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Molecule
ID:2675
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₈FN₃O₄
Molecular Mass
217.1545232
Exact Mass
217.04988397
Charge
0
InChI
InChI=1S/C7H8FN3O4/c8-3-1-11(2-4(9)6(13)14)7(15)10-5(3)12/h1,4H,2,9H2,(H,13,14)(H,10,12,15)/t4-/m0/s1
InChIKey
DBWPFHJYSTVBCZ-BYPYZUCNSA-N
Canonic Smiles
OC(=O)[C@H](Cn1cc(F)c(=O)[nH]c1=O)N
Isomeric Smiles
N[C@@H](Cn1cc(F)c(=O)[nH]c1=O)C(=O)O
Calculated Properties
JChem
Acid pKa
1.7217033
H Acceptors
5
H Donor
3
LogD (pH = 5.5)
-3.803562
LogD (pH = 7.4)
-3.998828
Log P
-3.801658
Molar Refractivity
44.8486
Polarizability
17.23067
Polar Surface Area
112.73
Rotatable Bonds
3
Lipinski's Rule of Five
true
ALOGPS 2.1
Log P
-1.73
LOG S
-1.75
Solubility (Water)
3.83e+00 g/l
Data Source
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Properties
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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ALOGPS 2.1
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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PubChem CID
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PubChem SID
Properties
Related Proteins
Molecular Spectra
Molecule Details
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DrugBank
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
DrugBank
DB02966
PubChem
126569
Names and Identifiers
IUPAC Traditional name
@fluoro-willardiine
IUPAC name
(2S)-2-amino-3-(5-fluoro-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)propanoic acid
Synonyms
Fluoro-Willardiine
Registration numbers
PubChem CID
126569
PubChem SID
160966124
46506706
Molecule Details
DrugBank
DB02966
Drug information: experimental
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay