylsulfamide, and arylsulfamate conjugates for selective targeting of human carbonic anhydrase IX

Carbonic anhydrase inhibitors

Carbonic anhydrase inhibitors: novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX.

In vitro and in vivo evaluation of bifunctional bisthiosemicarbazone 64Cu-complexes for the positron emission tomography imaging of hypoxia.

Labeling biomolecules with radiorhenium: a review of the bifunctional chelators.

Ultrahigh resolution crystal structures of human carbonic anhydrases I and II complexed with "two-prong" inhibitors reveal the molecular basis of high affinity.

Porphyrin substituted phosphoramidites: new building blocks for porphyrin-oligonucleotide syntheses.

Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moietie

Fluorescent gallium and indium bis(thiosemicarbazonates) and their radiolabelled analogues: synthesis, structures and cellular confocal fluorescence imaging investigations.

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10.1039/C4DT03206C

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English

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Sofia I Pascu

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2015-03-01T00:00:00Z

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272841737

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Synthesis of sulfonamide conjugates of Cu(II), Ga(III), In(III), Re(V) and Zn(II) complexes: carbonic anhydrase inhibition studies and cellular imaging investigations.

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P2860

P2860

Synthesis of sulfonamide conjugates of Cu(II), Ga(III), In(III), Re(V) and Zn(II) complexes: carbonic anhydrase inhibition studies and cellular imaging investigations.

description

name

type

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P1433

P1476

P2093

P2860

P304

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P356

P407

P433

P478

P50

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P5875

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

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P478

P50

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P698