CHEBI:86128 - 2-methyl-L-tryptophan

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ChEBI Name 2-methyl-L-tryptophan
ChEBI ID CHEBI:86128
ChEBI ASCII Name 2-methyl-L-tryptophan
Definition An L-tryptophan derivative in which the hydrogen at position 2 on the indole ring is replaced by a methyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H14N2O2
Net Charge 0
Average Mass 218.25180
Monoisotopic Mass 218.106
InChI InChI=1S/C12H14N2O2/c1-7-9(6-10(13)12(15)16)8-4-2-3-5-11(8)14-7/h2-5,10,14H,6,13H2,1H3,(H,15,16)/t10-/m0/s1
InChIKey BXJSOEWOQDVGJW-JTQLQIEISA-N
SMILES Cc1[nH]c2ccccc2c1C[C@H](N)C(O)=O
Metabolite of Species Details
Streptomyces laurentii (NCBI:txid39478) See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-methyl-L-tryptophan (CHEBI:86128) has role bacterial metabolite (CHEBI:76969)
2-methyl-L-tryptophan (CHEBI:86128) is a L-tryptophan derivative (CHEBI:47994)
2-methyl-L-tryptophan (CHEBI:86128) is tautomer of 2-methyl-L-tryptophan zwitterion (CHEBI:85908)
Incoming 2-methyl-L-tryptophan zwitterion (CHEBI:85908) is tautomer of 2-methyl-L-tryptophan (CHEBI:86128)
IUPAC Name
2-methyl-L-tryptophan
Synonyms Sources
2-Methyltryptophan ChemIDplus
L-2-Methyltryptophan KEGG COMPOUND
Manual Xrefs Databases
C16831 KEGG COMPOUND
CPD-392 MetaCyc
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Registry Numbers Types Sources
10551509 Reaxys Registry Number Reaxys
33468-32-5 CAS Registry Number KEGG COMPOUND
33468-32-5 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
23064318 PubMed citation Europe PMC
2321967 PubMed citation Europe PMC
7549921 PubMed citation Europe PMC
Last Modified
22 June 2015