Autor: |
Harsha, Kachigere B., Swaroop, Toreshettahally R., Roopashree, Rangaswamy, Jagadish, Swamy, Rangappa, Kanchugarakoppal S. |
Zdroj: |
Chemical Data Collections; August 2018, Vol. 15 Issue: 1 p223-228, 6p |
Abstrakt: |
Synthesis of a series of 2-(arylmethylthio)-6-ethyl-7H-pyrrolo[2,3-d]pyrimidin-4-ol and their cytotoxic activity on HCT-116 and A-549 cell lines using MTT assay is reported. The 6-ethyl-2-((4-fluorobenzyl)thio)-7H-pyrrolo[2,3-d]pyrimidin-4-ol 3dis the most active compound on HCT-116 with IC50of 8.65 ± 0.36 µM. On the other hand, 6-ethyl-2-((3-nitrobenzyl)thio)-7H-pyrrolo[2,3-d]pyrimidin-4-ol 3iand 2-((2-bromo‑3,4-dimethoxybenzyl)thio)-6-ethyl-7H-pyrrolo[2,3-d]pyrimidin-4-ol 3jexhibited high activities on A-549 with IC50values 2.7 ± 0.49 µM and 2.21 ± 0.66 µM respectively. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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