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Molecule
ID:1418
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₁₄O₆
Molecular Mass
194.18246
Exact Mass
194.07903817
Charge
0
InChI
InChI=1S/C7H14O6/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-11H,2H2,1H3/t3-,4-,5+,6-,7-/m1/s1
InChIKey
HOVAGTYPODGVJG-XUUWZHRGSA-N
Canonic Smiles
CO[C@@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O
Isomeric Smiles
CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Calculated Properties
JChem
LogD (pH = 7.4)
-2.29
LogD (pH = 5.5)
-2.29
Log P
-2.29
Rotatable Bonds
2
H Donor
4
H Acceptors
6
Lipinski's Rule of Five
true
Acid pKa
12.21
Polar Surface Area
99.38
Polarizability
18.37
Molar Refractivity
40.67
LOG S
0.56
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
No Data Available
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Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
•
Commercial Catalog
Names and Identifiers
•
Brand Name
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
•
DrugBank
•
Sigma Aldrich
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
PubChem
445238
DrugBank
DB01642
ChEBI
CHEBI:320055
Commercial Catalog
Sigma Aldrich
M0779
66950
TRC
M309500
Names and Identifiers
Brand Name
MGL
Methyl beta-d-glucopyranoside
M0779_SIGMA
Beta-methyl-d-glucoside
Methyl-beta-d-glucopyranoside
Methyl beta-d-glucoside
IUPAC Traditional name
O1-methyl-glucose
methyl β-d-glucoside
IUPAC name
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol
Synonyms
O1-Methyl-Glucose
β-Methyl-D-glucoside hemihydrate
Methyl-β-D-glucopyranoside hemihydrate
Methyl β-D-glucoside
Methyl β-D-glucopyranoside
NSC 403457
1-O-Methyl-β-D-glucopyranoside
Methyl β-D-Glucopyranoside
beta-Methylglucoside
Beta-methyl-d-glucoside
methyl beta-D-glucopyranoside
1-O-Methyl-beta-D-glucopyranoside
Methyl beta-d-glucoside
beta-d-Methylglucopyranoside
Methyl hexopyranoside
Properties
Safety Information
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
MSDS Link
Download link
Source
Download link
Source
Storage Condition
-20°C Freezer, Under Inert Atmosphere
Source
Product Information
Purity
≥99% (HPLC and GC)
Source
≥99.0% (sum of enantiomers, HPLC)
Source
Empirical Formula (Hill Notation)
C7H14O6 · 0.5H2O
Source
Certificate of Analysis
Download link
Source
Physical Property
Melting Point
107-111 °C
Source
103-105°C
Source
Solubility
H2O: soluble0.1 g/mL, clear, colorless
Source
Methanol
Source
Water
Source
Optical Rotation
[α]20/D -33±1°, c = 10% in H2O
Source
Apperance
White to Off-White Solid
Source
Related Proteins
PDB Bank
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1E5J
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1FCE
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7VL4
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2BOD
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1QJW
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1GZ1
2VI0
1QK2
1UP3
1Q2E
2A8U
3WLP
1OC5
2BOG
Molecule Details
DrugBank
DB01642
Drug information: experimental
Sigma Aldrich
66950
Application
Methyl-β-D-glucopyranoside is used as a starting material for the biosynthesis of long-chain alkyl glucosides. Methyl-β-D-glucopyranoside is used as a substrate to identify, differentiate and characterize β-D-glucosidase(s).
ChEBI
CHEBI:320055
A beta-D-glucopyranoside having a methyl substituent at the anomeric position.
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
MDL Number
•
CAS Number
•
EC Number
•
Beilstein Number
•
PubChem CID
•
BKMS React Database
•
BRENDA Database
•
DrugBank ID
•
SABIO-RK Database
•
BRENDA Ligand Database
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MetaboLights Database
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CompTox Database
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Protein Data Bank
•
BindingDB Database
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PubMed Citation Links
•
ACToR Database
•
UniProt Database
•
CHEBI ID
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Gmelin ID
•
SureChEMBL Database
•
CHEMBL
Registration numbers
PubChem SID
24896570
24885055
160964878
46507087
87351049
MDL Number
MFCD00006602
CAS Number
709-50-2
7000-27-3
EC Number
211-909-9
Beilstein Number
81567
PubChem CID
445238
BKMS React Database
29812
103856
30182
9002
43864
5184
101894
101997
2083
1829
8470
BRENDA Database
2.4.1.19
3.2.1.108
2.4.99.6
1.1.3.10
1.1.99.29
2.7.1.199
2.3.1.79
3.2.1.28
3.2.1.45
2.4.1.25
3.2.1.75
2.4.1.281
2.4.1.34
3.2.1.21
DrugBank ID
DB01642
SABIO-RK Database
6942
7933
12927
BRENDA Ligand Database
101894
48426
2557
8408
2580
94057
2204
103856
8470
3478
101997
29812
2083
1829
MetaboLights Database
MTBLS14
MTBLS804
MTBLS4099
MTBLS2224
MTBLS926
MTBLS1866
MTBLS45
MTBLS2145
CompTox Database
DTXSID20883559
Protein Data Bank
1e5j
1fce
7vl4
2bod
1qjw
1gz1
2vi0
1qk2
1up3
1q2e
2a8u
3wlp
1oc5
2bog
BindingDB Database
50454778
PubMed Citation Links
19630436
7504304
17929936
11671987
ACToR Database
7000-27-3
UniProt Database
Q53922
Q57071
CHEBI ID
CHEBI:43887
CHEBI:320055
Gmelin ID
408559
SureChEMBL Database
SCHEMBL166332
CHEMBL
CHEMBL132186
2557
2204
3478
2580
94057
104267
48426
8408
2.4.1.20
5.4.2.5
3.2.1.B40
2.4.1.30
3.2.1.147
2.4.1.2
2.4.1.31
2.4.1.49
3.2.1.10
3.7.1.4
3.1.1.6
2.4.1.140
2.4.1.12
1.1.3.9
2.7.1.85
3.1.1.3
2.4.99.B6
1.1.99.13
3.2.1.62
30182
43864
9002
104267
5184