Porreca et al., 2003 - Google Patents
Novel Mu, Delta, and Kappa Agonists: Potential for Development of Novel Analgesic AgentsPorreca et al., 2003
- Document ID
- 10986517122435704189
- Author
- Porreca F
- Hruby V
- Publication year
- Publication venue
- Pain
External Links
Snippet
Current opioid analgesics such as morphine are known to exert their specific pharmacological effects through the mu (µ) opioid receptor. Although powerful and effective pain killers, opioid µ-agonists have many undesirable side effects including analgesic …
- 239000000556 agonist 0 title abstract description 29
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/50—Cyclic peptides containing at least one abnormal peptide link
- C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
- C07K7/56—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring the cyclisation not occurring through 2,4-diamino-butanoic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/665—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans derived from pro-opiomelanocortin, pro-enkephalin or pro-dynorphin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1027—Tetrapeptides containing heteroatoms different from O, S, or N
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/07—Tetrapeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/10—Peptides having 12 to 20 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/18—Kallidins; Bradykinins; Related peptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Janecka et al. | Opioid receptors and their ligands | |
Ananthan | Opioid ligands with mixed μ/δ opioid receptor interactions: an emerging approach to novel analgesics | |
Dietis et al. | Simultaneous targeting of multiple opioid receptors: a strategy to improve side-effect profile | |
Schiller | 6 Development of Receptor-Specific Opioid Peptide Analogues | |
Schiller et al. | The TIPP opioid peptide family: development of δ antagonists, δ agonists, and mixed μ agonist/δ antagonists | |
Hruby et al. | Conformation–activity relationships of opioid peptides with selective activities at opioid receptors | |
US5610271A (en) | Kappa receptor selective opioid peptides | |
Arttamangkul et al. | Synthesis and opioid activity of conformationally constrained dynorphin A analogues. 2. Conformational constraint in the “address” sequence | |
Janecka et al. | Conformationally restricted peptides as tools in opioid receptor studies | |
Anand et al. | Modulation of opioid receptor ligand affinity and efficacy using active and inactive state receptor models | |
De Marco et al. | Strategies to improve bioavailability and in vivo efficacy of the endogenous opioid peptides endomorphin-1 and endomorphin-2 | |
Ballet et al. | Multiple ligands in opioid research | |
Gisemba et al. | Conformational constraint between aromatic residue side chains in the “message” sequence of the peptide arodyn using ring closing metathesis results in a potent and selective kappa opioid receptor antagonist | |
Kawasaki et al. | Design and synthesis of highly potent and selective cyclic dynorphin A analogs. 2. New analogs | |
Proteau-Gagné et al. | Exploring the backbone of enkephalins to adjust their pharmacological profile for the δ-opioid receptor | |
EP0853484B1 (en) | Novel mu opioid receptor ligands: agonists and antagonists | |
Porreca et al. | Novel Mu, Delta, and Kappa Agonists: Potential for Development of Novel Analgesic Agents | |
Schiller et al. | Opioid peptide analogs with novel activity profiles as potential therapeutic agents for use in analgesia | |
Wang et al. | Differential antinociceptive effects of intrathecal administration of C‐terminal esterified endomorphin‐2 analogues in mice | |
Davis | Opioid receptor targeting ligands for pain management: a review and update | |
Weltrowska et al. | N‐Methylated cyclic enkephalin analogues retain high opioid receptor binding affinity | |
Ioja et al. | Novel diastereomeric opioid tetrapeptides exhibit differing pharmacological activity profiles | |
Janecka et al. | Structure-activity relationship, conformation and pharmacology studies of morphiceptin analogues-selective μ-opioid receptor ligands | |
Joshi | Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides | |
Schlechtingen et al. | Structure–activity relationships of dynorphin analogs substituted in positions 2 and 3 |