Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H35NO4 |
Molecular Weight | 437.5711 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@@H](O)C[C@@]1([H])C3=C(N[C@H]2C)C=C(O[C@H](C)CCCC4=CC=CC=C4)C=C3OC(C)=O
InChI
InChIKey=FFVXQGMUHIJQAO-BFKQJKLPSA-N
InChI=1S/C27H35NO4/c1-17(8-7-11-20-9-5-4-6-10-20)31-22-15-25-27(26(16-22)32-19(3)29)24-14-21(30)12-13-23(24)18(2)28-25/h4-6,9-10,15-18,21,23-24,28,30H,7-8,11-14H2,1-3H3/t17-,18+,21-,23+,24-/m1/s1
Molecular Formula | C27H35NO4 |
Molecular Weight | 437.5711 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Levonantradol is a synthetic cannabinoid analogue of delta (9)-tetrahydrocannabinol (delta(9)-THC) administered intramuscularly. It has antiemetic and anti-analgesic properties. Although its precise mechanism of action is unknown, levonantradol appears to bind and activate the cannabinoid receptors CB1 and/or CB2. Antiemetic effect of levonantradol significantly superior to chlorpromazine. However, its adverse central effects limit its utility. The main adverse events are drowsiness and dizziness. Levonantradol, administered intramuscularly to the patients suffering from postoperative pain, manifested significant analgesic efficacy. Analgesia persisted for more than 6 h with the 2.5 and 3 mg doses of levonantradol. Drowsiness was frequent but few other psychoactive effects were reported.
Approval Year
PubMed
Title | Date | PubMed |
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Cannabinoids for control of chemotherapy induced nausea and vomiting: quantitative systematic review. | 2001 Jul 7 |
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Cannabinoid receptor agonist and antagonist effects on motor function in normal and 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP)-treated non-human primates. | 2001 Jun |
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Cannabinoids in medicine: A review of their therapeutic potential. | 2006 Apr 21 |
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A review of nabilone in the treatment of chemotherapy-induced nausea and vomiting. | 2008 Feb |
|
Therapeutic use of Cannabis sativa on chemotherapy-induced nausea and vomiting among cancer patients: systematic review and meta-analysis. | 2008 Sep |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16540272
Single doses: 1.5; 2; 2.5 and 3 mg
Route of Administration:
Intramuscular
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:00:12 GMT 2023
by
admin
on
Fri Dec 15 16:00:12 GMT 2023
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Record UNII |
03S640ADSK
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Record Status |
Validated (UNII)
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Record Version |
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-
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NCI_THESAURUS |
C267
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SUB08482MIG
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CHEMBL2111116
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100000082280
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5361881
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C1385
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4791
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71048-87-8
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DTXSID80221271
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LEVONANTRADOL
Created by
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C025490
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03S640ADSK
Created by
admin on Fri Dec 15 16:00:12 GMT 2023 , Edited by admin on Fri Dec 15 16:00:12 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |