[HTML][HTML] The novel bis-benzylisoquinoline PY35 reverses P-glycoprotein-mediated multidrug resistance

Z Cao, M Wright, J Cheng, X Huang… - Oncology …, 2014 - spandidos-publications.com
Multidrug resistance (MDR) to chemotherapeutic drugs is the main cause of chemotherapy
failure in cancer treatment, and it generally results from expression of ATP-dependent efflux …

Reversal of P-glycoprotein-mediated multidrug resistance by the novel tetrandrine derivative W6

H Sun, XD Liu, Q Liu, FP Wang, XQ Bao… - Journal of Asian natural …, 2015 - Taylor & Francis
Overexpression of ATP-dependent efflux pump P-glycoprotein (P-gp) is the main cause of
multidrug resistance (MDR) and chemotherapy failure in cancer treatment. Inhibition of P-gp …

[HTML][HTML] ZD6474 reverses multidrug resistance by directly inhibiting the function of P-glycoprotein

Y Mi, L Lou - British journal of cancer, 2007 - nature.com
Abstract P-glycoprotein (P-gp) pumps multiple types of drugs out of the cell, using energy
generated from ATP, and confers multidrug resistance (MDR) on cancer cells. ZD6474 is an …

[HTML][HTML] Development of a novel quinoline derivative as a P-glycoprotein inhibitor to reverse multidrug resistance in cancer cells

Y Zhou, P Chung, JY Ma, AK Lam, S Law, K Chan… - Biology, 2019 - mdpi.com
Multidrug resistance (MDR) is one of conventional cancer chemotherapy's limitations. Our
group previously synthesized a series of quinoline-based compounds in an attempt to …

In Vitro and in Vivo Reversal of P-Glycoprotein-mediated Multidrug Resistance by a Novel Potent Modulator, XR9576

P Mistry, AJ Stewart, W Dangerfield, S Okiji, C Liddle… - Cancer research, 2001 - AACR
The overexpression of P-glycoprotein (P-gp) on the surface of tumor cells causes multidrug
resistance (MDR). This protein acts as an energy-dependent drug efflux pump reducing the …

H1, a novel derivative of tetrandrine reverse P-glycoprotein-mediated multidrug resistance by inhibiting transport function and expression of P-glycoprotein

N Wei, H Sun, F Wang, G Liu - Cancer chemotherapy and pharmacology, 2011 - Springer
Purpose H1 is a novel derivative of tetrandrine (Tet). Here we investigate the ability of H1 to
reverse P-glycoprotein (Pgp)-mediated multidrug resistance (MDR) and its mechanisms …

HZ08 inhibits the multi-drug resistance on multiple sites as the substrate of p-glycoprotein

Y Feng, Y Hu, J Cen, KN Darshika, W Fang, Y Li… - European journal of …, 2013 - Elsevier
Overexpression of p-glycoprotein (p-gp) leads to the production of multi-drug resistance
(MDR) which could discharge various anti-tumor chemicals with structural heterogeneity …

[HTML][HTML] Novel quinoline compound derivatives of NSC23925 as potent reversal agents against P-glycoprotein-mediated multidrug resistance

X Quan, H Du, J Xu, X Hou, X Gong, Y Wu… - Frontiers in …, 2019 - frontiersin.org
Multidrug resistance is a serious problem and a common cause of cancer treatment failure,
leading to patient death. Although numerous reversal resistance inhibitors have been …

Simplified derivatives of tetrandrine as potent and specific P-gp inhibitors to reverse multidrug resistance in cancer chemotherapy

R Zeng, XM Yang, HW Li, X Li, Y Guan… - Journal of Medicinal …, 2023 - ACS Publications
Targeted inhibition of a drug efflux transporter P-glycoprotein (P-gp) is an important strategy
to reverse multidrug resistance in cancer chemotherapy. In this study, a rationally structural …

Substituted tetrahydroisoquinoline compound B3 inhibited P-glycoprotein-mediated multidrug resistance in-vitro and in-vivo

W Fang, Y Li, Y Cai, K Kang, F Yan… - Journal of Pharmacy …, 2007 - academic.oup.com
Abstract P-glycoprotein (P-gp) mediated multidrug resistance (MDR) is one of the main
obstacles in tumour chemotherapy. A promising approach to reverse MDR is the combined …