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M0534
5-Methyl-DL-tryptophan
tryptophan analog
Synonim(y):
5-Methyltryptophan
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| Gabaryty przesyłki | SKU | Dostępność | Cena netto |
|---|---|---|---|
| 250 mg | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 1140,00 zł | |
| 1 g | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 2350,00 zł |
Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C12H14N2O2
Numer CAS:
Masa cząsteczkowa:
218.25
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
EC Number:
213-453-6
Beilstein/REAXYS Number:
20225
MDL number:
1140,00 zł
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
Pomoc techniczna
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Pozwól nam pomócQuality Level
assay
≥97% (HPLC)
form
powder
color
white to faint yellow
mp
280-282 °C
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
Cc1ccc2[nH]cc(CC(N)C(O)=O)c2c1
InChI
1S/C12H14N2O2/c1-7-2-3-11-9(4-7)8(6-14-11)5-10(13)12(15)16/h2-4,6,10,14H,5,13H2,1H3,(H,15,16)
InChI key
HUNCSWANZMJLPM-UHFFFAOYSA-N
Application
- Amelioration of colitis through modulation of gut microbiota: The metabolite 5-Methyl-ᴅʟ-tryptophan (5-MT), derived from Angelica sinensis polysaccharides, was found to ameliorate colitis by modulating gut microbiota and the TLR4/MyD88/NF-κB signaling pathway. This suggests a potential application of 5-MT in inflammatory bowel disease research and therapy (Zou et al., 2023).
- Enzymatic synthesis of tryptophan derivatives: A study on the one-pot enantioselective synthesis of (S)-spirobrassinin and non-natural (S)-methylspirobrassinin from amino acids highlights a method using a turnip enzyme. This research outlines a novel approach to synthesizing tryptophan derivatives, potentially useful in biochemical assays (Ryu et al., 2021).
Biochem/physiol Actions
5-Methyl-DL-tryptophan inhibits the synthesis of anthranilate compounds that are the first steps in the biosynthesis of tryptophan in Neurospora crassa.[1] 5-Methyl-DL-tryptophan is a corepressor of the E. coli trp repressor.[2][3]
5-Methyl-DL-tryptophan may be used to select genetic mutants of PS strain of Methanococcus voltae (archaebacteria). 5-Methyl-tryptophan is a repressor trp operon expression. 5-Methyl-tryptophan is a substrate for tryptophanase. 5-Methyl-tryptophan inhibits the induction of anthranilate synthase activity by elicitors in oats.
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Ta pozycja | |||
|---|---|---|---|
| form powder | form powder | form powder or crystals | form solid |
| assay ≥97% (HPLC) | assay ≥98% (TLC) | assay ≥95% (HPLC) | assay ≥98% (HPLC) |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C |
| mp 280-282 °C | mp 204-206 °C (dec.) (lit.) | mp - | mp - |
| color white to faint yellow | color - | color slightly off-white to brown | color white to off-white |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 100 |
Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
X H Zhang et al.
Plant physiology, 127(1), 131-141 (2001-09-13)
Anthranilate synthase (AS), the control enzyme of the tryptophan (Trp) biosynthetic pathway, is encoded by nuclear genes, but is transported into the plastids. A tobacco (Nicotiana tabacum) cDNA (ASA2) encoding a feedback-insensitive tobacco AS alpha-subunit was transformed into two different
E I Hyde et al.
European journal of biochemistry, 201(3), 569-579 (1991-11-01)
The Escherichia coli trp repressor binds to the trp operator in the presence of tryptophan, thereby inhibiting tryptophan biosynthesis. Tryptophan analogues lacking the alpha-amino group act as inducers of trp operon expression. We have used one- and two-dimensional 1H-NMR spectroscopy
Tetsuya Matsukawa et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 57(1-2), 121-128 (2002-04-03)
Oat phytoalexins, avenanthramides, are a series of substituted hydroxycinnamic acid amides with anthranilate. The anthranilate in avenanthramides is biosynthesized by anthranilate synthase (AS, EC 4.1.3.27). Induction of anthranilate synthase activity was investigated in oat leaves treated with oligo-N-acetylchitooligosaccharide elicitors. AS
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| M0534-1G | 04061833993347 |
| M0534-250MG | 04061833993354 |