-
-
ChemBase ID:
73167
-
Molecular Formular:
C16H30N2O14S
-
Molecular Mass:
506.4794
-
Monoisotopic Mass:
506.14177465
-
SMILES and InChIs
SMILES:
[C@H]1(C([C@@H]([C@H]([C@@H](O1)O[C@@H]1[C@H]([C@@H](O[C@@H]([C@@H]1O)COS(=O)(=O)O)OC)NC(=O)C)O)O)C)C(=O)O.N
Canonical SMILES:
CO[C@@H]1O[C@H](COS(=O)(=O)O)[C@@H]([C@@H]([C@H]1NC(=O)C)O[C@@H]1O[C@H](C(=O)O)C([C@@H]([C@H]1O)O)C)O.N
InChI:
InChI=1S/C16H27NO14S.H3N/c1-5-9(19)11(21)16(30-12(5)14(22)23)31-13-8(17-6(2)18)15(27-3)29-7(10(13)20)4-28-32(24,25)26;/h5,7-13,15-16,19-21H,4H2,1-3H3,(H,17,18)(H,22,23)(H,24,25,26);1H3/t5?,7-,8-,9+,10+,11-,12+,13-,15-,16+;/m1./s1
InChIKey:
ZDBCVOJEOPFJES-GYRBVNGNSA-N
-
Cite this record
CBID:73167 http://www.chembase.cn/molecule-73167.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
CAS Number
|
|
PubChem SID
|
|
PubChem CID
|
|
DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
PROPERTIES
PROPERTIES
Safety Information
Product Information
Bioassay(PubChem)
Storage Condition
|
-20°C
|
Show
data source
|
|
Salt Data
|
Free Base
|
Show
data source
|
|
DETAILS
DETAILS
Selleck Chemicals
Selleck Chemicals -
S2416
|
Research Area: Immunology Biological Activity: Chondroitin sulfate is a kind of sulfated glycosaminoglycan (GAG) which is composed of a chain of alternating sugars including N-acetylgalactosamine and glucuronic acid. As part of a proteoglycan, it is usually attached to some particular proteins. The chondroitin chain contains over one hundred individual sugars sulfated in different positions and quantities. Chondroitin sulfate plays an important role in the structural constituent of cartilage. And chondroitin sulfate produces much of its resistance to compression. Chondroitin sulfate has become a broadly used dietary supplement for treatment of osteoarthritis in comination with glucosamine. Chondroitin sulfate chains are unbranched polysaccharides of variable length containing two alternating monosaccharides: D-glucuronic acid (GlcA) and N-acetyl-D-galactosamine (GalNAc). Some GlcA residues are epimerized into L-iduronic acid (IdoA); the resulting disaccharide is then referred to as dermatan sulfate. Chondroitin’s functions depend largely on the properties of the overall proteoglycan of which it is a part. These functions can be widely divided into structural and regulatory functions. [1] |
PATENTS
PATENTS
PubChem Patent
Google Patent