dbo:abstract |
Gusperimus is an immunosuppressive drug. It is a derivative of the naturally occurring HSP70 inhibitor spergualin, and inhibits the interleukin-2-stimulated maturation of T cells to the S and G2/M phases and the polarization of the T cells into IFN-gamma-secreting Th1 effector T cells, resulting in the inhibition of growth of activated naive CD4 T cells. Gusperimus was developed by Bristol-Myers Squibb. Currently, it is manufactured and sponsored for use as an orphan drug and for clinical studies by the Japanese company Euro Nippon Kayaku. The patent claim (see quotation) is that Gusperimus may be useful for a variety of hyperreactive inflammatory diseases such as autoimmune diseases. The drug is available in vials containing 100 mg each. There is little information about the pharmacokinetic properties of gusperimus. (en) |
dbo:alternativeName |
N-[2-[4-(3-Aminopropylamino)butylamino]-1-hydroxy-2-oxoethyl]-7-(diaminomethylideneamino)heptanamide (en) |
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http://ec.europa.eu/enterprise/pharmaceuticals/register/o034.htm http://www.ingentaconnect.com/content/adis/rea/2005/00000001/00001080/art00040 https://web.archive.org/web/20060109201017/http:/www.als.net/research/treatments/treatmentDetail.asp%3FtreatmentID=858 https://web.archive.org/web/20120204123305/http:/www.bizbozos.com/nci_Gusperimus |
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Gusperimus.svg (en) |
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Skeletal formula of a gusperimus minor tautomer (en) |
dbp:othernames |
N-[2-[4-butylamino]-1-hydroxy-2-oxoethyl]-7-heptanamide (en) |
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rdfs:comment |
Gusperimus is an immunosuppressive drug. It is a derivative of the naturally occurring HSP70 inhibitor spergualin, and inhibits the interleukin-2-stimulated maturation of T cells to the S and G2/M phases and the polarization of the T cells into IFN-gamma-secreting Th1 effector T cells, resulting in the inhibition of growth of activated naive CD4 T cells. There is little information about the pharmacokinetic properties of gusperimus. (en) |
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Gusperimus (en) |
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