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107751

Sigma-Aldrich

5-Hydroxy-L-tryptophan

98% (calc. on dried substance)

Sinónimos:

(S)-5-Hydroxytryptophan, 5-Hydroxytryptophan, L-5-HTP, L-5-Hydroxytryptophan

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About This Item

Fórmula empírica (notación de Hill):
C11H12N2O3
Número de CAS:
4350-09-8
Peso molecular:
220.22
Beilstein/REAXYS Number:
88200
EC Number:
224-411-1
MDL number:
MFCD00064341
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24846778
NACRES:
NA.22

assay

98% (calc. on dried substance)

form

solid

optical activity

[α]22/D −30°, c = 1 in H2O

reaction suitability

reaction type: solution phase peptide synthesis

refractive index

n20/D 1.4850 (lit.)

mp

270 °C (dec.) (lit.)

density

0.902 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

SMILES string

N[C@@H](Cc1c[nH]c2ccc(O)cc12)C(O)=O

InChI

1S/C11H12N2O3/c12-9(11(15)16)3-6-5-13-10-2-1-7(14)4-8(6)10/h1-2,4-5,9,13-14H,3,12H2,(H,15,16)/t9-/m0/s1

InChI key

LDCYZAJDBXYCGN-VIFPVBQESA-N

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pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Huixi Zou et al.
Journal of natural products, 72(1), 44-52 (2008-12-31)
This study reports that a series of tryptophan derivatives with modifications on the side chain or at the indole ring were accepted by two cyclic dipeptide prenyltransferases, CdpNPT and FtmPT1, and converted to prenylated derivatives. The structures of the enzymatic
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