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HM-30181
Known as:
HM30181
National Institutes of Health
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2019
2019
Affinity-based Protein Profiling Reveals Cellular Targets of Photoreactive Anticancer Inhibitors.
Nan Ma
,
Zhi-Min Zhang
,
+7 authors
Zhengqiu Li
ACS Chemical Biology
2019
Corpus ID: 208185478
Affinity-based protein profiling has proven to be a powerful method in target identification of bioactive molecules. Here this…
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2016
2016
Effect of HM30181 mesylate salt-loaded microcapsules on the oral absorption of paclitaxel as a novel P-glycoprotein inhibitor.
Jin Cheul Kim
,
Kyeong Soo Kim
,
+9 authors
Han‐Gon Choi
International journal of pharmaceutics
2016
Corpus ID: 12499999
Highly Cited
2015
Highly Cited
2015
HM30181 Derivatives as Novel Potent and Selective Inhibitors of the Breast Cancer Resistance Protein (BCRP/ABCG2).
Sebastian C Köhler
,
M. Wiese
Journal of Medicinal Chemistry
2015
Corpus ID: 31017883
The breast cancer resistance protein (BCRP, ABCG2) belongs to the superfamily of ATP binding-cassette (ABC) proteins. In addition…
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2014
2014
Effects of HM30181, a P-glycoprotein inhibitor, on the pharmacokinetics and pharmacodynamics of loperamide in healthy volunteers.
Tae-Eun Kim
,
Howard Lee
,
+8 authors
Joo-Youn Cho
British Journal of Clinical Pharmacology
2014
Corpus ID: 1284879
AIMS HM30181 is a third generation P-glycoprotein (P-gp) inhibitor currently under development. The objectives of this study were…
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2013
2013
Sustained Increase in the Oral Bioavailability of Loperamide after a Single Oral Dose of HM30181, a P‐glycoprotein Inhibitor, in Healthy Male Participants
Y. Cha
,
Howard Lee
,
+8 authors
Joo-Youn Cho
Basic & Clinical Pharmacology & Toxicology
2013
Corpus ID: 44404979
HM30181 is a new P‐glycoprotein (P‐gp) inhibitor. This study was conducted to investigate the effect of HM30181 and its duration…
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2012
2012
Interaction of HM30181 with P-glycoprotein at the murine blood-brain barrier assessed with positron emission tomography.
Florian Bauer
,
T. Wanek
,
+8 authors
T. Erker
European Journal of Pharmacology
2012
Corpus ID: 28354135
Highly Cited
2010
Highly Cited
2010
Selective inhibition of MDR1 (ABCB1) by HM30181 increases oral bioavailability and therapeutic efficacy of paclitaxel.
Jin-Oh Kwak
,
Sung Hee Lee
,
+6 authors
Min Goo Lee
European Journal of Pharmacology
2010
Corpus ID: 3040524
2007
2007
Characterization of Human Liver Cytochrome P-450 Enzymes Involved in the O-demethylation of a New P-glycoprotein Inhibitor HM-30181
I. Paek
,
S. Kim
,
M. Kim
,
John Kim
,
Gwansun Lee
,
Hye Suk Lee
Journal of Toxicology and Environmental Health…
2007
Corpus ID: 1927513
HM-30181, 4-oxo-4H-chromene-2-carboxylic acid [2-(2-{4-[2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-phenyl}-2H…
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2006
2006
Simultaneous determination of paclitaxel and a new P-glycoprotein inhibitor HM-30181 in rat plasma by liquid chromatography with tandem mass spectrometry.
I. Paek
,
H. Ji
,
Maeng Seop Kim
,
Gwan Sun Lee
,
H. Lee
Journal of Separation Science
2006
Corpus ID: 23531293
An LC-MS/MS method for the simultaneous determination of a new P-glycoprotein inhibitor 4-oxo-4H-chromene-2-carboxylic acid [2-(2…
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2006
2006
Metabolism of a new P-glycoprotein inhibitor HM-30181 in rats using liquid chromatography/electrospray mass spectrometry.
I. Paek
,
H. Ji
,
M. Kim
,
Gwansun Lee
,
H. Lee
Rapid Communications in Mass Spectrometry
2006
Corpus ID: 6406737
HM-30181, 4-oxo-4H-chromene-2-carboxylic acid, [2-(2-{4-[2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-phenyl}-2H…
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