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Vangala Santhosh Reddy

Researcher at Indian Institute of Chemical Technology

Publications -  17
Citations -  352

Vangala Santhosh Reddy is an academic researcher from Indian Institute of Chemical Technology. The author has contributed to research in topics: Tubulin & Cancer. The author has an hindex of 11, co-authored 17 publications receiving 301 citations. Previous affiliations of Vangala Santhosh Reddy include Council of Scientific and Industrial Research.

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Synthesis of β-carboline–benzimidazole conjugates using lanthanum nitrate as a catalyst and their biological evaluation

TL;DR: An in silico study of these β-carboline-benzimidazole conjugates reveals that they possess drug-like properties and substantiate the cytotoxic activity and the nature of interaction of these conjugate with DNA.
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Synthesis of phenstatin/isocombretastatin–chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers

TL;DR: A series of phenstatin/isocombretastatin–chalcones synthesized and screened for their cytotoxic activity against various human cancer cell lines showed a broad spectrum of antiproliferative efficacy on most of the cell lines in the sub-micromolar range.
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Synthesis of arylpyrazole linked benzimidazole conjugates as potential microtubule disruptors.

TL;DR: Investigations reveal that such conjugates having pyrazole and benzimidazole moieties have the potential in the development of newer chemotherapeutic agents.
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Design, synthesis and biological evaluation of imidazopyridine/imidazopyrimidine-benzimidazole conjugates as potential anticancer agents

TL;DR: The present study demonstrates that the synthesis of imidazopyridine/imidZopyrimidine-benzimidazole conjugates as promising tubulin inhibitors with G2/M phasecell cycle arrest and apoptotic-inducing ability.
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Synthesis and Biological Evaluation of Imidazopyridine–Oxindole Conjugates as Microtubule‐Targeting Agents

TL;DR: Flow cytometric analysis showed that MCF‐7 cells treated by these compounds arrested in the G2/M phase of the cell cycle in a concentration‐dependent manner, and docking of compound 10 f with tubulin protein suggested that the imidazo[1,2‐a]pyridine moiety occupies the colchicine binding site of tubulin.