Glucosamine sulfateProduct ingredient for Glucosamine

Name
Glucosamine sulfate
Drug Entry
Glucosamine

Osteoarthritis (OA) is a progressive and degenerative joint disease marked by loss of cartilage, bone changes, and synovial membrane inflammation.14 Treatment with chondroprotective drugs, such as glucosamine sulfate may offer additional benefits to nonsteroidal anti-inflammatory drugs treating the painful symptoms of OA. Glucosamine is commonly used over the counter as a treatment for arthritic joint pain, although its acceptance as a medical therapy varies due to contradictory and findings with unclear clinical significance during clinical trials.6,14 It is currently not approved as a prescription product by the FDA, but is widely available over the counter.

Accession Number
DBSALT001596
Structure
Synonyms
Not Available
UNII
1FW7WLR731
CAS Number
14999-43-0
Weight
Average: 456.42
Monoisotopic: 456.126124764
Chemical Formula
C12H28N2O14S
InChI Key
WLNBMPZUVDTASE-HXIISURNSA-N
InChI
InChI=1S/2C6H13NO5.H2O4S/c2*7-3(1-8)5(11)6(12)4(10)2-9;1-5(2,3)4/h2*1,3-6,9-12H,2,7H2;(H2,1,2,3,4)/t2*3-,4+,5+,6+;/m00./s1
IUPAC Name
bis((2R,3R,4S,5R)-2-amino-3,4,5,6-tetrahydroxyhexanal); sulfuric acid
SMILES
OS(O)(=O)=O.N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO.N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO
ChemSpider
20100842
Wikipedia
Glucosamine
Predicted Properties
PropertyValueSource
Water Solubility195.0 mg/mLALOGPS
logP-2.6ALOGPS
logP-3.7Chemaxon
logS0.04ALOGPS
pKa (Strongest Acidic)12.77Chemaxon
pKa (Strongest Basic)6.86Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count6Chemaxon
Hydrogen Donor Count5Chemaxon
Polar Surface Area124.01 Å2Chemaxon
Rotatable Bond Count10Chemaxon
Refractivity39 m3·mol-1Chemaxon
Polarizability16.65 Å3Chemaxon
Number of Rings0Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon