Evidence map›Paper›PMID 36119972›Full record

ArticleACS omega2022

1,2,3-Triazole Tethered Hybrid Capsaicinoids as Antiproliferative Agents Active against Lung Cancer Cells (A549).

Arif Khan, Fatima Naaz, Rafia Basit, Deepak Das, Piyush Bisht, Majeed Shaikh, Bilal Ahmad Lone, Yuba Raj Pokharel, Qazi Naveed Ahmed, Shazia Parveen and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in ACS omega, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Arif KhanDepartment of Chemistry, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.
Fatima NaazDepartment of Chemistry, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.
Rafia BasitPharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India.
Deepak DasDepartment of Chemistry, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.
Piyush BishtFaculty of Life Sciences and Biology, South Asian University, New Delhi 110021, India.
Majeed ShaikhNatural product and Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India.
Bilal Ahmad LoneFaculty of Life Sciences and Biology, South Asian University, New Delhi 110021, India.
Yuba Raj PokharelFaculty of Life Sciences and Biology, South Asian University, New Delhi 110021, India.
Qazi Naveed AhmedNatural product and Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India.ORCID https://orcid.org/0000-0002-6890-7587
Shazia ParveenFaculty of Science, Chemistry Department, Taibah University, Yanbu Branch, Yanbu 46423, Saudi Arabia.ORCID https://orcid.org/0000-0002-2213-2958
Intzar AliDepartment of Microbiology, Hamdard Institute of Medical Sciences and Research, Jamia Hamdard, New Delhi 110062, India.
Shashank Kumar SinghPharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India.
Gousia ChashooPharmacology Division, CSIR-Indian Institute of Integrative Medicine, Jammu 180001, India.
Syed ShafiDepartment of Chemistry, School of Chemical and Life Sciences, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.ORCID https://orcid.org/0000-0001-7657-0630
Indian Institute of Integrative Medicine · INJamia Hamdard · INSouth Asian University · INYanbu University College · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of novel 1,2,3-triazole derivatives of capsaicin and its structural isomer (new natural product hybrid capsaicinoid) were synthesized by exploiting one-/two-point modification of capsaicin without altering the amide linkage (neck). The newly synthesized compounds were screened for their antiproliferative activity against an NCI panel of 60 cancer cell lines at a single dose of 10 μM. Most of the compounds have demonstrated reduced growth between 55 and 95%, whereas capsaicin (

Identifiers

PMID36119972
PMCPMC9476207
OpenAlexW4294012479

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.