Description:
Lactosylsphingosine, a sphingolipid, is a vital biomarker characterizing diverse lysosomal storage disorders such as Niemann-Pick disease and Gaucher disease due to its accumulation within the tissues and blood of affected people. Detection through blood examination or imaging studies makes identification possible. Therapy options include substrate reduction and enzyme replacement therapy. Furthermore, tracking variations in lactosylsphingosine may be employed to monitor therapy response and trace disease advancement, imparting substantial clinical value in disease management.
- Molecular Weight: 623.77
- Molecular Formula: C30H57NO12
Purity: >99%
Canonical SMILES:
CCCCCCCCCCCCCC=CC(C(COC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O)N)O
InChI:
InChI=1S/C30H57NO12/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(34)19(31)18-40-29-27(39)25(37)28(22(17-33)42-29)43-30-26(38)24(36)23(35)21(16-32)41-30/h14-15,19-30,32-39H,2-13,16-18,31H2,1H3/b15-14+/t19-,20+,21+,22+,23-,24-,25+,26+,27+,28+,29+,30-/m0/s1
InChIKey: MQKSCOKUMZMISB-GPWKTZPCSA-N
- Boiling Point: 845.8±65.0 °C at 760 mmHg
- Appearance: Powder
- Storage: Store at -20°C
Synonyms:
D-lactosyl-beta1-1'-D-erythro-sphingosine; Lactosyl(beta) Sphingosine (d18: 1); 2S,3R1-beta-lactosyl-sphing-4-enine; lyso-Lactosylceramide; 1-b-Lactosyl-sphing-4-enine; lyso-LC
More details are to be found on supplier website
