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Molecule
ID:44452
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₃N₃O₅
Molecular Mass
243.21662
Exact Mass
243.08552053
Charge
0
InChI
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)
InChIKey
UHDGCWIWMRVCDJ-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(C(C1O)O)n1ccc(nc1=O)N
Isomeric Smiles
n1(C2C(C(C(O2)CO)O)O)c(=O)nc(cc1)N
Calculated Properties
JChem
Acid pKa
12.553241
H Acceptors
7
H Donor
4
LogD (pH = 5.5)
-2.7975256
LogD (pH = 7.4)
-2.7975204
Log P
-2.7975173
Molar Refractivity
54.5448
Polarizability
21.48729
Polar Surface Area
128.61
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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From Data Sources
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Data Source
Commercial Catalog
MP Biomedicals
02101459
Matrix Scientific
047887
Academic Data
PubChem
596
Names and Identifiers
IUPAC name
4-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2-dihydropyrimidin-2-one
IUPAC Traditional name
cytarabine hydrochloride
cytidine
Synonyms
Cytarabine
CYTIDINE FREE BASE
Cytosine-1-β-D-ribofuranoside
Cytosine-β-D-riboside
Registration numbers
EC Number
200-610-9
CAS Number
65-46-3
69-74-9
PubChem SID
162049215
PubChem CID
596
MDL Number
MFCD00066487
Molecule Details
MP Biomedicals
02101459
Free Base
Crystalline
References
PubChem Literature
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Bioactivity
PubChem BioAssay
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PubChem SID
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Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
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MSDS Link
Download link
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RTECS
UW7370000
Source
Room Temperature (15-30°C), Desiccate
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Product Information
>95%
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Physical Property
215-216°C
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Storage Condition
Purity
Certificate of Analysis
Melting Point