2022
DOI: 10.1007/s43440-021-00345-w
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Antiproliferative pharmacophore azo-hydrazone analogue BT-1F exerts death signalling pathway targeting STAT3 in solid tumour

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Cited by 4 publications
(3 citation statements)
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“…Furthermore, compound 10 attenuated solid tumor growth without inducing significant toxicological side effects. Recently, Banumathi et al showed that the azo-hydrazone analog 10 (Figure 9) exerted chemosensitivity specifically against EAC and A549 cells without altering their normal counterpart [113]. It was found that the antiproliferative activity of 10 was due to the induction of apoptosis by inhibiting the STAT3 signal.…”
Section: Antitumor Actionmentioning
confidence: 99%
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“…Furthermore, compound 10 attenuated solid tumor growth without inducing significant toxicological side effects. Recently, Banumathi et al showed that the azo-hydrazone analog 10 (Figure 9) exerted chemosensitivity specifically against EAC and A549 cells without altering their normal counterpart [113]. It was found that the antiproliferative activity of 10 was due to the induction of apoptosis by inhibiting the STAT3 signal.…”
Section: Antitumor Actionmentioning
confidence: 99%
“…According to the evaluation of Lis et al, acylhydrazone 9 (Figure 8) induced apoptosis in erlotinib-resistant neoplasms as a result of selective STAT3 inhibition [40]. Recently, Banumathi et al showed that the azo-hydrazone analog 10 (Figure 9) exerted chemosensitivity specifically against EAC and A549 cells without altering their normal counterpart [113]. It was found that the antiproliferative activity of 10 was due to the induction of apoptosis by inhibiting the STAT3 signal.…”
Section: Antitumor Actionmentioning
confidence: 99%
“…1 Introduction 4-Hydrazonyl quinazolines are compounds that hybridize two pharmacophore cores: a quinazoline 1,2 and a hydrazone. 3,4 Quinazolines constitute a class of heterocycles that contain two fused aromatic benzene and pyrimidine rings and exhibit a plethora of biological activities. [5][6][7][8][9][10] Hydrazones contain a characteristic R 1 R 2 CvN-NHR 3 functional group which due to its isomerization and nucleophilic, electrophilic and acidic sites gives rise to versatile uses of their carrier compounds.…”
mentioning
confidence: 99%