Structure and antimalarial activity of adducts of 11-azaartemisinin with conjugated terminal acetylenes (Q58476973)

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2 November 2019

title

Structure and antimalarial activity of adducts of 11-azaartemisinin with conjugated terminal acetylenes (English)

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2 November 2019

3

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2 November 2019

author name string

E Katz

series ordinal

1

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2 November 2019

J Ma

series ordinal

2

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2 November 2019

H Ziffer

series ordinal

4

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2 November 2019

language of work or name

English

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publication date

1 October 1999

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2 November 2019

number of pages

4

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Bioorganic & Medicinal Chemistry Letters

inferred from page(s)

published in

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2 November 2019

volume

9

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2 November 2019

issue

20

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2 November 2019

page(s)

2969-2972

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The chemistry, pharmacology, and clinical applications of qinghaosu (artemisinin) and its derivatives

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

Antimalarial activity of artemisinin (qinghaosu) and related trioxanes: mechanism(s) of action

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

Syntheses and antimalarial activities of N-substituted 11-azaartemisinins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

Structure-activity relationships of the antimalarial agent artemisinin. 2. Effect of heteroatom substitution at O-11: synthesis and bioassay of N-alkyl-11-aza-9-desmethylartemisinins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

Synthesis and biological activity of a new class of cytotoxic agents: N-(3-oxoprop-1-enyl)-substituted pyrimidines and purines

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

Antimalarial activity of new dihydroartemisinin derivatives. 7. 4-(p-substituted phenyl)-4(R or S)-[10(alpha or beta)-dihydroartemisininoxy]butyric acids.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2899%2900506-5

7 January 2021

10.1016/S0960-894X(99)00506-5

Identifiers

DOI

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2 November 2019

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