Basic Description

Synonyms	Methyl L-tryptophanate \| L-Tryptophan methyl ester \| 4299-70-1 \| L-Tryptophan, methyl ester \| L-Tryptophane methyl ester \| (S)-methyl 2-amino-3-(1H-indol-3-yl)propanoate \| methyl (2S)-2-amino-3-(1H-indol-3-yl)propanoate \| Tryptophan methyl ester \| (S)-2-Amino-3-(1H-indol
Specifications & Purity	Reagent grade
Grade	Reagent Grade

Associated Targets(Human)

RAD51 Tchem DNA repair protein RAD51 homolog 1 (0 Activities)

Discover Target: RAD51

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC16A10 Tbio Monocarboxylate transporter 10 (0 Activities)

Discover Target: SLC16A10

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GRIN3A Tclin Glutamate receptor ionotropic, NMDA 3A (0 Activities)

Discover Target: GRIN3A

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

PBMC (10003 Activities)

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RAD51 Tchem DNA repair protein RAD51 homolog 1 (504 Activities)

Discover Target: RAD51

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC16A10 SLC16A10 protein (28 Activities)

Discover Target: SLC16A10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Leishmania donovani (89745 Activities)

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Grin1 Glutamate NMDA receptor (6467 Activities)

Discover Target: Grin1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc16a10 Monocarboxylate transporter 10 (73 Activities)

Discover Target: Slc16a10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Names and Identifiers

IUPAC Name	methyl (2S)-2-amino-3-(1H-indol-3-yl)propanoate
INCHI	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
InChi Key	KCUNTYMNJVXYKZ-JTQLQIEISA-N
Canonical SMILES	COC(=O)C(CC1=CNC2=CC=CC=C21)N
Isomeric SMILES	COC(=O)[C@H](CC1=CNC2=CC=CC=C21)N
PubChem CID	77980
Molecular Weight	218.256

Certificates

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Citations of This Product

1. Qiao Chong, Chen Fei, Liu Zhan, Huang Tianfang, Li Wei, Zhang Guolin, Luo Yinggang. (2022) Functional characterization of a catalytically promiscuous tryptophan decarboxylase from camptothecin-producing Camptotheca acuminata. Frontiers in Plant Science, 13 [PMID:36061783]

References

1. Albish K Paul,Suneesh C Karunakaran,Joshy Joseph,Danaboyina Ramaiah. (2015-10-24) Amino Acid-Porphyrin Conjugates: Synthesis and Study of their Photophysical and Metal Ion Recognition Properties.. Photochemistry and photobiology, 91 ((6)): (1348-1355). [PMID:26494428]
2. Qiao Chong, Chen Fei, Liu Zhan, Huang Tianfang, Li Wei, Zhang Guolin, Luo Yinggang. (2022) Functional characterization of a catalytically promiscuous tryptophan decarboxylase from camptothecin-producing Camptotheca acuminata. Frontiers in Plant Science, 13 [PMID:36061783]

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(S)-2-Amino-3-(1H-indol-3-yl)-propionic acid methyl ester - Reagent Grade, high purity , CAS No.4299-70-1