Guzelj et al., 2021 - Google Patents
Structural fine-tuning of desmuramylpeptide NOD2 agonists defines their in vivo adjuvant activityGuzelj et al., 2021
View PDF- Document ID
- 17196921157249001745
- Author
- Guzelj S
- Nabergoj S
- Gobec M
- Pajk S
- Klančič V
- Slütter B
- Frkanec R
- Štimac A
- Šket P
- Plavec J
- Mlinarič-Raščan I
- Jakopin Z
- Publication year
- Publication venue
- Journal of medicinal chemistry
External Links
Snippet
We report on the design, synthesis, and biological evaluation of a series of nucleotide- binding oligomerization-domain-containing protein 2 (NOD2) desmuramylpeptide agonists with improved in vitro and in vivo adjuvant properties. We identified two promising …
- 230000000694 effects 0 title abstract description 152
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
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives
- A61K47/48—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers, inert additives the non-active ingredient being chemically bound to the active ingredient, e.g. polymer drug conjugates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Guzelj et al. | Structural fine-tuning of desmuramylpeptide NOD2 agonists defines their in vivo adjuvant activity | |
Bhandari et al. | The role of ClpP protease in bacterial pathogenesis and human diseases | |
Bersch et al. | Bacterial peptidoglycan fragments differentially regulate innate immune signaling | |
Gobec et al. | Discovery of nanomolar desmuramylpeptide agonists of the innate immune receptor nucleotide-binding oligomerization domain-containing protein 2 (NOD2) possessing immunostimulatory properties | |
Bergan et al. | Shiga toxins | |
Geddes et al. | Unleashing the therapeutic potential of NOD-like receptors | |
RU2668560C2 (en) | Conjugate vaccine on basis of antigen wt1 peptide | |
Alpdundar Bulut et al. | Human gut commensal membrane vesicles modulate inflammation by generating M2-like macrophages and myeloid-derived suppressor cells | |
Kaur et al. | TLR2 agonistic small molecules: detailed structure–activity relationship, applications, and future prospects | |
Zom et al. | Dual synthetic peptide conjugate vaccine simultaneously triggers TLR2 and NOD2 and activates human dendritic cells | |
Agnihotri et al. | Structure− activity relationships in nucleotide oligomerization domain 1 (Nod1) agonistic γ-glutamyldiaminopimelic acid derivatives | |
Morin et al. | Diprovocims: a new and exceptionally potent class of toll-like receptor agonists | |
Jakopin et al. | Immunomodulatory properties of novel nucleotide oligomerization domain 2 (Nod2) agonistic desmuramyldipeptides | |
BR112013018046B1 (en) | PEPTIDE CONJUGATE, PHARMACEUTICAL COMPOSITION, IN VITRO METHODS TO BLOCK SIGNALING BY ONE OR MORE CYTOKINE-YC FAMILY MEMBERS AND TO INHIBIT BINDING OF CYTOKINE-YC TO THE YC-SUBSUIT AND USE OF PEPTIDE CONJUGATE OR PHARMACEUTICAL COMPOSITION | |
Morin et al. | Discovery and structure–activity relationships of the neoseptins: a new class of Toll-like receptor-4 (TLR4) agonists | |
Fujimoto et al. | Structures, synthesis, and human Nod1 stimulation of immunostimulatory bacterial peptidoglycan fragments in the environment | |
AU2008302356A1 (en) | Compositions and methods for treating inflammation and inflammation-related disorders by Plectranthus Amboinicus extracts | |
Effenberg et al. | Nonpyrogenic molecular adjuvants based on norAbu-muramyldipeptide and norAbu-glucosaminyl muramyldipeptide: Synthesis, molecular mechanisms of action, and biological activities in vitro and in vivo | |
van de Graaff et al. | Conditionally controlling human TLR2 activity via trans-cyclooctene caged ligands | |
Cai et al. | Convergent synthesis of novel muramyl dipeptide analogues: inhibition of porphyromonas gingivalis-induced pro-inflammatory effects by high doses of muramyl dipeptide | |
Madge et al. | Structure–activity analysis of cyclic multicomponent lipopeptide self-adjuvanting vaccine candidates presenting group A streptococcus antigens | |
CN114956977B (en) | A biphenyl compound, pharmaceutical composition and preparation method and application thereof | |
Szekely et al. | Design, synthesis, and immunological evaluation of a multicomponent construct based on a glycotripeptoid core comprising B and T cell epitopes and a toll-like receptor 7 agonist that elicits potent immune responses | |
US8569245B2 (en) | Protease inhibitors, compositions and methods of use | |
Yang et al. | Next-generation diprovocims with potent human and murine TLR1/TLR2 agonist activity that activate the innate and adaptive immune response |