Evidence map›Paper›PMID 30779584›Full record

ArticleOrganic letters2019

Discovery of Amantamide, a Selective CXCR7 Agonist from Marine Cyanobacteria.

Xiao Liang, Danmeng Luo, Jia-Lei Yan, Mohammad A Rezaei, Lilibeth A Salvador-Reyes, Sarath P Gunasekera, Chenglong Li, Tao Ye, Valerie J Paul, Hendrik Luesch

Open access · greenAbstract read
In one paragraph

Article in Organic letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 19 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

10 authors at 4 institutions in 3 countries.

Xiao LiangDepartment of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , Gainesville , Florida 32610 , United States.
Danmeng LuoDepartment of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , Gainesville , Florida 32610 , United States.
Jia-Lei YanState Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics , Peking University Shenzhen Graduate School , Xili, Nanshan District, Shenzhen 518055 , China.
Mohammad A RezaeiDepartment of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , Gainesville , Florida 32610 , United States.
Lilibeth A Salvador-ReyesMarine Science Institute, College of Science , University of the Philippines , Diliman, Quezon City 1101 , Philippines.
Sarath P GunasekeraSmithsonian Marine Station , Fort Pierce , Florida 34949 , United States.
Chenglong LiDepartment of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , Gainesville , Florida 32610 , United States.
Tao YeState Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics , Peking University Shenzhen Graduate School , Xili, Nanshan District, Shenzhen 518055 , China.ORCID 0000-0002-2780-9761
Valerie J PaulSmithsonian Marine Station , Fort Pierce , Florida 34949 , United States.ORCID 0000-0002-4691-1569
Hendrik LueschDepartment of Medicinal Chemistry and Center for Natural Products, Drug Discovery and Development (CNPD3) , University of Florida , Gainesville , Florida 32610 , United States.ORCID 0000-0002-4091-7492
University of Florida · USPeking University · CNSmithsonian Marine Station · USUniversity of the Philippines Diliman · PH

Funding

Novel Targeted Anticancer Agents from Marine CyanobacteriaR01CA172310 · NCI · UNIVERSITY OF FLORIDA · PI HENDRIK LUESCH · 2013 to 2026
$5.8M
NCI NIH HHS R01 CA172310
6 · The paper itself

Abstract

CXCR7 plays an emerging role in several physiological processes. A linear peptide, amantamide (1), was isolated from marine cyanobacteria, and the structure was determined by NMR and mass spectrometry. The total synthesis was achieved by solid-phase method. After screening two biological target libraries, 1 was identified as a selective CXCR7 agonist. The selective activation of CXCR7 by 1 could provide the basis for developing CXCR7-targeted therapeutics and deciphering the role of CXCR7 in different diseases.

Indexed as

AmidesCyanobacteriaMolecular StructurePeptidesReceptors, CXCRACKR3 protein, humanAmidesPeptidesReceptors, CXCR

Identifiers

PMID30779584
PMCPMC7327960
OpenAlexW2915662325

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.