Unknown

Dataset Information

0

Synthesis of Curcuminoids and Evaluation of Their Cytotoxic and Antioxidant Properties.


ABSTRACT: Curcumin (1) and ten derivatives (2-11) were synthesized and evaluated as cytotoxic and antioxidant agents. The results of primary screening by Sulforhodamine B assay against five human cancer cell lines (U-251 MG, glioblastoma; PC-3, human prostatic; HCT-15, human colorectal; K562, human chronic myelogenous leukemia; and SKLU-1, non-small cell lung cancer) allowed us to calculate the half maximal inhibitory concentration (IC50) values for the more active compounds against HCT-15 and K562 cell lines. Compounds 2 and 10 were the most active against both cell lines and were more active than curcumin itself. Thiobarbituric acid reactive substances (TBARS) assay showed that 7 has potent activity; even stronger than curcumin, ?-tocopherol, and quercetin.

SUBMITTER: Lozada-Garcia MC 

PROVIDER: S-EPMC6154528 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications


Curcumin (<b>1</b>) and ten derivatives (<b>2</b>-<b>11</b>) were synthesized and evaluated as cytotoxic and antioxidant agents. The results of primary screening by Sulforhodamine B assay against five human cancer cell lines (U-251 MG, glioblastoma; PC-3, human prostatic; HCT-15, human colorectal; K562, human chronic myelogenous leukemia; and SKLU-1, non-small cell lung cancer) allowed us to calculate the half maximal inhibitory concentration (IC<sub>50</sub>) values for the more active compound  ...[more]

Similar Datasets

| S-EPMC8003642 | biostudies-literature
| S-EPMC8624111 | biostudies-literature
| S-EPMC8588455 | biostudies-literature
| S-EPMC6100566 | biostudies-literature
| S-EPMC6155822 | biostudies-other
| S-EPMC5942545 | biostudies-literature
| S-EPMC8229286 | biostudies-literature
| S-EPMC5373518 | biostudies-literature
| S-EPMC6271338 | biostudies-literature
| S-EPMC4265329 | biostudies-literature