Chemical Name: (2R,3R,4R,5R)-2-(Hydroxymethyl)-3,4,5-piperidinetriol hydrochloride
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Selective inhibitor of α-mannosidase I.
Technical Data
M. Wt
199.63
Formula
C6H13NO4.HCl
Storage
Desiccate at RT
CAS Number
73465-43-7
PubChem ID
11019872
InChI Key
ZJIHMALTJRDNQI-MVNLRXSJSA-N
Smiles
Cl[H].OC[C@H]1NC[C@@H](O)[C@@H](O)[C@@H]1O
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
water
9.98
50
Preparing Stock Solutions
The following data is based on the product molecular weight 199.63. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
5.01 mL
25.05 mL
50.09 mL
5 mM
1 mL
5.01 mL
10.02 mL
10 mM
0.5 mL
2.5 mL
5.01 mL
50 mM
0.1 mL
0.5 mL
1 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
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References
References are publications that support the products' biological activity.
Bischoffet al (1986) The use of 1-deoxymannojirimycin to evaluate the role of various α-mannosidases in oligosaccharide processing in intact cells. J.Biol.Chem. 261 4766 PMID: 2937779
Bischoff and Kornfeld
(1984) The effect of 1-deoxymannojirimycin on rat liver α-mannosidases. Biochem.Biophys.Res.Commun. 125 324 PMID: 6239623
Fuhrmannet al (1984) Novel mannosidase inhibitor blocking conversion of high mannose to complex oligosaccharides. Nature 307 755 PMID: 6230538