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Molecule
ID:2842
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₁₀O₅
Molecular Mass
150.1299
Exact Mass
150.05282342
Charge
0
InChI
InChI=1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4+,5+/m0/s1
InChIKey
HMFHBZSHGGEWLO-QMKXCQHVSA-N
Canonic Smiles
OC[C@@H]1O[C@H]([C@@H]([C@H]1O)O)O
Isomeric Smiles
OC[C@@H]1O[C@@H](O)[C@H](O)[C@H]1O
Calculated Properties
JChem
Acid pKa
11.305696
H Acceptors
5
H Donor
4
LogD (pH = 5.5)
-2.3022048
LogD (pH = 7.4)
-2.3022583
Log P
-2.3022044
Molar Refractivity
29.9609
Polarizability
12.6405
Polar Surface Area
90.15
Rotatable Bonds
1
Lipinski's Rule of Five
true
ALOGPS 2.1
Log P
-2.57
LOG S
0.91
Solubility (Water)
1.22e+03 g/l
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
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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Synonyms
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IUPAC name
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IUPAC Traditional name
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
DB03142
PubChem
445935
Names and Identifiers
Synonyms
Alpha-L-Arabinose
IUPAC name
(2R,3R,4R,5S)-5-(hydroxymethyl)oxolane-2,3,4-triol
IUPAC Traditional name
α-L-arabinofuranose
Registration numbers
PubChem CID
445935
PubChem SID
162103333
Molecule Details
DrugBank
DB03142
Drug information: experimental
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay