An Expedition on Synthetic Methodology of FDA-approved Anticancer Drugs (2018-2021)

被引:1
|
作者
Vishakha, S. [1 ]
Navneesh, N. [1 ]
Das Kurmi, Balak [2 ]
Das Gupta, Ghanshyam [2 ]
Verma, Sant Kumar [1 ]
Jain, Ankit [3 ]
Patel, Preeti [1 ]
机构
[1] ISF Coll Pharm, Dept Pharmaceut Chem & Anal, Moga 142001, Punjab, India
[2] ISF Coll Pharm, Dept Pharmaceut, Moga 142001, Punjab, India
[3] Texas A&M Univ, Dept Anim Sci, Kingsville, TX 78363 USA
关键词
FDA<bold>-</bold>approved anticancer drugs; synthetic approaches; target selectivity; anticancer agents; FDA between 2018 to 2021; therapeutic indication; INHIBITOR; DISCOVERY; POTENT; SELUMETINIB; NANOPARTICLES; RESISTANCE; LYMPHOMA; DELIVERY;
D O I
10.2174/0118715206259585240105051941
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New drugs being established in the market every year produce specified structures for selective biological targeting. With medicinal insights into molecular recognition, these begot molecules open new rooms for designing potential new drug molecules. In this review, we report the compilation and analysis of a total of 56 drugs including 33 organic small molecules (Mobocertinib, Infigratinib, Sotorasib, Trilaciclib, Umbralisib, Tepotinib, Relugolix, Pralsetinib, Decitabine, Ripretinib, Selpercatinib, Capmatinib, Pemigatinib, Tucatinib, Selumetinib, Tazemetostat, Avapritinib, Zanubrutinib, Entrectinib, Pexidartinib, Darolutamide, Selinexor, Alpelisib, Erdafitinib, Gilteritinib, Larotrectinib, Glasdegib, Lorlatinib, Talazoparib, Dacomitinib, Duvelisib, Ivosidenib, Apalutamide), 6 metal complexes (Edotreotide Gallium Ga-68, fluoroestradiol F-18, Cu 64 dotatate, Gallium 68 PSMA-11, Piflufolastat F-18, 177Lu (lutetium)), 16 macromolecules as monoclonal antibody conjugates (Brentuximabvedotin, Amivantamab-vmjw, Loncastuximabtesirine, Dostarlimab, Margetuximab, Naxitamab, Belantamabmafodotin, Tafasitamab, Inebilizumab, SacituzumabGovitecan, Isatuximab, Trastuzumab, Enfortumabvedotin, Polatuzumab, Cemiplimab, Mogamulizumab) and 1 peptide enzyme (Erwiniachrysanthemi-derived asparaginase) approved by the U.S. FDA between 2018 to 2021. These drugs act as anticancer agents against various cancer types, especially non-small cell lung, lymphoma, breast, prostate, multiple myeloma, neuroendocrine tumor, cervical, bladder, cholangiocarcinoma, myeloid leukemia, gastrointestinal, neuroblastoma, thyroid, epithelioid and cutaneous squamous cell carcinoma. The review comprises the key structural features, approval times, target selectivity, mechanisms of action, therapeutic indication, formulations, and possible synthetic approaches of these approved drugs. These crucial details will benefit the scientific community for futuristic new developments in this arena.
引用
收藏
页码:590 / 626
页数:37
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