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Molecule
ID:111826
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₈O₆
Molecular Mass
306.31052
Exact Mass
306.1103383
Charge
0
InChI
InChI=1S/C16H18O6/c17-8-12-13(18)14(19)15(20)16(22-12)21-11-7-3-5-9-4-1-2-6-10(9)11/h1-7,12-20H,8H2/t12-,13-,14+,15-,16-/m1/s1
InChIKey
CVAOQMBKGUKOIZ-IBEHDNSVSA-N
Canonic Smiles
OC[C@H]1O[C@@H](Oc2cccc3c2cccc3)[C@@H]([C@H]([C@@H]1O)O)O
Isomeric Smiles
O(c1cccc2c1cccc2)[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)CO
Calculated Properties
JChem
LogD (pH = 7.4)
0.39
LogD (pH = 5.5)
0.39
Log P
0.39
Rotatable Bonds
3
H Donor
4
H Acceptors
6
Lipinski's Rule of Five
true
Acid pKa
12.20
Polar Surface Area
99.38
Polarizability
30.70
Molar Refractivity
76.63
LOG S
-3.29
Data Source
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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IUPAC name
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
05221196
Academic Data
PubChem
7573796
ChEBI
CHEBI:136775
Names and Identifiers
IUPAC name
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(naphthalen-1-yloxy)oxane-3,4,5-triol
Synonyms
1-NAPHTHYL-β-D-GLUCOPYRANOSIDE
1-naphthyl beta-D-glucoside
1-Naphthylglucoside
naphthalen-1-yl beta-D-glucoside
1-naphthol glucoside
1-Naphthyl beta-D-glucopyranoside
IUPAC Traditional name
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(naphthalen-1-yloxy)oxane-3,4,5-triol
Registration numbers
CAS Number
65174-63-2
19939-82-3
PubChem SID
162097107
85336505
PubChem CID
7573796
BKMS React Database
83760
110613
129137
110008
103402
BRENDA Database
3.2.1.23
2.4.1.237
2.4.1.91
2.4.1.35
2.4.1.358
BRENDA Ligand Database
83760
110613
129137
103402
110008
CHEBI ID
CHEBI:136775
MetaboLights Database
MTBLS312
SureChEMBL Database
SCHEMBL1004201
PubMed Citation Links
6845360
9000339
Reaxys Registry
34364
Properties
Product Information
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Safety Information
MSDS Link
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Molecule Details
MP Biomedicals
05221196
MP Biomedicals Rare Chemical collection
ChEBI
CHEBI:136775
A beta-D-glucoside that is beta-D-glucopyranose in which the anomeric hydroxy hydrogen has been replaced by a 1-naphthyl group.
References
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Bioactivity
PubChem BioAssay
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CAS Number
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PubChem SID
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PubChem CID
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BKMS React Database
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BRENDA Database
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BRENDA Ligand Database
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CHEBI ID
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MetaboLights Database
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SureChEMBL Database
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PubMed Citation Links
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Reaxys Registry