about
P3364
In Vitro Tests For Workplace Cocarcinogens, Final ReportIn Vitro Tests For Workplace Cocarcinogens, Final ReportInhibition of Metabolic Cooperation in V79 Cells: Potential Correlations with Tumor PromotionD-amino acids indirectly inhibit biofilm formation in Bacillus subtilis by interfering with protein synthesis.Three new cytochalasins from the marine-derived fungus Spicaria elegans KLA03 by supplementing the cultures with L- and D-tryptophan.Alteration in the plasma concentration of a DAAO inhibitor, 3-methylpyrazole-5-carboxylic acid, in the ketamine-treated rats and the influence on the pharmacokinetics of plasma D-tryptophan.Unraveling complex small-molecule binding mechanisms by using simple NMR spectroscopy
P921
Q26372015-AFD739BC-AE4B-4F5E-A57F-88B22DA7E671Q26372165-4B9E472A-2738-49DF-B9C7-45C554D41A11Q26377429-7F93BC33-9E5E-4BC4-8C92-FC529149BE63Q33283055-83169428-C0E4-4F15-A889-FC0FCCB96E3FQ39544790-DFEF4639-6D9B-4C3F-9AE4-8D8011A69356Q41995548-01E65DA6-6727-4C12-AFD0-163836517FBAQ83453738-2DD9E82A-977B-4AC3-8D85-812611C9E69B
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
D-Tryptophan
@en
D-tryptofan
@nn
D-tryptofan
@pl
type
label
D-Tryptophan
@en
D-tryptofan
@nn
D-tryptofan
@pl
altLabel
(2R)-2-amino-3-(1H-indol-3-yl)propanoic acid
@en
(R)-2-amino-3-(3-indolyl)propansyre
@nn
(R)-2-amino-3-(3-indolyl)propionsyre
@nn
(R)-tryptofan
@nn
(R)-tryptophan
@en
D(+)-tryptofan
@nn
D-Trp
@en
D-Trp
@nn
D-W
@nn
DTR
@en
prefLabel
D-Tryptophan
@en
D-tryptofan
@nn
D-tryptofan
@pl
P279
P638
P592
P661
P662
P1579
P2017
C1=CC=C2C(=C1)C(=CN2)C[C@H](C(=O)O)N
P2057
HMDB0013609
P2067
P231
P232
P233
C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N
P234
1S/C11H12N2O2/c12-9(11(14)15)5 ...... 13H,5,12H2,(H,14,15)/t9-/m1/s1
P235
QIVBCDIJIAJPQS-SECBINFHSA-N
P2566
100.005.292
P274
C₁₁H₁₂N₂O₂
P2840
P3117
DTXSID0046989