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Molecule
ID:131523
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₁₆N₂O₅
Molecular Mass
220.22304
Exact Mass
220.10592162
Charge
0
InChI
InChI=1S/C8H16N2O5/c1-3(12)10-5-7(14)6(13)4(2-11)15-8(5)9/h4-8,11,13-14H,2,9H2,1H3,(H,10,12)
InChIKey
MCGXOCXFFNKASF-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(N)C(C(C1O)O)NC(=O)C
Isomeric Smiles
CC(=O)NC1C(C(C(OC1N)CO)O)O
Calculated Properties
JChem
Acid pKa
12.507108
H Acceptors
6
H Donor
5
LogD (pH = 5.5)
-4.792502
LogD (pH = 7.4)
-3.4623196
Log P
-3.3274562
Molar Refractivity
48.6822
Polarizability
20.21645
Polar Surface Area
125.04
Rotatable Bonds
2
Lipinski's Rule of Five
true
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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
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IUPAC Traditional name
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IUPAC name
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Sigma Aldrich
A7397
Academic Data
PubChem
897
Names and Identifiers
Synonyms
N-Acetyl-D-glucosylamine
2-Acetamido-1-amino-1,2-dideoxy-β-D-glucopyranose
IUPAC Traditional name
N-[2-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
IUPAC name
N-[2-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
Registration numbers
PubChem SID
162225801
PubChem CID
897
MDL Number
MFCD00057751
CAS Number
4229-38-3
Properties
Safety Information
German water hazard class
3
Source
Storage Temperature
-20°C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay