14403-45-3
14403-45-3
Chemical Structure
L-β-Imidazolelactic acid
- CAS No.: 14403-45-3
- Formula:C6H8N2O3
- Molecular Weight:156.14
IUPAC Name: (S)-2-hydroxy-3-(1H-imidazol-5-yl)propanoic acid
InChIKey: ACZFBYCNAVEFLC-YFKPBYRVSA-N
SMILES: C(C1=CN=CN1)[C@@H](C(=O)O)O
Biological Activity: L-β-Imidazolelactic acid is an inhibitor of Cholinesterase and Monoamine oxidase, and also the final metabolite of L-Histidine (HY-N0832). L-β-Imidazolelactic acid increases the activity of Superoxide dismutase. L-β-Imidazolelactic acid is applicable to research related to liver cirrhosis and histidinemia[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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L-β-Imidazolelactic acid | 99.93% | L-β-Imidazolelactic acid is an inhibitor of Cholinesterase and Monoamine oxidase, and also the final metabolite of L-Histidine (HY-N0832). L-β-Imidazolelactic acid increases the activity of Superoxide dismutase. L-β-Imidazolelactic acid is applicable to research related to liver cirrhosis and histidinemia. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.88
HY-W010209SDL-Histidine-13C6,15N3 -
Similarity Score 0.88
HY-W010209S1DL-Histidine-15N -
Similarity Score 0.88
HY-W012572RD-Histidine (Standard) -
Similarity Score 0.86
HY-W142156D-Histidine monohydrochloride -
Similarity Score 0.84
HY-W012572AD-Histidine hydrochloride hydrate -
Similarity Score 0.84
HY-W014422DL-Histidine hydrochloride hydrate -
Similarity Score 0.84
HY-W014423RL-Histidine hydrochloride hydrate (Standard) -
Similarity Score 0.84
HY-W014423SL-Histidine-13C hydrochloride hydrate -
Similarity Score 0.84
HY-W014423S2L-Histidine-13C6 hydrochloride hydrate -
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References
- [1]. Odoko M, et al. Bis [2-hydroxy-3-(1H-imidazol-4-yl) propionato] nickel (II)[J]. Structure Reports, 2002, 58(1): m7-m9.
- [2]. Tansini CM, et al. Effects of histidine and imidazolelactic acid on various parameters of the oxidative stress in cerebral cortex of young rats. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience. 2004 Apr;22(2):67-72. [Content Brief]
