(Q44416628)

English

Structure-based approach to falcipain-2 inhibitors: synthesis and biological evaluation of 1,6,7-trisubstituted dihydroisoquinolines and isoquinolines

scientific article published in May 2003

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scholarly article

1 reference

Europe PubMed Central

2 December 2017

Structure-based approach to falcipain-2 inhibitors: synthesis and biological evaluation of 1,6,7-trisubstituted dihydroisoquinolines and isoquinolines (English)

1 reference

Europe PubMed Central

2 December 2017

Philip J Rosenthal

3

object named as

Philip J Rosenthal

1 reference

Europe PubMed Central

2 December 2017

object named as

Sanjay Batra

1

1 reference

ORCID Public Data File 2021

author name string

Yogesh A Sabnis

2

1 reference

Europe PubMed Central

2 December 2017

Mitchell A Avery

4

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Europe PubMed Central

2 December 2017

language of work or name

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publication date

1 May 2003

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Europe PubMed Central

2 December 2017

Bioorganic & Medicinal Chemistry

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Europe PubMed Central

2 December 2017

11

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Europe PubMed Central

2 December 2017

10

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Europe PubMed Central

2 December 2017

2293-2299

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Europe PubMed Central

2 December 2017

Epidemiology of drug-resistant malaria

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Mechanisms of resistance of Plasmodium falciparum to antimalarial drugs

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A new class of potential chloroquine-resistance reversal agents for Plasmodia: syntheses and biological evaluation of 1-(3'-diethylaminopropyl)-3-(substituted phenylmethylene)pyrrolidines.

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An overview of chemotherapeutic targets for antimalarial drug discovery

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Aspartic proteases of Plasmodium falciparum and other parasitic protozoa as drug targets.

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Cysteine protease inhibitors as chemotherapy for parasitic infections

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Identification and characterization of falcilysin, a metallopeptidase involved in hemoglobin catabolism within the malaria parasite Plasmodium falciparum

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Characterization of native and recombinant falcipain-2, a principal trophozoite cysteine protease and essential hemoglobinase of Plasmodium falciparum

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The role of aminopeptidases in haemoglobin degradation in Plasmodium falciparum-infected erythrocytes

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The aspartic proteinase from the rodent parasite Plasmodium berghei as a potential model for plasmepsins from the human malaria parasite, Plasmodium falciparum.

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Hemoglobin metabolism in the malaria parasite Plasmodium falciparum

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Proteases of malaria parasites: new targets for chemotherapy

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Cysteine Proteases and Their Inhibitors

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Structure-based inhibitor design by using protein models for the development of antiparasitic agents

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Anti-malarial drug development using models of enzyme structure

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Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity

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Structure-based design, synthesis and evaluation of conformationally constrained cysteine protease inhibitors.

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Antimalarial effects in mice of orally administered peptidyl cysteine protease inhibitors

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Homology modeling of falcipain-2: validation, de novo ligand design and synthesis of novel inhibitors

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Cysteine proteases of parasitic organisms

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A geometric approach to macromolecule-ligand interactions

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The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000.

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A general method applicable to the search for similarities in the amino acid sequence of two proteins

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Predicting antibody hypervariable loop conformation. I. Ensembles of random conformations for ringlike structures

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Identifiers

10.1016/S0968-0896(03)00117-2

1 reference

Europe PubMed Central

2 December 2017

1 reference

Europe PubMed Central

2 December 2017

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