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pravadoline
Known as:
Methanone, (4-methoxyphenyl)(2-methyl-1-(2-(4-morpholinyl)ethyl)-1H-indol-3-yl)-
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Indoles
pravadoline maleate
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Use of SPME-HS-GC-MS for the analysis of herbal products containing synthetic cannabinoids.
A. Cox
,
R. Daw
,
+7 authors
J. Huffman
Journal of Analytical Toxicology
2012
Corpus ID: 15736664
The increasing prevalence and use of herbal mixtures containing synthetic cannabinoids presents a growing public health concern…
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Highly Cited
1998
Highly Cited
1998
The bioactive conformation of aminoalkylindoles at the cannabinoid CB1 and CB2 receptors: insights gained from (E)- and (Z)-naphthylidene indenes.
P. Reggio
,
S. Basu-Dutt
,
+9 authors
M. Abood
Journal of Medicinal Chemistry
1998
Corpus ID: 35926724
The aminoalkylindoles (AAIs) are agonists at both the cannabinoid CB1 and CB2 receptors. To determine whether the s-trans or s…
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1998
1998
Structure-Activity Relationships of Indole-and Pyrrole-Derived Cannabinoids 1
J. Wiley
,
D. R. Compton
,
+4 authors
B. Martin
1998
Corpus ID: 20342580
Early molecular modeling studies with D-tetrahydrocannabinol (D-THC) reported that three discrete regions which interact with…
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1996
1996
(Aminoalkyl)indole isothiocyanates as potential electrophilic affinity ligands for the brain cannabinoid receptor.
K. Yamada
,
K. Rice
,
+4 authors
A. Howlett
Journal of Medicinal Chemistry
1996
Corpus ID: 28657840
A series of (aminoalkyl)indole compounds, naphthalene analogs of pravadoline (1), has been shown to exhibit cannabinoid agonist…
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Highly Cited
1992
Highly Cited
1992
Conformationally restrained analogues of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor.
T. D'ambra
,
K. Estep
,
+7 authors
Beglin Nc
Journal of Medicinal Chemistry
1992
Corpus ID: 42366456
Pravadoline (1) is an (aminoalkyl)indole analgesic agent which is an inhibitor of cyclooxygenase and, in contrast to other NSAIDs…
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Highly Cited
1992
Highly Cited
1992
Aminoalkylindole analogs: cannabimimetic activity of a class of compounds structurally distinct from delta 9-tetrahydrocannabinol.
D. R. Compton
,
Lisa H. Gold
,
Susan J. Ward
,
R. Balster
,
Billy R. Martin
Journal of Pharmacology and Experimental…
1992
Corpus ID: 23195692
Six novel aminoalkylindole analogs, related structurally to the dual cyclooxygenase inhibitor and nonopioid analgesic pravadoline…
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Highly Cited
1991
Highly Cited
1991
Antinociceptive (aminoalkyl)indoles.
M. Bell
,
T. D'ambra
,
+7 authors
D. Hlasta
Journal of Medicinal Chemistry
1991
Corpus ID: 41173624
The (aminoalkyl)indole (AAI) derivative pravadoline (1a) inhibited prostaglandin (PG) synthesis in mouse brain microsomes in…
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1990
1990
Pharmacology of pravadoline: a new analgesic agent.
D. Haubrich
,
S. Ward
,
+7 authors
J. K. Saelens
Journal of Pharmacology and Experimental…
1990
Corpus ID: 6750746
Pravadoline is a new chemical entity with analgesic activity in humans. This report describes the pharmacology of pravadoline and…
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1990
1990
Pravadoline: profile in isolated tissue preparations.
S. Ward
,
D. Mastriani
,
F. Casiano
,
R. Arnold
Journal of Pharmacology and Experimental…
1990
Corpus ID: 2165644
Pravadoline is a novel cyclooxygenase-inhibiting analgesic with a preclinical profile of activity in vivo clearly distinct from…
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1989
1989
Pravadoline and aminoalkylindole (AAI) analogues: actions which suggest a receptor interaction.
S. Ward
,
S. Childers
,
M. Pacheco
British Journal of Pharmacology
1989
Corpus ID: 34448319
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