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Annapurna S Pendri

from South Glastonbury, CT

Also known as:
  • Anjaneyulu Pendri
  • Annapurna J Pendri
  • Annapurna R Pendri
Phone and address:
54 Aspen Dr, South Glastonbury, CT 06073
(860)6595800

Annapurna Pendri Phones & Addresses

  • 54 Aspen Dr, South Glastonbury, CT 06073 • (860)6595800
  • Middletown, CT
  • Matawan, NJ
  • Wallingford, CT
  • Denton, TX
  • Old Bridge, NJ
  • 54 Aspen Dr, South Glastonbury, CT 06073

Us Patents

  • Terminally-Branched Polymeric Linkers And Polymeric Conjugates Containing The Same

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  • US Patent:
    6395266, May 28, 2002
  • Filed:
    Apr 16, 1999
  • Appl. No.:
    09/293624
  • Inventors:
    Anthony J. Martinez - Hamilton Square NJ
    Annapurna Pendri - Middletown CT
    Richard B. Greenwald - Somerset NJ
    Yun H. Choe - Piscataway NJ
  • Assignee:
    Enzon, Inc. - Piscataway NJ
  • International Classification:
    A61K 31785
  • US Classification:
    424 783, 5147723, 514283, 514506, 514513, 514515
  • Abstract:
    The present invention is directed to polymeric-prodrug transport forms of the formula: wherein: E are independently selected from the group consisting of hydrogen, C alkyls, C branched alkyls, C cycloalkyls, C substituted alkyls, C substituted cycloalkyls, aryls, substituted aryls, aralkyls, C heteroalkyls, substituted C heteroalkyls, C alkoxy, phenoxy, C heteroalkoxy, and at least one of E includes a B moiety, wherein B is a leaving group, OH, a residue of a hydroxyl-or amino-containing moiety or wherein J is the same as J, or another member of the group defining J and E is the same as E , or another member of the group defining E ; Y are independently O, S or NR ; M is a heteroatom selected from either X or Q; wherein X is an electron withdrawing group and Q is a moiety containing a free electron pair positioned three to six atoms from C(=Y ); R and R are independently selected from the group consisting of hydrogen, C alkyls, C branched alkyls, C cycloalkyls, C substituted alkyls, C substituted cycloalkyls, aryls, substituted aryls, aralkyls, C heteroalkyls, substituted C heteroalkyls, C alkoxy, phenoxy and C heteroalkoxy; (m1) and (m2) are independently zero or one; (n1), (n2), (p1), (p2) and (q) are independently zero or a positive integer, Z is an electron withdrawing group; and R is a polymeric residue. which is optionally capped with a moiety of the formula:.
  • Terminally-Branched Polymeric Linkers And Polymeric Conjugates Containing The Same

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  • US Patent:
    6638499, Oct 28, 2003
  • Filed:
    Feb 6, 2002
  • Appl. No.:
    10/067930
  • Inventors:
    Anthony J. Martinez - Hamilton Square NJ
    Annapurna Pendri - Middletown CT
    Richard B. Greenwald - Somerset NJ
    Yun H. Choe - Piscataway NJ
  • Assignee:
    Enzon, Inc. - Bridgewater NJ
  • International Classification:
    A61K 31785
  • US Classification:
    424 783, 5147723, 514283, 514506, 514513, 514515
  • Abstract:
    The present invention is directed to polymeric-prodrug transport forms of the formula: wherein: E are independently selected from the group consisting of hydrogen, C alkyls, C branched alkyls, C cycloalkyls, C substituted alkyls, C substituted cycloalkyls, aryls, substituted aryls, aralkyls, C heteroalkyls, substituted C heteroalkyls, C alkoxy, phenoxy, C heteroalkoxy, and at least one of E includes a B moiety, wherein B is a leaving group, OH, a residue of a hydroxyl-or amino-containing moiety or wherein J is the same as J, or another member of the group defining J and E is the same as E , or another member of the group defining E , Y are independently O, S or NR ; M is a heteroatom selected from either X or Q; wherein X is an electron withdrawing group and Q is a moiety containing a free electron pair positioned three to six atoms from C( Y ); R and R are independently selected from the group consisting of hydrogen, C alkyls, C branched alkyls, C cycloalkyls, C substituted alkyls, C substituted cycloalkyls, aryls, substituted aryls, aralkyls, C heteroalkyls, substituted C heteroalkyls, C alkoxy, phenoxy and C heteroakoxy; (m ) and (m ) are independently zero or one; (n ), (n ), (p ), (p ) and (q) are independently zero or a positive integer, Z is an electron withdrawing group; and R is a polymeric residue. which is optionally capped with a moiety of the formula:.
  • Hiv Integrase Inhibitors

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  • US Patent:
    7109186, Sep 19, 2006
  • Filed:
    Jul 9, 2003
  • Appl. No.:
    10/616031
  • Inventors:
    Michael A. Walker - Durham CT, US
    Zhuping Ma - Chandler AZ, US
    B. Narasimhulu Naidu - Durham CT, US
    Margaret E. Sorenson - Meriden CT, US
    Annapurna Pendri - Glastonbury CT, US
    Jacques Banville - St-Hubert, CA
    Serge Plamondon - Ste-Catherine, CA
    Roger Remillard - Napierville, CA
  • Assignee:
    Bristol-Myers Squibb Company - Princeton NJ
  • International Classification:
    A61K 31/675
    A61K 31/496
    A61K 31/4015
    A61K 31/541
    C07D 403/06
    C07D 413/06
    C07D 417/06
    C07D 207/36
  • US Classification:
    514 91, 5142278, 5142322, 5142355, 51425401, 514326, 514343, 514397, 514422, 514423, 544 585, 544 60, 544 82, 544141, 544372, 546208, 5462787, 548112, 5483147, 548427, 548517, 548537
  • Abstract:
    The present invention describes novel compounds of Formula I which inhibit HIV integrase. The invention also describes compositions and treatments of AIDS or ARC by using these compounds.
  • Releasable Polymeric Conjugates Based On Aliphatic Biodegradable Linkers

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  • US Patent:
    7122189, Oct 17, 2006
  • Filed:
    Aug 13, 2002
  • Appl. No.:
    10/218167
  • Inventors:
    Hong Zhao - Edison NJ, US
    Richard B. Greenwald - Somerset NJ, US
    Annapurna Pendri - South Glastonbury CT, US
  • Assignee:
    Enzon, Inc. - Bridgewater NJ
  • International Classification:
    A61K 39/395
    A01N 33/08
    A01N 31/06
    A61K 39/44
  • US Classification:
    4241791, 4241811, 4241931, 4241941, 514668, 514715, 514716
  • Abstract:
    Activated polymeric bicine derivatives such as.
  • Pyrazine Modulators Of Cannabinoid Receptors

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  • US Patent:
    7326706, Feb 5, 2008
  • Filed:
    Aug 12, 2004
  • Appl. No.:
    10/917199
  • Inventors:
    Bruce A. Ellsworth - Princeton NJ, US
    Chongqing Sun - East Windsor NJ, US
    Annapurna Pendri - Glastonbury CT, US
  • Assignee:
    Bristol-Myers Squibb Company - Princeton NJ
  • International Classification:
    A01N 43/64
    A61K 31/53
    A61K 31/4965
    C07D 401/00
    C07D 241/02
  • US Classification:
    514241, 514242, 51425505, 51425506, 544180, 544182, 544295, 544405, 544406
  • Abstract:
    The present application describes compounds according to Formula I, wherein A, G, Gand Rare described herein. Additionally, the present application describes pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents. Finally, the present application describes methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents.
  • Azabicyclic Heterocycles As Cannabinoid Receptor Modulators

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  • US Patent:
    7378418, May 27, 2008
  • Filed:
    Dec 17, 2004
  • Appl. No.:
    11/016135
  • Inventors:
    Guixue Yu - Princeton Junction NJ, US
    William R. Ewing - Yardley PA, US
    Amarendra B. Mikkilineni - Easton PA, US
    Annapurna Pendri - Glastonbury CT, US
    Philip M. Sher - Plainsboro NJ, US
    Samuel Gerritz - Guilford CT, US
    Bruce A. Ellsworth - Princeton NJ, US
    Gang Wu - Princeton NJ, US
    Yanting Huang - Pennington NJ, US
    Chongqing Sun - East Windsor NJ, US
    Natesan Murugesan - Princeton Junction NJ, US
    Zhengxiang Gu - Princeton NJ, US
    Ying Wang - Princeton NJ, US
    Doree Sitkoff - Dresher PA, US
    Stephen R. Johnson - Erdenheim PA, US
    Ximao Wu - Princeton Junction NJ, US
  • Assignee:
    Bristol-Myers Squibb Company - Princeton NJ
  • International Classification:
    C07D 487/04
    A61K 31/4162
    A61P 3/04
    A61P 43/00
  • US Classification:
    514248, 544236
  • Abstract:
    The present application describes compounds according to Formula I, pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents and methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents. The compounds have the general Formula I:.
  • Pyrazole Derivatives As Cannabinoid Receptor Modulators

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  • US Patent:
    7517900, Apr 14, 2009
  • Filed:
    Oct 6, 2004
  • Appl. No.:
    10/959866
  • Inventors:
    Annapurna Pendri - South Glastonbury CT, US
    Samuel Gerritz - Guilford CT, US
    Dharmpal S. Dodd - Princeton NJ, US
    Chongqing Sun - East Windsor NJ, US
  • Assignee:
    Bristol-Myers Squibb Company - Princeton NJ
  • International Classification:
    A61K 31/415
    C07D 231/00
  • US Classification:
    514404, 5483561
  • Abstract:
    The present application describes compounds according to Formula I, wherein A, B, E, R, R, R, R, Y and Z are described herein. Additionally, the present application describes pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents. Finally, the present application describes methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents.
  • Tetrahydroquinoline Cannabinoid Receptor Modulators

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  • US Patent:
    7709647, May 4, 2010
  • Filed:
    Apr 17, 2008
  • Appl. No.:
    12/104553
  • Inventors:
    Chongqing Sun - East Windsor NJ, US
    William R. Ewing - Yardley PA, US
    Yanting Huang - Pennington NJ, US
    Annapurna Pendri - Glastonbury CT, US
    Samuel Gerritz - Guilford CT, US
    Bruce A. Ellsworth - Princeton NJ, US
    Natesan Murugesan - Princeton Junction NJ, US
  • Assignee:
    Bristol-Myers Squibb Company - Princeton NJ
  • International Classification:
    C07D 215/38
    A61K 31/4709
  • US Classification:
    546159, 514313
  • Abstract:
    The present application describes compounds according to Formula I, pharmaceutical compositions comprising at least one compound according to Formula I and optionally one or more additional therapeutic agents and methods of treatment using the compounds according to Formula I both alone and in combination with one or more additional therapeutic agents. The compounds have the general Formula I:.

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Annapurna Pendri Photo 3

Annapurna Pendri South G...

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