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CAS	9007-28-7
Chinese Name	硫酸软骨素
English Name	Chondroitin sulfate
Synonym	Chonsurid;Chondroitin polysulfate
Purity	HPLC≥98%
Unit	Bottle
Molecular Formula	(C₁₄H₂₁NO₁₄S)n
Appearance	White to yellow solid
Storage	Powder : 2-8℃, 2 years; In solvent(mother liquid): -20℃, 1 month; -80℃, 6 months
Solubility	Soluble in water≥25mg/ml
EC	EINECS 232-696-9
MDL	MFCD00146419
InChIKey	KXKPYJOVDUMHGS-OSRGNVMNSA-N
InChI	InChI=1S/C13H21NO15S/c1-2(15)14-3-8(7(19)13(28-11(3)22)29-30(23,24)25)26-12-6(18)4(16)5(17)9(27-12)10(20)21/h3-9,11-13,16-19,22H,1H3,(H,14,15)(H,20,21)(H,23,24,25)/t3-,4+,5+,6-,7-,8-,9+,11-,12-,13-/m1/s1
PubChem CID	24766
SMILES	O=S(O)=O.O=S(O)=O.OC([C@@H]1[C@@H](OC)[C@H](O)[C@@H](O)[C@H](O[C@@H]2[C@@H](NC(C)=O)[C@H](OC)O[C@H](CO[R])[C@@H]2O[R])O1)=O.[R].[R].[=].[=].[R2=].[R1=].[n].[or]
Description	It is a class of glycosaminoglycans that are covalently attached to proteins to form proteoglycans. It has been reported to reduce inflammatory mediators and apoptotic processes, and to reduce the production of inflammatory cytokines, iNOS and MMPs.
Target Point	NO Synthase
Passage	Immunology & Inflammation
Data Literature Source	[1]. Mikami T, et al. Biosynthesis and function of chondroitin sulfate. Biochim Biophys Acta. 2013 Oct;1830(10):4719-33. [2]. Martel-Pelletier J, et al.Discrepancies in composition and biological effects of different formulations of chondroitin sulfate. Molecules. 2015 Mar 6;20(3):4277-89. [3]. Monfort J, et al. Biochemical basis of the effect of chondroitin sulphate on osteoarthritis articular tissues. Ann Rheum Dis. 2008 Jun;67(6):735-40. [4]. Campo GM, et al. Glycosaminoglycans modulate inflammation and apoptosis in LPS-treated chondrocytes. J Cell Biochem. 2009 Jan 1;106(1):83-92. [5]. Henrotin Y, et al. Chondroitin sulfate in the treatment of osteoarthritis: from in vitro studies to clinicalrecommendations. Ther Adv Musculoskelet Dis. 2010 Dec;2(6):335-48.
Specification	100mg 10mM*1mL in Water 500mg