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Synthesis and Anticancer Activity Study of Some Novel Substituted and Fused Pyridotriazepine Derivatives
Author(s) -
ElDeeb Moshira A.,
ElZoghbi Mona S.
Publication year - 2019
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.3447
Subject(s) - chemistry , derivative (finance) , pyrimidine , stereochemistry , cisplatin , in vitro , cell culture , combinatorial chemistry , biochemistry , medicine , surgery , chemotherapy , biology , financial economics , economics , genetics
Various new substituted and fused pyridotriazepine analogues have been synthesized via different synthetic pathways. Among which are different heterocyclic compounds consisting of the pyridotriazepine backbone fused to different heterocyclic systems comprising either substituted pyrimidine nucleus such as compounds 3 – 9 or substituted 4‐aminopyridine nucleus such as compounds 10 – 16 . Besides, the tetrahydroquinoline derivative 17 , [1,2,4]triazolopyrimidine derivative 18 , thienodiazocine derivative 19 , dihydrobenzofuropyridine derivative 20 , and the substituted pyrrole derivative 21 were synthesized. In addition, different substituted pyridotriazepine derivatives as indicated in compounds 22 – 25 were designed and synthesized. Twenty‐five of the newly synthesized compounds were subjected to in vitro anticancer screening against mammalian colon carcinoma HCT‐116 cell line using Cisplatin as a reference drug. The anticancer activity screening results revealed that among the tested compounds, the tetrahydropyrido[1,2‐ b ]pyrimido[4,5‐ e ][1,2,4]triazepine derivative 4 substituted at C 2 and C 4 positions with S ‐methyl and amino moieties, respectively, and the 2,4‐dithioxo analogue 9 and the 2‐thioxodipyrido[1,2‐ b :2′,3′‐ e ][1,2,4]triazepine derivative 11 substituted at C 3 and C 4 with a cyano and amino moieties, respectively, exhibited moderate to strong anticancer activity against mammalian colon carcinoma HCT‐116 cell line.