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Inventor:
Ni; Zhi-Jie
Address:
Fremont, CA
No. of patents:
11
Patents:












Patent Number Title Of Patent Date Issued
7855295 Tetrahydrocarboline compounds as anticancer agents December 21, 2010
Tetrahydrocarboline compounds, pharmaceutically acceptable salts, and prodrugs thereof; compositions that include a pharmaceutically acceptable carrier and one or more of the tetrahydrocarboline compounds, either alone or in combination with at least one additional therapeutic agent.
7521062 Thiosemicarbazones as anti-virals and immunopotentiators April 21, 2009
The present invention is directed to novel immune potentiators, novel vaccine adjuvants, novel compounds and pharmaceutical compositions, novel methods for treating viral infections, including HCV, by administering the compounds, and novel methods for modulating an immune response by
7470709 Benzimidazole quinolinones and uses thereof December 30, 2008
Methods of inhibiting various enzymes and treating various conditions are provided that include administering to a subject a compound of Structure I or IB, a pharmaceutically acceptable salt thereof, a tautomer thereof, or a pharmaceutically acceptable salt of the tautomer. Compounds hav
7368422 Semi-synthetic rearranged vancomycin/desmethyl-vancomycin-based glycopeptides with antibiotic ac May 6, 2008
Semi-synthetic glycopeptides that have antibacterial activity are based on modifications of a rearranged vancomycin or desmethyl-vancomycin scaffold, in particular, alkylation or acylation of the amino substituent on the amino-substituted sugar moiety on this scaffold with certain acyl
7250443 Pyrrole based inhibitors of glycogen synthase kinase 3 July 31, 2007
New pyrrole based compounds, compositions and methods of inhibiting the activity of glycogen synthase kinase (GSK3) in vitro and of treatment of GSK3 mediated disorders in vivo are provided. The methods, compounds and compositions of the invention may be employed alone, or in combination
6852752 Urea compounds, compositions and methods of use and preparation February 8, 2005
Novel hydroxamic acid compounds are disclosed. These hydroxamates inhibit peptide deformylase (PDF), an enzyme present in prokaryotes and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and of use of the compounds are also disclosed.
6797820 Succinate compounds, compositions and methods of use and preparation September 28, 2004
Novel hydroxamic acid compounds are disclosed. These hydroxamates inhibit peptidyl deformylase (PDF), an enzyme present in prokaryotes. The hydroxymates are useful as antimicrobials and antibiotics. The compounds of the invention display selective inhibition of peptidyl deformylase v
6638927 Guanidinobenzamides October 28, 2003
Compounds of formula IA and IB are new ##STR1##where the variables R.sup.1 through R.sup.10 have the values set forth herein. Such compounds have use in treating diseases such as obesity and type II diabetes, and may be provided as pharmaceutical formulations in conjunction with a ph
6562844 Oxazolidinone combinatorial libraries, compositions and methods of preparation May 13, 2003
Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable composi
6531470 Oxazolidinone combinatorial libraries, compositions and methods of preparation March 11, 2003
Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable composi
6239152 Oxazolidinone combinatorial libraries, compositions and methods of preparation May 29, 2001
Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable composi










 
 
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