TY - JOUR
T1 - Calixarenes and their Relevance in Anticancer Drug Development
AU - Paul, Soumyajeet
AU - Jeyaprakash, Ramaiah Selladurai
AU - Pai, Aravinda
AU - Venkatachalam, Hillemane
AU - Jayashree, Bellur Srinivas
N1 - Publisher Copyright:
© 2023 Bentham Science Publishers.
PY - 2023
Y1 - 2023
N2 - Calixarenes have always captured the attention of several researchers. They have the ability to entrap multiple molecules and form inclusion complexes with drugs due to their unique structure. Due to this property, they are being widely used in the development of several classes of drugs, most notably anticancer drugs. This review attempted to summarize the potential applications of calixarenes and its derivatives in the development of anticancer drugs, with a focus on the delivery of drug classes such as DNA intercalators, taxanes, DNA alkylators, and topoisomerase inhibitors. Calixarene-based macromolecular chemistry could therefore have a high potential for overcoming the toxicity of cancer chemotherapy and achieving targeted drug delivery.
AB - Calixarenes have always captured the attention of several researchers. They have the ability to entrap multiple molecules and form inclusion complexes with drugs due to their unique structure. Due to this property, they are being widely used in the development of several classes of drugs, most notably anticancer drugs. This review attempted to summarize the potential applications of calixarenes and its derivatives in the development of anticancer drugs, with a focus on the delivery of drug classes such as DNA intercalators, taxanes, DNA alkylators, and topoisomerase inhibitors. Calixarene-based macromolecular chemistry could therefore have a high potential for overcoming the toxicity of cancer chemotherapy and achieving targeted drug delivery.
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U2 - 10.2174/1573406419666230703114605
DO - 10.2174/1573406419666230703114605
M3 - Short survey
C2 - 37403386
AN - SCOPUS:85175724870
SN - 1573-4064
VL - 19
SP - 939
EP - 945
JO - Medicinal Chemistry
JF - Medicinal Chemistry
IS - 10
ER -