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Cited by 470

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Anti-AIDS Agents, 11. Betulinic Acid and Platanic Acid as Anti-HIV Principles from Syzigium claviflorum, and the Anti-HIV Activity of Structurally Related Triterpenoids

Open access
Fujioka, Toshihiro, Kashiwada, Yoshiki, Kilkuskie, Robert E., Cosentino, L. Mark, Ballas, Lawrence M., Jiang, Jack B., Janzen, William P., Chen, Ih-Sheng, Lee, Kuo-Hsiung·1994·Journal of Natural Products

Abstract

Betulinic acid [1] and platanic acid [2], isolated from the leaves of Syzigium claviforum, were found to be inhibitors of HIV replication in H9 lymphocyte cells. Evaluation of anti-HIV activity with eight derivatives of 1 revealed that dihydrobetulinic acid [3] was also a potent inhibitor of HIV replication. The C-3 hydroxy group and C-17 carboxylic acid group, as well as the C-19 substituents, contribute to enhanced anti-HIV activity. The inhibitory activity of these compounds against protein kinase C (PKC) was also examined, since a correlation between anti-HIV and anti-PKC activities has been suggested. However, there was no apparent correlation between anti-HIV activity and the inhibition of PKC among these compounds.

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Metadata

Authors
Fujioka, T., Kashiwada, Y., Kilkuskie, R. E., Cosentino, L. M., Ballas, L. M., Jiang, J. B., Janzen, W. P., Chen, I.-S., & Lee, K.-H.
Venue
Journal of Natural Products
Published
1994-02
Volume
57
Issue
2
Pages
243-247
ISSN
  • 0163-3864 (ISSN-L)
  • 1520-6025
OpenAlex
W2015002417
Cited by
470
References
0
FWCI
1.72
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Anti-AIDS Agents, 11. Betulinic Acid and Platanic Acid as Anti-HIV Principles from Syzigium claviflorum, and the Anti-HIV Activity of Structurally Related Triterpenoids. https://app.cochat.ai/papers/10.1021/np50104a008
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Fujioka, T., Kashiwada, Y., Kilkuskie, R. E., Cosentino, L. M., Ballas, L. M., Jiang, J. B., Janzen, W. P., Chen, I.-S., & Lee, K.-H. (1994). Anti-AIDS Agents, 11. Betulinic Acid and Platanic Acid as Anti-HIV Principles from Syzigium claviflorum, and the Anti-HIV Activity of Structurally Related Triterpenoids. Journal of Natural Products. https://doi.org/10.1021/np50104a008

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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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