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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H14N2O2
Molecular Weight 218.2518
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Methyl L-tryptophanate

SMILES

COC(=O)[C@@H](N)CC1=CNC2=CC=CC=C12

InChI

InChIKey=KCUNTYMNJVXYKZ-JTQLQIEISA-N
InChI=1S/C12H14N2O2/c1-16-12(15)10(13)6-8-7-14-11-5-3-2-4-9(8)11/h2-5,7,10,14H,6,13H2,1H3/t10-/m0/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Stereochemistry and mechanism of reactions catalyzed by indolyl-3-alkane alpha-hydroxylase.
1979 Jul 25
Synthesis of "no-carrier-added" alpha-[11C]methyl-L-tryptophan.
1988 Mar
Synthesis of enantiomerically pure alpha-[14C]methyl-L-tryptophan.
1993 Sep
Patents
Name Type Language
Methyl L-tryptophanate
Systematic Name English
Methyl tryptophanate
Common Name English
L-Tryptophan, methyl ester
Systematic Name English
Tryptophan, methyl ester, L-
Systematic Name English
Code System Code Type Description
PUBCHEM
77980
Created by admin on Sat Dec 16 20:11:27 GMT 2023 , Edited by admin on Sat Dec 16 20:11:27 GMT 2023
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CAS
4299-70-1
Created by admin on Sat Dec 16 20:11:27 GMT 2023 , Edited by admin on Sat Dec 16 20:11:27 GMT 2023
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ECHA (EC/EINECS)
224-309-7
Created by admin on Sat Dec 16 20:11:27 GMT 2023 , Edited by admin on Sat Dec 16 20:11:27 GMT 2023
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FDA UNII
ZP5C4VEH76
Created by admin on Sat Dec 16 20:11:27 GMT 2023 , Edited by admin on Sat Dec 16 20:11:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID30884057
Created by admin on Sat Dec 16 20:11:27 GMT 2023 , Edited by admin on Sat Dec 16 20:11:27 GMT 2023
PRIMARY