(Q53768940)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

title

Antitrypanosomal activities and cytotoxicity of 5-nitro-2-furancarbohydrazides (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

0 references

Elisabeth Davioud-Charvet

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

Régis Millet

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

author name string

Louis Maes

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

Valérie Landry

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

Christian Sergheraert

4

1 reference

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15 December 2019

language of work or name

English

0 references

publication date

1 December 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

number of pages

4

1 reference

Bioorganic & Medicinal Chemistry Letters

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

volume

12

1 reference

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15 December 2019

issue

24

1 reference

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15 December 2019

page(s)

3601-3604

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

1,2,5-Oxadiazole N-oxide derivatives and related compounds as potential antitrypanosomal drugs: structure-activity relationships.

15 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Synthesis and antitrypanosomal evaluation of E-isomers of 5-nitro-2-furaldehyde and 5-nitrothiophene-2-carboxaldehyde semicarbazone derivatives. structure-activity relationships

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Nitrofuran drugs as common subversive substrates of Trypanosoma cruzi lipoamide dehydrogenase and trypanothione reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Chinifur, a selective inhibitor and "subversive substrate" for Trypanosoma congolense trypanothione reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Antitubercular substances. III. Nonpyridinoid heterocyclic hydrazides

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Chemotherapy of Experimental Tuberculosis. VIII. The Synthesis of Acid Hydrazides, their Derivatives and Related Compounds1,2

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

PyBOP®: A new peptide coupling reagent devoid of toxic by-product

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Charge is the major discriminating factor for glutathione reductase versus trypanothione reductase inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Trypanothione reductase from Trypanosoma cruzi. Purification and characterization of the crystalline enzyme.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Purification and characterization of lipoamide dehydrogenase from Trypanosoma cruzi

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Flavoprotein structure and mechanism. 5. Trypanothione reductase and lipoamide dehydrogenase as targets for a structure-based drug design.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

"Subversive" substrates for the enzyme trypanothione disulfide reductase: alternative approach to chemotherapy of Chagas disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Trypanothione reductase from Trypanosoma cruzi. Catalytic properties of the enzyme and inhibition studies with trypanocidal compounds

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

2- and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: synthesis and correlation between redox cycling activities and in vitro cytotoxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

Structure-based design of parasitic protease inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2802%2900788-6

7 January 2021

10.1016/S0960-894X(02)00788-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12443785%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference