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7521529 |
Differentially protected orthogonal lanthionine technology
The present invention provides a method of synthesizing an intramolecularly bridged polypeptide comprising at least one intramolecular bridge. The present invention further provides a method of...
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7335642 |
Method for treating a viral infection related or a chemical toxin related hepatic injury with deltorphin D
A method of modulating cytokine mediated hepatic injury by administering compound-D SEQ ID NO:1 to a mammal. A concentration of the compound in the range of about 0.5 mg/kg to about 20 mg/kg in a...
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6908617 |
Glycosylated modified primate lentivirus envelope polypeptides
A modified polypeptide corresponding to an envelope glycoprotein of a primate lentivirus is described. The polypeptide has been modified from the wild-type structure so that it has at least two of...
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6875742 |
Method for treating cytokine mediated hepatic injury
A method of modulating cytokine mediated hepatic injury by administering compound-D SEQ ID NO:1 to a mammal. A concentration of the compound in the range of about 0.5 mg/kg to about 20 mg/kg in a...
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6852834 |
Fusion peptides isolatable by phase transition
Genetically-encodable, environmentally-responsive fusion proteins comprising ELP peptides. Such fusion proteins exhibit unique physico-chemical and functional properties that can be modulated as a...
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6740639 |
Inclusion complees of a high potent opioid peptide, pharmaceutical compositions and method of treatment
The invention provides novel inclusion complexes of highly potent opioid peptide of L-Tyrosyl-D-alanyl-glycyl-N-methylphenylalanyl-glycyl-isopro
pylamide with cyclodextrin, pharmaceutical...
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6737397 |
Control of cancer growth through the interaction of &lsqb MET5&rsqb -enkephalin and the zeta receptor
The present invention is related to the treatment and prevention of cancer including particularly gastrointestinal cancer. More specifically, the present invention describes the use of naltrexone,...
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6673769 |
Lanthionine bridged peptides
Disclosed are lanthionine bridged peptides having the structure methods of their preparation and their use as pharmacologically active agents.
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6596778 |
β-endorphin peptides for treating muscle-wasting diseases
An active β-endorphin fragment or an analog of such a fragment is provided to a patient for alleviating the effect of muscle-wasting disease and for inhibiting or reducing leakage of an enzyme...
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6506730 |
Nasal transmucosal delivery of peptide conjugated with biocompatible polymers
The present invention relates to a pharmaceutical composition for the nasal transmucosal delivery of a biocompatible polymer-biologically active peptide conjugate. The pharmaceutical composition of...
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6359111 |
Opioid receptor targeting
A compound comprising a ligand portion which has binding affinity for an opioid receptor, and a therapeutically or diagnostically effective group selected from radionuclide chelating agents,...
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6337319 |
&mgr -Selective opioid peptides
This invention relates to novel opioid peptides for the treatment of pain as well as a method for the preparation thereof and pharmaceutically acceptable compositions comprising these peptides. The...
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6303578 |
Mu-opiate receptor peptides
This invention relates to certain peptides and linear and cyclic analogs thereof that bind to the mu (morphine) opiate receptor with higher affinity, selectivity and potency than currently...
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6251625 |
Process for preparing peptides and N-carbamoyl-protected peptides
The invention concerns a process for the enzymatic preparation of protected di- and oligopeptides and the separation of the protective groups used. The process according to the invention enables...
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6136780 |
Control of cancer growth through the interaction of [Met.sup.5 ]-enkephalin and the zeta (ζ) receptor
The present invention is related to the treatment and prevention of cancer including particularly gastrointestinal cancer. More specifically, the present invention describes the use of naltrexone,...
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6054557 |
Fluorescent peptides
The invention provides biologically active compounds of the formula: ##STR1## where R 1 is a light-emitting moiety and R 7 is a peptide of between 2 and 200 amino acids. X is selected from the...
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5776903 |
Peptide derivatives usable as zinc endopeptidase 24-15 inhibitors
Peptide derivatives usable as zinc endopeptidase 24-15 inhibitors. These peptide derivatives have the following amino acid sequence: -Pheψ(PO 2 CH 2 )- (L,D) Xaa'-Yaa'-Zaa'- in which ψ(PO 2 ...
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5747261 |
Protein related to but distinct from EGF receptor and antibodies reactive therewith
The isolation, cloning and characterization of a human gene related to but distinct from EGF receptor gene has been described. Nucleotide sequence of the gene and amino acid sequence of the...
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5733881 |
Opioid peptide antagonists
Compounds of the formula I as well as methods for their preparation, their pharmaceutical preparations and their use. ##STR1## The compounds of formula I are useful in therapy, especially as...
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5652335 |
Physiologically active substance well capable of permeating biomembrane
A physiologically active substance well capable of permeating biomembrane according to the present invention is represented by: ##STR1## where R represents a residue of a physiologically active...
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5627268 |
Hemoglobin comprising globin fusion proteins
The present invention relates to a novel method for making a predetermined, desired peptide in transgenic animals and can be advantageously used for the production of large quantities of the...
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5558987 |
Blood levels of CCK peptides relative to panic disorder treatment
A method of treating a patient having a panic disorder, the patient having an elevated CCK peptide plasma level, by lowering the plasma CCK peptide level of the patient. A further method provides a...
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5428128 |
Site specific synthesis of conjugated peptides
Processes for synthesizing polypeptides containing substantially non-antigenic polymers, preferably poly(alkylene glycols) in specifically predetermined sites are disclosed. Polypeptides prepared...
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5276137 |
Analgesic peptides with a trifluoronorvaline modification
The present invention relates to analgesic enkephalin derivatives represented by the following formula: Tyr-A 1 -A 2 -A 3 -A 4 SEQ ID NO:5 (1) and the acid salts thereof, wherein Tyr...
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5169833 |
Substituted cyclic pentapeptides
The present invention provides substituted cyclic pentapeptide compounds of general Formula I: ##STR1## and the pharmaceutically-acceptable slats, esters and amides thereof, which are useful for...
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5061691 |
Enkephalin analogs
The invention relates to enkephalin analogs of the formula ##STR1## wherein in case of X is D-Val, D-Phe, Pro, D-Met, D-Met(O), D-Leu, D-Glu, D-Glu(Obzl), D-Lys, D-Lys(Z), or D-Arg, Y is Gly or...
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5017689 |
Dynorphin analogs specific for kappa opioid receptors
Cyclic disulfide and linear dynorphin Dyn A 1 -11 and dynorphin Dyn A 1 -13 analogs which are highly specific for κ opioid receptors. These analogs are useful in pharmaceutical compositions and...
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H000810 |
Biologically active amides
The present invention provides novel peptides of formula (I): R--(X 1 ) m --(X 2 ) n --X 3 --X 4 --X 5 --X 6 --X 7 --(X 8 ) p --(X 9 ) q --R 1 (I) together with their salts, esters,...
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4933324 |
Fatty acid-neuroactive drug conjugate as a prodrug
The invention involves the formation of a prodrug from a fatty acid carrier and a neuroactive drug. The prodrug is stable in the environment of both the stomach and the bloodstream and may be...
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4902505 |
Chimeric peptides for neuropeptide delivery through the blood-brain barrier
Chimeric peptides adapted for delivering neuropharmaceutical agents, such as neuropeptides into the brain by receptor-mediated transcytosis through the blood-brain barrier. The chimeric peptides...
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4767744 |
Substituted tyrosyl methionyl dipeptide amides
This invention relates to novel substituted tyrosyl alanine dipeptide amides of the formula: ##STR1## and the pharmaceutically acceptable addition salts thereof, wherein R 1 is --OH, --OCH 3 or...
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4757153 |
Sulfide, sulfinyl and sulfone dipeptide amides
The invention relates to novel substituted tyrosyl alanine dipeptide amides of the formula: ##STR1## and the pharmaceutically acceptable acid addition salts thereof wherein R 1 is hydrogen, lower...
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4707468 |
Polypeptide
A novel polypeptide is defined by the below shown formula and is useful as an analgesic. ##STR1## wherein R 1 and R 2 may be the same or different and each represents a hydrogen atom or a lower...
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4684620 |
Cyclic polypeptides having mu-receptor specificity
Novel compounds which are capable of binding with enhanced specificity to the mu opioid receptor are disclosed. The compounds are analogs of somatostain and have the formula: ##STR1## wherein X is...
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4658013 |
Analgesic and/or opiate antagonist tripeptide amides and processes for preparation and compositions thereof
A genus of tripeptide amides and fifteen species thereof of Examples 4-18, which are useful as analgesics and/or opiate antagonists, three processes for preparation thereof, pharmaceutical...
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4657892 |
Pharmacologically active peptides
Pharmacologically active peptides of the following formulas are described: L--Tyr--X--L--Phe--X--T L--Tyr--X--L--Phe--X--A--T L--Tyr--X--L--Phe--X--A--X--T L--Tyr--X--L--Phe--X--A--X--B--T...
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4649039 |
Radiolabeling of methionine-containing proteins and peptides
A process for radiolabeling methionine-containing peptides and proteins.
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4631270 |
Therapeutically useful pseudopeptides, compositions containing the same and methods of preparation and use
Therapeutically useful pseudopeptides characterized by the replacement of at least one peptide group, both in a naturally occurring peptide or protein by a thiomethylene group are useful in the...
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4603121 |
Enkephalin analogs
The invention relates to novel enkephalin analogs of the formula: ##STR1## which are useful as analgesic agents.
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4594329 |
CRF analogs
Analogs of rCRF and oCRF are disclosed that can be administered to achieve a substantial elevation of ACTH, β-endorphin, β-lipotropin, other products of the pro-opiomelanocortin gene and...
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4593017 |
Methods of treating patients using a pharmaceutical preparation containing an α-endorfine fragment
The invention relates to the use of (2-9)-α-endorfine for dopaminergic and vasopressin-releasing properties.
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4568640 |
Method of inserting amino acid analogs into proteins
A method for substituting one amino acid for another in a protein chain to improve selected properties of the protein. Initially, an mRNA molecule capable of producing an unmodified protein of the...
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4518711 |
Conformationally constrained cyclic enkephalin analogs with delta receptor specificity
Novel compounds which are capable of binding with enhanced specificity to the delta receptor are disclosed. The compounds are a series of cyclic, conformationally constrained analogs of enkephalins...
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4510082 |
Pharmacologically active peptides
Compounds of the formula ##STR1## and pharmaceutically acceptable non-toxic acid addition salts thereof, in which R is hydrogen, methyl, ethyl, cyclopropylmethyl, or allyl; A is a residue of...
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4483988 |
Substituted derivatives of 4-t-alkoxycarbonyl-piperazin-2-ones
Novel analgesic and antipsychotic agents having the formula ##STR1## in which R 1 is hydrogen, hydroxy or halogen and R 4 is hydrogen or, R 1 and R 4 are both hydroxy; Z is hydrogen or straight...
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4469631 |
Fusion peptides comprising an expressible bacterial gene and β-endorphin
DNA comprising the naturally occurring nucleotide sequence coding for amino acids 44-90 of β-lipotropin and including the entire coding region for β-endorphin with the exception of the C-terminal...
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4468383 |
Dimeric enkephalins
The compounds of the invention are symmetrical dimers of enkephalin polypeptides comprising enkephalin polypeptide monomers linked at the C-termini thereof with a difunctional amino bridging group....
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4464358 |
Homocyclic derivatives
Compounds of the formula: ##STR1## wherein R 1 stands for hydrogen or a defined hydrocarbyl or halogenoalkenyl radical, R 2 stands for a defined hydrocarbyl, halogenoalkenyl or furylmethyl...
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4462941 |
Dynorphin amide analogs
Dynorphin(1-13) has been previously reported to antagonize the analgesia induced by narcotics in naive hosts. Novel compounds are provided which differ from dynorphin(1-13) by neither potentiating...
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4448717 |
Pharmacologically active peptides
Compounds of the formula ##STR1## and pharmaceutically acceptable non-toxic acid addition salts thereof, in which R is hydrogen, methyl, ethyl, cyclopropylmethyl, or allyl; A is a residue of...
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