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About This Item
Empirical Formula (Hill Notation):
C10H16N4O3 · HNO3
CAS Number:
Molecular Weight:
303.27
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
233-079-7
MDL number:
Product Name
L-Anserine nitrate salt, hydroxyl radical scavenger
Quality Level
assay
≥98%
form
powder
color
white
application(s)
detection
SMILES string
O[N+]([O-])=O.Cn1cncc1C[C@H](NC(=O)CCN)C(O)=O
InChI
1S/C10H16N4O3.HNO3/c1-14-6-12-5-7(14)4-8(10(16)17)13-9(15)2-3-11;2-1(3)4/h5-6,8H,2-4,11H2,1H3,(H,13,15)(H,16,17);(H,2,3,4)/t8-;/m0./s1
InChI key
OLWOKAYJAHHSNY-QRPNPIFTSA-N
Biochem/physiol Actions
L-Anserine s a dipeptide found in most animal tissues. In model systems it is a potent antioxidant and scavener of hydroxyl radicals. It inhibits nonenzymatic protein glycation induced by aldose and ketose reducing sugars. It is much less potent than L-carnosine as an inhibitor of protein-protein crosslinking.
Other Notes
Anserine is a naturally occurring methylated analog of carnosine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Wieslaw Kopec et al.
Antioxidants (Basel, Switzerland), 9(11) (2020-11-12)
The objective of the study was to test the effect of diets supplemented with β-alanine, L-histidine, and carnosine on the histidine dipeptide content and the antioxidative status of chicken breast muscles and blood. One-day-old Hubbard Flex male chickens were assigned
Daiki Kubomura et al.
Nutritional neuroscience, 13(4), 183-188 (2010-07-31)
Anserine and L-carnosine are similar dipeptides synthesized by muscles of vertebrates. The functional role of anserine is unknown, although previous studies showed hypoglycemic effects of carnosine through autonomic nerves. Thus, we evaluated the effects of anserine on blood glucose levels
Angelo Zinellu et al.
Talanta, 84(3), 931-935 (2011-04-13)
A field amplified sample injection (FASI) capillary electrophoresis method with UV detection was developed for the separation and detection of carnosine-related peptides carnosine (Car), anserine (Ans) and homocarnosine (Hcar). The imidazole dipeptides were baseline-separated within 10 min by using 50
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A1131-250MG | 04061833335581 |
| A1131-100MG | 04061833335574 |
