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Molecule
ID:103406
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₆H₁₈O₈
Molecular Mass
338.30932
Exact Mass
338.10016754
Charge
0
InChI
InChI=1S/C16H18O8/c1-7-4-12(18)23-10-5-8(2-3-9(7)10)22-16-15(21)14(20)13(19)11(6-17)24-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13-,14+,15-,16+/m1/s1
InChIKey
YUDPTGPSBJVHCN-JZYAIQKZSA-N
Canonic Smiles
OC[C@H]1O[C@H](Oc2ccc3c(c2)oc(=O)cc3C)[C@@H]([C@H]([C@@H]1O)O)O
Isomeric Smiles
O=c1oc2cc(O[C@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)CO)ccc2c(c1)C
Calculated Properties
JChem
Acid pKa
12.20014
H Acceptors
7
H Donor
4
LogD (pH = 5.5)
-0.4888793
LogD (pH = 7.4)
-0.48888606
Log P
-0.4888792
Molar Refractivity
79.9559
Polarizability
31.877827
Polar Surface Area
125.68
Rotatable Bonds
3
Lipinski's Rule of Five
true
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General Information
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IUPAC name
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Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02151683
Sigma Aldrich
M9766
69591
Academic Data
PubChem
87330
Names and Identifiers
IUPAC Traditional name
4-methyl-7-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-2-one
IUPAC name
4-methyl-7-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one
Synonyms
4-Methylumbelliferyl α-D-glucopyranoside
4-METHYLUMBELLIFERYL α-D-GLUCOSIDE
4-Methylumbelliferyl α-D-glucopyranoside
4-Methylumbelliferyl α-D-glucoside
Registration numbers
EC Number
241-794-0
CAS Number
17833-43-1
Beilstein Number
1690776
MDL Number
MFCD00067661
PubChem SID
24897365
162090394
24885954
PubChem CID
87330
Molecule Details
MP Biomedicals
02151683
Crystalline Substrate for the fluorometric, phosphorimetric and spectrophotometric assay of α-D-glucosidase.
Sigma Aldrich
69591
Other Notes
Substrate for determination of α-D-glucosidase activity1
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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EC Number
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CAS Number
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Beilstein Number
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MDL Number
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PubChem SID
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PubChem CID
Properties
Safety Information
MSDS Link
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Storage Condition
-20°C, Protect from light
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Storage Temperature
-20°C
Source
German water hazard class
3
Source
Product Information
Certificate of Analysis
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Quality Level
PREMIUM
Source
Description
α-glucosidase substrate
Source
Purity
≥99.0% (TLC)
Source
Grade
for fluorescence
Source
suitable as substrate for α-D-glucosidase test
Source
C16H18O8
Source
Physical Property
Solubility
DMSO: soluble50 mg/mL, clear, colorless to faintly yellow
Source
Fluorescence
λex 317 nm; λem 374 nm (pH9.0)
Source
λex 365 nm; λem 445 nm in 0.1 M Tris pH 8.0 (α-glucosidase)
Source
λex 316 nm; λem 375 nm (Reaction product)
Source
λex 360 nm; λem 449 nm
Source
Suitability
Empirical Formula (Hill Notation)