| Name | castanospermine |
|---|---|
| Synonyms |
1,6,7,8-Indolizinetetrol, octahydro-, (1S,6S,7R,8R,8aR)-
Castanospermine (1S,6S,7R,8R,8aR)-Octahydro-1,6,7,8-indolizinetetrol Castanospermine,[1S-(1α,6β,7α,8β,8aβ)]-Octahydro-1,6,7,8-indolizinetetrol (1S,6S,7R,8R,8aR)-Octahydroindolizine-1,6,7,8-tetrol MFCD00017555 |
| Description | Castanospermine inhibits all forms of α- and β-glucosidases, especially glucosidase l (required for glucoprotein processing by transfer of mannose and glucose from asparagine-linked lipids).target:α- and β-glucosidases.IC 50: 1.2 uM [2] in vitro :Castanospermine, [(1 S,6S,7R,8R,8aR)-1 ,6,7,8-tetrahydroxyoctahydroindolizine]is a potent and specific inhibitor of mammalian and plant α-and β-D-glucosidases in vitro [1] in vivo: Experiments in vivo with castanospermine, an inhibitor of the glucosidases that convert protein N-linked high mannose carbohydrates to complex oligosaccharides, resulted in significant inhibition of tumor growth in nude mice.[3] |
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| Related Catalog | |
| References |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 421.9±45.0 °C at 760 mmHg |
| Melting Point | 213-217 °C(lit.) |
| Molecular Formula | C8H15NO4 |
| Molecular Weight | 189.209 |
| Flash Point | 267.6±27.4 °C |
| Exact Mass | 189.100113 |
| PSA | 84.16000 |
| LogP | -1.61 |
| Vapour Pressure | 0.0±2.3 mmHg at 25°C |
| Index of Refraction | 1.647 |
| Storage condition | 2-8°C |
| Water Solubility | 1 M HCl: 20 mg/mL, clear, very faintly yellow |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H312-H332 |
| Precautionary Statements | P280 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn: Harmful;Xi: Irritant; |
| Risk Phrases | 20/21/22 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| Precursor 1 | |
|---|---|
| DownStream 3 | |