The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 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 |
| 25466177 |
24 |
The SAR development of substituted purine derivatives as selective CB2 agonists for the treatment of chronic pain. |
Eli Lilly |
| 23865723 |
169 |
Therapeutic utility of cannabinoid receptor type 2 (CB(2)) selective agonists. |
Arena Pharmaceuticals |
| 23350768 |
196 |
Design, synthesis, and pharmacological properties of new heteroarylpyridine/heteroarylpyrimidine derivatives as CB(2) cannabinoid receptor partial agonists. |
Universit£ |
| 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 |
| 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£ |
| 22765893 |
32 |
Discovery and optimization of novel purines as potent and selective CB2 agonists. |
Eli Lilly |
| 22370265 |
63 |
Synthesis and evaluation of 2-amido-3-carboxamide thiophene CB2 receptor agonists for pain management. |
Abbott Laboratories |
| 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 |
| 18006322 |
43 |
Imine derivatives as new potent and selective CB2 cannabinoid receptor agonists with an analgesic action. |
Taisho Pharmaceutical |
| 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 |
| 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 |
| 20137936 |
7 |
Radiosynthesis of novel carbon-11-labeled triaryl ligands for cannabinoid-type 2 receptor. |
National Institute Of Radiological Sciences |
| 19919895 |
54 |
Novel sulfamoyl benzamides as selective CB(2) agonists with improved in vitro metabolic stability. |
Adolor |
| 19921781 |
220 |
Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity. |
Abbott Laboratories |
| 19736007 |
31 |
Novel pyridine derivatives as potent and selective CB2 cannabinoid receptor agonists. |
Adolor |
| 19331413 |
54 |
New resorcinol-anandamide"hybrids" as potent cannabinoid receptor ligands endowed with antinociceptive activity in vivo. |
Universita Degli Studi Di Siena |
| 17582659 |
22 |
Synthesis and cannabinoid activity of 1-substituted-indole-3-oxadiazole derivatives: novel agonists for the CB1 receptor. |
Monash University (Parkville Campus) |
| 17477516 |
115 |
Discovery of 2-[(2,4-dichlorophenyl)amino]-N-[(tetrahydro- 2H-pyran-4-yl)methyl]-4-(trifluoromethyl)- 5-pyrimidinecarboxamide, a selective CB2 receptor agonist for the treatment of inflammatory pain. |
Glaxosmithkline |
| 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 |
| 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 |
| 23808805 |
42 |
Carbonic anhydrase inhibitors. Phenols incorporating 2- or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae ß-carbonic anhydrase. |
Ataturk 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 |
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