C122106
Cytidine
99%
Synonyme(s) :
Cytosine β-D-riboside, Cytosine-1-β-D-ribofuranoside
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A propos de cet article
Formule empirique (notation de Hill) :
C9H13N3O5
Numéro CAS:
Poids moléculaire :
243.22
UNSPSC Code:
41106305
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-610-9
Beilstein/REAXYS Number:
89173
MDL number:
Assay:
99%
Form:
powder
Storage temp.:
2-8°C
Service technique
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assay
99%
form
powder
optical activity
[α]20/D +33°, c = 2 in H2O
mp
210-220 °C (dec.) (lit.)
storage temp.
2-8°C
SMILES string
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O
InChI
1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7-,8-/m1/s1
InChI key
UHDGCWIWMRVCDJ-XVFCMESISA-N
Gene Information
mouse ... Uck1(22245)
General description
Cytidine also known as cytosine β-D-riboside, is a nucleoside, commonly used in organic synthesis.
Application
Cytidine can be used as a building block to synthesize 5‘-hydroxy-5‘-phosphonate derivatives of cytidine. Additionally, it is used to regulate the phosphatidate phosphatase activity by nucleotides.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Regulation of phosphatidate phosphatase activity from the yeast Saccharomyces cerevisiae by nucleotides.
The Journal of Biological Chemistry, 269, 29495-29501 (1994)
Stereoselective synthesis of the 5 `-hydroxy-5 `-phosphonate derivatives of cytidine and cytosine arabinoside
X Chen
The Journal of Organic Chemistry, 67, 9331-9339 (2002)
Takayuki Ohira et al.
The Journal of biological chemistry, 288(11), 7645-7652 (2013-01-31)
Non-universal genetic codes are frequently found in animal mitochondrial decoding systems. In squid mitochondria, four codons deviate from the universal genetic code, namely AUA, UGA, and AGA/AGG (AGR) for Met, Trp, and Ser, respectively. To understand the molecular basis for