U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C8H15NO3
Molecular Weight 173.2096
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETYLLEUCINE

SMILES

CC(C)CC(NC(C)=O)C(O)=O

InChI

InChIKey=WXNXCEHXYPACJF-UHFFFAOYSA-N
InChI=1S/C8H15NO3/c1-5(2)4-7(8(11)12)9-6(3)10/h5,7H,4H2,1-3H3,(H,9,10)(H,11,12)

HIDE SMILES / InChI

Molecular Formula C8H15NO3
Molecular Weight 173.2096
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Acetylleucine is a drug that is used for symptomatic treatment of acute vestibular vertigo and dizziness. Its pharmacodynamics are not fully understood. The hypothesis is that it restores the membrane potential, via an interaction with membrane phospholipids on the injured side of vestibular neurons mainly in the thalamus or parietal region of the cortex. Clinical trials on animals showed an improvement in locomotor balance after forced rotation or unilateral vestibular neurotomy. Acetylleucine has a marketing authorisation in France although there is no evidence of its efficacy on human. Acetylleucine neither reduced the nausea associated with this provocative stimulus, nor hastened the acquisition or retention of vestibular habituation of motion sickness and nystagmus.

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro effects of acetyl-DL-leucine (tanganil) on central vestibular neurons and vestibulo-ocular networks of the guinea-pig.
2001 Feb
Effects of acetyl-DL-leucine in vestibular patients: a clinical study following neurotomy and labyrinthectomy.
2009

Sample Use Guides

1.5 g - 2 g per day, 3 or 4 tablets taken twice a day morning and evening. The duration of treatment is variable according to clinical advice (between 10 days and 5 - 6 weeks).
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:59:27 GMT 2023
Edited
by admin
on Fri Dec 15 16:59:27 GMT 2023
Record UNII
K76S41V71X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETYLLEUCINE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
N-ACETYL-DL-LEUCINE
Systematic Name English
acetylleucine [INN]
Common Name English
NSC-122020
Code English
NSC-758152
Code English
ACETYLLEUCINE [MART.]
Common Name English
ACETYLLEUCINE [MI]
Common Name English
ACETYLLEUCINE, DL-
Common Name English
Acetylleucine [WHO-DD]
Common Name English
TANGANIL
Brand Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 640818
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
FDA ORPHAN DRUG 631918
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
FDA ORPHAN DRUG 653218
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
FDA ORPHAN DRUG 626218
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
NCI_THESAURUS C73539
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
WHO-VATC QN07CA04
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
EU-Orphan Drug EU/3/18/2059
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
WHO-ATC N07CA04
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
Code System Code Type Description
MERCK INDEX
m1361
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY Merck Index
NSC
122020
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
CAS
99-15-0
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
WIKIPEDIA
ACETYLLEUCINE
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
DRUG BANK
DB13226
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
SMS_ID
100000084620
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID40859594
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
NCI_THESAURUS
C72679
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
DRUG CENTRAL
71
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
INN
5209
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
ChEMBL
CHEMBL1875805
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
PUBCHEM
1995
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
CHEBI
17786
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-734-9
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
NSC
758152
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
FDA UNII
K76S41V71X
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
EVMPD
SUB05231MIG
Created by admin on Fri Dec 15 16:59:27 GMT 2023 , Edited by admin on Fri Dec 15 16:59:27 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY