![4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde - chemical structure image](https://media.scbt.com/product/4-2-4-chlorophenyl-5-methyl-1-3-oxazol-4-yl-methoxybenzaldehyde-structure_23_12_b_231274.jpg)
![4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde - chemical structure image](https://media.scbt.com/product/4-2-4-chlorophenyl-5-methyl-1-3-oxazol-4-yl-methoxybenzaldehyde-structure_23_12_t_231274.jpg "Molecular structure of 4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde")
Molecular structure of 4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde
4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde
Molecular Weight:
327.76
Molecular Formula:
C18H14ClNO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
1-Deoxymannojirimycin hydrochloride is a selective inhibitor of alpha(1rarr2)-mannosidases. Mannosidases are broken into two subtypes: I and II, which display a wide expression pattern. Mannosidase I hydrolyzes (1,2)-linked alpha-D-mannose residues in the oligo-mannose oligosaccharide Man9(GlcNAc)2 and mannosidase II hydrolyzes (1,3)- and (1,6)-linked α-D-mannose residues in Man5(GlcNAc)3. Both mannosidase I and mannosidase II of require a divalent cation cofactor. 1-Deoxymannojirimycin hydrochloride selectively inhibits mannosidase I, but not mannosidase II.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-{[2-(4-Chlorophenyl)-5-methyl-1,3-oxazol-4-yl]-methoxy}benzaldehyde, 500 mg | sc-315569 | 500 mg | $180.00 |