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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
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

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.

Originator

Approval Year

PubMed

Sample Use Guides

In Vivo Use Guide
Single doses: 1.5; 2; 2.5 and 3 mg
Route of Administration: Intramuscular
Substance Class Chemical
Record UNII
03S640ADSK
Record Status Validated (UNII)
Record Version