Evidence map›Paper›PMID 32785052›Full record

ArticleMolecules (Basel, Switzerland)2020

Structural Basis of Beneficial Design for Effective Nicotinamide Phosphoribosyltransferase Inhibitors.

Sei-Ichi Tanuma, Kiyotaka Katsuragi, Takahiro Oyama, Atsushi Yoshimori, Yuri Shibasaki, Yasunobu Asawa, Hiroaki Yamazaki, Kosho Makino, Miwa Okazawa, Yoko Ogino and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Anticancer Inhibitors.Molecules (Basel, Switzerland) · 2022
    Article
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  5. Review
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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

18 authors at 4 institutions in 1 country.

Sei-Ichi TanumaDepartment of Genomic Medicinal Science, Research Institute for Science and Technology, Organization for Research Advancement, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Kiyotaka KatsuragiDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Takahiro OyamaHinoki Shinyaku Co., Ltd., Chiyoda-ku, Tokyo 102-0084, Japan.
Atsushi YoshimoriInstitute for Theoretical Medicine Inc., Fujisawa, Kanagawa 251-0012, Japan.
Yuri ShibasakiDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Yasunobu AsawaLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Kanagawa 226-8503, Japan.
Hiroaki YamazakiHinoki Shinyaku Co., Ltd., Chiyoda-ku, Tokyo 102-0084, Japan.
Kosho MakinoDepartment of Medicinal Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Miwa OkazawaDepartment of Genomic Medicinal Science, Research Institute for Science and Technology, Organization for Research Advancement, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Yoko OginoDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Yoshimi SakamotoDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Miyagi 981-1293, Japan.
Miyuki NomuraDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Miyagi 981-1293, Japan.
Akira SatoDepartment of Biochemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.ORCID 0000-0002-2239-6208
Hideaki AbeHinoki Shinyaku Co., Ltd., Chiyoda-ku, Tokyo 102-0084, Japan.
Hiroyuki NakamuraLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Kanagawa 226-8503, Japan.ORCID 0000-0002-4511-2984
Hideyo TakahashiDepartment of Medicinal Chemistry, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Nobuhiro TanumaDivision of Cancer Chemotherapy, Miyagi Cancer Center Research Institute, Natori, Miyagi 981-1293, Japan.
Fumiaki UchiumiDepartment of Gene Regulation, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Tokyo University of Science · JPMiyagi Prefectural Hospital Organization · JPNippon Shinyaku (Japan) · JPTokyo Institute of Technology · JP

Funding

Japan Agency for Medical Research and Development 18cm0106133h0001
6 · The paper itself

Abstract

Inhibition of nicotinamide phosphoribosyltransferase (NAMPT) is an attractive therapeutic strategy for targeting cancer metabolism. So far, many potent NAMPT inhibitors have been developed and shown to bind to two unique tunnel-shaped cavities existing adjacent to each active site of a NAMPT homodimer. However, cytotoxicities and resistances to NAMPT inhibitors have become apparent. Therefore, there remains an urgent need to develop effective and safe NAMPT inhibitors. Thus, we designed and synthesized two close structural analogues of NAMPT inhibitors, azaindole-piperidine (

Indexed as

Drug DesignBinding SitesCatalytic DomainEnzyme InhibitorsHumansIndolesKineticsMolecular Docking SimulationNicotinamide PhosphoribosyltransferasePiperazinePiperidinesEnzyme InhibitorsindoleIndolesNicotinamide PhosphoribosyltransferasePiperazinepiperidinePiperidinesanticancer drugazacyclohexanedrug designenthalpy effectinhibitorNAD+ biosynthesisnicotinamide phosphoribosyltransferase

Identifiers

PMID32785052
PMCPMC7464552
OpenAlexW3048123077

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.