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Robert Merrifield Ph.D.

Robert Merrifield Ph.D.

The Nobel Prize in Chemistry 1984

Award: “for his development of methodology for chemical synthesis on a solid matrix”

Biography
Patents

Patents

Publication: 1/13
Publication No: US 5714467 A
Title: Antibacterial and antimalarial hybrid peptides
Publication Type: Grant
Publication Date: Feb 3, 1998
Filing Date: Mar 26, 1993
Inventors: Hans G. Boman, Robert B. Merrifield, David Andreu
Original Assignee: The Rockefeller University
Abstract: The invention relates to antibacterial and antimalarial peptides which are
hybrids peptides which a of naturally occurring peptides such as cecropins, attacins, magainins, sarcotoxin, sapecin, bactenecins, alamethidicins, defensins
and PGLa, and toxins such as streptolysins, melittin, barbatolysin, paradaxins and
delta hemolysin. The hybrid peptides of the present invention are easily synthesized and have reduced toxicity.
Also included in the invention are pharmaceutical compositions containing such hybrid peptides, and methods of treating patients infected with an organism against which these peptides are active.
Representative Figure: No Figure
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Publication: 2/13
Publication No: US 5585353 A
Title: Antibiotic peptides containing D-amino acids
Publication Type: Grant
Publication Date: Dec 17, 1996
Filing Date: Sep 16, 1994
Inventors: Robert B. Merrifield, David Wade, Hans G. Boman
Original Assignee: The Rockefeller University
Abstract: Antibiotically and/or antimalarially active D-peptides of naturally occurring antibiotics such as cecropin A, B and D, melittin,
and Magainin I and II and their addition, deletion and replacement analogs including homologous and heterologous analogs thereof.
Representative Figure: No Figure
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Espacenet
Publication: 3/13
Publication No: US 5480867 A
Title: Glucagon analogs with serine replacements
Publication Type: Grant
Publication Date: Jan 2, 1996
Filing Date: Jun 8, 1994
Inventors: Robert B. Merrifield, Cecilia G. Unson
Original Assignee: The Rockefeller University
Abstract: Glucagon analogs characterized principally by the removal or replacement of the 9-aspartic acid residue or its replacement with
another amino acid residue together with replacement of the 16-serine residue and possible replacement of the 11-serine residue and 21-aspartic acid residue with or without a histidine at the amino terminal
are useful adjuncts to insulin therapy.
Representative Figure: No Figure
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Espacenet
Publication: 4/13
Publication No: US 5258454 A
Title: Peptide synthesis method and solid support for use in the method
Publication Type: Grant
Publication Date: Nov 2, 1993
Filing Date: May 12, 1992
Inventors: Rolf H. Berg, Kristoffer Almdal, Walther B. Pedersen, Arne Holm, James P. Tam, Robert B. Merrifield
Original Assignee: Riso National Laboratory
Abstract: A method for the solid-phase synthesis of peptides or proteins in high yield and high purity uses a solid-support consisting of a
functionalized polystyrene-grafted polymer substrate, the grafted polystyrene chains being substantially non-cross-linked and having a chain molecular weight, not including optional non-reactive substituents,
of at least 200,000, preferably in the range of 600,000-1,200,000. Particularly suitable polymer substrates are substrates of a polyolefin such as polyethylene. The method is particularly well-suited to the
compartmentalized synthesis of a multitude of peptides or proteins in a parallel and substantially simultaneous fashion. Preferred embodiments of a solid support for performing the synthesis are prepared from thin polyethylene sheet or film which has been grafted with polystyrene chains in a radical-initiated process in which the polyethylene sheet or film is immersed in a solution of optionally substituted styrene monomer in an alcohol such as methanol, the volume percentage of styrene in the solution preferably being about 30% v/v, and subjected to gamma irradiation.
Representative Figure: No Figure
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Espacenet
Publication: 5/13
Publication No: US 5143902 A
Title: Glucagon analogs with ASP9 replacements or deletions
Publication Type: Grant
Publication Date: Sep 1, 1992
Filing Date: Dec 16, 1991
Inventors: Robert B. Merrifield, Cecilia G. Unson
Original Assignee: The Rockefeller University
Abstract: Glucagon analogs characterized principally by the removal of the 9-aspartic acid residue or its replacement with an amino acid residue
other than an L- dibasic amino acid containing up to five carbon atoms with or without a histidine at the amino terminal are useful adjuncts to insulin therapy.
Representative Figure: No Figure
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Espacenet
Publication: 6/13
Publication No: US 4879273 A
Title: Glucagon homologs and therapeutic use thereof
Publication Type: Grant
Publication Date: Nov 7, 1989
Filing Date: May 22, 1987
Inventors: Robert B. Merrifield
Original Assignee: The Rockefeller University
Abstract: Glucagon analogs characterized principally by deletion of the number one histidine and replacement of the number nine aspartic acid
with glutamic acid are useful adjuncts to insulin therapy.
Representative Figure: No Figure
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Espacenet
Publication: 7/13
Publication No: US 4560676 A
Title: N.sup.α -desacetylthymosinα1 and process
Publication Type: Grant
Publication Date: Dec 24, 1985
Filing Date: Apr 13, 1981
Inventors: Robert B. Merrifield
Original Assignee: The Rockefeller University
Abstract: The preparation of N.sup.α -desacetylthymosinα1 and its use as a hormonally active agent participating in the regulation, differentiation
and function of thymic dependent lymphocytes (T-cells) is described.
Representative Figure: No Figure
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Espacenet
Publication: 8/13
Publication No: US 4507230 A
Title: Peptide synthesis reagents and method of use
Publication Type: Grant
Publication Date: Mar 26, 1985
Filing Date: May 12, 1982
Inventors: James P. Tam, William F. Heath, Jr., Robert B. Merrifield
Original Assignee: Research Corporation
Abstract: A method of releasing a functional group present in an amino acid or amino acyl residue from a resin or protecting residue which is
bonded to the functional group by a linkage having proton affinity, which comprises: reacting the functional group bonded to the organic residue, with a mixture of HF and a base for a time and under conditions
effective to produce the release; wherein the amounts of HF and base in the mixture are adjusted so that said release occurs substantially by an SN 2 mechanism.
Representative Figure: No Figure
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Espacenet
Publication: 9/13
Publication No: US 4293455 A
Title: N.sup.α -Desacetylthymosinα1 and process
Publication Type: Grant
Publication Date: Oct 6, 1981
Filing Date: Apr 7, 1980
Inventors: Robert B. Merrifield, Tai W. Wong
Original Assignee: Rockefeller University
Abstract: The preparation of N.sup.α -desacetylthymosinα1 and its use as a hormonally active agent participating in the regulation, differentiation
and function of thymic dependent lymphocytes (T-cells) is described.
Representative Figure: No Figure
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Espacenet
Publication: 10/13
Publication No: US 3531258 A
Title: Apparatus for the automated synthesis of peptides
Publication Type: Grant
Publication Date: Sep 29, 1970
Filing Date: Nov 16, 1967
Inventors: Nils Jernberg, Robert Bruce Merrifield, John M Stewart
Original Assignee: Us Health Education & Welfare
Abstract: No Abstract
Representative Figure: No Figure
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Espacenet
Publication: 11/13
Publication No: WO 9204042 A1
Title: Glucagon analogs with asp9 replacements or deletions
Publication Type: Grant
Publication Date: Mar 19, 1992
Filing Date: Aug 8, 1991
Inventors: Robert Bruce Merrifield, Cecilia G Unson
Original Assignee: Univ Rockefeller
Abstract: Glucagon analogs characterized principally by the removal of the 9-aspartic acid residue or its replacement with an amino acid residue
other than an L- dibasic amino acid containing up to five carbon atoms with or without a histidine at the amino terminal are useful adjuncts to insulin therapy.
Representative Figure: No Figure
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Espacenet
Publication: 12/13
Publication No: WO 9011771 A1
Title: Antibacterial and antimalarial peptides
Publication Type: Grant
Publication Date: Oct 13, 1990
Filing Date: Apr 12, 1990
Inventors: Hans G Boman, Robert Bruce Merrifield
Original Assignee: Univ Rockefeller
Abstract: Antibiotically and/or antimalarially active hybrid peptides containing from about 20 to about 40 amino acid residues are prepared by
rearranging selected sequences of known peptides.
Representative Figure: No Figure
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Espacenet
Publication: 13/13
Publication No: WO 9002749 A1
Title: Peptide synthesis method and solid support for use in the method
Publication Type: Grant
Publication Date: Mar 22, 1990
Filing Date: Aug 31, 1989
Inventors: Rolf H Berg, Kristoffer Almdal, Walther Batsberg Pedersen, Arne Holm, James P Tam, Robert Bruce Merrifield
Original Assignee: Risoe Forskningscenter
Abstract: A method for the solid-phase synthesis of peptides or proteins in high yield and high purity uses a solid support consisting of a
functionalized polystyrene-grafted polymer substrate, the grafted polystyrene chains being substantially non-cross-linked and having a chain molecular weight, not including optional non-reactive substituents,
of at least 200,000, preferably in the range of 600,000-1,200,000. Particularly suitable polymer substrates are substrates of a polyolefin such as polyethylene. The method is particularly well-suited to the
compartmentalized synthesis of a multitude of peptides or proteins in a parallel and substantially simultaneous fashion. Preferred embodiments of a solid support for performing the synthesis are prepared from
thin polyethylene sheet or film which has been grafted with polystyrene chains in a radical-initiated process in which the polyethylene sheet or film is immersed in a solution of optionally substituted styrene
monomer in an alcohol such as methanol, the volume percentage of styrene in the solution preferably being about 30 % v/v, and subjected to gamma irradiation.
Representative Figure: No Figure
Family
Details Google Patents
Espacenet