178622-38-3Relevant articles and documents
Semisynthetic cyclopamine analogues as potent and orally bioavailable hedgehog pathway antagonists
Tremblay, Martin R.,Nevalainen, Marta,Nair, Somarajan J.,Porter, James R.,Castro, Alfredo C.,Behnke, Mark L.,Yu, Lin-Chen,Hagel, Margit,White, Kerry,Faia, Kerrie,Grenier, Louis,Campbell, Matthew J.,Cushing, Jill,Woodward, Caroline N.,Hoyt, Jennifer,Foley, Michael A.,Read, Margaret A.,Sydor, Jens R.,Tong, Jeffrey K.,Palombella, Vito J.,McGovern, Karen,Adams, Julian
supporting information; experimental part, p. 6646 - 6649 (2009/11/30)
Herein is reported the synthesis of a novel class of hedgehog antagonists derived from cyclopamine. The acid sensitive D-ring of cyclopamine was homologated utilizing a sequence of chemoselective cyclopropanation and stereoselective acid-catalyzed rearran
REGULATORS OF THE HEDGEHOG PATHWAY, COMPOSITIONS AND USES RELATED THERETO
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Page/Page column 52, (2008/06/13)
The present invention makes available, inter alia, methods and reagents for modulating smoothened-dependent pathway activation. In certain embodiments, the subject methods can be used to counteract the phenotypic effects of unwanted activation of a hedgeh
Composition containing a penem or carbapenem antibiotic
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, (2008/06/13)
Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. The composition may be prepared by simple mixing.