Evidence map›Paper›PMID 20673723›Full record

ArticleBioorganic & medicinal chemistry2010

Conjugates of betulin derivatives with AZT as potent anti-HIV agents.

Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Juan XiongGraduate School of Pharmaceutical Sciences, University of Tokushima, Tokushima 770-8505, Japan.
Yoshiki Kashiwada
Chin-Ho Chen
Keduo Qian
Susan L Morris-Natschke
Kuo-Hsiung Lee
Yoshihisa Takaishi
Tokushima University · JPUniversity of North Carolina at Chapel Hill · USDuke Medical Center · US

Funding

Modified Triterpines as Potent HIV Fusion InhibitorsR01AI077417 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LEE, KUO-HSIUNG · 2008 to 2012
$2.4M
NIAID NIH HHS AI-077417NIAID NIH HHS R01 AI077417
6 · The paper itself

Abstract

Fourteen novel conjugates of 3,28-di-O-acylbetulins with AZT were prepared as anti-HIV agents, based on our previously reported potent anti-HIV triterpene leads, including 3-O-acyl and 3,28-di-O-acylbetulins. Nine of the conjugates (49-53, 55, 56, 59, and 60) exhibited potent anti-HIV activity at the submicromolar level, with EC(50) values ranging from 0.040 to 0.098muM in HIV-1(NL4-3) infected MT-4 cells. These compounds were equipotent or more potent than 3-O-(3',3'-dimethylsuccinyl)betulinic acid (2), which is currently in Phase IIb anti-AIDS clinical trial.

Indexed as

Anti-HIV AgentsBetulinic AcidCD4-Positive T-LymphocytesCell LineHIV-1HumansPentacyclic TriterpenesTriterpenesZidovudineAnti-HIV AgentsbetulinBetulinic AcidPentacyclic TriterpenesTriterpenesZidovudine

Identifiers

PMID20673723
PMCPMC3016297
OpenAlexW1974197466

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.