DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/24430917https://www.ncbi.nlm.nih.gov/pubmed/17630726Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/23621668 | https://www.ncbi.nlm.nih.gov/pubmed/22954177 | https://www.ncbi.nlm.nih.gov/pubmed/24525548 | https://www.ncbi.nlm.nih.gov/pubmed/25777582 | https://www.ncbi.nlm.nih.gov/pubmed/23401746
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24430917https://www.ncbi.nlm.nih.gov/pubmed/17630726
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/23621668 | https://www.ncbi.nlm.nih.gov/pubmed/22954177 | https://www.ncbi.nlm.nih.gov/pubmed/24525548 | https://www.ncbi.nlm.nih.gov/pubmed/25777582 | https://www.ncbi.nlm.nih.gov/pubmed/23401746
CB-13 is a cannabinoid drug, which acts as a potent agonist at both the CB1 and CB2 receptors, but has poor blood-brain barrier penetration, and so produces only peripheral effects at low doses, with symptoms of central effects such as catalepsy only appearing at much higher dose ranges. CB-13 displays antihyperalgesic activity in a rat model of neuropathic pain with no CNS side effects.
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1097148https://www.google.com/patents/WO2002042248A2
Curator's Comment: # Novartis Ag, Novartis Pharma Gmbh
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL218 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17630726 |
6.1 nM [EC50] | ||
Target ID: CHEMBL253 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17630726 |
27.9 nM [EC50] | ||
Target ID: CHEMBL3397 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17630726 |
80800.0 nM [IC50] | ||
Target ID: CHEMBL218 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22284817 |
10.0 nM [Ki] | ||
Target ID: CHEMBL253 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26000707 |
42.0 nM [Ki] | ||
Target ID: CHEMBL4794 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25029033 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17630726 |
Primary | Unknown Approved UseUnknown |
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Primary | Sativex Approved UseUnknown |
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Primary | Sativex Approved UseUnknown |
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Primary | Sativex Approved UseUnknown |
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Primary | Sativex Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
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. | 2007 Aug 9 |
|
Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol. | 2014 May 25 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT03087201
2.7 mg delta-9-tetrahydrocannabinol (THC) and 2.5 mg cannabidiol (CBD), maximum dose (12 puffs): 32.4 mg THC/30 mg CBD
Route of Administration:
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C29631
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All of the following components must be present:
SUBSTANCE RECORD