Evidence map›Paper›PMID 26363638›Full record

ArticleInflammation2016

3,5-Disubstituted Isoxazole Derivatives: Potential Inhibitors of Inflammation and Cancer.

Kodagahalli Sathya Rakesh, Swamy Jagadish, Kyathegowdanadoddi Srinivas Balaji, Farhan Zameer, Toreshettahally Ramesh Swaroop, Chakrabhavi Dhanajaya Mohan, Shankar Jayarama, Kanchugarakoppal Subbegowda Rangappa

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2016. 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, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Isoxazole Derivatives as Regulators of Immune Functions.Molecules (Basel, Switzerland) · 2018
    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

8 authors at 1 institution in 1 country.

Kodagahalli Sathya RakeshDepartment of Studies in Chemistry, University of Mysore, Crawford Hall, Mysore, 570 006, Karnataka, India.
Swamy JagadishDepartment of Studies in Chemistry, University of Mysore, Crawford Hall, Mysore, 570 006, Karnataka, India.
Kyathegowdanadoddi Srinivas BalajiDepartment of Biotechnology, Terresian College, University of Mysore, Mysore, 570 011, Karnataka, India.
Farhan ZameerDepartment of Biotechnology, Biochemistry and Microbiology, Mahajana Research Foundation, SBRR Mahajana First Grade College, University of Mysore, JL Puram, Mysore, 570 012, Karnataka, India.
Toreshettahally Ramesh SwaroopDepartment of Studies in Chemistry, University of Mysore, Crawford Hall, Mysore, 570 006, Karnataka, India.
Chakrabhavi Dhanajaya MohanDepartment of Studies in Chemistry, University of Mysore, Crawford Hall, Mysore, 570 006, Karnataka, India.
Shankar JayaramaDepartment of Biotechnology, Terresian College, University of Mysore, Mysore, 570 011, Karnataka, India.
Kanchugarakoppal Subbegowda RangappaDepartment of Studies in Chemistry, University of Mysore, Crawford Hall, Mysore, 570 006, Karnataka, India. rangappaks@gmail.com.
University of Mysore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The products of arachidonic acid metabolism by lipoxygenase (LOX) and cyclooxygenase (COX) significantly contribute to inflammation and carcinogenesis. Particularly, overproduction of leukotrienes and prostaglandins contribute to tumor growth by inducing formation of new blood vessels that sustain tumor cell viability and growth. Hence, search for novel anticancer drug via inhibition of LOX and COX enzymes constitutes an impressive strategy till date. In this context, a series of isoxazole derivatives were synthesized and screened for their anti-inflammatory activity via LOX and COX inhibition. Among these, 3-(3-methylthiophen-2-yl)-5-(3,4,5-trimethoxyphenyl)isoxazole (2b) showed significant inhibitory activity toward LOX and COX-2. Additionally, 2b showed a good inhibition of tumor growth, peritoneal angiogenesis, and ascite formation in Ehrlich ascites carcinoma (EAC) cell mouse model. Further, the in silico molecular studies also revealed that the compound 2b binds to the catalytic domain of LOX and COX-1 and COX-2 strongly with high atomic contact energy (ACE) score compared to standard drug. These initial pharmacological data support the fact that the compound 2b serves as the basis in developing anti-inflammatory and anticancer agents.

Indexed as

Angiogenesis InhibitorsAnimalsAnti-Inflammatory AgentsAntineoplastic AgentsBinding SitesCarcinoma, Ehrlich TumorCatalytic DomainCell Line, TumorCell SurvivalCyclooxygenase 2Cyclooxygenase 2 InhibitorsDisease Models, AnimalHeLa CellsHumansInflammationIsoxazoles3-(3-methylthiophen-2-yl)-5-(3,4,5-trimethoxyphenyl)isoxazoleAngiogenesis InhibitorsAnti-Inflammatory AgentsAntineoplastic AgentsCyclooxygenase 2Cyclooxygenase 2 InhibitorsIsoxazolesLipoxygenaseLipoxygenase InhibitorsPtgs2 protein, mouseThiophenes3,5-disubstituted isoxazolescarcinogenesiscyclooxygenaseinflammationlipoxygenaseperitoneal angiogenesis

Identifiers

PMID26363638
OpenAlexW2241507036

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.