Biochemicals

Deoxyfuconojirimycin HCl is a potent and selective inhibitor of FUCA (α-L-fucosidases).A potent and selective inhibitor of α-L-fucosidases.

1-Deoxymannojirimycin hydrochloride is a selective inhibitor of α(1→2)-mannosidases. Mannosidases are broken into two subtypes: I and II, which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked α-D-mannose residues in the

1-Deoxymannojirimycin hydrochloride is a selective inhibitor of α(1→2)-mannosidases. Mannosidases are broken into two subtypes: I and II, which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked α-D-mannose residues in the

1-Deoxymannojirimycin hydrochloride is a selective inhibitor of α(1→2)-mannosidases. Mannosidases are broken into two subtypes: I and II, which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked α-D-mannose residues in the

1-Deoxymannojirimycin hydrochloride is a selective inhibitor of α(1→2)-mannosidases. Mannosidases are broken into two subtypes: I and II, which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked α-D-mannose residues in the

DescriptionChemical structure: glucosamineApplication：1-Deoxynojirimycin hydrochloride has been usedto study its effects on the loss-of-function of N-glycosylation pathway on hair cell regenerationas an endoplasmic reticulum (ER) α-glucosidase I and

DescriptionChemical structure: glucosamineApplication：1-Deoxynojirimycin hydrochloride has been usedto study its effects on the loss-of-function of N-glycosylation pathway on hair cell regenerationas an endoplasmic reticulum (ER) α-glucosidase I and

DescriptionChemical structure: glucosamineApplication：1-Deoxynojirimycin hydrochloride has been usedto study its effects on the loss-of-function of N-glycosylation pathway on hair cell regenerationas an endoplasmic reticulum (ER) α-glucosidase I and

DescriptionChemical structure: glucosamineApplication：1-Deoxynojirimycin hydrochloride has been usedto study its effects on the loss-of-function of N-glycosylation pathway on hair cell regenerationas an endoplasmic reticulum (ER) α-glucosidase I and

1-deoxysphinganine is synthesized by the condensation of palmitic acid with alanine or glycine in the presence of enzyme serine palmitoyltransferase (SPT). It is metabolized to 1-deoxyceramides.Application1-deoxysphinganine may be used for the

1-deoxysphinganine is synthesized by the condensation of palmitic acid with alanine or glycine in the presence of enzyme serine palmitoyltransferase (SPT). It is metabolized to 1-deoxyceramides.Application1-deoxysphinganine may be used for the

1-deoxysphingosine (m18:1).