5-bromo-1-[3-hydroxy-5-(hydroxymethyl)-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione
AlkaPlorer ID: AK524023
Synonym: None
IUPAC Name: 5-bromo-1-[3-hydroxy-5-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-yl]pyrimidine-2,4-dione
Structure
SMILES: O=C1N=C(O)C(Br)=CN1C1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C1O
InChI: InChI=1S/C15H21BrN2O11/c16-4-1-18(15(26)17-12(4)25)13-10(24)11(6(3-20)27-13)29-14-9(23)8(22)7(21)5(2-19)28-14/h1,5-11,13-14,19-24H,2-3H2,(H,17,25,26)
InChIKey: SLVUBEQZZWHSHM-UHFFFAOYSA-N
Reference
Formation of 3′-<i>O</i>-β-Galactosyl Compounds of 5-Bromouridine by<i>Sporobolomyces singularis</i>
PubChem CID: 139586276
LOTUS: LTS0185933
COCONUT: CNP0356129.1
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Hamamotoa singularis | Hamamotoa | Chrysozymaceae | None | Microbotryomycetes | Basidiomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 485.2400000000001
TPSA？: 204.19
MolLogP？: -3.8529
Number of H-Donors: 7
Number of H-Acceptors: 13
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|