Abstract: Cyclic lactam peptides are disclosed which inhibit at various levels of antagonism the melanocortin 1 receptor (MC1R), melanocortin 3 receptor (MC3R), melanocortin 4 receptor (MC4R), and Melanocortin 4 receptor (MC5R).
Type:
Grant
Filed:
November 28, 1997
Date of Patent:
April 25, 2000
Assignee:
The Arizona Board of Regents on Behalf of the University of Arizona
Abstract: A method of forming a pharmaceutical composition of antimicrobial sterol conjugates having the following formulae: ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4 and Y are as defined in the specification. Also disclosed is a method of inducing an antimicrobial effect by administrating these pharmaceutical compositions.
Abstract: A series of 5,5-disubstituted Hydantoin derivatives synthesized by alkylating 5,5-bis(thiomethyl)-2,4-imidazolidinedione with halomethyl aromatic or halomethyl heteroaromatic precursors or by using the Buchener-Berg procedure on the required ketone. This series of 5,5-disubstituted Hydantoin derivatives are biologically active in their ability to inhibit HIV-induced death and virus production in mammalian (human) cells.
Type:
Grant
Filed:
March 14, 1995
Date of Patent:
June 16, 1998
Assignee:
Southern Research Institute
Inventors:
Robert N. Comber, Robert C. Reynolds, Robert W. Buckheit, Jr.
Abstract: In accordance with the disclosure there is described herein a simultaneous vision lens that incorporates both continuous aspheric and concentric bifocal optics into a single optical lens that may be configured as a contact lens or an intraocular lens.
Abstract: The present invention relates to new and useful nucleoside thiophosphoroamidites and polynucleotide phosphorodithioate compounds as well as the processes whereby these compounds may be used for synthesizing new mononucleotides and polynucleotides having phosphorothioate and phosphorodithioate internucleotide linkages.
Type:
Grant
Filed:
October 31, 1994
Date of Patent:
May 12, 1998
Assignee:
Competitve Technologies, Inc.
Inventors:
Marvin H. Caruthers, Wolfgang K.-D Brill, Eric Yau, Michael Ma, John Nielsen
Abstract: A surgical drape apparatus that incorporates means to alleviate a patient's "suffocation anxiety" by providing for continued circulation of air to the patient's nose and mouth while the patient is draped for surgery, especially the field of surgery is the eye, is described.
Type:
Grant
Filed:
August 1, 1994
Date of Patent:
March 24, 1998
Assignee:
Stanley Chang
Inventors:
Stanley Chang, Nancy Cimitile, Clarice Jaget, Liebert Turner
Abstract: Linear and Cyclic Alpha-MSH fragment analogues of Ac-Nle.sup.4 -Glu.sup.5 -His.sup.6 -D-Phe.sup.7 -Arg.sup.8 -Try.sup.9 -Gly.sup.10 -NH.sub.2. The method of stimulating melanocytes by the transdermal application of these biologically-active analogues and compositions comprising these analogues for use in the method are disclosed.
Type:
Grant
Filed:
April 7, 1997
Date of Patent:
February 3, 1998
Assignee:
Competitive Technologies, Inc.
Inventors:
Victor J. Hruby, Mac E. Hadley, Fahad Al-Obeidi
Abstract: The present invention describes a method for the inhibition of reverse transcriptase by contacting said reverse transcriptase with oligonucleotides having have at least one phosphorodithioate internucleotide linkage of the formula ##STR1## within the phosphorus backbone of the oligonucleotide.
Type:
Grant
Filed:
March 28, 1995
Date of Patent:
December 9, 1997
Assignee:
Competitive Technologies, Inc.
Inventors:
Marvin H. Caruthers, William S. Marshall, Wolfgang Brill, John Nielsen
Abstract: A novel class of cyclic bridged analogs of .alpha.-MSH are described herein. With the described analogs, when administered in pharmaceutical compositions, it is now possible to achieve normalization of hypopigmentation dysfunctions and to achieve darkening of the skin in the total absence of sun or UV light irradiation.
Type:
Grant
Filed:
June 6, 1995
Date of Patent:
November 4, 1997
Assignee:
Competitive Technologies, Inc.
Inventors:
Mac E. Hadley, Victor J. Hruby, Shubh D. Sharma
Abstract: The present invention relates to new and useful nucleoside thiophosphoroamidites and polynucleotide phosphorodithioate compounds as well as the processes whereby these compounds may be used for synthesizing new mononucleotides and polynucleotides having phosphorothioate and phosphorodithioate internucleotide linkages.
Type:
Grant
Filed:
May 17, 1995
Date of Patent:
November 4, 1997
Assignee:
Competitive Technologies, Inc.
Inventors:
Marvin H. Caruthers, Wolfgang K. D. Brill, Eric Yau, Michael Ma, John Nielsen
Abstract: Cyclic Alpha-MSH fragment analogues of Ac-Nle.sup.4 -Glu.sup.5 -His.sup.6 -D-Phe.sup.7 -Arg.sup.8 -Try.sup.9 -Gly.sup.10 -NH.sub.2. The method of stimulating melanocytes by the transdermal application of these biologically-active analogues and compositions comprising these analogues for use in the method are disclosed.
Type:
Grant
Filed:
December 6, 1994
Date of Patent:
October 7, 1997
Assignee:
Competitive Technologies, Inc.
Inventors:
Victor J. Hruby, Mac E. Hadley, Fahad Al-Obeidi
Abstract: The present invention relates to an enzyme reagent ticket for conducting diagnostic or serological tests. More particularly, the present invention relates to an enzyme reagent device which allows for a low-cost, disposable, rapid and convenient system for use in the determination of various components in test fluids, and to a diagnostic kit including the device according to the present invention for conducting certain immunochemical, diagnostic or serological testing.
Abstract: The present invention relates to the pretreatment and treatment of biodegradable wastewater utilizing a series of treatment modes within a single variable depth reactor apparatus to biologically reduce the biochemical oxygen and chemical oxygen demand in domestic and industrial wastewater.
Abstract: Described herein is a method, and the resulting compound, for the synthesis of improved amphiphilic antibiotic agents achieved by altering the chemical structure of amphiphilic polyene macrolide compounds with an oligo(ethylene glycol) conjugate in order to raise the critical micelle concentration of the compound.
Abstract: Dinucleoside phosphorodithioate phosphoramidite precursors useful in the synthesis of oligonucleotide phosphorodithioate which can be used as antisense inhibitors of translation.
Type:
Grant
Filed:
May 8, 1995
Date of Patent:
February 11, 1997
Assignee:
Competitive Technologies, Inc.
Inventors:
Marvin H. Caruthers, Wolfgang K.-D. Brill, Eric Yau, Michael Ma, John Nielsen
Abstract: The invention discloses steroid conjugates having the following structure: ##STR1## where Y is NHCH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 NH.sub.2, NH(CH.sub.2).sub.3 NH(CH.sub.2).sub.4 NH(CH.sub.2).sub.3 NH.sub.2, or NHCH.sub.2 CH.sub.2 NHCH.sub.2 CH.sub.2 NHCH.sub.2 CH.sub.2 NH.sub.2, and each of R.sub.1, R.sub.2, R.sub.3 and R.sub.4 is individually H, OH and OSO.sub.3 H. These conjugates posses antimicrobial properties and are, therefore, useful as antibiotics.
Abstract: The present invention is directed to a group of linear and cyclic peptides having the structures: ##STR1## These peptides, when systemically administered to animals will bring about a sexual response and are thus useful for the diagnosis and treatment of psychogenic sexual dysfunction in the male.