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Merck
CN

T90204

L-色氨酸

99%

别名:

(S)-2-氨基-3-(3-吲哚基)丙酸, L-α-氨基-3-吲哚丙酸

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经验公式(希尔记法):
C11H12N2O2
化学文摘社编号:
分子量:
204.23
EC Number:
200-795-6
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
86197
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assay

99%

optical activity

[α]20/D −31.5°, c = 1 in H2O

optical purity

ee: 99% (GLC)

mp

280-285 °C (dec.) (lit.)

SMILES string

N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O

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-/m0/s1

InChI key

QIVBCDIJIAJPQS-VIFPVBQESA-N

Application

用于合成桥联吲哚生物碱。

Other Notes

血清素和褪黑素的氨基酸前体


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存储类别

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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Journal of the Chemical Society. Chemical Communications, 1559-1559 (1994)
Claudia Temperini et al.
Bioorganic & medicinal chemistry, 16(18), 8373-8378 (2008-09-09)
An activation study of mammalian carbonic anhydrase (CA, EC 4.2.1.1) isoforms I-XIV with D- and L-tryptophan has been performed both by means of kinetic and X-ray crystallographic techniques. These compounds show a time dependent activity against isozyme CA II, with
Rafat M Mohareb et al.
Bioorganic & medicinal chemistry, 19(9), 2966-2974 (2011-04-16)
There is a great deal of interest in neurotrophin therapy to prevent neuronal degeneration. The present study aimed at synthesizing new functionalized indole derivatives with structures justifying neuroprotective activity using L-tryptophan (TRP) as starting material. The potential neuroprotective effect of