Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 221,021,028 papers from all fields of science
Search
Sign In
Create Free Account
zosuquidar trihydrochloride
Known as:
(2R)-anti-5-(3-(4-(10,11-difluoromethanodibenzo-suber-5-yl)piperazin-1-yl)2-hydroxypropoxy)quinoline trihydrochloride
, (R)-4-((1aR,6R,10bS)-1,2-Difluoro-1,1a,6,10b-tetrahydrodibenzo(a,e)cyclopropa(c)cycloheptan-6-yl)-alpha-((5-quinoloyloxy)methyl)-1-piperazineethanol, Trihydrochloride
A difluorocyclopropyl quinoline. Zosuquidar trihydrochloride binds with high affinity to P-glycoprotein and inhibits P-glycoprotein-mediated…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
5 relations
Broader (2)
Dibenzocycloheptenes
Quinolines
Narrower (1)
LY335979
Zosuquidar
cytarabine/daunorubicin/zosuquidar trihydrochloride
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Nucleus Accumbens AMPA Receptors Are Necessary for Morphine-Withdrawal-Induced Negative-Affective States in Rats
Shayla Russell
,
Daniel J. Puttick
,
+4 authors
E. Chartoff
Journal of Neuroscience
2016
Corpus ID: 41268587
Dependence is a hallmark feature of opiate addiction and is defined by the emergence of somatic and affective withdrawal signs…
Expand
Highly Cited
2011
Highly Cited
2011
Endoxifen, the Active Metabolite of Tamoxifen, Is a Substrate of the Efflux Transporter P-Glycoprotein (Multidrug Resistance 1)
W. Teft
,
Sara E. Mansell
,
R. Kim
Drug Metabolism And Disposition
2011
Corpus ID: 15964155
Tamoxifen is widely prescribed to patients with estrogen receptor-positive breast cancer, and it is a prodrug that requires…
Expand
2003
2003
A population pharmacokinetic model for doxorubicin and doxorubicinol in the presence of a novel MDR modulator, zosuquidar trihydrochloride (LY335979)
S. Callies
,
D. D. de Alwis
,
James G. Wright
,
A. Sandler
,
Michael F. Burgess
,
L. Aarons
Cancer Chemotherapy and Pharmacology
2003
Corpus ID: 21463021
Abstract Purpose. To develop a population pharmacokinetic model for doxorubicin and doxorubicinol in the presence of zosuquidar…
Expand
Highly Cited
2001
Highly Cited
2001
Effects of WAY100635, a selective 5-HT1A-receptor antagonist on the micturition-reflex pathway in the rat.
H. Kakizaki
,
M. Yoshiyama
,
T. Koyanagi
,
W. D. de Groat
American Journal of Physiology. Regulatory…
2001
Corpus ID: 7980221
5-Hydroxytryptamine (5-HT) receptors in the central nervous system have been implicated in the control of micturition. The…
Expand
Highly Cited
2000
Highly Cited
2000
Selective inhibition of cyclooxygenase-2 enhances mitomycin-C-induced apoptosis
C. Hsueh
,
C. Chiu
,
D. Kelsen
,
G. Schwartz
Cancer Chemotherapy and Pharmacology
2000
Corpus ID: 7666645
Purpose: Cyclooxygenase-2 (COX-2) is involved in antiapoptosis signaling, and its induction may require activation of protein…
Expand
1999
1999
The 5-HT1A receptor agonist Bay x 3702 inhibits apoptosis induced by serum deprivation in cultured neurons.
B. Ahlemeyer
,
A. Glaser
,
C. Schaper
,
I. Semkova
,
J. Krieglstein
European Journal of Pharmacology
1999
Corpus ID: 23298337
Highly Cited
1997
Highly Cited
1997
Autoradiographic localization of 5-HT1A receptors in the post-mortem human brain using [3H]WAY-100635 and [11C]WAY-100635
H. Hall
,
C. Lundkvist
,
+8 authors
G. Sedvall
Brain Research
1997
Corpus ID: 7232072
Highly Cited
1997
Highly Cited
1997
Postsynaptic 5-HT1A receptors mediate 5-hydroxytryptamine release in the amygdala through a feedback to the caudal linear raphe.
F. Bosker
,
A. Klompmakers
,
H. Westenberg
European Journal of Pharmacology
1997
Corpus ID: 24592128
Highly Cited
1994
Highly Cited
1994
Evaluation of [O-methyl-3H]WAY-100635 as an in vivo radioligand for 5-HT1A receptors in rat brain.
S. Hume
,
S. Ashworth
,
+6 authors
A. C. White
European Journal of Pharmacology
1994
Corpus ID: 4550717
Highly Cited
1978
Highly Cited
1978
Diacridines, bifunctional intercalators. Chemistry and antitumor activity.
T. K. Chen
,
R. Fico
,
E. Canellakis
Journal of Medicinal Chemistry
1978
Corpus ID: 29897429
The synthesis and the characterization of a number of diacridines connected through the 9-amino position of the acridine rings by…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE