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Pyridine indole hybrids as novel potent CYP17A1 inhibitors

Pyridine indole hybrids as novel potent CYP17A1 inhibitors

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2b0f63253cc24dfc970b0890757145a1

Pyridine indole hybrids as novel potent CYP17A1 inhibitors

About this item

Full title

Pyridine indole hybrids as novel potent CYP17A1 inhibitors

Publisher

England: Taylor & Francis

Journal title

Journal of enzyme inhibition and medicinal chemistry, 2025-12, Vol.40 (1), p.2463014

Language

English

Formats

Publication information

Publisher

England: Taylor & Francis

More information

Scope and Contents

Contents

Prostate cancer (PCa) is one of the most prevalent malignancies affecting men worldwide, and androgen deprivation therapy (ADT) is a primary treatment approach. CYP17A1 inhibitors like abiraterone target the steroidogenic pathway to reduce androgen levels, but their clinical efficacy is limited by drug resistance and adverse effects. This study rep...

Alternative Titles

Full title

Pyridine indole hybrids as novel potent CYP17A1 inhibitors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2b0f63253cc24dfc970b0890757145a1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2b0f63253cc24dfc970b0890757145a1

Other Identifiers

ISSN

1475-6374,1475-6366

E-ISSN

1475-6374

DOI

10.1080/14756366.2025.2463014

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