21138-24-9
21138-24-9
Chemical Structure
L-Inosine
- CAS No.: 21138-24-9
- Formula:C10H12N4O5
- Molecular Weight:268.23
IUPAC Name: 2,2'-((2Z,2'Z)-((4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2,7-diyl)bis(methanylylidene))bis(6-fluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile
InChIKey: UGQMRVRMYYASKQ-DEGSGYPDSA-N
SMILES: O[C@@H]1[C@H](O)[C@@H](N2C3=C(C(N=CN3)=O)N=C2)O[C@H]1CO
Biological Activity: L-Inosine is the L-configuration of Inosine (HY-N0092). Inosine is an endogenous purine nucleoside produced by catabolism of adenosine[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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L-Inosine | 99.91% | L-Inosine is the L-configuration of Inosine (HY-N0092). Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. | ||||||||||||||||||||
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References
- [1]. Filipe Marques Gonçalves, et al. Signaling pathways underlying the antidepressant-like effect of inosine in mice. Purinergic Signal. 2017 Jun; 13(2): 203-214. [Content Brief]
- [2]. Sara Cipriani, et al. Protection by inosine in a cellular model of Parkinson’s disease. Neuroscience. 2014 Aug 22; 274: 242-249. [Content Brief]
Keywords
