Synthesis and cytotoxicity of diastereomeric benzylamides derived from maslinic acid, augustic acid and bredemolic acid
Tài liệu tham khảo
Siewert, 2013, Esters and amides of maslinic acid trigger apoptosis in human tumor cells and alter their mode of action with respect to the substitution pattern at C-28, Eur. J. Med. Chem., 70, 259, 10.1016/j.ejmech.2013.10.016
Siewert, 2014, Towards cytotoxic and selective derivatives of maslinic acid, Bioorg. Med. Chem., 22, 594, 10.1016/j.bmc.2013.10.047
Cheng, 2008, Practical synthesis of bredemolic acid, a natural inhibitor of glycogen phosphorylase, J. Nat. Prod., 71, 1877, 10.1021/np8003886
Sommerwerk, 2015, Straightforward partial synthesis of four diastereomeric 2,3-dihydroxy-olean-12-en-28-oic acids from oleanolic acid, Tetrahedron, 71, 8528, 10.1016/j.tet.2015.09.037
Tschesche, 1963, Structure of bredemolic acid and the partial synthesis of its methyl ester from methyl oleanolate, Tetrahedron Lett., 4, 613, 10.1016/S0040-4039(01)90684-7
Tschesche, 1960, The sapogenins of Bredemeyera floribunda, Ber., 93, 1903
Choudhary, 2021, Medicinal uses of maslinic acid: a review, J. Drug Delivery Ther., 11, 237, 10.22270/jddt.v11i2.4588
Jing, 2021, Review of the biological activity of maslinic acid, Curr. Drug Targets, 22, 1496, 10.2174/1389450122666210308111159
Lin, 2018, Maslinic acid as an effective anticancer agent, Cell Mol. Biol. (Noisy-le-grand), 64, 87, 10.14715/cmb/2018.64.10.14
Lozano-Mena, 2014, Maslinic acid, a natural phytoalexin-type triterpene from olives - a promising nutraceutical?, Molecules, 19, 11538, 10.3390/molecules190811538
Qian, 2021, Corosolic acid and its structural analogs: A systematic review of their biological activities and underlying mechanism of action, Phytomedicine, 91, 10.1016/j.phymed.2021.153696
Yu, 2021, The anticancer potential of maslinic acid and its derivatives: a review, Drug Des. Devel. Ther., 15, 3863, 10.2147/DDDT.S326328
Alam, 1996, Oleanene and stigmasterol derivatives from Ambroma augusta, Phytochemistry, 41, 1197, 10.1016/0031-9422(95)00774-1
Briskorn, 1970, Presence of three additional triterpenic acids in Rosmarinus officinalis leaves, Pharmazie, 25, 488
Wen, 2008, Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies, J. Med. Chem., 51, 3540, 10.1021/jm8000949
Bag, 2020, Terpenoids, ano-entities and molecular self-assembly, Pure Appl. Chem., 92, 567, 10.1515/pac-2019-0812
Kahnt, 2018, Transformation of asiatic acid into a mitocanic, bimodal-acting rhodamine B conjugate of nanomolar cytotoxicity, Eur. J. Med. Chem., 159, 143, 10.1016/j.ejmech.2018.09.066
Sommerwerk, 2017, Rhodamine B conjugates of triterpenoic acids are cytotoxic mitocans even at nanomolar concentrations, Eur. J. Med. Chem., 127, 1, 10.1016/j.ejmech.2016.12.040
Sommerwerk, 2016, Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell lines, Eur. J. Med. Chem., 119, 1, 10.1016/j.ejmech.2016.04.051
Zheng, 2010, Inhibition of DNA topoisomerases I and II and cytotoxicity of compounds from Ulmus davidiana var. japonica, Arch. Pharm. Res., 33, 1307, 10.1007/s12272-010-0903-0
