(Q40638565)

22 September 2017

title

Synthesis and cytotoxic activity of A-ring modified betulinic acid derivatives (English)

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22 September 2017

1

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22 September 2017

Yong Kim

2

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22 September 2017

Nguyen-Hai Nam

series ordinal

3

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22 September 2017

Byung-Zun Ahn

series ordinal

4

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22 September 2017

language of work or name

English

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publication date

1 October 2003

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Bioorganic & Medicinal Chemistry Letters

22 September 2017

published in

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22 September 2017

volume

13

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22 September 2017

issue

19

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22 September 2017

page(s)

3137-3140

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Betulinic acid and dihydrobetulinic acid derivatives as potent anti-HIV agents

22 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Anti-AIDS agents, 11. Betulinic acid and platanic acid as anti-HIV principles from Syzigium claviflorum, and the anti-HIV activity of structurally related triterpenoids

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Inhibitory effect of glycyrrhetinic acid derivatives on lipoxygenase and prostaglandin synthetase

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Preparation of amino acid conjugates of betulinic acid with activity against human melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Synthesis of betulinic acid derivatives with activity against human melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Discovery of betulinic acid as a selective inhibitor of human melanoma that functions by induction of apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Betulinic acid induces apoptosis in human neuroblastoma cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Novel synthetic oleanane and ursane triterpenoids with various enone functionalities in ring A as inhibitors of nitric oxide production in mouse macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Synthetic oleanane and ursane triterpenoids with modified rings A and C: a series of highly active inhibitors of nitric oxide production in mouse macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

Design and synthesis of tricyclic compounds with enone functionalities in rings A and C: a novel class of highly active inhibitors of nitric oxide production in mouse macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2803%2900724-8

7 January 2021

10.1016/S0960-894X(03)00724-8

Identifiers

DOI

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22 September 2017

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