2-acylaminopropanamides as tachykinin receptor antagonists
申请人:Eli Lilly and Company
公开号:US05565568A1
公开(公告)日:1996-10-15
This invention provides a series of novel substituted propanamides which are useful in the treatment or prevention of a physiological disorder associated with an excess of tachykinins. This invention also provides methods for the treatment of such physiological disorders as well as pharmaceutical formulations which employ these novel compounds.
2-Acylaminopropanamides as growth hormone secretagogues
申请人:ELI LILLY AND COMPANY
公开号:EP0761220A1
公开(公告)日:1997-03-12
This invention provides a series of substituted propanamides which are useful in the treatment of a physiological condition which may be modulated by an increase in growth hormone. This invention also provides methods for the treatment of such physiological conditions which comprise administering a growth hormone secretagogue as described in the present invention in combination with growth hormone releasing hormone.
2-acylaminopropanamides as growth hormone secretagogues
申请人:Eli Lilly and Company
公开号:US05773441A1
公开(公告)日:1998-06-30
This invention provides a series of novel substituted propanamides which are useful in the a physiological condition which may be modulated by an increase in growth hormone. This invention also provides methods for the treatment of such physiological conditions which comprise administering a growth hormone secretagogue as described in the present invention in combination with growth hormone releasing hormone.
The present invention is directed to peptidomimetic macrocyclic compounds which inhibit prenyl-protein transferase and the prenylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting prenyl-protein transferase and the prenylation of the oncogene protein Ras.
Intramolecular Aza-Wittig Reaction: A New Efficient Tool for the Construction of Piperazine 2,5-Dione Derivatives
作者:K. Majumdar、Krishanu Ray、Sintu Ganai
DOI:10.1055/s-0030-1258519
日期:2010.9
A new efficient approach for the synthesis of unsymmetricaly substituted piperazine 2,5-dione derivatives is described by using intramolecular aza-Wittig reaction as the key step. The reaction conditions are very simple, offer easy isolation, and excellent yields of the products.