产品名称

英文名称：3′-Sialyl-Lewis-X tetrasaccharide

同义词

Sialyl-Lewis X、sialyl Lewis x、98603-84-0、3'-Sialyl-Lewis X、SLex、SialylLewisX、sialyl LewisX、Sialyl lewis-x、Sialyl Lex tri、3'-Sialyl-Lewis-X tetrasaccharide、Sialyl LeX、3'-SLeX、SSEA 1、0PS35WG8U3、(2S,4S,5R,6R)-5-acetamido-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R)-、唾液酸化酶X

产品性质

CAS编号：98603-84-0

分子式：C31H52N2O23

分子量：820.74

MDL号：MFCD00270073

PubChem编号：643990

别名：唾液酸化酶X

英文别名：Sialyl-Lewis X|sialyl Lewis x|98603-84-0|3'-Sialyl-Lewis X|SLex|SialylLewisX|sialyl LewisX|Sialyl lewis-x|Sialyl Lex tri|3'-Sialyl-Lewis-X tetrasaccharide|Sialyl LeX|3'-SLeX|SSEA 1|0PS35WG8U3|(2S,4S,5R,6R)-5-acetamido-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R)-

规格或纯度：95%

英文名称：3′-Sialyl-Lewis-X tetrasaccharide

储存温度：-20°C储存,充氩

运输条件：超低温冰袋运输

产品介绍：Enzymatically prepared tetrasaccharide which acts as a minimal binding ligand for E-selectins. SLex reduces injury following ischemia, reperfusion and immune complex-induced acute lung injury in animal models. In both of these models, SLex is presumed to act by blocking E-selectin-mediated neutrophil recruitment to sites of inflammation.生化/生理作用与内皮粘附分子 E-选择素结合的抗原。Enzymatically prepared tetrasaccharide which acts as a minimal binding ligand for E-selectins. SLex reduces injury following ischemia, reperfusion and immune complex-induced acute lung injury in animal models. In both of these models, SLex is presumed to act by blocking E-selectin-mediated neutrophil recruitment to sites of inflammation.

IUPAC Name：(2S,4S,5R,6R)-5-acetamido-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R)-5-acetamido-1,2-dihydroxy-6-oxo-4-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhexan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

INCHI：InChI=1S/C31H52N2O23/c1-9-18(43)21(46)22(47)28(51-9)53-24(12(5-34)32-10(2)38)25(15(42)7-36)54-29-23(48)27(20(45)16(8-37)52-29)56-31(30(49)50)4-13(40)17(33-11(3)39)26(55-31)19(44)14(41)6-35/h5,9,12-29,35-37,40-48H,4,6-8H2,1-3H3,(H,32,38)(H,33,39)(H,49,50)/t9-,12-,13-,14+,15+,16+,17+,18+,19+,20-,21+,22-,23+,24+,25+,26+,27-,28-,29-,31-/m0/s1

InChi Key：LAQPKDLYOBZWBT-NYLDSJSYSA-N

Canonical SMILES：CC1C(C(C(C(O1)OC(C(C=O)NC(=O)C)C(C(CO)O)OC2C(C(C(C(O2)CO)O)OC3(CC(C(C(O3)C(C(CO)O)O)NC(=O)C)O)C(=O)O)O)O)O)O

Isomeric SMILES：C[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@H]([C@H](C=O)NC(=O)C)[C@@H]([C@@H](CO)O)O[C@H]2[C@@H]([C@H]([C@H]([C@H](O2)CO)O)O[C@@]3(C[C@@H]([C@H]([C@@H](O3)[C@@H]([C@@H](CO)O)O)NC(=O)C)O)C(=O)O)O)O)O)O

WGK Germany：3

PubChem CID：643990

溶解性：Methanol (Slightly), Water (Slightly)

个人防护装备：Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter

产品包装