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Details

Stereochemistry ABSOLUTE
Molecular Formula C11H12N2O2
Molecular Weight 204.2252
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRYPTOPHAN

SMILES

N[C@@H](CC1=CNC2=C1C=CC=C2)C(O)=O

InChI

InChIKey=QIVBCDIJIAJPQS-VIFPVBQESA-N
InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1

HIDE SMILES / InChI
Molecular Formula C11H12N2O2
Molecular Weight 204.2252
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:03:31 UTC 2023
Edited
by admin
on Fri Dec 15 16:03:31 UTC 2023
Record UNII
8DUH1N11BX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRYPTOPHAN
EP   HSDB   II   INCI   INN   MART.   MI   USAN   USP   VANDF  
INN   INCI   USAN  
Official Name English
TRYPTOPHAN [HSDB]
Common Name English
L-TRYPTOPHAN [VANDF]
Common Name English
NSC-13119
Code English
TRYPTOPHAN [INCI]
Common Name English
TRYPTOPHAN [EP MONOGRAPH]
Common Name English
TRYTOPHAN-
Common Name English
TRYPTOPHAN [II]
Common Name English
TRYPTOPHAN [VANDF]
Common Name English
N-ACETYLTRYPTOPHAN IMPURITY A [EP IMPURITY]
Common Name English
TRYPTOPHAN [MART.]
Common Name English
L-TRYPTOPHAN [USP-RS]
Common Name English
tryptophan [INN]
Common Name English
TRYPTOPHAN, L-
WHO-DD  
Systematic Name English
L-TRYPTOPHAN [FCC]
Common Name English
L-TRYPTOPHAN
FCC   USP-RS   VANDF  
Systematic Name English
TRYPTOPHAN ((-),L,S)
Common Name English
1H-INDOLE-3-PROPANOIC ACID, .ALPHA.-AMINO-, (S)-
Systematic Name English
(-)-TRYPTOPHAN
Common Name English
TRYPTOPHAN [USAN]
Common Name English
L-TRYPTOPHAN [JAN]
Common Name English
TRYPTOPHAN [USP MONOGRAPH]
Common Name English
L-.ALPHA.-AMINO-3-INDOLEPROPIONIC ACID
Common Name English
TRYPTOPHAN [MI]
Common Name English
Classification Tree Code System Code
LOINC 25546-3
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 34384-8
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 3072-6
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 3071-8
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 17752-7
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 53159-0
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 28608-8
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 20659-9
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 15130-8
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 26602-3
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
NCI_THESAURUS C68442
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 56993-9
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 3070-0
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 15145-6
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
WHO-ATC N06AX02
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 9325-2
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
FDA ORPHAN DRUG 796220
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 44414-1
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 27334-2
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 32275-0
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 13418-9
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 27135-3
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 3068-4
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 25139-7
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 3069-2
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 25994-5
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
DSLD 199 (Number of products:65)
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
CFR 21 CFR 172.320
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 24457-4
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
DSLD 2783 (Number of products:447)
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 13817-2
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
WHO-VATC QN06AX02
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
LOINC 74767-5
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
Code System Code Type Description
CAS
73-22-3
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
CHEBI
29954
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
EVMPD
SUB15631MIG
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
CHEBI
57912
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
FDA UNII
8DUH1N11BX
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
RXCUI
10898
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
200-795-6
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
INN
6173
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
ChEMBL
CHEMBL54976
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
CHEBI
16828
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
NCI_THESAURUS
C29603
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
DAILYMED
8DUH1N11BX
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
HSDB
4142
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
NSC
13119
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
DRUG BANK
DB00150
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
CHEBI
57719
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
RS_ITEM_NUM
1700501
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID5021419
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
MESH
D014364
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
DRUG CENTRAL
2780
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
WIKIPEDIA
TRYPTOPHAN
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
MERCK INDEX
m11247
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY Merck Index
SMS_ID
100000091926
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
CHEBI
27897
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
PUBCHEM
6305
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
EVMPD
SUB12377MIG
Created by admin on Fri Dec 15 16:03:31 UTC 2023 , Edited by admin on Fri Dec 15 16:03:31 UTC 2023
PRIMARY
Related Record Type Details
INDOLEAMINE 2,3-DIOXYGENASE 1
METABOLIC ENZYME -> SUBSTRATE
Structure of .ALPHA.-METHYL-L-TRYPTOPHAN C-11
RADIOLIGAND->TARGET
Used to monitor tryptophan uptake and metabolism
INDOLEAMINE 2,3-DIOXYGENASE 2
METABOLIC ENZYME -> INDUCER
Related Record Type Details
Structure of INDOXYL SULFATE
METABOLITE TOXIC -> PARENT
Metabolised to indole by gut lactobacilli then to indoxyl sulfate in the liver by cypE1 and a sulfation enzyme.
Structure of KYNURENINE
METABOLITE -> PARENT
Structure of OXITRIPTAN
METABOLITE -> PARENT
Structure of INDOLE
METABOLITE -> PARENT
Formed from tryptophanase from gut bacteria.
Structure of FORMYLKYNURENINE
METABOLITE -> PARENT
Structure of 3-INDOLINONE
METABOLITE -> PARENT
Metabolized from indole in the liver.
Structure of INDOLE-3-CARBOXALDEHYDE
METABOLITE -> PARENT
Structure of 5-METHOXYTRYPTOPHAN
METABOLITE -> PARENT
Structure of SEROTONIN
METABOLITE ACTIVE -> PARENT
Related Record Type Details
Structure of 1,2,3,4-TETRAHYDRO-BETA-CARBOLINE-3-CARBOXYLIC ACID
IMPURITY -> PARENT
EP
Structure of N-ACETYL-DL-TRYPTOPHAN
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 2-(2,3-DIHYDROXY-1-(1H-INDOL-3-YL)PROPYL)-L-TRYPTOPHAN
IMPURITY -> PARENT
EP
Structure of 2,3,4,9-TETRAHYDRO-1-(1H-INDOL-3-YLMETHYL)-1H-PYRIDO(3,4-B)INDOLE-3-CARBOXYLIC ACID
IMPURITY -> PARENT
EP
Structure of KYNURENINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of FORMYLKYNURENINE
IMPURITY -> PARENT
EP
Structure of OXITRIPTAN
IMPURITY -> PARENT
EP
Structure of DIOXYINDOLYLALANINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of IRON
IMPURITY -> PARENT
EP
Structure of (2S)-2-AMINO-3-(PHENYLAMINO)PROPANOIC ACID
IMPURITY -> PARENT
EP
Structure of 2-(3-INDOLYLMETHYL)-L-TRYPTOPHAN
IMPURITY -> PARENT
EP
Structure of SULFATE ION
IMPURITY -> PARENT
EP
Structure of 1,1'-ETHYLIDENEBIS(L-TRYPTOPHAN)
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of 2-HYDROXYTRYPTOPHAN
IMPURITY -> PARENT
EP
Structure of CHLORIDE ION
IMPURITY -> PARENT
EP
Related Record Type Details
Structure of TRYPTOPHAN
ACTIVE MOIETY
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