Evidence map›Paper›PMID 41028273›Full record

ArticleScientific reports2025

Probing into 9'-substituted Suzuki-coupled noscapine ionic liquids as potent microtubule targeting anticancer agents with hemoglobin affinity.

Shubham Sewariya, Nistha Mishra, Sagar Panchal, Shrikant Kukreti, Ramesh Chandra

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shubham SewariyaDepartment of Chemistry, University of Delhi, Delhi, 110007, India.
Nistha MishraDepartment of Chemistry, University of Delhi, Delhi, 110007, India.
Sagar PanchalDepartment of Chemistry, University of Delhi, Delhi, 110007, India.
Shrikant KukretiDepartment of Chemistry, University of Delhi, Delhi, 110007, India.
Ramesh ChandraDepartment of Chemistry, University of Delhi, Delhi, 110007, India. acbrdu@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

On a global scale, lung cancer accounts for 18% of all cancer deaths making it the most lethal cancer. To restrain this, there has been continual research in the domain of microtubule-targeting anticancer agents but issues like toxicity, immunosuppression, effective delivery to tumor site, etc. persist to impede their clinical success. Unlike the other existing drugs in this regime; noscapine (a non-opioid alkaloid) is testified to be an intrinsically safer drug with minimal side effects. In this work, we have synthesized and evaluated novel 9'-substituted suzuki-coupled noscapine ionic liquid(s) as effectual anticancer drug(s) against non-small cell (H1299) lung cancer. We have devised a synthetic route (employed suzuki coupling for subsuming the biaryl pharmacophore and combined it with the idea of active pharmaceutical ingredient-based ionic liquids (API-ILs)) to yield the desired API-ILs followed by their characterization using associated analytical techniques like NMR, HRMS, etc. Following this, we have performed SAR analysis of the API-ILs using molecular docking with the target tubulin protein and preliminary in vitro screening against H1299 (non-small cancer) cells to opt for the most promising analogue i.e., [p-NO

Indexed as

Antineoplastic AgentsHemoglobinsIonic LiquidsMicrotubulesNoscapineCell Line, TumorHumansMolecular Docking SimulationStructure-Activity RelationshipTubulinAntineoplastic AgentsHemoglobinsIonic LiquidsNoscapineTubulinAPI-ILBiaryl pharmacophoreHemoglobinLung cancerMicrotubulesNoscapine

Identifiers

PMID41028273
PMCPMC12484645

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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.