Timothy F. Walseth - Roseville MN Antonio De Flora - Genoa, IT Elena Zocchi - Genoa, IT Marina Podesta - Genoa, IT Long Wong - Roseville MN Robert A. Aarhus - Coon Rapids MN Hon Cheung Lee - Woodbury MN
Assignee:
Regents of the University of Minnesota - Minneapolis MN
International Classification:
A61K 3170
US Classification:
514 47, 514 46, 514 45, 536 2611
Abstract:
The present invention provides a compound of formula I: wherein A, D, R , and R are as defined in the specification; or a salt or a detectably labeled derivative thereof. The invention also provides methods of using the compound of formula I or a salt or a detectably labeled derivative thereof for promoting the proliferation of hemopoietic progenitor cells without cell differentiation.
Kyle R. Gee - Springfield OR Hon Cheung Lee - Woodbury MN Robert Aarhus - Brooklyn Park MN Richard P. Haugland - Eugene OR Timothy F. Walseth - Roseville MN Richard M. Graeff - St. Paul MN
Assignee:
Molecular Probes, Inc. - Eugene OR The Regents of the University of Minnesota - Minneapolis MN
International Classification:
C07H 100 C07H 2100
US Classification:
536 2623
Abstract:
The present invention describes a family of photolabile caged nucleotides, including cyclic nucleotides. The compounds of the present invention are caged analogs and derivatives of NAD. sup. +, NADH, NADP, NADPH, NAADP and cADPR. The photolysis of the present compounds allows the release of the free nucleotide in vivo or in vitro with precise spatial and temporal control. The compounds are useful for the photolytic generation of free nucleotides in aqueous samples, for example, in the study of calcium mobilization in cells and cell homogenates.
Timothy F. Walseth - Roseville MN Robert A. Aarhus - Brooklyn Park MN
Assignee:
Regents of the University of Minnesota - Minneapolis MN
International Classification:
C07H 1923 A61K 5100
US Classification:
536 2613
Abstract:
Cyclic ADP-ribose (cADPR) analogs block cADPR from releasing Ca. sup. +2, and also inhibit cADPR from potentiating Ca. sup. +2 release induced by either divalent cations or by caffeine. 8-amino-cADPR and two other 8-substituted analogs were also synthesized. Both 8-Br- and 8-azido-cADPR were also antagonists, although with less potency than 8-amino-cADPR. These results show that alterations at the 8-position of the adenine group do not inhibit cADPR from binding to its receptor but do eliminate the ability of the metabolite to activate the Ca. sup. +2 release mechanism.