Evidence map›Paper›PMID 35859880›Full record

ArticleACS medicinal chemistry letters2022

Indolactam Dipeptides as Nanomolar Gli Inhibitors.

Manuel Mendoza, UyenPhuong Tran, Grace C Zhang, Jeffrey Leister, Kyle To, Theodore Malepeai-Tofaeono, Alison E Ondrus, Kelvin L Billingsley

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Design of PKC-Targeting Benzolactams as Gli Inhibitors.ACS medicinal chemistry letters · 2026
    Article
  2. Article
  3. Article
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

8 authors at 3 institutions in 1 country.

Manuel MendozaDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.
UyenPhuong TranDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.
Grace C ZhangDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.ORCID https://orcid.org/0000-0002-2044-9230
Jeffrey LeisterDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.
Kyle ToDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.
Theodore Malepeai-TofaeonoDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.
Alison E OndrusDepartment of Chemistry, University of Illinois Chicago, Chicago, Illinois 60607, United States.ORCID https://orcid.org/0000-0002-6023-3290
Kelvin L BillingsleyDepartment of Chemistry and Biochemistry, California State University Fullerton, Fullerton, California 92831, United States.ORCID https://orcid.org/0000-0001-9071-5170
California State University, Fullerton · USCalifornia Institute of Technology · USUniversity of Illinois Chicago · US

Funding

PREDOCTORAL TRAINING IN BIOLOGY AND CHEMISTRYT32GM007616 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI STERNBERG, PAUL WARREN · 1985 to 2019
$22.9M
NIGMS NIH HHS T32 GM007616
6 · The paper itself

Abstract

The Gli transcription factors within the Hedgehog (Hh) signaling pathway play essential roles in human development. However, the reactivation of Gli proteins in adult tissue is tumorigenic and drives the progression of several cancers, including the majority of basal cell carcinomas. Here we describe a novel set of indolactam dipeptides that target protein kinase C (PKC), exploiting the unique capacity of PKC isozymes to act as regulators of Gli. We devised an efficient synthetic route for the indolactam-based natural product (-)-pendolmycin and a series of analogues, and we evaluated these analogues in mechanistically distinct Gli reporter assays. The lead compound from these studies,

Identifiers

PMID35859880
PMCPMC9290001
OpenAlexW4281932519

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.