Emeritus Professor
- About
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- Email Address
- rgp@abdn.ac.uk
- Office Address
School of Medical Sciences Institute of Medical Sciences University of Aberdeen Foresterhill Aberdeen AB25 2ZD Scotland, UK
- School/Department
- School of Medicine, Medical Sciences and Nutrition
Biography
Roger Pertwee has three degrees from the University of Oxford: MA (in biochemistry), D.Phil. (in pharmacology) and D.Sc. (in physiological sciences). He is now an Emeritus Professor at the University of Aberdeen, where he is still actively engaged in scientific research. He is also co-chairman of the International Union of Basic and Clinical Pharmacology (IUPHAR) Subcommittee on Cannabinoid Receptors, a co-ordinator of the British Pharmacological Society’s Special Interest Group on Cannabinoids, a co-founder of the International Cannabinoid Research Society (ICRS) <http://icrs.co/> , and an invited scientific advisor on cannabinoid pharmacology/therapeutics to the Beckley Foundation <http://beckleyfoundation.org/about/advisory-boards/>, has had formal cannabinoid pharmacology-related links with several pharmaceutical companies, and currently has such a link with GW Pharmaceuticals. He has served too, twice as President of the ICRS (1997-1998 and 2007-2008), and once as Chairman of the International Association for Cannabinoid Medicines (IACM; 2005-2007), and is also currently ICRS International Secretary, and a member of the IACM Board of Directors <http://www.cannabis-med.org/index.php?tpl=page&id=74&lng=en>. He was the recipient of the 2002 Mechoulam Award “for his outstanding contributions to cannabinoid research”. He was also awarded the 2011 Wellcome Gold Medal by the British Pharmacological Society (BPS) “for outstanding contributions to pharmacology, based mainly on research achievements”, and the 2013 IACM Special Award “for his major contributions to the re-introduction of cannabis as a medicine”, and is an Honorary Fellow of the BPS: this fellowship is awarded to BPS members who have “demonstrated distinction and peer recognition in science, or have given long and valuable service to the Society”. In addition, he was identified by Thomson Reuters in 2005 to be a “Highly Cited Researcher” and hence among “the world's most cited and influential researchers”. He also received (1) a Highly Cited Researcher Award from Thomson Reuters in September 2014 “in recognition of ranking among the top 1% of researchers for most cited documents in their specific field” (see Pertwee in “Archives” at <http://hcr.stateofinnovation.thomsonreuters.com/page/archives> and from Clarivate Analytics in 2018 “in recognition of exceptional research performance demonstrated by production of multiple highly cited papers, those that rank in the top 1% by citations for field and year in Pharmacology and Toxicology” and (2) the 2018 Lifetime Achievement Award from the International Cannabinoid Research Society "for outstanding contributions to cannabinoid research and the ICRS".
Roger Pertwee presented evidence on cannabis in person at the House of Lords to the Science and Technology Committee which published its report on cannabis in 1998. He is the author of numerous review articles on the cannabinoids and is often invited to speak on the pharmacology of cannabinoids at international conferences. He is also interested in the therapeutic potential of cannabinoids. Indeed, he was a contributing author of the British Medical Association book entitled "Therapeutic Uses of Cannabis." and served on the Royal Pharmaceutical Society working party that recommended and helped to design clinical trials with cannabis and THC that were carried out in the UK and funded by the Medical Research Council. Together with Drs Rik Musty and Paul Consroe he also carried out the first large survey of multiple sclerosis patients who self-medicate with cannabis [Eur Neurol (1997) 38: 44]. His contributions to the "medicalization of cannabis" are summarized in a Witness Seminar Transcript (Vol 40), co-authored by Crowther, S.M., Reynolds, L.A. and Tansey, E.M. and published in 2010 by The Wellcome Trust Centre for the History of Medicine at UCL. This book is freely downloadable at <http://www.history.qmul.ac.uk/research/modbiomed/wellcome_witnesses/volume40/index.html>.
Roger Pertwee's research focuses on the pharmacology of cannabinoids. He began his work in this area in 1968 as a post-doc with Professor Sir William Paton at the Department of Pharmacology, Oxford University. He initially worked with cannabis and also with delta-9-tetrahydrocannabinol (THC) and cannabidiol, both of which were extracted from tincture of cannabis, then still a legal medicine in the UK. This research led to the demonstration that cannabidiol is a highly effective inhibitor of hepatic microsomal enzymes and to the development of the "ring immobility test", still widely used as a behavioural bioassay.
After moving to Aberdeen in 1974, Roger Pertwee continued with his cannabinoid research, initially investigating the basis for the hypothermic effect of THC. This work provided evidence that THC lowers the thermoregulatory set point such that animals regulate their core temperature at a lower level than normal by adjusting heat gain and heat loss both autonomically and behaviourally. In other research carried out during this time he found that cannabinoids interact synergistically with benzodiazepines and also identified the globus pallidus as one of the sites at which cannabinoids alter motor function.
Opioid research with the mouse isolated vas deferens being carried out in Professor Hans Kosterlitz's laboratory in Aberdeen gave Roger Pertwee the opportunity to establish whether this tissue would also serve as a bioassay for cannabinoids. The mouse vas deferens turned out to be an extremely sensitive quantitative assay for CB1 agonists. He presented some of the initial vas deferens data at a cannabinoid meeting in Palm Beach in 1991 and this led to a collaboration with Professor Raphael Mechoulam who was also at the meeting. As a result, using the mouse vas deferens, Roger Pertwee (with Graeme Griffin) was able to provide the first evidence that anandamide not only binds to cannabinoid receptors (Dr William Devane's data) but also activates these receptors, greatly strengthening the argument that anandamide is an endogenous cannabinoid/endocannabinoid [Science (1992) 258:1946]. Other research in his laboratory, led by Dr Angela Coutts, was directed at mapping out the distribution of cannabinoid receptors in brain and gut using immunohistochemical techniques.
His research has also played major roles in
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the discovery that ethanolamides that are formed from dietary omega-3 polyunsaturated fatty acids and that seem to be endocannabinoids, have the capacity to inhibit cancer cell growth and proliferation;
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the discovery of a cannabinoid CB1 receptor allosteric site;
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the discovery that delta-9-tetrahydrocannabivarin is a plant cannabinoid (phytocannabinoid) - and that this compound is both a cannabinoid CB1 receptor blocker (antagonist) and a cannabinoid CB2 receptor activator (agonist) that has the potential to treat drug dependence, Parkinson’s disease, stroke, obesity and liver diseases, and to reduce health risks associated with liver transplantation;
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the pharmacological characterization of other phytocannabinoids, including cannabidiol, cannabidiolic acid & cannabigerol, and the further pharmacological characterization of THCV;
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the discovery/pharmacological characterization of novel synthetic cannabinoids many of which are widely used by cannabinoid researchers as experimental tools, e.g.
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methanandamide, the first CB1 receptor-selective agonist (with Dr Alexandros Makriyannis);
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two other CB1-selective agonists: ACEA & ACPA (with Dr Cecelia Hillard);
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HU-308, a CB2-selective agonist (with Dr Raphael Mechoulam);
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AM281, a widely-used CB1 receptor antagonist, and AM630, a widely-used CB2 receptor antagonist (with Dr Alexandros Makriyannis);
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CB1 receptor “neutral” antagonists;
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O-1057, the first water-soluble cannabinoid receptor ligand (with Drs Billy Martin and Raj Razdan);
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novel positive and negative allosteric modulators of the CB1 receptor (with Dr Ganesh Thakur).
Research now being carried out in Roger Pertwee's laboratory is directed (i) at seeking out further pharmacological actions of phytocannabinoids, (ii) at elucidating the pharmacological actions of other constituents of cannabis, and (iii) at exploring the actions and therapeutic potential of novel synthetic allosteric modulators of cannabinoid receptors. This research, which is being conducted mainly using radioligand binding assays and in vitro bioassays that measure drug effects on cannabinoid receptor signalling (e.g. [35S]GTPgammaS binding assays), is currently supported by the US National Institute on Drug Abuse (part of NIH) and by GW Pharmaceuticals. He is also presently collaborating with colleagues at Aberdeen University in cannabinoid research funded by Diabetes UK and by Medical Research Scotland.
- Research
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Research Overview
Primary research interests:
· pharmacology and therapeutic potential of plant cannabinoids
· pharmacology of allosteric sites on cannabinoid receptors
· novel cannabinoid CB1 and CB2 receptor ligands
· new pharmacological targets for cannabinoids
· roles of the endocannabinoid system in health and disease
Current Research
Roger Pertwee's current research is directed at seeking out pharmacological actions of phytocannabinoids, and at elucidating the pharmacological actions of other constituents of cannabis. In addition, he is currently following up a discovery made in his laboratory that there is at least one allosteric site on the cannabinoid CB1 receptor, by exploring the actions and therapeutic potential of novel synthetic allosteric modulators of cannabinoid receptors.
- Publications
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Page 1 of 6 Results 1 to 50 of 269
Cyclic AMP Assay Using Human Cannabinoid CB2 Receptor-Transfected Cells
Endocannabinoid Signaling.. Maccarrone, M. (ed.). HUMANA PRESS INC, pp. 171-179, 9 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-1-0716-2728-0_13
- [ONLINE] View publication in Scopus
Displacement Binding Assay Using Human Cannabinoid CB2 Receptor-Transfected Cells
Endocannabinoid Signaling.: Methods in Molecular Biology. Maccarrone, M. (ed.). HUMANA PRESS INC, pp. 111-118, 8 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-1-0716-2728-0_8
- [ONLINE] View publication in Scopus
The Plant Derived 3-3′-Diindolylmethane (DIM) Behaves as CB2 Receptor Agonist in Prostate Cancer Cellular Models
International Journal of Molecular Sciences, vol. 24, no. 4, 3620Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.3390/ijms24043620
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/20232/1/Tucci_etal_ijms_Plant_Derived_33_VOR.pdf
- [ONLINE] View publication in Scopus
M3 Receptor Pathway Stimulates Rapid Transcription of the CB1 Receptor Activation through Calcium Signalling and the CNR1 Gene Promoter
International Journal of Molecular Sciences, vol. 24, no. 2, 1308Contributions to Journals: ArticlesMotor-like Tics are Mediated by CB2 Cannabinoid Receptor-dependent and Independent Mechanisms Associated with Age and Sex
Molecular Neurobiology, vol. 59, pp. 5070-5083Contributions to Journals: ArticlesOsteogenic growth peptide is a potent anti-inflammatory and bone preserving hormone via cannabinoid receptor type 2
eLife, e65834Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.7554/eLife.65834
- [ONLINE] View publication in Scopus
Synthetic bioactive olivetol-related amides: The influence of the phenolic group in cannabinoid receptor activity
Bioorganic and Medicinal Chemistry, vol. 28, no. 11, 115513Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.bmc.2020.115513
- [ONLINE] View publication in Scopus
Anticancer effects of n-3 EPA and DHA and their endocannabinoid derivatives on breast cancer cell growth and invasion
Prostaglandins, Leukotrienes and Essential Fatty Acids, vol. 156, pp. 102024Contributions to Journals: ArticlesDisease associated polymorphisms within the conserved ECR1 enhancer differentially regulate the tissue specific activity of the cannabinoid‐1 receptor gene promoter; implications for cannabinoid pharmacogenetics
Human Mutation, vol. 41, no. 1, pp. 291-298Contributions to Journals: ArticlesFatty acid suppression of glial activation prevents central neuropathic pain after spinal cord injury
Pain, vol. 160, no. 12, pp. 2724-2742Contributions to Journals: Articles- [ONLINE] http://links.lww.com/PAIN/A854
- [ONLINE] DOI: https://doi.org/10.1097/j.pain.0000000000001670
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/14798/1/PAIN_D_19_00177_R1.pdf
- [ONLINE] http://Insights.ovid.com/crossref?an=00006396-900000000-98626
- [ONLINE] View publication in Mendeley
- [ONLINE] View publication in Scopus
Disruption of an enhancer associated with addictive behaviour within the cannabinoid receptor-1 gene suggests a possible role in alcohol intake, cannabinoid response and anxiety-related behaviour
Psychoneuroendocrinology, vol. 109, pp. 104407Contributions to Journals: ArticlesA synthetic analogue of cannabidiolic acid that acts like a positive allosteric modulator at 5-HT1A receptors
British-Pharmacology-Society Meeting (Pharmacology), pp. 3011-3012Contributions to Journals: Abstracts- [ONLINE] DOI: https://doi.org/10.1111/bph.14681
- [ONLINE] View publication in Mendeley
Identification of the First Synthetic Allosteric Modulator of the CB2 Receptors and Evidence of Its Efficacy for Neuropathic Pain Relief
Journal of Medicinal Chemistry, vol. 62, no. 1, pp. 276-287Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/acs.jmedchem.8b00368
- [ONLINE] View publication in Scopus
- [ONLINE] View publication in Mendeley
Positive Allosteric Modulation of Cannabinoid Receptor Type 1 Suppresses Pathological Pain Without Producing Tolerance or Dependence
Biological Psychiatry, vol. 84, no. 10, pp. 722-733Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.biopsych.2017.06.032
- [ONLINE] View publication in Scopus
Enantiospecific Allosteric Modulation of Cannabinoid 1 Receptor
ACS Chemical Neuroscience, vol. 8, no. 6, pp. 1188-1203Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/acschemneuro.6b00310
- [ONLINE] View publication in Scopus
Synthesis, radio-synthesis and in vitro evaluation of terminally fluorinated derivatives of HU-210 and HU-211 as novel candidate PET tracers
Organic & Biomolecular Chemistry, vol. 15, no. 9, pp. 2086-2096Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1039/C6OB02796B
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/10024/1/C6OB02796B.pdf
The pharmacology and therapeutic potential of plant cannabinoids
Cannabis sativa L. - Botany and Biotechnology. Chandra, S., Lata, H., ElSohly, M. (eds.). Springer, Biomedicine & Life Sciences, pp. 207-225, 19 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-3-319-54564-6_9
Exploring the Benzimidazole Ring as a Substitution for Indole in Cannabinoid Allosteric Modulators
Cannabis and Cannabinoid Research, vol. 1, no. 1, pp. 196-201Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1089/can.2016.0003
- [ONLINE] View publication in Scopus
Pure Δ9-tetrahydrocannabivarin and a Cannabis sativa extract with high content in Δ9-tetrahydrocannabivarin inhibit nitrite production in murine peritoneal macrophages
Pharmacological Research, vol. 113, no. A, pp. 199-208Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.phrs.2016.07.045
- [ONLINE] View publication in Scopus
Mapping Cannabinoid 1 Receptor Allosteric Site(s): Critical Molecular Determinant and Signaling Profile of GAT100, a Novel, Potent, and Irreversibly Binding Probe
ACS Chemical Neuroscience, vol. 7, no. 6, pp. 776-798Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1021/acschemneuro.6b00041
The Displacement Binding Assay Using Human Cannabinoid CB2 Receptor-Transfected Cells
Endocannabinoid Signaling: Methods and Protocols. Maccarrone, M. (ed.). Springer Science+Business Media, pp. 57-63, 7 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-1-4939-3539-0_6
Effect of cannabis on glutamate signalling in the brain: A systematic review of human and animal evidence
Neuroscience & Biobehavioral Reviews, vol. 64, pp. 359-381Contributions to Journals: Literature Reviews- [ONLINE] DOI: https://doi.org/10.1016/j.neubiorev.2016.03.010
Novel Electrophilic and Photoaffinity Covalent Probes for Mapping the Cannabinoid 1 Receptor Allosteric Site(s)
Journal of Medicinal Chemistry, vol. 59, no. 1, pp. 44-60Contributions to Journals: ArticlesThe Cyclic AMP Assay Using Human Cannabinoid CB2 Receptor-Transfected Cells
Endocannabinoid Signaling: Methods and Protocols. Maccarrone, M. (ed.). Springer Science+Business Media, pp. 85-93, 9 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-1-4939-3539-0_9
Increasing levels of the endocannabinoid 2-AG is neuroprotective in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson's disease
Experimental Neurology, vol. 273, pp. 36-44Contributions to Journals: ArticlesCB2 cannabinoid receptor agonist enantiomers HU-433 and HU-308: An inverse relationship between binding affinity and biological potency
PNAS, vol. 112, no. 28, pp. 8774-8779Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1073/pnas.1503395112
Modulation of food consumption and sleep-wake cycle in mice by the neutral CB1 antagonist ABD459
Behavioural Pharmacology, vol. 26, no. 3, pp. 289-303Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1097/FBP.0000000000000108
The phytocannabinoid, Δ(9) -tetrahydrocannabivarin, can act through 5-HT1 A receptors to produce antipsychotic effects
British Journal of Pharmacology, vol. 172, no. 5, pp. 1305-1318Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/bph.13000
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/5584/1/bph13000.pdf
Tricyclic fused pyrazoles with a 'Click' 1,2,3-triazole substituent in position 3 are nanomolar CB1 receptor ligands
Synthesis, vol. 47, no. 6, pp. 817-826Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1055/s-0034-1379887
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/5583/1/Synthesis.docx
- [ONLINE] View publication in Scopus
Are cannabidiol and Delta(9)-tetrahydrocannabivarin negative modulators of the endocannabinoid system? A systematic review
British Journal of Pharmacology, vol. 172, no. 3, pp. 737-753Contributions to Journals: Literature Reviews- [ONLINE] DOI: https://doi.org/10.1111/bph.12944
Endocannabinoids
Vol. 231, Springer. 30 pagesBooks and Reports: Books- [ONLINE] DOI: https://doi.org/10.1007/978-3-319-20825-1
Early phytocannabinoid chemistry to endocannabinoids and beyond
Nature reviews neuroscience, vol. 15, no. 11, pp. 757-764Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1038/nrn3811
Pyrazoles with a "click" 4-[N-(4-fluorobutyl)-1,2,3-triazole] substituent in position 3 are nanomolar CB1 receptor ligands
Journal of Fluorine Chemistry, vol. 167, pp. 184-191Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.jfluchem.2014.07.010
- [ONLINE] View publication in Scopus
Structure-affinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonist
Behavioral and Brain Sciences, vol. 22, no. 17, pp. 4770-4783Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.bmc.2014.07.006
The phytocannabinoid, Δ9-tetrahydrocannabivarin, can act trough 5HT1A receptors to produce anti-psychotic effects
Contributions to Conferences: PostersInhibition of colon carcinogenesis by a standardized Cannabis sativa extract with high content of cannabidiol
Phytomedicine, vol. 21, no. 5, pp. 631-639Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.phymed.2013.11.006
In-vivo pharmacological evaluation of the CB1-receptor allosteric modulator Org-27569
Behavioural Pharmacology, vol. 25, no. 2, pp. 182-185Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1097/FBP.0000000000000027
Elevating endocannabinoid levels: pharmacological strategies and potential therapeutic applications
Proceedings of the Nutrition Society, vol. 73, no. 1, pp. 96-105Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1017/S0029665113003649
Handbook of Cannabis
Vol. 1, OXFORD UNIV PRESS, OxfordBooks and Reports: BooksMotor effects of the non-psychotropic phytocannabinoid cannabidiol that are mediated by 5-HT1A receptors
Neuropharmacology, vol. 75, pp. 155-163Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.neuropharm.2013.07.024
Cannabidivarin-rich cannabis extracts are anticonvulsant in mouse and rat via a CB1 receptor-independent mechanism
British Journal of Pharmacology, vol. 170, no. 3, pp. 679-692Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/bph.12321
Effects of Δ9-tetrahydrocannabivarin at serotoninergic 5-HT1A receptors, and of its 11-Hydroxy-metabolite at cannabinoid CB1 and CB2 receptors
Contributions to Conferences: PostersCharacterization of cannabinoid receptor ligands in tissues natively expressing cannabinoid CB2 receptors
British Journal of Pharmacology, vol. 169, no. 4, pp. 887-899Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/bph.12191
The cannabinoid TRPA1 agonist cannabichromene inhibits nitric oxide production in macrophages and ameliorates murine colitis
British Journal of Pharmacology, vol. 169, no. 1, pp. 213-229Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/bph.12120
Cannabidiolic acid prevents vomiting in Suncus murinus and nausea-induced behaviour in rats by enhancing 5-HT(1A) receptor activation
British Journal of Pharmacology, vol. 168, no. 6, pp. 1456-1470Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/bph.12043
CB1 Receptor Allosteric Modulators Display Both Agonist and Signaling Pathway Specificity
Molecular Pharmacology, vol. 83, no. 2, pp. 322-338Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1124/mol.112.080879
Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?
British Journal of Clinical Pharmacology, vol. 75, no. 2, pp. 323-333Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1111/j.1365-2125.2012.04341.x
Cannabinoids and omega-3/6 endocannabinoids as cell death and anticancer modulators
Progress in Lipid Research, vol. 52, no. 1, pp. 80-109Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.plipres.2012.10.001
- [ONLINE] View publication in Scopus
Targeting the endocannabinoid system with cannabinoid receptor agonists: pharmacological strategies and therapeutic possibilities
Philosophical Transactions of the Royal Society B: Biological Sciences, vol. 367, no. 1607, pp. 3353-3363Contributions to Journals: Literature Reviews- [ONLINE] DOI: https://doi.org/10.1098/rstb.2011.0381
Investigations on the 4-quinolone-3-carboxylic acid motif. 6. Synthesis and pharmacological evaluation of 7-substituted quinolone-3-carboxamide derivatives as high affinity ligands for cannabinoid receptors
European Journal of Medicinal Chemistry, vol. 58, pp. 30-43Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1016/j.ejmech.2012.09.035