alpha-L-Fucp-(1->3)-[beta-D-Galp4Cl-(1->4)]-beta-D-GlcpNAc-OMe

chemical compound

C₂₁H₃₆ClNO₁₄

alpha-L-Fucp-(1->3)-[beta-D-Galp4Cl-(1->4)]-beta-D-GlcpNAc-OMe is …
instance of (P31):
type of chemical entityQ113145171

sublass of (P279):
chemical compoundQ11173

External links are
P233canonical SMILESCC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)CO)Cl)O)O)CO)OC)NC(=O)C)O)O)O
P683ChEBI ID77193
P661ChemSpider ID30786204
P234InChIInChI=1S/C21H36ClNO14/c1-6-12(27)14(29)16(31)20(33-6)37-18-11(23-7(2)26)19(32-3)35-9(5-25)17(18)36-21-15(30)13(28)10(22)8(4-24)34-21/h6,8-21,24-25,27-31H,4-5H2,1-3H3,(H,23,26)/t6-,8+,9+,10-,11+,12+,13-,14+,15+,16-,17+,18+,19+,20-,21-/m0/s1
P235InChIKeyHTGFVLHXIHYVMP-ZVLVVNEPSA-N
P2017isomeric SMILESC[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H](O[C@@H]([C@H]2O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)Cl)O)O)CO)OC)NC(=O)C)O)O)O
P662PubChem CID86289158
P1579Reaxys registry number22800897
P11089UniChem compound ID69466150

P2067mass561.182433

Reverse relations

main subject (P921)
Q91010790Recognition of Lewis X by Anti-Lex Monoclonal Antibody IG5F6
Q36281169Synthesis of 4” manipulated Lewis X trisaccharide analogues
Q42709282Understanding the recognition of Lewis X by anti-Le(x) monoclonal antibodies

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