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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H13NO4
Molecular Weight 223.2252
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETYL L-TYROSINE

SMILES

CC(=O)N[C@@H](CC1=CC=C(O)C=C1)C(O)=O

InChI

InChIKey=CAHKINHBCWCHCF-JTQLQIEISA-N
InChI=1S/C11H13NO4/c1-7(13)12-10(11(15)16)6-8-2-4-9(14)5-3-8/h2-5,10,14H,6H2,1H3,(H,12,13)(H,15,16)/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C11H13NO4
Molecular Weight 223.2252
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:52:22 UTC 2023
Edited
by admin
on Fri Dec 15 15:52:22 UTC 2023
Record UNII
DA8G610ZO5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETYL L-TYROSINE
Common Name English
N-ACETYLTYROSINE
EP  
Systematic Name English
(+)-(2S)-2-(ACETYLAMINO)-3-(4-HYDROXYPHENYL)PROPANOIC ACID
Systematic Name English
TYR-EXCEL
Brand Name English
L-N-ACETYLTYROSINE
Common Name English
N-ACETYLTYROSINE [EP MONOGRAPH]
Common Name English
L-TYROSINE, N-ACETYL
Common Name English
N-acetyltyrosin [WHO-DD]
Common Name English
N-ACETYL-L-TYROSINE [USP-RS]
Common Name English
ACETYL TYROSINE [INCI]
Common Name English
N-ACETYLTYROSIN
WHO-DD  
Systematic Name English
MELANOWHITE-A
Brand Name English
(2S)-2-ACETYLAMINO-3-(4-HYDROXYPHENYL)PROPANOIC ACID
Systematic Name English
N-ACETYL-L-TYROSINE
USP-RS  
Systematic Name English
TANOGEN HB
Brand Name English
NSC-10853
Code English
ACETYL TYROSINE
INCI  
INCI  
Official Name English
N-ACETYL-TYROSINE
Systematic Name English
Classification Tree Code System Code
DSLD 3506 (Number of products:19)
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
LOINC 79514-6
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
DSLD 3129 (Number of products:660)
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
LOINC 25119-9
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
LOINC 13780-2
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
LOINC 29632-7
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
NCI_THESAURUS C73539
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
Code System Code Type Description
NSC
10853
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
DRUG BANK
DB11102
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
PUBCHEM
68310
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
EPA CompTox
DTXSID7046045
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
NCI_THESAURUS
C61853
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
SMS_ID
100000088304
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
MESH
C025787
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
WIKIPEDIA
N-Acetyl-L-tyrosine
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
CHEBI
21563
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
FDA UNII
DA8G610ZO5
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
ECHA (EC/EINECS)
208-671-3
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
DAILYMED
DA8G610ZO5
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
EVMPD
SUB12166MIG
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
DRUG CENTRAL
4481
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
RS_ITEM_NUM
1010106
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
RXCUI
31005
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY RxNorm
CHEBI
68561
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
CAS
537-55-3
Created by admin on Fri Dec 15 15:52:23 UTC 2023 , Edited by admin on Fri Dec 15 15:52:23 UTC 2023
PRIMARY
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY