The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
25470070 |
81 |
Probing the carboxyester side chain in controlled deactivation (-)-d(8)-tetrahydrocannabinols. |
Northeastern University |
1732519 |
15 |
Conformationally restrained analogues of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor. |
Sterling Research Group |
1317925 |
6 |
A novel probe for the cannabinoid receptor. |
Hebrew University |
1659638 |
8 |
Synthesis and pharmacological evaluation of ether and related analogues of delta 8-, delta 9-, and delta 9,11-tetrahydrocannabinol. |
Virginia Commonwealth University |
27096053 |
4 |
Discovery of KLS-13019, a Cannabidiol-Derived Neuroprotective Agent, with Improved Potency, Safety, and Permeability. |
Kannalife Sciences |
26890113 |
41 |
Tricyclic pyrazoles. Part 8. Synthesis, biological evaluation and modelling of tricyclic pyrazole carboxamides as potential CB2 receptor ligands with antagonist/inverse agonist properties. |
Universit£ |
26275680 |
68 |
Synthesis and biological evaluation of (3',5'-dichloro-2,6-dihydroxy-biphenyl-4-yl)-aryl/alkyl-methanone selective CB2 inverse agonist. |
University of Tennessee Health Science Center |
25935384 |
26 |
New quinolone- and 1,8-naphthyridine-3-carboxamides as selective CB2 receptor agonists with anticancer and immuno-modulatory activity. |
University of Pisa |
25760146 |
49 |
3'-functionalized adamantyl cannabinoid receptor probes. |
University of Hawaii At Manoa |
25703248 |
3 |
Cannabidiol (CBD) and its analogs: a review of their effects on inflammation. |
University of Massachusetts Medical School |
25701254 |
48 |
Novel tail and head group prostamide probes. |
Northeastern University |
23902803 |
9 |
Peripherally restricted CB1 receptor blockers. |
Jenrin Discovery |
25575658 |
83 |
Selective CB2 receptor agonists. Part 3: the optimization of a piperidine-based series that demonstrated efficacy in an in vivo neuropathic pain model. |
Boehringer Ingelheim Pharmaceuticals |
25488844 |
154 |
Discovery of 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalen-4-carboxamides as potent and selective CB2 receptor agonists. |
Arena Pharmaceuticals |
24900848 |
11 |
C-ring cannabinoid lactones: a novel cannabinergic chemotype. |
Northeastern University |
23865723 |
169 |
Therapeutic utility of cannabinoid receptor type 2 (CB(2)) selective agonists. |
Arena Pharmaceuticals |
23621789 |
69 |
Novel adamantyl cannabinoids as CB1 receptor probes. |
Northeastern University |
23350768 |
196 |
Design, synthesis, and pharmacological properties of new heteroarylpyridine/heteroarylpyrimidine derivatives as CB(2) cannabinoid receptor partial agonists. |
Universit£ |
19249138 |
142 |
Development of CoMFA and CoMSIA models of affinity and selectivity for indole ligands of cannabinoid CB1 and CB2 receptors. |
Universidade Federal Do Rio De Janeiro |
15149681 |
3 |
Synthesis and CB1 receptor activities of novel arachidonyl alcohol derivatives. |
University of Kuopio |
23147076 |
163 |
Structure-activity relationships of 2-arylamido-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide derivatives as cannabinoid receptor agonists and their analgesic action. |
Nycomed Pharma |
23083016 |
20 |
Sulfonyl fluoride inhibitors of fatty acid amide hydrolase. |
Northeastern University |
22738638 |
59 |
Assay and inhibition of diacylglycerol lipase activity. |
Northeastern University |
22738271 |
250 |
7-Oxo-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxamides as selective CB(2) cannabinoid receptor ligands: structural investigations around a novel class of full agonists. |
Universit£ |
22796181 |
51 |
C3-heteroaroyl cannabinoids as photolabeling ligands for the CB2 cannabinoid receptor. |
University of Hawaii At Manoa |
22370265 |
63 |
Synthesis and evaluation of 2-amido-3-carboxamide thiophene CB2 receptor agonists for pain management. |
Abbott Laboratories |
20943404 |
24 |
1-Bromo-3-(1',1'-dimethylalkyl)-1-deoxy-¿(8)-tetrahydrocannabinols: New selective ligands for the cannabinoid CB(2) receptor. |
Clemson University |
19278853 |
67 |
Synthesis and pharmacological evaluation of coumarin derivatives as cannabinoid receptor antagonists and inverse agonists. |
University of Bonn |
18680277 |
198 |
Discovery and optimization of a novel series of N-arylamide oxadiazoles as potent, highly selective and orally bioavailable cannabinoid receptor 2 (CB2) agonists. |
Amgen |
18448340 |
27 |
Aminopyrazine CB1 receptor inverse agonists. |
Neurogen |
17919913 |
55 |
Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940. |
Clemson University |
18337096 |
37 |
Tetrazole-biarylpyrazole derivatives as cannabinoid CB1 receptor antagonists. |
Reen Cross |
17630726 |
32 |
Naphthalen-1-yl-(4-pentyloxynaphthalen-1-yl)methanone: a potent, orally bioavailable human CB1/CB2 dual agonist with antihyperalgesic properties and restricted central nervous system penetration. |
Novartis Institutes For Biomedical Research |
16451075 |
6 |
New cannabidiol derivatives: synthesis, binding to cannabinoid receptor, and evaluation of their antiinflammatory activity. |
Ben-Gurion University of The Negev |
16451053 |
37 |
Synthesis and activity of 1,3,5-triphenylimidazolidine-2,4-diones and 1,3,5-triphenyl-2-thioxoimidazolidin-4-ones: characterization of new CB1 cannabinoid receptor inverse agonists/antagonists. |
Universit£ |
16190764 |
24 |
Potent cannabinergic indole analogues as radioiodinatable brain imaging agents for the CB1 cannabinoid receptor. |
Northeastern University |
16078824 |
48 |
The endocannabinoid system: drug targets, lead compounds, and potential therapeutic applications. |
Universit£ |
15139773 |
3 |
Discovery of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-3-hexyl-1h-1,2,4-triazole, a novel in vivo cannabinoid antagonist containing a 1,2,4-triazole motif. |
Instituto De Qu£Mica M£Dica |
12672252 |
104 |
Design, synthesis, and biological evaluation of new inhibitors of the endocannabinoid uptake: comparison with effects on fatty acid amidohydrolase. |
Universidad Complutense |
11741470 |
40 |
Design, synthesis and biological evaluation of novel arachidonic acid derivatives as highly potent and selective endocannabinoid transporter inhibitors. |
Universidad Complutense |
9057852 |
74 |
Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptor. |
Hebrew University |
8809166 |
10 |
Unsaturated side chain beta-11-hydroxyhexahydrocannabinol analogs. |
University of Hawaii |
22284817 |
82 |
¿-Carbolines: a novel class of cannabinoid agonists with high aqueous solubility and restricted CNS penetration. |
Astrazeneca R&D Montreal |
21962575 |
8 |
Characterization of a novel and selective CB1 antagonist as a radioligand for receptor occupancy studies. |
Bristol-Myers Squibb |
21880487 |
21 |
Conformationally constrained analogs of BAY 59-3074 as novel cannabinoid receptor ligands. |
Northeastern University |
21885167 |
3 |
Novel indole and azaindole (pyrrolopyridine) cannabinoid (CB) receptor agonists: design, synthesis, structure-activity relationships, physicochemical properties and biological activity. |
Abbott Healthcare Products |
21741835 |
41 |
Structure-activity relationship studies of novel pyrazole and imidazole carboxamides as cannabinoid-1 (CB1) antagonists. |
Dr. Reddy'S Laboratories |
21420857 |
115 |
Decahydroquinoline amides as highly selective CB2 agonists: role of selectivity on in vivo efficacy in a rodent model of analgesia. |
Merck Research Laboratories |
21420860 |
34 |
Imidazopyridine CB2 agonists: optimization of CB2/CB1 selectivity and implications for in vivo analgesic efficacy. |
Merck Research Laboratories |
20845959 |
94 |
Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor. |
Research Triangle Institute |
20925434 |
43 |
Novel 1',1'-chain substituted hexahydrocannabinols: 9ß-hydroxy-3-(1-hexyl-cyclobut-1-yl)-hexahydrocannabinol (AM2389) a highly potent cannabinoid receptor 1 (CB1) agonist. |
Northeastern University |
20673729 |
60 |
Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist. |
Green Cross |
20621488 |
13 |
Synthesis and pharmacology of 1-methoxy analogs of CP-47,497. |
Clemson University |
20593789 |
47 |
Heteroadamantyl cannabinoids. |
University of Hawaii At Manoa |
20584609 |
13 |
Rational design of a novel peripherally-restricted, orally active CB(1) cannabinoid antagonist containing a 2,3-diarylpyrrole motif. |
Sanofi-Aventis R&D |
20423086 |
93 |
Discovery of N-[(4R)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-2,2-dimethyl-3,4-dihydro-2H-pyrano[2,3-b]pyridin-4-yl]-5-methyl-1H-pyrazole-3-carboxamide (MK-5596) as a novel cannabinoid-1 receptor (CB1R) inverse agonist for the treatment of obesity. |
Merck Research Laboratories |
20045337 |
117 |
Synthesis and structure-activity relationship of 1,2,4-triazole-containing diarylpyrazolyl carboxamide as CB1 cannabinoid receptor-ligand. |
Green Cross |
19921781 |
220 |
Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity. |
Abbott Laboratories |
19850473 |
30 |
Pentacycle derivatives as cannabinoid CB1 receptor ligands. |
Green Cross |
19683918 |
36 |
Bioisosteric replacement of the hydrazide pharmacophore of the cannabinoid-1 receptor antagonist SR141716A. Part I: potent, orally-active 1,4-disubstituted imidazoles. |
Pfizer |
19762126 |
16 |
Synthesis and pharmacological evaluation of sulfamide-based analogues of anandamide. |
Instituto De Qu£Mica M£Dica |
19596576 |
60 |
Substituted pyrimidines as cannabinoid CB1 receptor ligands. |
Green Cross |
19527048 |
19 |
Chemical and biological investigation of cyclopropyl containing diaryl-pyrazole-3-carboxamides as novel and potent cannabinoid type 1 receptor antagonists. |
Gedeon Richter |
| 4 |
Synthesis of (+)- and (−)-2-methylarachidonyl-2′-fluoroethylamide (O-689) |
TBA |
| 11 |
Morpholinoalkylindenes as antinociceptive agents: Novel cannabinoid receptor agonists |
TBA |
19457667 |
17 |
Hit-to-lead optimization of pyrrolo[1,2-a]quinoxalines as novel cannabinoid type 1 receptor antagonists. |
Gedeon Richter |
19331413 |
54 |
New resorcinol-anandamide"hybrids" as potent cannabinoid receptor ligands endowed with antinociceptive activity in vivo. |
Universita Degli Studi Di Siena |
19328001 |
49 |
Synthesis and structure-activity relationship of novel diarylpyrazole imide analogues as CB1 cannabinoid receptor ligands. |
Green Cross |
19320488 |
171 |
1-Sulfonyl-4-acylpiperazines as selective cannabinoid-1 receptor (CB1R) inverse agonists for the treatment of obesity. |
Merck Research Laboratories |
19269817 |
28 |
Oxadiazole-diarylpyrazole 4-carboxamides as cannabinoid CB1 receptor ligands. |
Green Cross |
19128970 |
18 |
Synthesis and characterization of a peripherally restricted CB1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in mice. |
University of California |
19097888 |
11 |
Synthesis and CB1 cannabinoid receptor affinity of 4-alkoxycarbonyl-1,5-diaryl-1,2,3-triazoles. |
University of New Orleans |
19022666 |
71 |
Diarylimidazolyl oxadiazole and thiadiazole derivatives as cannabinoid CB1 receptor antagonists. |
Green Cross |
18954042 |
117 |
Biarylpyrazolyl oxadiazole as potent, selective, orally bioavailable cannabinoid-1 receptor antagonists for the treatment of obesity. |
Green Cross |
18826296 |
12 |
Bornyl- and isobornyl-Delta8-tetrahydrocannabinols: a novel class of cannabinergic ligands. |
Northeastern University |
18723350 |
37 |
Development of novel tail-modified anandamide analogs. |
Northeastern University |
18243711 |
76 |
Design, synthesis and biological evaluation of piperazine analogues as CB1 cannabinoid receptor ligands. |
Central Research Institute |
18077343 |
2 |
Hemopressin is an inverse agonist of CB1 cannabinoid receptors. |
Proteimax Biotechnology |
17582659 |
22 |
Synthesis and cannabinoid activity of 1-substituted-indole-3-oxadiazole derivatives: novel agonists for the CB1 receptor. |
Monash University (Parkville Campus) |
14575438 |
4 |
Semiplenamides A-G, fatty acid amides from a Papua New Guinea collection of the marine cyanobacterium Lyngbya semiplena. |
Oregon State University |
18038967 |
12 |
Cannabilactones: a novel class of CB2 selective agonists with peripheral analgesic activity. |
Northeastern University |
17826996 |
5 |
Conformationally constrained analogues of 2-arachidonoylglycerol. |
Northeastern University |
17672444 |
22 |
C1'-cycloalkyl side chain pharmacophore in tetrahydrocannabinols. |
National Hellenic Research Foundation |
17513109 |
32 |
Discovery of pyrazine carboxamide CB1 antagonists: the introduction of a hydroxyl group improves the pharmaceutical properties and in vivo efficacy of the series. |
Pharmaceutical Research Institute |
17293109 |
69 |
Substituted acyclic sulfonamides as human cannabinoid-1 receptor inverse agonists. |
Merck Research Laboratories |
16889960 |
56 |
1-Alkyl-2-aryl-4-(1-naphthoyl)pyrroles: new high affinity ligands for the cannabinoid CB1 and CB2 receptors. |
Clemson University |
16387492 |
26 |
Structural modifications of the cannabinoid side chain towards C3-aryl and 1',1'-cycloalkyl-1'-cyano cannabinoids. |
National Hellenic Research Foundation |
16134948 |
15 |
Synthesis and structure-activity relationship of a novel series of aminoalkylindoles with potential for imaging the neuronal cannabinoid receptor by positron emission tomography. |
National Institute On Drug Abuse |
16005223 |
64 |
1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles. |
Clemson University |
15999995 |
12 |
Adamantyl cannabinoids: a novel class of cannabinergic ligands. |
Northeastern University |
12951114 |
18 |
Arachidonylsulfonyl derivatives as cannabinoid CB1 receptor and fatty acid amide hydrolase inhibitors. |
University of California |
12852753 |
17 |
Pharmacophoric requirements for the cannabinoid side chain. Probing the cannabinoid receptor subsite at C1'. |
National Hellenic Research Foundation |
12781177 |
7 |
Hemisynthesis and preliminary evaluation of novel endocannabinoid analogues. |
Umr Cnrs 5074 |
12570386 |
15 |
Synthesis, structure-activity relationship, and evaluation of SR141716 analogues: development of central cannabinoid receptor ligands with lower lipophilicity. |
National Institute On Drug Abuse |
12467613 |
15 |
Homologues and isomers of noladin ether, a putative novel endocannabinoid: interaction with rat cannabinoid CB(1) receptors. |
Discaff |
12443781 |
22 |
Novel 1',1'-chain substituted Delta(8)-tetrahydrocannabinols. |
National Hellenic Research Foundation |
12166944 |
48 |
Oxygenated metabolites of anandamide and 2-arachidonoylglycerol: conformational analysis and interaction with cannabinoid receptors, membrane transporter, and fatty acid amide hydrolase. |
Utrecht University |
12061874 |
60 |
Synthesis and structure-activity relationships of amide and hydrazide analogues of the cannabinoid CB(1) receptor antagonist N-(piperidinyl)- 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (SR141716). |
Research Triangle Institute |
11906286 |
34 |
Molecular interaction of the antagonist N-(piperidin-1-yl)-5-(4-chlorophenyl)-1- (2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide with the CB1 cannabinoid receptor. |
University of South Carolina |
32551012 |
18 |
P2Y |
Saint Louis University School of Medicine |
11229744 |
7 |
Synthesis and biological evaluation of novel amides of polyunsaturated fatty acids with dopamine. |
Institute of Bioorganic Chemistry Ras |
27482723 |
73 |
Peripherally Selective Cannabinoid 1 Receptor (CB1R) Agonists for the Treatment of Neuropathic Pain. |
Research Triangle Institute |
27624523 |
33 |
Synthesis, molecular modeling and SAR study of novel pyrazolo[5,1-f][1,6]naphthyridines as CB |
Universit£ |
27367336 |
78 |
Novel C-Ring-Hydroxy-Substituted Controlled Deactivation Cannabinergic Analogues. |
Northeastern University |
30816712 |
78 |
Plant-Based Modulators of Endocannabinoid Signaling. |
Concordia University Wisconsin |
10465529 |
9 |
Novel conformationally restricted tetracyclic analogs of delta8-tetrahydrocannabinol. |
University of Connecticut |
10354405 |
31 |
Unique analogues of anandamide: arachidonyl ethers and carbamates and norarachidonyl carbamates and ureas. |
Organix |
10072686 |
25 |
Substrate specificity and stereoselectivity of rat brain microsomal anandamide amidohydrolase. |
University of Connecticut |
10052983 |
40 |
Structure-activity relationships of pyrazole derivatives as cannabinoid receptor antagonists. |
University of Connecticut |
31756109 |
108 |
Application of Fluorine- and Nitrogen-Walk Approaches: Defining the Structural and Functional Diversity of 2-Phenylindole Class of Cannabinoid 1 Receptor Positive Allosteric Modulators. |
Northeastern University |
9876105 |
75 |
Novel analogues of arachidonylethanolamide (anandamide): affinities for the CB1 and CB2 cannabinoid receptors and metabolic stability. |
University of Connecticut |
9873517 |
4 |
Enantioselective synthesis and pharmacology of 11-hydroxy-(1'S,2'R)-dimethylheptyl-delta 8-THC. |
Clemson University |
31220675 |
88 |
Preparation of bivalent agonists for targeting the mu opioid and cannabinoid receptors. |
Biological Research Centre of The Hungarian Academy of Sciences |
9784095 |
4 |
Derivation of a pharmacophore model for anandamide using constrained conformational searching and comparative molecular field analysis. |
Saint Louis University School of Medicine |
9733485 |
16 |
Classical/nonclassical hybrid cannabinoids: southern aliphatic chain-functionalized C-6beta methyl, ethyl, and propyl analogues. |
University of Hawaii |
9544219 |
12 |
Pharmacophoric requirements for cannabinoid side chains: multiple bond and C1'-substituted delta 8-tetrahydrocannabinols. |
National Hellenic Research Foundation |
9379452 |
8 |
Importance of the C-1 substituent in classical cannabinoids to CB2 receptor selectivity: synthesis and characterization of a series of O,2-propano-delta 8-tetrahydrocannabinol analogs. |
Kennesaw State University |
9379442 |
61 |
Cannabinol derivatives: binding to cannabinoid receptors and inhibition of adenylylcyclase. |
Institute of Science |
8893848 |
21 |
Head group analogs of arachidonylethanolamide, the endogenous cannabinoid ligand. |
University of Connecticut |
8831752 |
9 |
Synthesis and pharmacology of a very potent cannabinoid lacking a phenolic hydroxyl with high affinity for the CB2 receptor. |
Clemson University |
8642555 |
11 |
(Aminoalkyl)indole isothiocyanates as potential electrophilic affinity ligands for the brain cannabinoid receptor. |
National Institute of Diabetes and Digestive and Kidney Diseases |
8411007 |
392 |
Chemistry, binding affinities, and behavioral properties of a new class of"antineophobic" mitochondrial DBI receptor complex (mDRC) ligands. |
Mayo Foundation |
24445310 |
25 |
Design, synthesis, biological evaluation, and comparative docking study of 1,2,4-triazolones as CB1 receptor selective antagonists. |
Zhejiang University |
24518874 |
61 |
1,2-Dihydro-2-oxopyridine-3-carboxamides: the C-5 substituent is responsible for functionality switch at CB2 cannabinoid receptor. |
Universit£ |
24286207 |
30 |
Controlled-deactivation cannabinergic ligands. |
Northeastern University |
23795771 |
94 |
Selective cannabinoid receptor type 2 (CB2) agonists: optimization of a series of purines leading to the identification of a clinical candidate for the treatment of osteoarthritic pain. |
Lilly Research Laboratories |
24125850 |
89 |
Mastering tricyclic ring systems for desirable functional cannabinoid activity. |
The University of Montana |
23807113 |
6 |
Discovery of novel tetrahydro-pyrazolo [4,3-c] pyridines for the treatment of neuropathic pain: synthesis and neuropharmacology. |
Birla Institute of Technology & Science - Pilani |
23697626 |
167 |
Discovery of 7-oxopyrazolo[1,5-a]pyrimidine-6-carboxamides as potent and selective CB(2) cannabinoid receptor inverse agonists. |
Universit£ |
7636873 |
62 |
Aminoalkylindoles: structure-activity relationships of novel cannabinoid mimetics. |
Sanofi Research Division |
21215643 |
20 |
Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists. |
University of Eastern Finland |
16466915 |
4 |
Alpha-methylated derivatives of 2-arachidonoyl glycerol: synthesis, CB1 receptor activity, and enzymatic stability. |
University of Kuopio |
16420041 |
24 |
3D-QSAR studies on cannabinoid CB1 receptor agonists: G-protein activation as biological data. |
University of Kuopio |
16190768 |
6 |
High affinity electrophilic and photoactivatable covalent endocannabinoid probes for the CB1 receptor. |
Northeastern University |
11448223 |
70 |
Volume learning algorithm artificial neural networks for 3D QSAR studies. |
Institute of Bioorganic & Petroleum Chemistry |
9804691 |
84 |
Three-dimensional quantitative structure-activity relationship study of the cannabimimetic (aminoalkyl)indoles using comparative molecular field analysis. |
Sanofi Research Division |
9357529 |
20 |
Synthesis and pharmacological comparison of dimethylheptyl and pentyl analogs of anandamide. |
Research Triangle Institute |
7966145 |
2 |
(-)-11-Hydroxy-7'-isothiocyanato-1',1'-dimethylheptyl-delta 8-THC: a novel, high-affinity irreversible probe for the cannabinoid receptor in the brain. |
University of Connecticut |
8021930 |
10 |
(R)-methanandamide: a chiral novel anandamide possessing higher potency and metabolic stability. |
University of Connecticut |
30122284 |
70 |
Oximes short-acting CB1 receptor agonists. |
Northeastern University |
30196704 |
90 |
( R)- N-(1-Methyl-2-hydroxyethyl)-13-( S)-methyl-arachidonamide (AMG315): A Novel Chiral Potent Endocannabinoid Ligand with Stability to Metabolizing Enzymes. |
Northeastern University |
29259753 |
70 |
Discovery of APD371: Identification of a Highly Potent and Selective CB |
Arena Pharmaceuticals |
28792219 |
61 |
Novel Diarylurea Based Allosteric Modulators of the Cannabinoid CB1 Receptor: Evaluation of Importance of 6-Pyrrolidinylpyridinyl Substitution. |
Research Triangle Institute |
28726401 |
55 |
Amidoalkylindoles as Potent and Selective Cannabinoid Type 2 Receptor Agonists with in Vivo Efficacy in a Mouse Model of Multiple Sclerosis. |
East China Normal University |
26808391 |
6 |
A Dual Non-ATP Analogue Inhibitor of Aurora Kinases A and B, Derived from Resorcinol with a Mixed Mode of Inhibition. |
Jawaharlal Nehru Centre For Advanced Scientific Research |
26833890 |
18 |
Synthesis, Biological Evaluation, and Molecular Docking of 8-imino-2-oxo-2H,8H-pyrano[2,3-f]chromene Analogs: New Dual AChE Inhibitors as Potential Drugs for the Treatment of Alzheimer's Disease. |
Yogi Vemana University |
26575582 |
15 |
Development of 2-(Substituted Benzylamino)-4-Methyl-1, 3-Thiazole-5-Carboxylic Acid Derivatives as Xanthine Oxidase Inhibitors and Free Radical Scavengers. |
Jamia Hamdard |
26469307 |
7 |
Phosphorylation of Capsaicinoid Derivatives Provides Highly Potent and Selective Inhibitors of the Transcription Factor STAT5b. |
University of Leipzig |
8022403 |
113 |
A binding site model and structure-activity relationships for the rat A3 adenosine receptor. |
National Institute of Diabetes, Digestive and Kidney Diseases |