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by IQAC KIITKIIT Deemed to be University — Internal Quality Assurance Cell

Publication2023

AKR1B1 inhibition using NARI-29-an Epalrestat analogue-alleviates Doxorubicin-induced cardiotoxicity via modulating Calcium/CaMKII/MuRF-1 axis

The record

Type
Publication
Date
25 August 2023
Level
National
Journal
Chemico Biological Interactions
Volume
381
Published
25 August 2023
DOI
10.1016/j.cbi.2023.110566
Scopus ID
85160412559
ISSN
00092797
Authors
9
Open access
No
Citations
23
International co-authorship
No
Co-author countries
IN

Classification

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UN Sustainable Development Goals

  1. 3.4 Reduce premature mortality from non-communicable diseases and promote mental health and well-being

    TargetPrimaryCertain confidenceJudged

    AKR1B1 inhibitor NARI-29 prevents doxorubicin-induced cardiotoxicity while enhancing breast cancer chemotherapy efficacy

    Certain confidence
    The record states the subject matter explicitly. A reader shown only the title and this goal would agree without hesitation. Example: a workshop titled "Renewable Energy and Smart Grid" against SDG 7.
    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

  1. vb-1.2 Health and well-being

    Sub-themePrimaryHigh confidenceJudged

    Cancer treatment toxicity mitigation improving patient outcomes and treatment tolerability

    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.
    Produced by
    claude-haiku-4-5-20251001, under kortex-publication-v1

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1

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Citing this record

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KIIT Deemed to be University. “AKR1B1 inhibition using NARI-29-an Epalrestat analogue-alleviates Doxorubicin-induced cardiotoxicity via modulating Calcium/CaMKII/MuRF-1 axis”. Kortex.

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