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Tetrahydroisoquinolines - an updated patent review for cancer treatment (2016-present)
被引:0
|作者:
Tanwar, Ankur Kumar
[1
]
Sengar, Neha
[1
]
Mase, Nobuyuki
[2
]
Singh, Inder Pal
[1
]
机构:
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Nat Prod, Sect 67, Sas Nagar 160062, Punjab, India
[2] Shizuoka Univ, Res Inst Green Sci & Technol, Hamamatsu, Shizuoka, Japan
关键词:
Cancer;
anticancer agents;
cancer targets;
1,2,3,4-tetrahydroisoquinoline;
PRMT5;
HPK1;
Bcl-xL;
HISTONE DEACETYLASE INHIBITORS;
X-LINKED INHIBITOR;
LUNG-CANCER;
ANTITUMOR-ACTIVITY;
ACID-DERIVATIVES;
PROTEIN;
PHOSPHODIESTERASE-4;
ACTIVATION;
KW2152;
RAS;
D O I:
10.1080/13543776.2024.2391288
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
IntroductionCancer is a prominent cause of death globally, triggered by both non-genetic and genetic alterations in genes influenced by various environmental factors. The tetrahydroisoquinoline (THIQ), specifically 1,2,3,4-tetrahydroisoquinoline serves as fundamental element in various alkaloids, prevalent in proximity to quinoline and indole alkaloids.Area coveredIn this review, the therapeutic applications of THIQ derivatives as an anticancer agent from 2016 to 2024 have been examined. The patents were gathered through comprehensive searches of the Espacenet, Google patent, WIPO, and Sci Finder databases. The therapeutic areas encompassed in the patents include numerous targets of cancer.Expert OpinionTHIQ analogues play a crucial role in medicinal chemistry, with many being integral to pharmacological processes and clinical trials. Numerous THIQ compounds have been synthesized for therapeutic purposes, notably in cancer treatment. They show great promise for developing anticancer drugs, demonstrating strong affinity and efficacy against various cancer targets. The creation of multi-target ligands is a compelling avenue for THIQ-based anticancer drug discovery.
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页码:873 / 906
页数:34
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