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Molecule
ID:2851
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General Information
Structure
Molecular Formula
C₁₄H₂₈O₆
Molecular Mass
292.36852
Exact Mass
292.18858862
Charge
0
InChI
InChI=1S/C14H28O6/c1-2-3-4-5-6-7-8-19-13-12(17)11(16)10(9-15)20-14(13)18/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14-/m1/s1
InChIKey
BVHPDIWLWHHJPD-RKQHYHRCSA-N
Canonic Smiles
CCCCCCCCO[C@H]1[C@H](O)O[C@@H]([C@H]([C@@H]1O)O)CO
Isomeric Smiles
[C@H]1(O)[C@H](OCCCCCCCC)[C@@H](O)[C@H](O)[C@H](O1)CO
Calculated Properties
JChem
Acid pKa
11.326057
H Acceptors
6
H Donor
4
LogD (pH = 5.5)
0.8127603
LogD (pH = 7.4)
0.8127095
Log P
0.81276095
Molar Refractivity
72.9522
Polarizability
29.735554
Polar Surface Area
99.38
Rotatable Bonds
9
Lipinski's Rule of Five
true
ALOGPS 2.1
Log P
1.2
LOG S
-1.28
Solubility (Water)
1.52e+01 g/l
Data Source
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Names and Identifiers
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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
•
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 Traditional name
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IUPAC 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
•
PubChem BioAssay
Data Source
Academic Data
DrugBank
DB03152
PubChem
445463
Names and Identifiers
Synonyms
B-2-Octylglucoside
IUPAC Traditional name
(2R,3R,4S,5S,6R)-6-(hydroxymethyl)-3-(octyloxy)oxane-2,4,5-triol
IUPAC name
(2R,3R,4S,5S,6R)-6-(hydroxymethyl)-3-(octyloxy)oxane-2,4,5-triol
Registration numbers
PubChem CID
445463
PubChem SID
46504476
160966298
Molecule Details
DrugBank
DB03152
Drug information: experimental
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay