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M4001

Sigma-Aldrich

5-Methoxy-DL-Tryptophan

≥98% (TLC)

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About This Item

Empirische Formel (Hill-System):
C12H14N2O3
CAS-Nummer:
28052-84-8
Molekulargewicht:
234.25
Beilstein:
26781
EG-Nummer:
248-800-0
MDL-Nummer:
MFCD00005650
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24896893
NACRES:
NA.26

product name

5-Methoxy-DL-Tryptophan,

Assay

≥98% (TLC)

Qualitätsniveau

200

Form

crystalline

Farbe

white to light beige

mp (Schmelzpunkt)

258-261 °C (dec.) (lit.)

Anwendung(en)

peptide synthesis

Lagertemp.

−20°C

SMILES String

COc1ccc2[nH]cc(CC(N)C(O)=O)c2c1

InChI

1S/C12H14N2O3/c1-17-8-2-3-11-9(5-8)7(6-14-11)4-10(13)12(15)16/h2-3,5-6,10,14H,4,13H2,1H3,(H,15,16)

InChIKey

KVNPSKDDJARYKK-UHFFFAOYSA-N

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Biochem./physiol. Wirkung

5-Methoxy-DL-tryptophan is an amino acid derivative.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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Sigma-Aldrich

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Anika Kremer et al.
Applied microbiology and biotechnology, 79(6), 951-961 (2008-05-16)
Recently, a gene for a 7-dimethylallyltryptophan synthase (7-DMATS) was identified in Aspergillus fumigatus and its enzymatic function was proven biochemically. In this study, the behaviour of 7-DMATS towards aromatic substrates was investigated and compared with that of the 4-dimethylallyltryptophan synthase
J van Benthem et al.
Journal of neural transmission, 67(1-2), 147-162 (1986-01-01)
Testes weight, plasma FSH and LH concentration and pineal methylating capacity were compared in hamsters housed under either long (LD14:10) or short (LD8:16) photoperiods. Hamsters housed for 14 weeks under short photoperiod showed gonadal atrophy, which was complete after 6
D J Morton
Journal of pineal research, 4(1), 7-11 (1987-01-01)
Pineal glands were incubated in the presence of [3H] methoxytryptophan with and without methoxamine, epinephrine, and norepinephrine. The beta-adrenoceptor-stimulated pineal glands were capable of converting methoxytryptophan to methoxytryptamine, melatonin, methoxyindole acetic acid, and methoxytryptophol, albeit in small quantities. Only methoxyindole
J van Benthem et al.
Journal of neural transmission, 61(3-4), 219-237 (1985-01-01)
Until now the day/night and seasonal rhythmicity in the synthesis of 5-methoxyindoles (MI) is thought to be regulated by environmental factors, especially photoperiod and temperature. Endogenous factors are also implicated in the generation of N-acetyltransferase and hydroxyindole-O-methyltransferase activity rhythms. In
G L Brammer
Life sciences, 55(10), 775-787 (1994-01-01)
Markedly increased melatonin levels in plasma have been observed in response to tryptophan administration. This post-tryptophan melatonin increase has been attributed to the duodenum. Because extra-pineal sources of melatonin may be important in interpreting the meaning of altered melatonin production
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