N-[(2R,3R,4R,5R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide

• ChemBase ID: 2811
• Molecular Formular: C8H15NO6
• Molecular Mass: 221.2078
• Monoisotopic Mass: 221.08993721
• SMILES: CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@H](O)[C@@H]1O
• Canonical SMILES: OC[C@H]1O[C@@H](O)[C@@H]([C@H]([C@H]1O)O)NC(=O)C
• InChI: InChI=1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6+,7-,8-/m1/s1
• InChIKey: OVRNDRQMDRJTHS-JAJWTYFOSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: N-[(2R,3R,4R,5R,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
• IUPAC Traditional name: N-acetyl-β-D-galactosamine
• Synonyms: N-Acetyl-D-Allosamine; N-Acetyl-2-Deoxy-2-Amino-Galactose; 2-(Acetylamino)-2-Deoxy-a-D-Glucopyranose

Database IDs

• PubChem SID: 160966259; 46504848; 46505390; 46508699
• PubChem CID: 440552

CALCULATED PROPERTIES

JChem

• Acid pKa: 11.60413
• H Acceptors: 6
• H Donor: 5
• LogD (pH = 5.5): -3.2205749
• LogD (pH = 7.4): -3.2206008
• Log P: -3.2205744
• Molar Refractivity: 47.0247 cm^3
• Polarizability: 19.398714 Å^3
• Polar Surface Area: 119.25 Å^2
• Rotatable Bonds: 2
• Lipinski's Rule of Five: true

ALOGPS 2.1

• Log P: -2.6
• LOG S: 0.06
• Solubility (Water): 2.54e+02 g/l

DETAILS

DrugBank - DB03567

• Drug Groups: experimental
• Description: The N-acetyl derivative of galactosamine. [PubChem]

DrugBank - DB03109

Drug information: experimental

DrugBank - DB03740

• Drug Groups: experimental
• Description: The N-acetyl derivative of glucosamine. [PubChem]