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Discovery of a potent and dual-selective bisubstrate inhibitor for protein arginine methyltransferase 4/5

Acta Pharmaceutica Sinica B(2020)10.1016/j.apsb.2020.10.013Source: DataRank Database

Discovery of a potent and dual-selective bisubstrate inhibitor for protein arginine methyltransferase 4/5 is a research paper published in Acta Pharmaceutica Sinica B (2020). On theSindex it has a DataRank of 0. It has been cited 27 times.

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Open Access27 citations

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Enrichment:Funding (5 grants)OA: goldTopics (20)IDs (PubMed, PMC)Annotations (1)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (5)

Dongxing Chen ORCID,Youchao Deng ORCID,Guangping Dong ORCID,Rong Huang ORCID,Ayad A. Al-Hamashi ORCID

Live enrichment

PubMed:34589391 PMC:PMC8463262

National Institutes of Health

Grant: P30 CA023168

National Institutes of Health

Grant: R01GM117275

National Institutes of Health

Grant: 5R01GM117275-04

Protein N-terminal Methylation Mechanisms and Inhibition

National Institutes of Health

Grant: 3P30CA023168-35S1

Cancer Center Support Grant (CORE) Renewal

Purdue University

goldLicense: cc-by-nc-nd

publisherhttps://doi.org/10.1016/j.apsb.2020.10.013

publisherhttps://api.elsevier.com/content/article/PII:S2211383520307656?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2211383520307656?httpAccept=text/plain

repositoryhttps://doaj.org/article/94de89932623487b8bf535b282a1cf58

repositoryhttp://europepmc.org/pmc/articles/PMC8463262

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

Protein Arginine MethyltransferaseProtein Arginine Methyltransferase 5Tlc, Thin-layer ChromatographyBisubstrate InhibitorSam, S-adenosylmethionineProtein Arginine Methyltransferase 4Bisubstrate AnalogueSah, S-(5′-adenosyl)-l-homocysteineGar, Glycine And ArginineNtmts, N-terminal MethyltransferasesPkmts, Protein Lysine MethyltransferasesPrmts, Protein Arginine MethyltransferasesSnf, SinofunginIc50, Half-maximal Inhibition ConcentrationOriginal ArticleTherapeutics. PharmacologyRM1-950

Sustainable Development Goals

SDG 3: 3. Good health