CAS 843651-89-8

Formel: C57H109NO10

InChl: InChI=1S/C57H109NO10/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-51(59)58-46-50-54(62)55(63)56(64)57(68-50)66-48-49(67-53(61)45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)47-65-52(60)44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h49-50,54-57,62-64H,4-48H2,1-3H3,(H,58,59)/t49-,50?,54+,55?,56?,57-/m0/s1

InChI Key: FQQGDOIXTUYSNI-LMRVJDJMSA-N

SMILES: CCCCCCCCCCCCCCCC(=O)NCC1[C@H](C(C([C@H](O1)OC[C@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)O)O)O

1,2-Dipalmitoyl-3-(N-palmitoyl-6''-amino-6''-deoxy-a-D-glucosyl)-sn-glycerol

CAS: 843651-89-8

Ref: 7W-GC6290

1,2-Dipalmitoyl-3-(N-palmitoyl-6'-amino-6'-deoxy-a-D-glucosyl)-sn-glycerol

CAS: 843651-89-8

Dipalmitoyl-3-(N-palmitoyl-6'-amino-6'-deoxy-a-D-glucosyl)-sn-glycerol is a marine glycoglycerolipid that has been shown to have potent inhibitory activity against human and bacterial enzymes. This molecule was synthesized using multistep, stereoselective synthetic methods. It is a lipid molecule with two domains: the first domain is palmitic acid and the second domain is a glycosylated amino acid. The first domain has been shown to inhibit human and bacterial enzyme activity.

Formel: C₅₇H₁₀₉NO₁₀

Reinheit: Min. 95%

Molekulargewicht: 968.48 g/mol

Ref: 3D-MD16700