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Molecule
ID:117427
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₁FN₂O₃S
Molecular Mass
294.3014432
Exact Mass
294.04744144
Charge
0
InChI
InChI=1S/C13H11FN2O3S/c14-10-4-2-1-3-8(10)7-20-13-15-9(6-12(18)19)5-11(17)16-13/h1-5H,6-7H2,(H,18,19)(H,15,16,17)
InChIKey
MGILZVKZKXAVIP-UHFFFAOYSA-N
Canonic Smiles
OC(=O)Cc1cc(=O)[nH]c(n1)SCc1ccccc1F
Isomeric Smiles
[nH]1c(nc(cc1=O)CC(=O)O)SCc1c(F)cccc1
Calculated Properties
JChem
Acid pKa
3.7407866
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
0.42908606
LogD (pH = 7.4)
-1.1002538
Log P
2.1884947
Molar Refractivity
74.0017
Polarizability
27.556973
Polar Surface Area
78.76
Rotatable Bonds
5
Lipinski's Rule of Five
true
Data Source
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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IUPAC Traditional name
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IUPAC name
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From Data Sources
Bioactivity
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Data Source
Academic Data
PubChem
33679543
Commercial Catalog
Life Chemicals
F2158-0425
Names and Identifiers
Synonyms
{2-[(2-fluorobenzyl)thio]-6-oxo-1,6-dihydropyrimidin-4-yl}acetic acid
IUPAC Traditional name
(2-{[(2-fluorophenyl)methyl]sulfanyl}-6-oxo-1H-pyrimidin-4-yl)acetic acid
IUPAC name
2-(2-{[(2-fluorophenyl)methyl]sulfanyl}-6-oxo-1,6-dihydropyrimidin-4-yl)acetic acid
Registration numbers
PubChem SID
162102075
PubChem CID
33679543
MDL Number
MFCD11986911
Properties
Physical Property
Partition Coefficient
1.922
Source
Product Information
Purity
95+%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay