Evidence map›Paper›PMID 26819495›Full record

ArticleMediators of inflammation2015

4-Isopropyl-2,6-bis(1-phenylethyl)aniline 1, an Analogue of KTH-13 Isolated from Cordyceps bassiana, Inhibits the NF-κB-Mediated Inflammatory Response.

Woo Seok Yang, Zubair Ahmed Ratan, Gihyeon Kim, Yunmi Lee, Mi-Yeon Kim, Jong-Hoon Kim, Jae Youl Cho

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Frontiers in pharmacology · 2020
    Review
  4. Antioxidant and Cytoprotective Effects of (-)-Epigallocatechin-3-(3″-International journal of molecular sciences · 2019
    Article
  5. Article
  6. Src Is a Prime Target Inhibited byEvidence-based complementary and alternative medicine : eCAM · 2018
    Article
  7. Beauvericin, a cyclic peptide, inhibits inflammatory responses in macrophages by inhibiting the NF-κB pathway.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  8. Article
  9. Journal of ginseng research · 2016
    Article
  10. 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

7 authors at 4 institutions in 2 countries.

Woo Seok YangDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of Korea.
Zubair Ahmed RatanDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of Korea; Department of Pediatrics, Institute of Child and Maternal Health (ICMH), Matuail, Dhaka 1362, Bangladesh.
Gihyeon KimDepartment of Chemistry, Kwangwoon University, Seoul 139-701, Republic of Korea.
Yunmi LeeDepartment of Chemistry, Kwangwoon University, Seoul 139-701, Republic of Korea.
Mi-Yeon KimSchool of Systems Biological Science, Soongsil University, Seoul 156-743, Republic of Korea.
Jong-Hoon KimDepartment of Physiology, College of Veterinary Medicine, Chonbuk National University, 79 Gobong-ro, Iksan 54596, Republic of Korea.
Jae Youl ChoDepartment of Genetic Engineering, Sungkyunkwan University, Suwon 440-746, Republic of Korea.
Sungkyunkwan University · KRKwangwoon University · KRJeonbuk National University · KRSoongsil University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Cordyceps species has been a good source of compounds with anticancer and anti-inflammatory activities. Recently, we reported a novel compound (4-isopropyl-2,6-bis(1-phenylethyl)phenol, KTH-13) with anticancer activity isolated from Cordyceps bassiana and created several derivatives to increase its pharmacological activity. In this study, we tested one of the KTH-013 derivatives, 4-isopropyl-2,6-bis(1-phenylethyl)aniline 1 (KTH-13-AD1), with regard to anti-inflammatory activity under macrophage-mediated inflammatory conditions. KTH-13-AD1 clearly suppressed the production of nitric oxide (NO) and reactive oxygen species (ROS) in lipopolysaccharide (LPS) and sodium nitroprusside- (SNP-) treated macrophage-like cells (RAW264.7 cells). Similarly, this compound also reduced mRNA expression of inducible NO synthase (iNOS) and tumor necrosis factor-α (TNF-α), as analyzed by RT-PCR and real-time PCR. Interestingly, KTH-13-AD1 strongly diminished NF-κB-mediated luciferase activities and nuclear translocation of NF-κB family proteins. In accordance, KTH-13-AD1 suppressed the upstream signaling pathway of NF-κB activation, including IκBα, IKKα/β, AKT, p85/PI3K, and Src in a time- and dose-dependent manner. The autophosphorylation of Src and NF-κB observed during the overexpression of Src was also suppressed by KTH-13-AD1. These results strongly suggest that KTH-13-AD1 has strong anti-inflammatory features mediated by suppression of the Src/NF-κB regulatory loop.

Indexed as

Aniline CompoundsAnimalsAnti-Inflammatory AgentsCells, CulturedCordycepsHumansMiceNF-kappa BNitric OxideTranscription Factor AP-14-isopropyl-2,6-bis(1-phenylethyl)anilineAniline CompoundsAnti-Inflammatory AgentsNF-kappa BNitric OxideTranscription Factor AP-1

Identifiers

PMID26819495
PMCPMC4706927
OpenAlexW2236107788

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.