Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,206,844 papers from all fields of science
Search
Sign In
Create Free Account
AT 1015
Known as:
AT-1015
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2004
Review
2004
Randomized trial of AT-1015 for treatment of intermittent claudication. A novel 5-hydroxytryptamine antagonist with no evidence of efficacy
William R. Hiatt
,
Alan T. Hirsch
,
John P. Cooke
,
Jeffrey W. Olin
,
D. Brater
,
M. Creager
Vascular Medicine
2004
Corpus ID: 35082535
AT-1015 is a novel selective 5-HT2A serotonin receptor antagonist that is known to impair platelet aggregation and…
Expand
2004
2004
Safety of AT-1015, a novel 5-HT2A antagonist, in combination with high-dose aspirin: an open-label study.
D. Anderson
,
N. Kato
,
+4 authors
J. Ilgenfritz
International journal of clinical pharmacology…
2004
Corpus ID: 30038506
OBJECTIVE To assess the safety of AT-1015 in combination with high-dose aspirin (300 mg daily). Study subjects were 17 healthy…
Expand
2003
2003
Insurmountable antagonism of AT‐1015, a 5‐HT2 antagonist, on serotonin‐induced endothelium‐dependent relaxation in porcine coronary artery
M. Rashid
,
M. Nakazawa
,
T. Nagatomo
The Journal of pharmacy and pharmacology
2003
Corpus ID: 26468911
The purpose of this study was to examine the inhibitory effects of AT‐1015, a newly synthesized 5‐HT2 receptor antagonist, on…
Expand
2002
2002
AT‐1015, a newly synthesized 5‐HT2 receptor antagonist, dissociates slowly from the 5‐HT2 receptor sites in rabbit cerebral cortex membrane
M. Rashid
,
Masatomo Watanabe
,
M. Nakazawa
,
T. Nagatomo
The Journal of pharmacy and pharmacology
2002
Corpus ID: 6005623
The purpose of this study was to investigate the association and dissociation kinetics of [3H]AT‐1015 from 5‐HT2 receptors in…
Expand
2001
2001
Assessment of affinity and dissociation ability of a newly synthesized 5-HT2 antagonist, AT-1015: comparison with other 5-HT2 antagonists.
M. Rashid
,
M. Watanabe
,
M. Nakazawa
,
T. Nakamura
,
K. Hattori
,
T. Nagatom
Japanese Journal of Pharmacology
2001
Corpus ID: 25555279
This study investigated the binding affinities of a newly synthesized 5-HT2 antagonist, AT-1015 (N-[2-[4-(5H-dibenzo[a,d…
Expand
2001
2001
Binding affinity of a newly synthesized 5-HT2 antagonist, AT-1015 (N-[2-[4-(5H-Dibenzo[a,d]cyclohepten-5-ylidene)-piperidino]ethyl]-1-formyl-4-piperidinecarboxamide monohydrochloride monohydrate), in…
Mamunur Rashid
,
Masatomo Watanabe
,
M. Nakazawa
,
T. Nagatomo
Biological and Pharmaceutical Bulletin
2001
Corpus ID: 40345401
The object of this study was to investigate the binding affinity of a newly synthesized 5-HT2 antagonist, (N-[2-[4-(5H-dibenzo[a…
Expand
2000
2000
Inhibitory effects of a newly synthesized 5-HT2 receptor antagonist, AT-1015 (N-[2-[4-(5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidino]-ethyl]-1-for myl-4-piperidinecarboxamide monohydrochloride…
H. Gong
,
M. Rashid
,
+5 authors
T. Nagatomo
Biological and Pharmaceutical Bulletin
2000
Corpus ID: 24223489
Inhibitory effects of a newly synthesized 5-HT2 receptor antagonist, AT-1015 (N-[2-[4-(5H-dibenzo[a,d]cyclohepten-5-ylidene…
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