Classifications

• • 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
  • C07K14/745—Blood coagulation or fibrinolysis factors
  • C07K14/75—Fibrinogen
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • A61K38/36—Blood coagulation or fibrinolysis factors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P17/00—Drugs for dermatological disorders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
  • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
  • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
  • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

• the present invention relates to peptides and peptide derivatives, to the production thereof as well as to their use for preparing a therapeutically and/or preventively active drug and to such a pharmaceutical drug.
• EP 15 865 86 describes the use of peptides from the sequence of fibrin possessing anti-inflammatory effects.
• Said effect may be based on the fact that the fibrin and fibrin fragments generated during the breakdown thereof bind to endothelial cells via its neo-N-terminus of the Bbeta-chain and to cells in the bloodstream via the sequence of the Aalpha-chain, thereby leading to the adhesion and transmigration of these cells into the tissue.
• the binding partner of the fibrin and fibrin fragments to the endothelial cells is the protein vascular endothelial (VE) cadherin, which is expressed exclusively in the adherens junction between neighboring endothelial cells.
• the peptides according to the invention block this interaction and thereby counteract the transmigration of blood cells.
• the natural defense against infections by the leukocytes in the blood is not adversely effected, however.
• the composition of the same such as granulocytes, lymphocytes and monocytes, remains unaffected so that the natural defense process is maintained.
• Fibrinogen is produced in the liver and, in this form, is biologically inactive and normally is provided in the blood at concentrations of around 3 g/l. Proteolytic cleavage of the proenzyme prothrombin results in the formation of thrombin, which cleaves off the fibrinopeptides A and B from the fibrinogen. In this way, fibrinogen is transformed into its biologically active form. Fibrin and fibrin cleavage products are generated.
• Thrombin is formed whenever blood coagulation is activated, i.e. with damage to the tissue, be it of inflammatory, traumatic or degenerative genesis.
• the formation of fibrin as mediated by thrombin is basically a protective process aimed at quickly sealing any defects caused to the vascular system.
• the formation of fibrin also is a pathogenic process.
• the appearance of a fibrin thrombus as the triggering cause of cardiac infarction is one of the most prominent problems in human medicine.
• Fibrin binds to endothelial cells via its neo-N-terminus of Bbeta by means of the sequence to Bbeta and to cells in the bloodstream by means of the sequence Aalpha, thereby leading to the adhesion and transmigration of cells into the tissue.
• the peptides or proteins according to the invention may prevent the adhesion of cells from the bloodstream to endothelial cells of the vascular wall and/or their subsequent transmigration from the blood into the tissue.
• WO9216221 describes polypeptides which are covalently linked to long-chain polymers, as for instance methoxy-polyethylene glycol (PEG).
• PEG methoxy-polyethylene glycol
• the binding of polypeptides to such polymers frequently results in a prolongation of the biological half-life of these polypeptides and delays their renal excretion.
• PEG-groups exerts this effect in a way proportional to the molecular weight of the PEGylated peptide, as, up to a certain size of the molecule, the glomular filtration rate is inversely proportional to the molecular weight.
• WO2004/101600 also describes new poly(ethylene glycol)-modified compounds and their use, in particular with emphasis on modified peptides activating the erythropoietin receptor.
• a prolonged biological half-life is advantageous for various therapeutic uses of peptides. This is in particular true in cases of chronic diseases where the administration of the active agent over a prolonged period of time is indicated. With such indications this may improve the patient's compliance, as applying the active agent once a day will for instance be accepted more easily than continuous infusion.
• a prolongation of the persistency of polypeptides may be obtained by modifying them in such a way that their degradation by proteolytic enzymes (e.g. exo- or endoproteases or peptidases) is prevented.
• Calcitonin Lee et al. Pharm. Res. 1999, 16, 813
• Growth Hormone Releasing Hormone Esposito et al., Advanced Drug Delivery Reviews, 2003, 55, 1279
• Glucagon like peptide 1 Lee et al., Bioconjugate Res. 2005, 16, 377
• Pegvisomant Ross et al., J. Clin. Endocrin. Metab.
• peptides derived from the chain of the Bbeta(15-42)fibrin fragment wherein one or several amino acids of the natural fibrin sequence have been substituted by other amino acids, as well as derivatives modified at the C-terminal end of the peptide sequence also have strong anti-inflammatory effects.
• peptides and peptide derivatives the modification of which prevents their destruction by proteases or peptidases, as well as to peptide-PEG-conjugates derived from the basic sequence of the Bbeta(15-42)fibrin fragment.
• modified peptides which are derived from the chain of the Bbeta(15-42)-fibrin fragment and wherein one or several of the amino acids of the sequence have been substituted by genetically encoded or not genetically encoded amino acids or peptidomimetics. They may exist as free peptides or as C-terminal derivative and/or being linked to a polyethylene glycol (PEG)-polymer, and have anti-inflammatory and/or endothelium stabilizing effects. Esters or amides may for instance be taken into consideration as C-terminal derivatives.
• the inventive compounds may have conservative substitutions of amino acids as compared to the natural sequence of fibrin of the warm blooded animals to be treated in one or several positions.
• a conservative substitution is defined as the side chain of the respective amino acid being replaced by a side chain of similar chemical structure and polarity, the side chain being derived from a genetically coded or not genetically coded amino acid. Families of amino acids of this kind having similar side chains are known in the art.
• amino acids having basic side chains lysins, arginins, histidine
• acidic side chains aspartic acid, glutamic acid
• uncharged polar side chains glycine, aspartamic acid, glutamine, serine, threonine, tyrosine, cysteine
• non-polar side chains alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan
• beta-branched side chains threonine, valine, isoleucine
• aromatic side chains tyrosine, phenylalanine, tryptophane, histidine.
• amino acids having basic side chains lysins, arginins, histidine
• acidic side chains aspartic acid, glutamic acid
• uncharged polar side chains glycine, aspartamic acid, glutamine, serine, threonine, tyrosine, cysteine
• the invention in particular concerns peptides and peptide derivatives of the following general formula I:
• a preferred subject matter of the invention are peptides and peptide derivatives of the general Formula I, wherein:
• X 1 , X 9 , X 10 , X 14 denote L, I, S, M or A
• X 2 , X 6 , X 7 denote E or D
• X 3 , X 4 , X 5 , X 11 denote R or K
• X 8 X 12 denote A, G, S, or L
• X 13 denotes I, L or V and wherein X 15 , X 16 and X 17 have the same meaning as given above, as well as the physiologically acceptable salts thereof.
• a particularly preferred subject matter of the invention are peptides and peptide derivates of Formula II,
• X 17 has the same meaning as given above for Formula I, as well as the physiologically acceptable salts thereof.
• a furthermore most highly preferred subject matter of the invention are peptide derivatives of Formula (III),
• residues X 19 , X 20 and X 21 each are a glycine residue and the remaining one is a residue C—(S-succinimido)-(PEG 5-40K ), the succinimido residue being linked to the sulfur atom of the cysteine residue via C-atom 3, and wherein X 17 denotes NR 2 R 3 , R 2 and R 3 being identical or different and being hydrogen or (C 1 -C 10 )-alkyl, as well as the physiologically acceptable salts thereof.
• a furthermore most highly preferred subject matter of the invention are peptide derivatives of Formula (III),
• residues X 19 , X 20 and X 21 each are a glycine residue and the remaining one is a residue K-(PEG 5-40K ), the PEG-residue being linked via the nitrogen atom in the side chain of the lysine residue, and wherein X 17 denotes NR 2 R 3 , R 2 and R 3 being identical or different and being hydrogen or (C 1 -C 10 )-alkyl, as well as the physiologically acceptable salts thereof.
• amino acid residues in the compounds of Formula I may either be present in their D or their L configuration.
• peptide refers to a polymer of these amino acids, which are linked via an amide linkage.
• “Physiologically acceptable” means that salts are formed with acids or bases the addition of which does not have undesirable effects when used for humans. Preferable are salts with acids or bases the use of which is listed for use with warm blooded animals, in particular humans, in the US Pharmacopoeia or any other generally recognized pharmacopoeia.
• PEG stands for a polyethylene glycol residue having a molecular weight of between 5.000 and 60.000 Dalton, this molecular weight being the maximum of a molecular weight distribution, so that individual components of the mixture may have a higher or lower molecular weight.
• the invention furthermore concerns processes for the production of the peptides and peptide derivatives of general Formula (I), characterized in that, either
• Embodiments of the respective processing steps are not new per se and will be clear to an experienced specialist in the field of organic synthesis.
• a cysteine (C)-residue may be reacted with PEG-maleimide, resulting in a succinimide residue as spacer for residue Z.
• a further possibility is reacting an optionally activated C-terminal carboxy residue with an aminoalkyl-substituted PEG residue.
• a further possibility is the introduction of a PEG residue by reacting an aldehyde-substituted PEG residue with the ⁇ -amino function of a lysine residue.
• Activated PEG reagents having suitable spacers and reactive groups may for instance be obtained from NOF Corporation (Tokyo, Japan).
• the substances according to the invention and the use of the substances according to the invention for the production of a pharmaceutical drug are of particular significance for the production of a pharmaceutical drug for the therapy of diseases resulting from the tissue-damaging effect of white blood cells, or wherein the integrity and full physiological integrity of the layer of endothelial cells lining the blood vessels is impaired.
• Diseases belonging to this group are those in context with autoimmunity, as for instance collagenoses, rheumatic diseases, inflammatory bowel diseases like Morbus Crohn or Colitis ulcerosa, psoriasis and psoriatic rheumatoid arthritis, and post/parainfectious diseases as well as diseases caused by a graft-versus-host reaction.
• a healing effect takes place as this medical drug blocks the migration of the white blood cells into the tissue.
• the white blood cells remain in the blood stream and cannot cause an autoreactive effect harmful to the tissue.
• This effect of the inventive substances is furthermore important for the treatment of shock conditions, in particular in case of septic shock triggered by infection with gram-positive or gram-negative bacterial pathogens as well as viral infections and haemorrhagic shock caused by heavy loss of blood because of severe injuries or bacterial or viral infections.
• inventive substances may generally be used in situations that can be described with the terms “Systemic Inflammatory Response Syndrome (SIRS)”, “Acute Respiratory Distress Syndrome (ARDS)” and organ- or multiorgan failure, respectively.
• SIRS Systemic Inflammatory Response Syndrome
• ARDS acute Respiratory Distress Syndrome
• organ- or multiorgan failure organ- or multiorgan failure
• a pharmaceutical drug for the therapy and/or prevention of reperfusion trauma following surgically or pharmaceutically induced re-supply with blood e.g. following percutaneous coronary intervention, stroke, vessel surgery, cardiac bypass surgery and organ transplants
• this pharmaceutical drug inhibits the migration of lymphocytes, neutrophils and monocytes into the wall of the vessel.
• Reperfusion trauma is caused by a lack of oxygen/acidosis of the cells of the vessel during its re-supply with blood, leading to their activation and/or damage. Because of this, lymphocytes, neutrophils and monocytes adhere to the vessel wall and migrate into it.
• Blocking the adherence and migration of lymphocytes, neutrophils and monocytes in the vessel wall causes the hypoxy/acidosis-induced damage to abate, without the subsequent inflammatory reaction causing a permanent damage to the vessel.
• the endothelium-stabilizing effect of the inventive compounds furthermore prevents the formation of oedemas as well as any further damage to the organs supplied via the respective blood vessels.
• the pharmaceutical drug according to the invention may also be used for the transportation of another drug.
• the inventive drug specifically binds a surface molecule on endothelial cells.
• drugs linked thereto may be delivered to endothelial cells in high concentrations without any danger of them having side effects at other sites.
• An example that may be cited here is the use of substances inhibiting the division of cells, which, specifically brought to endothelial cells, may have an antiangiogenetic effect. This brings about a healing effect in tumor patients, as tumor growth is blocked by preventing the proliferation of endothelial cells and thus by preventing neoangiogenesis.
• inventive compounds themselves may also develop an antiangiogenetic effect, as they, because of their endothelium-stabilizing effect, prevent the endothelial cells from changing into a proliferative phenotype and thus prevent the formation of new capillary blood vessels. Therefore they are themselves suitable for the treatment of all kinds of tumor diseases as well as the prevention and/or treatment of tumor metastases.
• inventive compounds of Formula (I) together with pharmaceutical adjuvants and additives may be formulated into pharmaceutical preparations which also are a subject matter of the present invention.
• a therapeutically effective dose of the peptide or peptide derivative is mixed with pharmaceutically acceptable diluents, stabilizers, solubilizers, emulsifying aids, adjuvants or carriers and brought into a suitable therapeutic form.
• Such preparations for instance contain a dilution of various buffers (e.g. Tris-HCl, acetate, phosphate) of different pH and ionic strength, detergents and solubilizers (e.g. Tween 80, Polysorbat 80), antioxidants (e.g. ascorbic acid), and fillers (e.g. lactose, mannitol).
• buffers e.g. Tris-HCl, acetate, phosphate
• solubilizers e.g. Tween 80, Polysorbat 80
• antioxidants e.g. as
• compositions according to the invention may be administered orally, parenterally (intramuscularly, intraperitoneally, intravenously or subcutaneously), transdermally or in an erodable implant of a suitable biologically degradable polymer (e.g. polylactate or polyglycolate).
• a suitable biologically degradable polymer e.g. polylactate or polyglycolate.
• the biological effect and applicability for the claimed use of the inventive compounds may for instance be determined in an assay in which a culture of human umbilical cord endothelial cells is examined microscopically after stimulation with the “N-terminal disulfide knot protein II” (NDSK-II) or with thrombin.
• the stimulation of endothelial cells causes the formation of gaps between the cells in a densely packed cell layer.
• Treatment with the inventive compounds may prevent the formation of these gaps, and is successful in closing gaps that have already been formed.
• This effect is predicative for the protective effect on the endothelium the inventive compounds have throughout the organism.
• the inventive compounds have an effect in the range of concentrations from 0.01 nM to 1 mM, preferably in the range from 1 nM to 0.1 mM in the bath solution of cells.
• the effectiveness in vivo may for instance be established using a model of acute pulmonitis in a rodent.
• the treatment of the animal and the administration of the substance are carried out as described in Example 7 below.
• the inventive compounds show an effect at a dose ranging from 0.001 mg/kg body weight to 500 mg/kg body weight, preferably at a dose ranging from 0.1 mg/kg to 50 mg/kg.
• mice are, as described in Example 8, for instance infected with a dose of Dengue viruses, wherein 50% of the animals die within a period of 5-20 days after infection.
• the inventive compounds bring about a reduction of this mortality at a dose ranging from 0.001 to 500 mg/kg body weight, preferably at a dose ranging from 0.1 to 50 mg/g body weight.
• Tentagel-S-RAM (Rapp-Polymere) at a load of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.
• the FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 ⁇ l DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3 ⁇ 900 ⁇ l 30% piperidine in DMF and thorough mixing for 4 minutes.
• DIC di-isopropy-carbodiimide
• DIPEA di-isopropy-ethylamine
• HOBt hydroxybenzotriazole
• Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.
• the amino acid derivatives FMOC-Ala, FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Lys(BOC), FMOC-Pro, FMOC-Ser(tBu) and FMOC-Tyr(tBu) (Orpegen) are employed.
• the peptide resin When synthesis is completed the peptide resin is dried.
• the peptide amide is subsequently cleaved off by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature.
• concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.
• the peptide is purified by RP-HPLC on Kromasil RP-18 250-20, 10 ⁇ m in 0.1% TFA with a gradient of 5 on 60% acetonitrile in 40 minutes at a flow rate of 12 ml/min and evaluation of the eluate by means of a UV detector at 215 nm.
• the purity of the individual fractions is determined by analyt.
• RP-HPLC and mass spectrometry Following combination of the purified fractions and lyophilisation 48 mg of pure product are obtained Maldi-TOF, 3036.6 m/z (m.i.).
• the monomeric peptide is synthesized as in Example 1, Tentagel (Rapp Polymere) being used as resin support here with FMOC-Cys(Trt) as the first amino acid.
• Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.
• the amino acid derivatives FMOC-Ala, FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Lys(BOC), FMOC-Pro, FMOC-Ser(tBu), FMOC-Cys(Trt) and FMOC-Tyr(tBu) (Orpegen) are employed.
• Tentagel-S-RAM (Rapp-Polymere) having a charge of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.
• the FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 ⁇ l DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3 ⁇ 900 ⁇ l 30% piperidine in DMF and thorough mixing for 4 minutes.
• Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.
• the amino acid derivatives FMOC-Ala, FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Lys(BOC), FMOC-Pro, FMOC-Ser(tBu), FMOC-Cys(Trt) and FMOC-Tyr(tBu) (Orpegen) are employed.
• the peptide resin When synthesis is completed the peptide resin is dried.
• the peptide amide is subsequently cleaved by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature.
• concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.
• the peptide is purified by RP-HPLC on Kromasil RP-18 250-20.
• the peptide thus obtained is reacted with maleinimido-PEG 20k .
• purification by means of gel chromatography and lyophilisation a pure product is obtained, the identity of which is confirmed by way of RP-HPLC and MALDI-MS.
• Example 1 The biological effect of the compound of Example 1 was established in a model of LPS-induced pneumonitis. C57 Black mice were randomized in two groups of 6 animals each and treated as follows:
• Group 1 received 100 ng/kg LPS intranasally, immediately after the administration of LPS the mice received 4.8 mg/kg of the agent of Example 1 (dissolved in 100 ⁇ l NaCl) i.p., a second dose followed 60 min after the administration of LPS.
• Group 2 received 100 ng/kg LPS intranasally, immediately after the administration of LPS the mice received 1001 NaCl i.p., 60 min after the LPS admininistration the mice again received 100 ⁇ l NaCl i.p. 6 hours after the application of LPS all groups were submitted to a bronchioalveolar lavage and the lungs were removed. From the lavage liquids the number of neutrophils (PMN) was determined. This brought the following results:
• mice The biological effect of the compound of Example 3 was established in a model of Dengue virus infection in mice.
• 5-week-old male BALB/c mice were divided into 2 groups. All animals were infected subcutaneously with a mouse-adapted Dengue virus (DEN-2, strain P23085 at a dose of 1-2 LD 50 .
• 15 mice received 0.1 ml of 0.8% saline as intramuscular injection (control).
• the treated animals received 4.8 mg/kg/day of the agent of Example 3 as an intramuscular injection (diluted in 0.1 ml of 0.8% saline) once a day for 5 days, starting on day 3 after the virus infection.
• Tentagel-S-RAM (Rapp-Polymere) at a load of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.
• the FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 ⁇ l DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3 ⁇ 900 ⁇ l 30% piperidine in DMF and thorough mixing for 4 minutes.
• DIC di-isopropy-carbodiimide
• DIPEA di-isopropy-ethylamine
• HOBt hydroxybenzotriazole
• Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.
• the amino acid derivatives FMOC-Ala, FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Lys(BOC), FMOC-Pro, FMOC-Ser(tBu), FMOC-Cys(Trt) and FMOC-Tyr(tBu) (Orpegen) are employed.
• Tentagel-S-RAM (Rapp-Polymere) at a charge of 0.24 mmol/g are transferred to a commercially available peptide synthesis device (PSMM(Shimadzu)), wherein the peptide sequence is constructed step-by-step according to the carbodiimide/HOBt method.
• the FMOC-amino acid derivatives are pre-activated by adding a 5-fold equimolar excess of di-isopropy-carbodiimide (DIC), di-isopropy-ethylamine (DIPEA) und hydroxybenzotriazole (HOBt) and, following their transfer into the reaction vessel, mixed with the resin support for 30 minutes. Washing steps are carried out by 5 additions of 900 ⁇ l DMF and thorough mixing for 1 minute. Cleavage steps are carried out by the addition of 3 ⁇ 900 ⁇ l 30% piperidine in DMF and thorough mixing for 4 minutes.
• DIC di-isopropy-carbodiimide
• DIPEA di-isopropy-ethylamine
• HOBt hydroxybenzotriazole
• Removal of the individual reaction and wash solutions is effected by forcing the solutions through the bottom frit of the reaction vessel.
• the amino acid derivatives FMOC-Ala, FMOC-Arg(Pbf), FMOC-Asp, FMOC-Gly, FMOC-His(Trt), FMOC-Ile, FMOC-Leu, FMOC-Lys(BOC), FMOC-Pro, FMOC-Ser(tBu), FMOC-Cys(Trt) and FMOC-Tyr(tBu) (Orpegen) are employed.
• the peptide resin When synthesis is completed the peptide resin is dried.
• the peptide amide is subsequently cleaved by treatment with trifluoracetic acid/TIS/EDT/water (95:2:2:1 vol) for 2 hours at room temperature.
• concentration of the solution and precipitation by the addition of ice-cold diethyl ether the crude product (75 mg) is obtained as a solid.
• the peptide is purified by RP-HPLC on Kromasil RP-18 250-20.
• the peptide thus obtained is reacted with O-(iodoacetyl)-N-hydroxysuccinimide, followed by amino-ethyl-oxi-PEG 20k .

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ID=38042580

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• 2007
  • 2007-02-23 US US12/280,543 patent/US20110098442A1/en not_active Abandoned
  • 2007-02-23 JP JP2008555560A patent/JP2009527502A/ja active Pending
  • 2007-02-23 EP EP07701338A patent/EP1987062B1/en not_active Not-in-force
  • 2007-02-23 KR KR1020087023213A patent/KR20090005300A/ko not_active Application Discontinuation
  • 2007-02-23 ZA ZA200807028A patent/ZA200807028B/xx unknown
  • 2007-02-23 WO PCT/AT2007/000095 patent/WO2007095660A1/en active Search and Examination
  • 2007-02-23 AU AU2007219031A patent/AU2007219031B2/en not_active Ceased
  • 2007-02-23 ES ES07701338T patent/ES2371038T3/es active Active
  • 2007-02-23 MX MX2008010930A patent/MX2008010930A/es unknown
  • 2007-02-23 AT AT07701338T patent/ATE513853T1/de active
  • 2007-02-23 EP EP10009684A patent/EP2256131A1/en not_active Withdrawn
  • 2007-02-23 CN CNA2007800063032A patent/CN101389653A/zh active Pending
  • 2007-02-23 RU RU2008137796/04A patent/RU2008137796A/ru not_active Application Discontinuation
  • 2007-02-23 CA CA002641908A patent/CA2641908A1/en not_active Abandoned
  • 2007-02-23 US US11/678,535 patent/US7799758B2/en not_active Expired - Fee Related
• 2008
  • 2008-08-13 IL IL193435A patent/IL193435A0/en unknown
  • 2008-09-19 NO NO20084002A patent/NO20084002L/no not_active Application Discontinuation
• 2010
  • 2010-06-22 US US12/820,804 patent/US20100279924A1/en not_active Abandoned

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