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XR9576
Known as:
XR 9576
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
tariquidar
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Reversal of multidrug resistance by co-delivery of tariquidar (XR9576) and paclitaxel using long-circulating liposomes.
Niravkumar R. Patel
,
Alok Rathi
,
D. Mongayt
,
V. Torchilin
International journal of pharmaceutics
2011
Corpus ID: 24283334
2010
2010
Synthesis and evaluation of [11C]XR9576 to assess the function of drug efflux transporters using PET
K. Kawamura
,
F. Konno
,
+8 authors
Ming-Rong Zhang
Annals of Nuclear Medicine
2010
Corpus ID: 23029831
ObjectiveXR9576 (tariquidar) is an anthranilic acid derivative and potent P-glycoprotein (P-gp) inhibitor. XR9576 has undergone…
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2009
2009
Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators.
W. Klinkhammer
,
Henrik Müller
,
C. Globisch
,
I. Pajeva
,
M. Wiese
Bioorganic & Medicinal Chemistry
2009
Corpus ID: 24378644
Highly Cited
2009
Highly Cited
2009
A Phase I Study of the P-Glycoprotein Antagonist Tariquidar in Combination with Vinorelbine
J. Abraham
,
M. Edgerly
,
+10 authors
T. Fojo
Clinical Cancer Research
2009
Corpus ID: 24734948
Purpose: P-glycoprotein (Pgp) antagonists have had unpredictable pharmacokinetic interactions requiring reductions of…
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2005
2005
The coupling mechanism of P‐glycoprotein involves residue L339 in the sixth membrane spanning segment
A. Rothnie
,
J. Storm
,
R. McMahon
,
Andrewf . Taylor
,
I. Kerr
,
R. Callaghan
FEBS Letters
2005
Corpus ID: 34032519
2005
2005
Alterations in respiration rate of isolated rainbow trout hepatocytes exposed to the P-glycoprotein substrate rhodamine 123.
Onkar S. Bains
,
C. Kennedy
Toxicology
2005
Corpus ID: 21601951
Highly Cited
2003
Highly Cited
2003
Increased 99mTc-sestamibi accumulation in normal liver and drug-resistant tumors after the administration of the glycoprotein inhibitor, XR9576.
M. Agrawal
,
J. Abraham
,
+5 authors
Clara C. Chen
Clinical Cancer Research
2003
Corpus ID: 32285021
99mTc-sestamibi, a substrate of the multidrug transporter P-glycoprotein (Pgp), has been used as a functional imaging agent for…
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Highly Cited
2003
Highly Cited
2003
Fluoro-, bromo-, and iodopaclitaxel derivatives: synthesis and biological evaluation.
D. Kiesewetter
,
E. Jagoda
,
+5 authors
W. Eckelman
Nuclear Medicine and Biology
2003
Corpus ID: 35970303
Highly Cited
2001
Highly Cited
2001
In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576.
P. Mistry
,
A. Stewart
,
+6 authors
P. Charlton
Cancer Research
2001
Corpus ID: 18917796
The overexpression of P-glycoprotein (P-gp) on the surface of tumor cells causes multidrug resistance (MDR). This protein acts as…
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Highly Cited
2000
Highly Cited
2000
Phase I trial of XR9576 in healthy volunteers demonstrates modulation of P-glycoprotein in CD56+ lymphocytes after oral and intravenous administration.
A. Stewart
,
J. Steiner
,
G. Mellows
,
B. Laguda
,
D. Norris
,
P. Bevan
Clinical Cancer Research
2000
Corpus ID: 6946367
XR9576 is a novel inhibitor of P-glycoprotein (P-gp) that has been shown to reverse P-gp-dependent multidrug-resistance in tumor…
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