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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
Structure of LEVONANTRADOL

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Delta(9)-tetrahydrocannabinol and synthetic cannabinoids prevent emesis produced by the cannabinoid CB(1) receptor antagonist/inverse agonist SR 141716A.
2001 Feb
Cannabinoids for control of chemotherapy induced nausea and vomiting: quantitative systematic review.
2001 Jul 7
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
Activation of G-proteins in brain by endogenous and exogenous cannabinoids.
2006 Mar 10
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

Single doses: 1.5; 2; 2.5 and 3 mg
Route of Administration: Intramuscular
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:00:12 UTC 2023
Edited
by admin
on Fri Dec 15 16:00:12 UTC 2023
Record UNII
03S640ADSK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVONANTRADOL
INN  
INN  
Official Name English
levonantradol [INN]
Common Name English
1,9-PHENANTHRIDINEDIOL, 5,6,6A,7,8,9,10,10A-OCTAHYDRO-6-METHYL-3-(1-METHYL-4-PHENYLBUTOXY)-, 1-ACETATE, (6S-(3(S*),6ALPHA,6AALPHA,9ALPHA,10ABETA))
Common Name English
(-)-(6S,6AR,9R,10AR)-5,6,6A,7,8,9,10,10A-OCTAHYDRO-6-METHYL-3-((R)-1-METHYL-4-PHENYLBUTOXY)-1,9-PHENANTHRIDINEDIOL 1-ACETATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C267
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
Code System Code Type Description
EVMPD
SUB08482MIG
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
ChEMBL
CHEMBL2111116
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
SMS_ID
100000082280
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
PUBCHEM
5361881
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
NCI_THESAURUS
C1385
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
INN
4791
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
CAS
71048-87-8
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
EPA CompTox
DTXSID80221271
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
WIKIPEDIA
LEVONANTRADOL
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
MESH
C025490
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
FDA UNII
03S640ADSK
Created by admin on Fri Dec 15 16:00:12 UTC 2023 , Edited by admin on Fri Dec 15 16:00:12 UTC 2023
PRIMARY
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SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY