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Cited by 381

The DOI matches its Crossref record; 108 of the 108 references it cites were found in a registry or an index.

Triterpenoids as new promising anticancer drugs

Petronelli, Alessia, Pannitteri, Gaetano, Testa, Ugo·2009·Anti-Cancer Drugs

Abstract

Triterpenoids are structurally diverse organic compounds, characterized by a basic backbone modified in multiple ways, allowing the formation of more than 20 000 naturally occurring triterpenoid varieties. Several triterpenoids, including ursolic and oleanolic acid, betulinic acid, celastrol, pristimerin, lupeol, and avicins possess antitumor and anti-inflammatory properties. To improve antitumor activity, some synthetic triterpenoid derivatives have been synthesized, including cyano-3,12-dioxooleana-1,9 (11)-dien-28-oic (CDDO), its methyl ester (CDDO-Me), and imidazolide (CDDO-Im) derivatives. Of these, CDDO, CDDO-Me, and betulinic acid have shown promising antitumor activities and are presently under evaluation in phase I studies. Triterpenoids are highly multifunctional and the antitumor activity of these compounds is measured by their ability to block nuclear factor-kappaB activation, induce apoptosis, inhibit signal transducer, and activate transcription and angiogenesis.

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Metadata

Authors
Petronelli, A., Pannitteri, G., & Testa, U.
Venue
Anti-Cancer Drugs
Published
2009-11
Volume
20
Issue
10
Pages
880-892
ISSN
0959-4973 (ISSN-L)
OpenAlex
W1977773503
Cited by
381
References
108
FWCI
9.12
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Triterpenoids as new promising anticancer drugs. https://app.cochat.ai/papers/10.1097/cad.0b013e328330fd90
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Petronelli, A., Pannitteri, G., & Testa, U. (2009). Triterpenoids as new promising anticancer drugs. Anti-Cancer Drugs. https://doi.org/10.1097/cad.0b013e328330fd90

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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