Patents by Inventor Tianwei Ma

Tianwei Ma has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20070105951
    Abstract: The present invention relates to novel, non-secosteroidal, phenyl-furan compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1?,25dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
    Type: Application
    Filed: November 16, 2004
    Publication date: May 10, 2007
    Inventors: Robert Gajewski, Charles Jones, Jianliang Lu, Tianwei Ma, Sunil Nagpal, Ying Yee
  • Publication number: 20060293385
    Abstract: The present invention relates to novel, non-secosteroidal, sulfonate and sulfonamide functional diaryl compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1?,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
    Type: Application
    Filed: November 8, 2004
    Publication date: December 28, 2006
    Inventors: Robert Gajewski, Charles Jones, Jared Linebarger, Jianliang Lu, Tianwei Ma, Sunil Nagpal, Ying Yee
  • Publication number: 20060287536
    Abstract: The present invention relates to novel, non-secosteroidal, phenyl-thiophene compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1?,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
    Type: Application
    Filed: May 22, 2003
    Publication date: December 21, 2006
    Inventors: Karl Dahnke, Robert Gajewski, Charles Jones, Jared Linebarger, Jianliang Lu, Tianwei Ma, Sunil Nagpal, Todd Simard, Ying Yee, Emilio Bunel, Ryan Stites
  • Publication number: 20060241157
    Abstract: The present invention is directed to compounds represented by the following structural formula, Formula I: wherein: (a) X is selected from the group consisting of a single bond, O, S, S(O)2 and N; (b) U is an aliphatic linker; (c) Y is selected from the group consisting of O, C, S, NH and a single bond; (d) E is C(R3)(R4)A or A and wherein (i) A is selected from the group consisting of carboxyl, tetrazole, C1-C6 alkylnitrile, carboxamide, sulfonamide and acylsulfonamide; (e) Z1 and Z2 are each independently selected from the group consisting of N, O, and C with the proviso that at least one of Z1 and Z2 is N; (f) Z3 is selected from the group consisting of N, O, and C. (g) R8 is selected from the group consisting of hydrogen, C1-C6 alkyl, C1-C4 alkylenyl and halo; (h) R9 is selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 alkylenyl, halo, aryl-C0-C4 alkyl, heteroaryl, C1-C6 allyl, and OR29.
    Type: Application
    Filed: December 31, 2003
    Publication date: October 26, 2006
    Inventors: Scott Conner, Tianwei Ma, Nathan Mantlo, Daniel Mayhugh, Jeffrey Schkeryantz, Alan Warshawsky, Guoxin Zhu