Publication2022
Design and synthesis of the novel, selective WZ4002 analogue as EGFR-L858R/T790M tyrosine kinase inhibitors for targeted drug therapy in non-small-cell lung cancer (NSCLC)
The record
- Type
- Publication
- Date
- 15 April 2022
- Level
- National
- Journal
- Journal of Molecular Structure
- Volume
- 1254
- Published
- 15 April 2022
- DOI
- 10.1016/j.molstruc.2021.132313
- Scopus ID
- 85122324807
- ISSN
- 00222860
- Authors
- 8
- Open access
- No
- Citations
- 28
- International co-authorship
- No
- Co-author countries
- IN
Classification
Every label below carries the reasoning it was assigned on, the confidence band it was assigned in, and what produced it. The rubric is published.
UN Sustainable Development Goals
3.4 Reduce premature mortality from non-communicable diseases and promote mental health and well-being
Novel WZ4002 analogue EGFR tyrosine kinase inhibitors achieve selective targeting of drug-resistant non-small-cell lung cancer.
- High confidence
- The subject matter is a strong and direct inference from the record type, the funding or organising body, or the programme context, even where the title alone is thin. Example: an ICMR-funded project against SDG 3, on the strength of the agency.
- Judged
- Judged against the published classification rubric, under the rubric and prompt versions recorded with the run that produced it.
- Produced by
- claude-haiku-4-5-20251001, under kortex-publication-v1
Viksit Bharat @2047
vb-1.2 Health and well-being
Targeted cancer drug development advances precision medicine and disease treatment outcomes.
- Produced by
- claude-haiku-4-5-20251001, under kortex-publication-v1
Each label above carries the instrument and the version that produced it. How each classification is reached.
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Provenance
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- Source rows resolved into this record
- 1
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Citing this record
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KIIT Deemed to be University. “Design and synthesis of the novel, selective WZ4002 analogue as EGFR-L858R/T790M tyrosine kinase inhibitors for targeted drug therapy in non-small-cell lung cancer (NSCLC)”. Kortex.