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Molecule
ID:84251
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₈ClNO₅S
Molecular Mass
323.79302
Exact Mass
323.05942136
Charge
0
InChI
InChI=1S/C12H17NO5S.ClH/c13-6-1-3-7(4-2-6)19-12-11(17)10(16)9(15)8(5-14)18-12;/h1-4,8-12,14-17H,5,13H2;1H/t8-,9-,10+,11+,12+;/m1./s1
InChIKey
HKAFWLFFBCRHQI-ZYVSMTKISA-N
Canonic Smiles
OC[C@H]1O[C@@H](Sc2ccc(cc2)N)[C@H]([C@H]([C@@H]1O)O)O.Cl
Isomeric Smiles
Cl.Nc1ccc(S[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)cc1
Calculated Properties
JChem
Acid pKa
12.4691
H Acceptors
6
H Donor
5
LogD (pH = 5.5)
-1.0460526
LogD (pH = 7.4)
-1.0296806
Log P
-1.029464
Molar Refractivity
71.4204
Polarizability
28.095398
Polar Surface Area
116.17
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Data Source
Commercial Catalog
Apollo Scientific
OR270T
Academic Data
PubChem
71299485
Names and Identifiers
IUPAC Traditional name
(2S,3S,4S,5S,6R)-2-[(4-aminophenyl)sulfanyl]-6-(hydroxymethyl)oxane-3,4,5-triol hydrochloride
Synonyms
4-Aminophenyl-beta-D-thiomannopyranoside hydrochloride
IUPAC name
(2S,3S,4S,5S,6R)-2-[(4-aminophenyl)sulfanyl]-6-(hydroxymethyl)oxane-3,4,5-triol hydrochloride
Registration numbers
PubChem CID
71299485
PubChem SID
162071367
MDL Number
MFCD00190751
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay