Antiviral and anticancer optimization studies of the DNA-binding marine natural product aaptamine (Q28829158)

6

object named as

Raymond F Schinazi

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author name string

John J Bowling

1

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Hari K Pennaka

2

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Kelly Ivey

3

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Subagus Wahyuono

4

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Frederick A Valeriote

7

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David E Graves

8

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Mark T Hamann

Chemical Biology and Drug Design

9

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language of work or name

English

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publication date

March 2008

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published in

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volume

71

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issue

3

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page(s)

205-15

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cites work

Marine natural products as novel antioxidant prototypes

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Natural products as sources of new drugs over the last 25 years

16 March 2017

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Modification at the C9 position of the marine natural product isoaaptamine and the impact on HIV-1, mycobacterial, and tumor cell activity

7 April 2017

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Fragment-based lead discovery

3 June 2018

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Antineoplastic agents 491. Synthetic conversion of aaptamine to isoaaptamine, 9-demethylaaptamine, and 4-methylaaptamine

3 June 2018

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Antineoplastic agents. 380. Isolation and X-ray crystal structure determination of isoaaptamine from the Republic of Singapore Hymeniacidon sp. and conversion to the phosphate prodrug hystatin 1.

3 June 2018

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Antineoplastic agents. 499. Synthesis of hystatin 2 and related 1H-benzo[de][1,6]-naphthyridinium salts from aaptamine

3 June 2018

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Influence of Substituent Modifications on DNA Binding Energetics of Acridine-Based Anticancer Agents

3 June 2018

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Marine natural products as lead anti-HIV agents

3 June 2018

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DNA and its associated processes as targets for cancer therapy

3 June 2018

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Analysis of drug-DNA binding data

3 June 2018

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Anti HSV-1 Alkaloids from a Feeding Deterrent Marine Sponge of the Genus Aaptos

3 June 2018

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Crossref

https://api.crossref.org/works/10.1111%2FJ.1747-0285.2008.00628.X

Discovery and development of anticancer agents from plants

21 January 2018

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Structures and cytotoxicity relationship of isoaaptamine and aaptamine derivatives

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18251774

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18251774