| Identification | Back Directory | [Name]
2'-Deoxycytidine | [CAS]
207121-53-7 | [Synonyms]
DC
Dbct
2'-DC
doublecortin
RP5-914P14.1
2'-DEOXYCYTIDINE
OTTMUSP00000020394
OTTMUSP00000020395
OTTMUSP00000020396
2'-DEOXY-D-CYTIDINE
2'-DEOXYCYTIDINE:H2O
CYTOSINE DEOXYRIBOSIDE
2'-Deoxycytidine USP/EP/BP
2-DEOXYCYTIDINE H2O (RIBOSE-1-13C)
Anti-DCX antibody produced in goat
Cytidine, 2'-deoxy-, hydrate (1:1)
1-(2'-DEOXY-BETA-D-RIBOFURANOSYL)CYTOSINE
4-Amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
4-amino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one:hydrate
4-aMino-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxyMethyl)oxolan-2-yl]-1,2-dihydropyriMidin-2-one
4-Amino-1-((2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one hydrate | [EINECS(EC#)]
213-454-1 | [Molecular Formula]
C9H15N3O5 | [MDL Number]
MFCD00006547 | [MOL File]
207121-53-7.mol | [Molecular Weight]
245.24 |
| Chemical Properties | Back Directory | [Melting point ]
209-211 °C(lit.) | [storage temp. ]
Keep in dark place,Sealed in dry,2-8°C | [solubility ]
Methanol (Slightly), Water (Slightly) | [form ]
Solid | [color ]
White | [biological source]
goat | [Stability:]
Hygroscopic | [InChI]
InChI=1/C9H13N3O4.H2O/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8;/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15);1H2/t5-,6+,8+;/s3 | [InChIKey]
HXBGOHZLZCFWLH-AZXCMKNYNA-N | [SMILES]
O=C1N=C(N)C=CN1[C@H]1C[C@H](O)[C@@H](CO)O1.O |&1:8,10,12,r| |
| Hazard Information | Back Directory | [Uses]
A deoxyribonucleoside as Eg5 kinesin modulator with antiproliferative and apoptosis-inducing activity. | [Definition]
ChEBI: 2'-deoxycytidine is a pyrimidine 2'-deoxyribonucleoside having cytosine as the nucleobase. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is functionally related to a cytosine. | [Purification Methods]
Purify 2'-deoxycytidine by recrystallisation from MeOH/Et2O or EtOH and dry it in air. [NMR: Miles J Am Chem Soc 85 1007 1963, UV: Fox & Shugar Biochim Biophys Acta 9 369 1952.] The hydrochloride crystallises from H2O/EtOH and has m 174o(dec, 169-173o). [Walker & Butler Can J Chem 34 1168 1956.] The picrate has m 208o(dec). [Fox et al. J Am Chem Soc 83 4066 1961, Beilstein 25 III/IV 3662.] |
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