(2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-{[(2R,3R,4S,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]sulfanyl}oxane-3,4,5-triol

• ChemBase ID: 2959
• Molecular Formular: C12H22O10S
• Molecular Mass: 358.36208
• Monoisotopic Mass: 358.0933679
• SMILES: OC[C@@H]1O[C@H](S[C@H]2[C@@H](CO)O[C@H](O)[C@@H](O)[C@@H]2O)[C@@H](O)[C@H](O)[C@H]1O
• Canonical SMILES: OC[C@H]1O[C@H](O)[C@H]([C@@H]([C@H]1S[C@H]1O[C@@H](CO)[C@@H]([C@H]([C@@H]1O)O)O)O)O
• InChI: InChI=1S/C12H22O10S/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4+,5-,6+,7-,8-,9-,10-,11-,12+/m0/s1
• InChIKey: VDQIIPZYLPYPNM-SYQMOTIOSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: (2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-{[(2R,3R,4S,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]sulfanyl}oxane-3,4,5-triol
• IUPAC Traditional name: @thiocellobiose
• Synonyms: Thiocellobiose

Database IDs

• PubChem SID: 160966406; 46507245
• PubChem CID: 46936622

CALCULATED PROPERTIES

JChem

• Acid pKa: 11.289908
• H Acceptors: 10
• H Donor: 8
• LogD (pH = 5.5): -4.392245
• LogD (pH = 7.4): -4.3923
• Log P: -4.392244
• Molar Refractivity: 74.6875 cm^3
• Polarizability: 31.24687 Å^3
• Polar Surface Area: 180.3 Å^2
• Rotatable Bonds: 4
• Lipinski's Rule of Five: false

ALOGPS 2.1

• Log P: -2.94
• LOG S: 0.08
• Solubility (Water): 4.31e+02 g/l

DETAILS

DrugBank - DB03263

Drug information: experimental