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Robert T Goegelman

Deceased

from Linden, NJ

Also known as:
  • Robt T Goegelman
  • Robert N
Phone and address:
437 Academy Ter, Tremley, NJ 07036
908-486-7625

Robert Goegelman Phones & Addresses

  • 437 Academy Ter, Linden, NJ 07036 • 908-486-7625
  • Englewood, FL

Us Patents

  • Immunosuppressive Cyclosporin Analogs With Modified Amino Acids At Position-8

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  • US Patent:
    51225115, Jun 16, 1992
  • Filed:
    Feb 27, 1990
  • Appl. No.:
    7/485920
  • Inventors:
    Arthur A. Patchett - Westfield NJ
    David Taub - Metuchen NJ
    Robert T. Goegelman - Linden NJ
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C07K 512
    C07K 764
    A61K 3700
  • US Classification:
    514 11
  • Abstract:
    New immunosuppressive cyclosporin analogs are disclosed consisting of [dehydro-Ala]. sup. 8 cyclosporins and derived therefrom cyclosporins having a sulfur containing amino acid at position-8.
  • Thienamycin Production

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  • US Patent:
    40060608, Feb 1, 1977
  • Filed:
    Nov 18, 1975
  • Appl. No.:
    5/632938
  • Inventors:
    Jean S. Kahan - Rahway NJ
    Frederick M. Kahan - Rahway NJ
    Edward O. Stapley - Metuchen NJ
    Robert T. Goegelman - Linden NJ
    Sebastian Hernandez - Madrid, ES
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C12D 914
  • US Classification:
    195 80R
  • Abstract:
    The antibiotic thienamycin is active against both gram-positive and gram-negative bacteria. The antibiotic is produced by growing a newly-found and hitherto undescribed species of Streptomyces on suitable fermentation media.
  • Process For Producing Antibiotics By Cultivation Of Streptomyces Flavogriseus

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  • US Patent:
    42359678, Nov 25, 1980
  • Filed:
    Apr 6, 1979
  • Appl. No.:
    6/027642
  • Inventors:
    Patrick J. Cassidy - Rahway NJ
    Robert T. Goegelman - Linden NJ
    Edward O. Stapley - Metuchen NJ
    Sebastian Hernandez - Madrid, ES
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C12P 1718
  • US Classification:
    435119
  • Abstract:
    The antibiotics MSD 890A. sub. 1 and MSD 890A. sub. 3 and pharmaceutically acceptable salts thereof (hereinafter referred to as antibiotics 890A. sub. 1 and 890A. sub. 3) are active against both gram-positive and gram-negative bacteria. The antibiotics are produced by growing species of Streptomyces on suitable fermentation media.
  • Antibiotics

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  • US Patent:
    40815480, Mar 28, 1978
  • Filed:
    Sep 3, 1976
  • Appl. No.:
    5/720483
  • Inventors:
    Jean S. Kahan - Rahway NJ
    Frederick M. Kahan - Rahway NJ
    Edward O. Stapley - Metuchen NJ
    Robert T. Goegelman - Linden NJ
    Sebastian Hernandez - Madrid, ES
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    A61K 3140
  • US Classification:
    424274
  • Abstract:
    The antibiotic thienamycin is active against both gram-positive and gram-negative bacteria. The antibiotic is produced by growing a newly-found and hitherto undescribed species of Streptomyces on suitable fermentation media.
  • Antibiotics

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  • US Patent:
    39503577, Apr 13, 1976
  • Filed:
    Nov 25, 1974
  • Appl. No.:
    5/526992
  • Inventors:
    Jean S. Kahan - Rahway NJ
    Frederick M. Kahan - Rahway NJ
    Edward O. Stapley - Metuchen NJ
    Robert T. Goegelman - Linden NJ
    Sebastian Hernandez - Madrid, ES
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C07D20712
  • US Classification:
    26032627
  • Abstract:
    The antibiotic thienamycin is active against both gram-positive and gram-negative bacteria. The antibiotic is produced by growing a newly-found and hitherto undescribed species of Streptomyces on suitable fermentation media.
  • Isolation Of Non-Ionic Lipophilic Materials On Macroreticular Polymeric Absorbents

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  • US Patent:
    43992749, Aug 16, 1983
  • Filed:
    Jul 2, 1981
  • Appl. No.:
    6/279633
  • Inventors:
    Robert T. Goegelman - Linden NJ
    Laszlo R. Treiber - Gillette NJ
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C07H 1708
  • US Classification:
    536 71
  • Abstract:
    Non-ionic, lipophilic substances are isolated from aqueous or aqueous-organic solution by treatment with a macroreticular polymeric absorbent followed by elution with additional or a different organic solvent.
  • Avermectin Bioconversion Products

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  • US Patent:
    46669370, May 19, 1987
  • Filed:
    Feb 20, 1986
  • Appl. No.:
    6/830333
  • Inventors:
    Robert T. Goegelman - Linden NJ
    Edward S. Inamine - Rahway NJ
    Raymond F. White - Englishtown NJ
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C07D49322
    A61K 31365
  • US Classification:
    514450
  • Abstract:
    There are disclosed novel compounds which are derived from 22,23-dihydro avermectin Bla aglycone, 13-deoxy-22,23 dihydro overmectin Bla aglycone and 13-deoxy-22,23-dihydro overmectin Blb aglycone. The six compounds are hydroxy adducts of the substrate avermectin compound at the 12a, 24, 24a, 26, 26a and 27 positions. The hydroxy adducts are prepared by incubating the substrate with the microorganism Cunninghamella blakesleeana and isolating the hydroxy adducts from the fermentation broth. The compounds are highly potent antiparasitic, insecticidal and anthelmintic agents.
  • Method For The Production Of A Modified "8-Amino Acid" Cyclosporin Derivative

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  • US Patent:
    53189019, Jun 7, 1994
  • Filed:
    Jul 10, 1992
  • Appl. No.:
    7/911433
  • Inventors:
    Arthur A. Patchett - Westfield NJ
    Raymond F. White - Englishtown NJ
    Robert T. Goegelman - Linden NJ
  • Assignee:
    Merck & Co., Inc. - Rahway NJ
  • International Classification:
    C12P 2104
  • US Classification:
    435 711
  • Abstract:
    A cyclosporin derivative with incorporated "8-(3-fluoro-D-alanine)" or "8-(2-deutero-3-fluoro-D-alanine)" has been isolated from the fermentation broth of incubating Tolypocladium inflatum MF5080 (NRRL 8044) with 3-fluoro-D-alanine or its 2-deuterated isomer respectively. The modified cyclosporins exhibit immunosuppressive properties.

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