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P-glycoprotein Inhibitor HM30181AK
Known as:
HM30181AK
, Pgp Inhibitor HM30181AK
, HM30181A
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An inhibitor of the adenosine triphosphate (ATP)-binding cassette (ABC) transporter P-glycoprotein (P-gp), with adjuvant activity. Upon oral…
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
KX-ORAX-001: An open label, randomized, multicenter, phase III registrational study to determine the safety, tolerability, and tumor response of oraxol (HM30181A + oral paclitaxel) and its…
Gerardo Antonio Umanzor Funez
,
R. Vassallo
,
+10 authors
F. J. Barrios
Journal of Clinical Oncology
2019
Corpus ID: 190859769
TPS1116 Background: Paclitaxel is used in multiple cancer types including the treatment of breast cancer after failure of…
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2018
2018
A phase I study to evaluate safety, tolerability, pharmacokinetics and activity of oraxol in patients (pts) with advanced malignancies.
W. Ma
,
N. Azad
,
+12 authors
A. Jimeno
2018
Corpus ID: 80810603
2526Background: Oraxol is an oral formulation of paclitaxel (PTX) co-administered with the potent, selective, poorly absorbed, P…
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2018
2018
Oral paclitaxel and HM30181A demonstrate clinical activity in metastatic breast cancer (MBC) patients.
M. Dai
,
T. Chao
,
+11 authors
T. Hung
Annals of Oncology
2018
Corpus ID: 81341121
2015
2015
Phase I/II Study of Weekly Oraxol for the Second-Line Treatment of Patients With Metastatic or Recurrent Gastric Cancer.
Keun-Wook Lee
,
K. Lee
,
+9 authors
Y. Bang
The Oncologist
2015
Corpus ID: 33922133
BACKGROUND Oraxol consists of paclitaxel and HM30181A, a P-glycoprotein inhibitor, to increase the oral bioavailability of…
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2014
2014
A Phase I Study of Oral Paclitaxel with a Novel P-Glycoprotein Inhibitor, HM30181A, in Patients with Advanced Solid Cancer
H. J. Lee
,
D. Heo
,
+9 authors
Y. Bang
Cancer research and treatment : official journal…
2014
Corpus ID: 11088269
Purpose The purpose of this study is to determine the maximum tolerated dose (MTD), safety, pharmacokinetics, and recommended…
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2008
2008
Oral paclitaxel chemotherapy for brain tumors: ideal combination treatment of paclitaxel and P-glycoprotein inhibitor.
K. Joo
,
Kwan Park
,
+5 authors
D. Nam
Oncology Report
2008
Corpus ID: 16128257
Oral chemotherapy has many advantages over parenteral chemotherapeutics administration. To use the advantages of the oral…
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2008
2008
Response of brain specific microenvironment to P-glycoprotein inhibitor: an important factor determining therapeutic effect of P-glycoprotein inhibitor on brain metastatic tumors.
K. Joo
,
S. Song
,
+7 authors
D. Nam
International Journal of Oncology
2008
Corpus ID: 18055481
P-glycoprotein (P-gp), a factor responsible for the multidrug resistance of tumors, is specifically expressed in brain…
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2008
2008
Effectively targeting BRAF in melanoma: a formidable challenge
L. Fecher
,
R. Amaravadi
,
L. Schuchter
Pigment Cell & Melanoma Research
2008
Corpus ID: 10287246
Since the finding of activating mutation of BRAF in cutaneous melanoma we have learned to appreciate the remarkable diversity of…
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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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