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1-(beta-D-Arabinofuranosyl)-5-ethyluracil

HCID 153103
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
70020-72-3
Standard SMILES
CCc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)c(=O)[nH]c1=O
InChIKey
LNVBVDVUTCPLIZ-BDNRQGISSA-N
Molecular formula
C11H16N2O6
Average molar mass
272.25 g/mol
Monoisotopic mass
272.10083623

Overview

structure

Names & identifiers

Preferred name
1-(beta-D-Arabinofuranosyl)-5-ethyluracil
IUPAC
1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-ethylpyrimidine-2,4-dione
English name
5-Ethyluracil arabinoside
Molecular formula
C11H16N2O6
Molecular weight
272.25

Names & synonyms

1-(beta-D-Arabinofuranosyl)-5-ethyluracil70020-72-3656CO4QR68DTXSID802203052,4(1H,3H)-Pyrimidinedione, 1-beta-D-arabinofuranosyl-5-ethyl-RefChem:907432DTXCID401427965-Ethyluracil arabinosideEt-araU1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-ethylpyrimidine-2,4-dioneUNII-656CO4QR68SCHEMBL3385371
Show more names
2,4(1H,3H)-Pyrimidinedione, 1-β-D-arabinofuranosyl-5-ethyl-
CHEMBL32287251-.BETA.-ARABINOFURANOSYL-5-ETHYLURACIL5-ETHYL-1-.BETA.-D-ARABINOFURANOSYLURACIL1-beta-D-Arabinofuranosyl-5-ethylpyrimidine-2,4(1H,3H)-dione1-.BETA.-D-ARABINOFURANOSYL-5-ETHYL-2,4(1H,3H)-PYRIMIDINEDIONE2,4(1H,3H)-PYRIMIDINEDIONE, 1-.BETA.-D-ARABINOFURANOSYL-5-ETHYL-1-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-5-ethyl-pyrimidine-2,4-dione

Database identifiers

CAS
70020-72-3
PubChem CID
153103
DTXSID
DTXSID80220305

Properties

Computed structural properties

XLogP
-1.2
Topological polar surface area
119 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
6
Rotatable bonds
3
Heavy atoms
19
Formal charge
0
Complexity
423

Physicochemical properties

Density
1.501 · 1.501±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka
9.61 · 9.610±0.10(predicted)
FDA UNII
656 CO4QR68 · 656CO4QR68

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 2 items

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly.

Compounds that inhibit cell production of DNA or RNA.

Suppliers1 total

HONEST JOY HOLDINGS LIMITED[email protected]

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
ChEMBL
CHEMBL3228725
UNII
656CO4QR68
Nikkaji
J1.001.489A