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Celgosivir

Catalog No. T10755L   CAS 121104-96-9
Synonyms: MX3253, MBI 3253, 6 O-butanoyl castanospermine, MDL 28574

Celgosivir (6 O-butanoyl castanospermine) is an inhibitor of α-glucosidase I. In vitro assay, it inhibits bovine viral diarrhoea virus (BVDV) ( IC50: 1.27 μM ).

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Celgosivir Chemical Structure
Celgosivir, CAS 121104-96-9
Pack Size Availability Price/USD Quantity
1 mg In stock $ 129.00
2 mg In stock $ 198.00
5 mg In stock $ 293.00
10 mg In stock $ 418.00
25 mg In stock $ 695.00
50 mg In stock $ 988.00
100 mg In stock $ 1,330.00
500 mg In stock $ 2,670.00
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Purity: 98.03%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Celgosivir (6 O-butanoyl castanospermine) is an inhibitor of α-glucosidase I. In vitro assay, it inhibits bovine viral diarrhoea virus (BVDV) ( IC50: 1.27 μM ).
Targets&IC50 α-glucosidase I:1.27 μM
In vitro Celgosivir exhibits potent antiviral activity against HIV-1 (IC50: 2.0±2.3 μM) [1]. Celgosivir inhibits DENV2 replication (EC50: 0.2 μM). The EC50 values against DENV1, 3 and 4 are less than 0.7 μM[3]. Celgosivir is more effective (IC50=20 μM) than the parent molecule (IC50=254 μM) at causing the accumulation of glucosylated oligosaccharides in HIV-infected cells by inhibition of glycoprotein processing. Bovine viral diarrhoea virus (BVDV) is a closely related virus of hepatitis C virus (HCV). In plaque assay and cytopathic effect assay, Celgosivir inhibits BVDV, with IC50 values of 16 and 47 μM , respectively[2].
In vivo Celgosivir demonstrates robust protection in AG129 mice against lethal infection from a mouse-adapted dengue virus, effectively administered at a dosage of 50 mg/kg twice daily (BID) for a duration of 5 days. This protective efficacy is maintained even when treatment onset is delayed by 48 hours. The outcomes suggest that celgosivir's protective capability is contingent upon both the dosage and the administration schedule, with a twice daily regimen of 50, 25, or 10 mg/kg proving superior to a single daily dose of 100 mg/kg in terms of survival. Specifically, during primary infection with the mouse-adapted DENV strain S221, there is a notable increase in viremia by day 3. However, an impressive 80% of mice survive until day 10, with the virus being completely eliminated by day 8[3].
Synonyms MX3253, MBI 3253, 6 O-butanoyl castanospermine, MDL 28574
Molecular Weight 259.3
Formula C12H21NO5
CAS No. 121104-96-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 1.8mg/mL (6.9mM)

TargetMolReferences and Literature

1. Taylor DL, et al. Inhibition of alpha-glucosidase I of the glycoprotein-processing enzymes by 6-O-butanoylcastanospermine (MDL 28,574) and its consequences in human immunodeficiency virus-infected T cells. Antimicrob Agents Chemother. 1994 Aug;38(8):1780-7. 2. Rathore AP, et al. Celgosivir treatment misfolds dengue virus NS1 protein, induces cellular pro-survival genes andprotects against lethal challenge mouse model. Antiviral Res. 2011 Dec;92(3):453-60. 3. Whitby K, et al. Action of celgosivir (6 O-butanoyl castanospermine) against the pestivirus BVDV: implications for the treatment of hepatitis C. Antivir Chem Chemother. 2004 May;15(3):141-51. 4. Watanabe S, et al. Dose- and schedule-dependent protective efficacy of celgosivir in a lethal mouse model for dengue virus infection informs dosing regimen for a proof of concept clinical trial. Antiviral Res. 2012 Oct;96(1):32-5.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Drug Repurposing Compound Library Bioactive Compounds Library Max Bioactive Compound Library Clinical Compound Library Kinase Inhibitor Library

Related Products

Related compounds with same targets
α-Glucosidase-IN-25 Pinoresinol diglucoside α-Glucosidase-IN-22 α-Glucosidase-IN-33 Castanospermine Ceftezole sodium α-Amylase/α-Glucosidase-IN-5 Viscidulin III

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Keywords

Celgosivir 121104-96-9 Metabolism Glucosidase MBI3253 MX3253 MX 3253 MDL28574 MBI 3253 6 O-butanoyl castanospermine MDL-28574 MDL 28574 MX-3253 MBI-3253 inhibitor inhibit

 

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