101110-74-1Relevant articles and documents
SYNTHESIS AND STRUCTURE CONFIRMATION OF RICCARDIN B, A MACROCYCLIC BIS(BIBENZYL) FROM THE LIVERWORT, RICCARDIA MULTIFIDA
Shiobara, Yoshinori,Sumitomo, Hisako,Tsukamoto, Michiyo,Harada, Chiemi,Kodama, Mitsuaki
, p. 1587 - 1588 (1985)
Riccardin B, a cytotoxic bis(bibenzyl) obtained from a liverwort was synthesized via an intramolecular Wittig-type reaction and the structure was established unequivocally.
Design, synthesis, biological evaluation and molecular modeling study of novel macrocyclic bisbibenzyl analogues as antitubulin agents
Sun, Bin,Li, Lin,Hu, Qing-wen,Zheng, Hong-bo,Tang, Hui,Niu, Huan-min,Yuan, Hui-qing,Lou, Hong-xiang
, p. 186 - 208 (2017/02/26)
A series of macrocyclic bisbibenzyls with novel skeletons was designed, synthesized, and evaluated for antiproliferative activity against five anthropic cancer cell lines. Among these novel molecules, compound 47 displayed excellent anticancer activity ag
Bisbibenzyl derivatives sensitize vincristine-resistant KB/VCR cells to chemotherapeutic agents by retarding P-gp activity
Xi, Guang-Min,Sun, Bin,Jiang, Hui-Hui,Kong, Feng,Yuan, Hui-Qing,Lou, Hong-Xiang
experimental part, p. 6725 - 6733 (2010/10/19)
P-glycoprotein (P-gp) is known to mediate multidrug resistance (MDR) by acting as an efflux pump to actively transport chemotherapeutic agents out of carcinoma cells. Inhibition of P-gp function may represent one of the strategies to reverse MDR. We have