Unknown

Dataset Information

0

The anti-HIV actions of 7- and 10-substituted camptothecins.


ABSTRACT: Camptothecin (CPT), a traditional anti-tumor drug, has been shown to possess anti-HIV-1 activity. To increase the antiviral potency, the anti-HIV activities of two CPT derivatives, 10-hydroxy-CPT and 7-hydroxymethyl-CPT, were evaluated in vitro. The therapy index (TI) of CPT, 10-hydroxy-CPT and 7-hydroxymethyl-CPT against HIV-1(IIIB) in C8166 were 24.2, 4.2 and 198.1, and against clinical isolated strain HIV-1(KM018) in PBMC were 10.3, 3.5 and 66.0, respectively. While the TI of CPT, 10-hydroxy-CPT and 7-hydroxymethyl-CPT against HIV-2(CBL-20) were 34.5, 10.7 and 317.0, respectively, and the TI of the three compounds against HIV-2(ROD) showed the similar values. However, when the antiviral mechanisms were considered, we found there was no inhibition of 7-hydroxymethyl-CPT on viral cell-to-cell transmission, and was no inhibition on reverse transcriptase, protease or integrase in cell-free systems. 7-Hydroxymethyl-CPT showed no selective killing of chronically infected cells after 3 days of incubation. In conclusion, 7-hydroxymethyl-CPT showed more potent anti-HIV activity, while 10-hydroxy-CPT had less efficient activity, compared with the parent CPT. Though the antiviral mechanisms remain to be further elucidated; the modification of -OH residues at C-7 of CPT could enhance the antiviral activity, while of -OH residues at C-10 of CPT had decreased the antiviral activity, which provides the preliminary modification strategy for anti-viral activities enhancement of this compound.

SUBMITTER: Li YY 

PROVIDER: S-EPMC6256925 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC4102066 | biostudies-literature
| S-EPMC1951479 | biostudies-literature
| S-EPMC7127420 | biostudies-literature
| S-EPMC5406285 | biostudies-literature
| S-EPMC6362671 | biostudies-other
| S-EPMC5890519 | biostudies-literature
| S-EPMC3785711 | biostudies-other
| S-EPMC7531226 | biostudies-literature
| S-EPMC5890500 | biostudies-literature
| S-EPMC9316519 | biostudies-literature