26524-60-7
Chemical Structure
L-Cytidine
- CAS No.: 26524-60-7
- Formula:C9H13N3O5
- Molecular Weight:243.22
IUPAC Name: 2,2'-((2Z,2'Z)-((4,4,9,9-tetrahexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2,7-diyl)bis(methanylylidene))bis(5,6-dichloro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile
InChIKey: UHDGCWIWMRVCDJ-PSQAKQOGSA-N
SMILES: OC[C@@H]1O[C@H](N2C(N=C(C=C2)N)=O)[C@@H](O)[C@H]1O
Biological Activity: L-Cytidine is the L-configurational form of Cytidine (HY-B0158). L-Cytidine is a pyrimidine nucleoside and a component of RNA. Cytidine regulates glial glutamate cycling, affects cephalin metabolism, catecholamine synthesis and mitochondrial function. L-Cytidine interacts with HSA, which may alter the structure and function of HSA[1][2][3].
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L-Cytidine | 99.98% | L-Cytidine is the L-configurational form of Cytidine (HY-B0158). L-Cytidine is a pyrimidine nucleoside and a component of RNA. Cytidine regulates glial glutamate cycling, affects cephalin metabolism, catecholamine synthesis and mitochondrial function. L-Cytidine interacts with HSA, which may alter the structure and function of HSA. | ||||||||||||||||||||
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- [1]. Liu C, et al. Study on the stereoselective binding of cytosine nucleoside enantiomers to human serum albumin. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 2020 Jan 05;224:117452. [Content Brief]
- [2]. Breslow R, et al. On the origin of terrestrial homochirality for nucleosides and amino acids. Proceedings of the National Academy of Sciences of the United States of America. 2009 Jun 09;106(23):9144-6. [Content Brief]
- [3]. Dantsu Y, et al. Synthesis and Structural Characterization of 2'-Deoxy-2'-fluoro-l-uridine Nucleic Acids. Org Lett. 2021 Jul 2;23(13):5007-5011. [Content Brief]
Keywords
