M9005
3-Methyl-L-histidine
≥98% (TLC)
Synonym(s):
π-Methyl-L-histidine, 1-Methyl-L-histidine (archaic), 3-(1-Methylimidazol-5-yl)-L-alanine
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About This Item
Empirical Formula (Hill Notation):
C7H11N3O2
CAS Number:
Molecular Weight:
169.18
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26
EC Number:
206-704-6
MDL number:
Product Name
3-Methyl-L-histidine,
assay
≥98% (TLC)
Quality Level
form
powder
color
white to off-white
mp
254 °C
application(s)
detection
SMILES string
Cn1cncc1C[C@H](N)C(O)=O
InChI
1S/C7H11N3O2/c1-10-4-9-3-5(10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1
InChI key
JDHILDINMRGULE-LURJTMIESA-N
Application
- Engineering mutually orthogonal PylRS/tRNA pairs for dual encoding of functional histidine analogues.: Exploring innovative genetic engineering techniques, this research advances the use of histidine analogues like 3-Methyl-L-histidine for producing novel proteins with enhanced functionalities, offering vast potential in therapeutic and industrial applications (Taylor et al., 2023).
- Improving the enzymatic activity of l-amino acid α-ligase for imidazole dipeptide production by site-directed mutagenesis.: This investigation enhances the enzymatic synthesis of imidazole dipeptides, crucial for understanding the role of modifications like those seen in 3-Methyl-L-histidine and its impact on biological activities (Kino et al., 2023).
Biochem/physiol Actions
3-Methyl-L-histidine is a non-proteinogenic amino acid and an index of muscle breakdown.
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Richard Lee et al.
Analytical chemistry, 82(7), 2959-2968 (2010-03-03)
Despite several decades of active research, the success of large-scale clinical trials involving antioxidants remains equivocal given the complex biological interactions of reactive oxygen/nitrogen species in human health. Herein, we outline a differential metabolomics strategy by capillary electrophoresis-electrospray ionization-mass spectrometry
S G A van der Drift et al.
Journal of dairy science, 95(9), 4911-4920 (2012-08-25)
The objective of this study was to obtain information on variation between dairy cows in muscle and fat tissue mobilization around parturition and to study the association between protein and fat mobilization and serum β-hydroxybutyrate (BHBA) concentrations (hyperketonemia) in this
Elin Chorell et al.
Journal of proteome research, 8(6), 2966-2977 (2009-03-26)
We have investigated whether postexercise ingestion of carbohydrates in combination with proteins generates a different systemic metabolic response, as compared to the sole ingestion of carbohydrate or water, in the early recovery phase following exercise. In addition, metabolic patterns related
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M9005-1G | 04061826061008 |
| M9005-100MG | 04061834063803 |
| M9005-250MG | 04061832417578 |