Evidence map›Paper›PMID 35905686›Full record

ArticleBioorganic & medicinal chemistry2022

Synthesis and evaluation of 3'- and 4'-substituted cyclohexyl noviomimetics that modulate mitochondrial respiration.

Penchala Narasimharao Meka, Eva Amatya, Sukhmanjit Kaur, Monimoy Banerjee, Ang Zuo, Rick T Dobrowsky, Brian S J Blagg

Open access · greenAbstract read
In one paragraph

Article in Bioorganic & medicinal chemistry, 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
0.4field-weighted citation impact, top 42% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Recent advances toward the development of Hsp90 C-terminal inhibitors.Bioorganic & medicinal chemistry letters · 2023
    Review
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

7 authors at 2 institutions in 1 country.

Penchala Narasimharao MekaDepartment of Chemistry and Biochemistry, 305 McCourtney Hall, The University of Notre Dame, Notre Dame, IN 46556, United States.
Eva AmatyaDepartment of Chemistry and Biochemistry, 305 McCourtney Hall, The University of Notre Dame, Notre Dame, IN 46556, United States.
Sukhmanjit KaurDepartment of Pharmacology and Toxicology Department, The University of Kansas, Lawrence, KS 66045, United States.
Monimoy BanerjeeDepartment of Chemistry and Biochemistry, 305 McCourtney Hall, The University of Notre Dame, Notre Dame, IN 46556, United States.
Ang ZuoDepartment of Chemistry and Biochemistry, 305 McCourtney Hall, The University of Notre Dame, Notre Dame, IN 46556, United States.
Rick T DobrowskyDepartment of Pharmacology and Toxicology Department, The University of Kansas, Lawrence, KS 66045, United States. Electronic address: dobrowsky@ku.edu.
Brian S J BlaggDepartment of Chemistry and Biochemistry, 305 McCourtney Hall, The University of Notre Dame, Notre Dame, IN 46556, United States. Electronic address: bblagg@nd.edu.
University of Notre Dame · USUniversity of Kansas · US

Funding

Chaperone therapeutics for the treatment of DPNR01NS075311 · NINDS · UNIVERSITY OF NOTRE DAME · PI BLAGG, BRIAN S J, DOBROWSKY, RICK T · 2012 to 2020
$2.8M
HSP90 InhibitorsU01CA109265 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI BLAGG, BRIAN S J · 2006 to 2014
$2.2M
Chaperones in Diabetic Peripheral NeuropathyR01DK095911 · NIDDK · UNIVERSITY OF KANSAS LAWRENCE · PI DOBROWSKY, RICK T · 2013 to 2016
$1.3M
A Novel Pharmacologic Approach to Treat CMT1XR33NS114355 · NINDS · UNIVERSITY OF KANSAS LAWRENCE · PI DOBROWSKY, RICK T · 2021 to 2022
$752k
A Novel Pharmacologic Approach to Treat CMT1XR61NS114355 · NINDS · UNIVERSITY OF KANSAS LAWRENCE · PI DOBROWSKY, RICK T · 2020 to 2020
$387k
NCI NIH HHS U01 CA109265NIDDK NIH HHS R01 DK095911NINDS NIH HHS R01 NS075311NINDS NIH HHS R33 NS114355NINDS NIH HHS R61 NS114355
6 · The paper itself

Abstract

KU-32 (2) and KU-596 (3), are first and second generation cytoprotective novologues that are derivatives of novobiocin (1), a heat shock protein 90 (Hsp90) C-terminal inhibitor. Although 2 and 3 improve mitochondrial bioenergetics and have demonstrated considerable cytoprotective activity, they contain a synthetically demanding noviose sugar. This issue was initially addressed by creating noviomimetics, such as KU-1202 (4), which replaced the noviose sugar with ether-linked cyclohexyl derivatives that retained some cytoprotective potential due to their ability to increase mitochondrial bioenergetics. Based on structure-activity relationship (SAR) studies of KU-1202 (4), the current study investigated 3'- and 4'-substituted cyclohexyl scaffolds as noviomimetics and determined their efficacy at increasing mitochondrial bioenergetic as a marker for cytoprotective potential.

Indexed as

HSP90 Heat-Shock ProteinsNovobiocinMitochondriaRespirationSugarsHSP90 Heat-Shock ProteinsNovobiocinSugarsHeat shock protein 70Heat shock protein 90Mitochondrial bioenergeticsMolecular chaperonesNoviomimeticsNovologues

Identifiers

PMID35905686
PMCPMC11664489
OpenAlexW4285678545

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.