Design and synthesis of Meldrum's acid based 7-azaindole anchored 1,2,3-triazole hybrids as anticancer agents

Vanga, Murali Krishna; Bhukya, Rambabu; Thumma, Vishnu; Ambadipudi, S. S. S. S. Sudha; Nayak, V. Lakshma; Andugulapati, Sai Balaji; Manga, Vijjulatha

doi:10.1039/d4md00015c

RSC Med. Chem.

2024

DOI: 10.1039/d4md00015c

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Design and synthesis of Meldrum's acid based 7-azaindole anchored 1,2,3-triazole hybrids as anticancer agents

Murali Krishna Vanga,

Rambabu Bhukya,

Vishnu Thumma

et al.

Abstract: A series of Meldrum’s acid, 7-azaindole and 1,2,3-triazole hybrids were synthesized and evaluated for their anticancer activity in five different cancer cell lines i.e.: MCF-7 (breast cancer), HeLa (cervical cancer),...

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Cited by 2 publications

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Synthesis, biological evaluation and molecular docking studies of tetrahydropyrido[3, 4-d]pyrimidine derivatives as anti-leukemic agents

Parashuram,

Aruna Kumari,

Charitha Mullaguri

et al. 2024

Results in Chemistry

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Synthesis, biological evaluation and molecular docking studies of tetrahydropyrido[3, 4-d]pyrimidine derivatives as anti-leukemic agents

Parashuram,

Aruna Kumari,

Charitha Mullaguri

et al. 2024

Results in Chemistry

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Design and synthesis of novel thiazolidinone hybrid as α-amylase inhibitor, glucose uptake and antioxidant activity

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Jakkawad,

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et al. 2024

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Design and synthesis of Meldrum's acid based 7-azaindole anchored 1,2,3-triazole hybrids as anticancer agents

Abstract: A series of Meldrum’s acid, 7-azaindole and 1,2,3-triazole hybrids were synthesized and evaluated for their anticancer activity in five different cancer cell lines i.e.: MCF-7 (breast cancer), HeLa (cervical cancer),...

Cited by 2 publications

References 55 publications

Synthesis, biological evaluation and molecular docking studies of tetrahydropyrido[3, 4-d]pyrimidine derivatives as anti-leukemic agents

Synthesis, biological evaluation and molecular docking studies of tetrahydropyrido[3, 4-d]pyrimidine derivatives as anti-leukemic agents

Design and synthesis of novel thiazolidinone hybrid as α-amylase inhibitor, glucose uptake and antioxidant activity

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