Evidence map›Paper›PMID 21197572›Full record

ReviewMolecular diversity2011

Chemical biology of histone acetyltransferase natural compounds modulators.

Fabrizio Dal Piaz, Antonio Vassallo, Osmany Cuesta Rubio, Sabrina Castellano, Gianluca Sbardella, Nunziatina De Tommasi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 29 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

6 authors at 3 institutions in 2 countries.

Fabrizio Dal PiazDipartimento di Scienze Farmaceutiche, Università di Salerno, Via Ponte Don Melillo, 84084, Fisciano (SA), Italy.
Antonio Vassallo
Osmany Cuesta Rubio
Sabrina Castellano
Gianluca Sbardella
Nunziatina De Tommasi
University of Salerno · ITUniversity of Basilicata · ITUniversity of Havana · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone acetyltransferases (HATs) are a class of epigenetic enzymes crucial for chromatin restructuring and transcriptional regulation in eukaryotic cells, thus being a promising target for therapeutic development. Nonetheless, differently from histone deacetylases (HDACs) inhibitors, there is still paucity of small-molecule modulators of HAT activity. After a decline during past decade, natural products and their derivatives could be once again a valuable tool in the lead discovery process and meet such need of Novel Chemical Entities (NCEs). In this review, we will provide a comprehensive summary on the discovery of small-molecule HAT modulators from naturally occurring molecular scaffolds.

Indexed as

AlkaloidsAnacardic AcidsAnimalsBenzophenonesBenzoquinonesBiological ProductsEnzyme InhibitorsFlavonoidsHistone AcetyltransferasesHumansPeptidesPhenolsPolyphenolsAlkaloidsAnacardic AcidsBenzophenonesBenzoquinonesBiological ProductsEnzyme InhibitorsFlavonoidsHistone AcetyltransferasesPeptidesPhenolspolyisoprenyl benzophenonePolyphenolsquinone

Identifiers

PMID21197572
OpenAlexW1976675316

What OpenQuestion holds

Textmetadata
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.