TRYPTOPHAN, D-

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

InChIKey=QIVBCDIJIAJPQS-SECBINFHSA-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-/m1/s1

Targets

Primary Target	Pharmacology	Condition	Potency
Escherichia coli 82 Target ID: CHEMBL354 Sources: https://www.ncbi.nlm.nih.gov/pubmed/29257726 \| https://www.ncbi.nlm.nih.gov/pubmed/25836411	Inhibitor 8504

PubMed

Title	Date	PubMed
Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A.	2010-05-21	20392128
Aromatic D-amino acids act as chemoattractant factors for human leukocytes through a G protein-coupled receptor, GPR109B.	2009-03-10	19237584
Prevention of severe menorrhagia in oncology patients with treatment-induced thrombocytopenia by luteinizing hormone-releasing hormone agonist and depo-medroxyprogesterone acetate.	2006-10-01	16944540
The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.	2003-08-08	12895062
Comparison of the responses of the chorda tympani and glossopharyngeal nerves to taste stimuli in C57BL/6J mice.	2003-03-04	12617752

Patents

Name

Type

Language

TRYPTOPHAN, D-

Systematic Name

English

NSC-97942

Preferred Name

English

(2R)-2-AMINO-3-(1H-INDOL-3-YL)PROPANOIC ACID

Systematic Name

English

D-TRYPTOPHAN

Systematic Name

English

(+)-TRYPTOPHAN

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID0046989