Celgosivir

Celgosivir
Clinical data
Other names	6-O-Butanoylcastanospermine; MDL-28574; MX-3253
Legal status
Legal status	Investigational;
Identifiers
	IUPAC name [(1S,6S,7S,8R,8aR)-1,7,8-Trihydroxy-1,2,3,5,6,7,8,8a-octahydroindolizin-6-yl] butanoate;
CAS Number	121104-96-9;
PubChem CID	60734; 3033824;
ChemSpider	54737;
UNII	895VG117HN;
CompTox Dashboard (EPA)	DTXSID70153153 ;
Chemical and physical data
Formula	C12H21NO5
Molar mass	259.302 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCCC(=O)O[C@H]1CN2CC[C@@H]([C@@H]2[C@H]([C@@H]1O)O)O;
	InChI InChI=1S/C12H21NO5/c1-2-3-9(15)18-8-6-13-5-4-7(14)10(13)12(17)11(8)16/h7-8,10-12,14,16-17H,2-6H2,1H3/t7-,8-,10+,11+,12+/m0/s1; Key:HTJGLYIJVSDQAE-VWNXEWBOSA-N;

Celgosivir, in development by Migenix for the treatment of hepatitis C virus (HCV) infection, is an oral prodrug of the natural product castanospermine that inhibits alpha-glucosidase I, an enzyme that plays a critical role in viral maturation by initiating the processing of the N-linked oligosaccharides of viral envelope glycoproteins. Celgosivir is well absorbed in vitro and in vivo, and is rapidly converted to castanospermine. Celgosivir has a novel mechanism of action (preventing the glycosylation of viral proteins by the host), and demonstrates broad antiviral activity in vitro.^[1]

Clinical trials

Celgosivir is not efficient as a monotherapy for the treatment of HCV, but has demonstrated a synergistic effect in combination with pegylated interferon alfa-2b plus ribavirin, both in vitro and in phase II clinical trials that last up to 1 year in patients with chronic HCV infection. Celgosivir may prove to be a valuable component for combination therapy and may help to prevent the apparition of drug resistance. Long-term toxicity studies are necessary to confirm the safety of celgosivir in humans.^[1]

Although generally safe and well tolerated, celgosivir does not seem to reduce viral load or fever burden in patients with dengue fever.^[2]

References

1 2 Durantel D (August 2009). "Celgosivir, an alpha-glucosidase I inhibitor for the potential treatment of HCV infection". Current Opinion in Investigational Drugs. 10 (8): 860–70. PMID 19649930.
↑ Low JG, Sung C, Wijaya L, Wei Y, Rathore AP, Watanabe S, et al. (August 2014). "Efficacy and safety of celgosivir in patients with dengue fever (CELADEN): a phase 1b, randomised, double-blind, placebo-controlled, proof-of-concept trial". The Lancet. Infectious Diseases. 14 (8): 706–715. doi:10.1016/S1473-3099(14)70730-3. PMID 24877997.

External links

KEGG DRUG: Celgosivir Hydrochloride

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[Durantel-1] 1 2 Durantel D (August 2009). "Celgosivir, an alpha-glucosidase I inhibitor for the potential treatment of HCV infection". Current Opinion in Investigational Drugs. 10 (8): 860–70. PMID 19649930.

[2] Low JG, Sung C, Wijaya L, Wei Y, Rathore AP, Watanabe S, et al. (August 2014). "Efficacy and safety of celgosivir in patients with dengue fever (CELADEN): a phase 1b, randomised, double-blind, placebo-controlled, proof-of-concept trial". The Lancet. Infectious Diseases. 14 (8): 706–715. doi:10.1016/S1473-3099(14)70730-3. PMID 24877997.

[1]

[2]