Glycorex Catalogue MODIFIED SACCHARIDES, AMINO ACID CONJUGATES

SEt, thioethyl group, commonly used in glycosyl donors for organic synthesis of saccharides.

4,6-OBn, 4,6-O-benzylidene group, commonly used protection group in acceptors for e.g. the chemical synthesis of 1-3-linked oligosaccharides or for preparation of 4- or 6-bensylated acceptor.

NPhth, N-phthaloyl group, and NTeoc, N-trichloroethoxycarbonyl group, are commonly used for temporary protection of the amino group in glucosamine in the chemical synthesis of complex saccharides.

If you are interested in other modified saccharides, in larger quantities, or in custom synthesis, please contact us.

Cat. No.	STRUCTURE	Quantity
M-8001	(4,6-OBn)Galß-SEt	(1 g)
M-8002	GlcNPhthß-OAc (peracetylated)	(1 g)
M-8003	(4,6-OBn)GlcNPhthß-SEt	(1 g)
M-8004	Fucá-SEt (peracetylated)	(1 g)
M-8005	Galß-OCH₂CH=CH₂	(1 g)
M-8006	Galß-OCH₂Ph	(1 g)
M-8007	Galß-OCH₂CH₂Si(Me)₃	(1 g)
M-8008	Galß1-4Glcß-SPhMe	(1 g)
M-8009	Galß1-4GlcNTeocß-SEt	(1 g)
P-6006	Galá-PMP	(1 g)
P-6007	Galß-PMP	(1 g)
A-7001	Galß-O-(N-^tBoc)-L-Serine N-tert-butyloxycarbonyl derivative of Serine ß-galactoside Galß-Ser is a common structure in glycoproteins	(5 mg) (20 mg)
M-8010	Galß-SEt	(1 g)
M-9000	GalNAcá-1-Phosphate (NEW)	(10 mg)

GalNAcá-O-L-Serine, GlcNAcß-O-L-Serine, Galß1-3GalNAcá-O-L-Serine: Please enquire