Evidence map›Paper›PMID 23241029›Full record

ArticleJournal of medicinal chemistry2013

Discovery of potent, selective multidrug and toxin extrusion transporter 1 (MATE1, SLC47A1) inhibitors through prescription drug profiling and computational modeling.

Matthias B Wittwer, Arik A Zur, Natalia Khuri, Yasuto Kido, Alan Kosaka, Xuexiang Zhang, Kari M Morrissey, Andrej Sali, Yong Huang, Kathleen M Giacomini

Open access · greenAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

66 citing papers in PubMed, 142 citations in OpenAlex.

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  6. Beyond SGLT2: proximal tubule transporters as potential drug targets for chronic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Review
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  20. Effects of 5-HTClinical and translational science · 2021
    Article

6 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Matthias B Wittwer *University of California, San Francisco, Department of Bioengineering and Therapeutic Sciences RH 581, 1550 4 Street San Francisco, CA 94158, United States of America.
Arik A Zur *University of California, San Francisco, Department of Bioengineering and Therapeutic Sciences RH 581, 1550 4 Street San Francisco, CA 94158, United States of America.
Natalia Khuri *University of California, San Francisco, Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, and California Institute for Quantitative Biosciences (QB3) BH 503B, 1700 4 Street San Francisco, CA 94158, United States of America.
Yasuto KidoDrug-Drug Interaction Group, Drug Metabolism and Pharmacokinetics, Shionogi & Co., Ltd. 3-1-1, Futaba-cho, Toyonaka-shi Osaka 561-0825, Japan.
Alan KosakaOptivia Biotechnology Inc. 115 Constitution Drive, Suite 7 Menlo Park, CA 94025.
Xuexiang ZhangOptivia Biotechnology Inc. 115 Constitution Drive, Suite 7 Menlo Park, CA 94025.
Kari M MorrisseyUniversity of California, San Francisco, Department of Bioengineering and Therapeutic Sciences RH 581, 1550 4 Street San Francisco, CA 94158, United States of America.
Andrej SaliUniversity of California, San Francisco, Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, and California Institute for Quantitative Biosciences (QB3) BH 503B, 1700 4 Street San Francisco, CA 94158, United States of America.
Yong HuangOptivia Biotechnology Inc. 115 Constitution Drive, Suite 7 Menlo Park, CA 94025.
Kathleen M GiacominiUniversity of California, San Francisco, Department of Bioengineering and Therapeutic Sciences RH 581, 1550 4 Street San Francisco, CA 94158, United States of America.
University of California, San Francisco · USOptivia Biotechnology (United States) · USShionogi (Japan) · JP

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
PHARMACOGENETICS OF MEMBRANE TRANSPORTERSU01GM061390 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GIACOMINI, KATHLEEN M · 2000 to 2009
$29.2M
SPECIALIZED CENTER FOR THE PROTEIN STRUCTURE INITIATIVEU54GM074929 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHOE, SENYON · 2005 to 2009
$16.6M
Pharmacogenomics of Membrane TransportersU19GM061390 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWOK, PUI-YAN · 2010 to 2014
$16.3M
PHARMACEUTICAL SCIENCES AND PHARMACOGENOMICST32GM007175 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AHITUV, NADAV, KROETZ, DEANNA L · 1985 to 2021
$7.1M
A Comprehensive Platform for Transporter Mediated Drug-Drug Interaction StudiesR44GM086970 · NIGMS · OPTIVIA BIOTECHNOLOGY, INC. · PI GIACOMINI, KATHLEEN M, HUANG, YONG · 2011 to 2012
$1.8M
NIDDK NIH HHS P30 DK026743NIGMS NIH HHS R44 GM086970NIGMS NIH HHS T32 GM007175NIGMS NIH HHS U01 GM061390NIGMS NIH HHS U01 GM61390NIGMS NIH HHS U19 GM061390NIGMS NIH HHS U54 GM074929
6 · The paper itself

Abstract

The human multidrug and toxin extrusion (MATE) transporter 1 contributes to the tissue distribution and excretion of many drugs. Inhibition of MATE1 may result in potential drug-drug interactions (DDIs) and alterations in drug exposure and accumulation in various tissues. The primary goals of this project were to identify MATE1 inhibitors with clinical importance or in vitro utility and to elucidate the physicochemical properties that differ between MATE1 and OCT2 inhibitors. Using a fluorescence assay of ASP(+) uptake in cells stably expressing MATE1, over 900 prescription drugs were screened and 84 potential MATE1 inhibitors were found. We identified several MATE1 selective inhibitors including four FDA-approved medications that may be clinically relevant MATE1 inhibitors and could cause a clinical DDI. In parallel, a QSAR model identified distinct molecular properties of MATE1 versus OCT2 inhibitors and was used to screen the DrugBank in silico library for new hits in a larger chemical space.

Indexed as

Computer SimulationPrescription DrugsFluorescent DyesOrganic Cation Transport ProteinsFluorescent DyesOrganic Cation Transport ProteinsPrescription DrugsSLC47A1 protein, human

Identifiers

PMID23241029
PMCPMC4068829
OpenAlexW2150254577

What OpenQuestion holds

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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.