4-Toluenesulfonylureido derivatives of amines, amino acids and dipeptides: a novel class of potential antitumor agents (Q58863318)

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1 November 2019

title

4-toluenesulfonylureido derivatives of amines, amino acids and dipeptides: a novel class of potential antitumor agents (English)

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1 November 2019

2

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1 November 2019

author name string

Mastrolorenzo A

series ordinal

1

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1 November 2019

Supuran CT

series ordinal

3

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1 November 2019

language of work or name

English

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publication date

1 October 2000

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European Journal of Pharmaceutical Sciences

1 November 2019

published in

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1 November 2019

volume

11

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1 November 2019

issue

4

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1 November 2019

page(s)

325-332

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Cellular pharmacology of chloroquinoxaline sulfonamide and a related compound in murine B16 melanoma cells

1 November 2019

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Novel agents effective against solid tumors: the diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships

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Clinical and pharmacology study of chloroquinoxaline sulfonamide given on a weekly schedule

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Effects of diarylsulfonylurea antitumor agents on the function of mitochondria isolated from rat liver and GC3/c1 cells

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Carbonic Anhydrase Inhibitors. Synthesis of Water-Soluble, Topically Effective, Intraocular Pressure-Lowering Aromatic/Heterocyclic Sulfonamides Containing Cationic or Anionic Moieties: Is the Tail More Important than the Ring?1

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Carbonic Anhydrase Inhibitors: Synthesis of Water-Soluble, Aminoacyl/Dipeptidyl Sulfonamides Possessing Long-Lasting Intraocular Pressure-Lowering Properties via the Topical Route1

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Carbonic anhydrase inhibitors. Arylsulfonylureido- and arylureido-substituted aromatic and heterocyclic sulfonamides: towards selective inhibitors of carbonic anhydrase isozyme I

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Carbonic anhydrase inhibitors: synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV.

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Carbonic anhydrase activators

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Protease inhibitors: synthesis of potent bacterial collagenase and matrix metalloproteinase inhibitors incorporating N-4-nitrobenzylsulfonylglycine hydroxamate moieties

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Markedly decreased binding of vincristine to tubulin in vinca alkaloid-resistant Chinese hamster cells is associated with selective overexpression of alpha and beta tubulin isoforms

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Carbonic anhydrase inhibitors - Part 94. 1,3,4-Thiadiazole-2-sulfonamide derivatives as antitumor agents?

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Sulfonimidamide analogs of oncolytic sulfonylureas

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Novel sulfonamides as potential, systemically active antitumor agents

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7 January 2021

10.1016/S0928-0987(00)00122-6

Identifiers

DOI

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1 November 2019

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