WO2010052718A9 - Composés lipidiques oxydés et leurs utilisations - Google Patents

Composés lipidiques oxydés et leurs utilisations Download PDF

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Publication number
WO2010052718A9
WO2010052718A9 PCT/IL2009/001049 IL2009001049W WO2010052718A9 WO 2010052718 A9 WO2010052718 A9 WO 2010052718A9 IL 2009001049 W IL2009001049 W IL 2009001049W WO 2010052718 A9 WO2010052718 A9 WO 2010052718A9
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Prior art keywords
carboxy
glycero
butyl
hexadecyl
disease
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PCT/IL2009/001049
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English (en)
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WO2010052718A1 (fr
Inventor
Eti Kovalevski-Ishai
Zeev Ziniuk
Gideon Halperin
Itzhak Mendel
Erez Feige
Niva Yacov
Eyal Breitbart
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Vascular Biogenics Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Priority to CN200980153378.2A priority Critical patent/CN102271517B/zh
Priority to NZ592357A priority patent/NZ592357A/xx
Application filed by Vascular Biogenics Ltd. filed Critical Vascular Biogenics Ltd.
Priority to AU2009312355A priority patent/AU2009312355C1/en
Priority to US13/127,717 priority patent/US9206206B2/en
Priority to ES09824498.1T priority patent/ES2534044T3/es
Priority to CA2740726A priority patent/CA2740726A1/fr
Priority to MX2011004773A priority patent/MX2011004773A/es
Priority to EP09824498.1A priority patent/EP2348866B1/fr
Priority to RU2011122729/04A priority patent/RU2532546C2/ru
Priority to JP2011535207A priority patent/JP5752599B2/ja
Publication of WO2010052718A1 publication Critical patent/WO2010052718A1/fr
Priority to ZA2011/02872A priority patent/ZA201102872B/en
Priority to IL212721A priority patent/IL212721A/en
Publication of WO2010052718A9 publication Critical patent/WO2010052718A9/fr
Priority to HK11109192.4A priority patent/HK1155906A1/xx
Priority to US13/828,883 priority patent/US20130203707A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
    • A—HUMAN NECESSITIES
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    • A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-nitrogen bonds
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    • A61P19/00—Drugs for skeletal disorders
    • A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
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    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00—Antineoplastic agents
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    • A61P9/00—Drugs for disorders of the cardiovascular system
    • 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
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/10—Phosphatides, e.g. lecithin
    • C07F9/106—Adducts, complexes, salts of phosphatides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
    • C07F9/44—Amides thereof
    • C07F9/4403—Amides thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4411—Amides of acyclic unsaturated acids

Definitions

  • the present invention in some embodiments thereof, relates to novel oxidized lipids and to methods employing oxidized lipids for treating or preventing an inflammation associated with endogenous oxidized lipids.
  • the methods of the present embodiments can be utilized in treating or preventing inflammation associated diseases and disorders such as, for example, atherosclerosis and related disorders, autoimmune diseases or disorders, and proliferative diseases or disorders.
  • Oxidized phospholipids have been previously described as useful in the treatment of medical conditions such as, for example, cardiovascular diseases, cerebrovascular diseases and inflammatory diseases and disorders.
  • PCT/IL02/00005 Publication No. WO 02/053092
  • PCT/IL08/000013 Publication No. WO 08/084472
  • etherified oxidized lipids which comprise a carbon backbone chain to which an alkyl chain, an alkyl chain substituted by an oxidized moiety and a phosphate-containing group are attached.
  • the alkyl chain which is substituted by an oxidized moiety is preferably attached to the carbon backbone via an ether bond (hence compounds are referred to as "etherified oxidized lipids), as such a bond imparts the compounds desired pharmacological properties, which are described in detail in the above-mentioned publications.
  • the present inventors have now designed and successfully prepared and tested novel oxidized phospholipids.
  • Ai, A 2 and A3 are each independently selected from the group consisting of O and S;
  • X is a Ci-25 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is alkyl
  • R 2 is selected from the group consisting of (4-methylcarboxy)butyl, (3- carboxy)propyl, (6-carboxy)hexanyl, (2-carboxy)ethyl, . 5,6- dihydroxyhexanyl, 5,5-diethoxypentyl and 5,5-dimethoxypentyl; and
  • R 3 is selected from the group consisting of H, acyl, alkyl, phosphate, phosphocholine, phosphoethanolamine, phosphoethanolamine-N-glutaric acid, phosphoserine, and phosphoinositol.
  • Ai, A 2 and A3 are each independently selected from the group consisting of O and S;
  • R] and R 2 are each independently selected from the group consisting of an alkyl chain being 2-28 carbons in length and
  • X is a C 1-2 5 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is C 1-4 alkyl
  • R 3 is selected from the group consisting of H, phosphate, phosphoethanolamine, phosphoethanolamine-N-glutaric acid and phosphoserine.
  • Ai, A 2 and A3 are each independently selected from the group consisting of O and S;
  • R] is selected from the group consisting of dodecyl, octadecyl, octyl, eicosanyl, cis-9-hexadecenyl, (2-octyl)dodecyl and (15-carboxy)pentadecyl;
  • R 2 is selected from the group consisting of an alkyl chain 2-28 carbons in length and
  • X is a Ci_25 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is C 1-4 alkyl
  • R 3 is selected from the group consisting of H, acyl, alkyl, phosphate, phosphocholine, phosphoethanolamine, phosphoethanolamine-N-glutaric acid, phosphoserine, and phosphoinositol.
  • Ai is S and A 2 and A3 are each O;
  • Ri and R 2 are each independently selected from the group consisting of an alkyl chain 2-28 carbons in length and
  • Z is selected from the group consisting of:
  • R' is CM alkyl
  • (iii) 3 is selected from the group consisting of H, acyl, alkyl, phosphate, phosphocholine, phosphoethanolamine, phosphoethanolamine -N-glutaric acid, phosphoserine, and phosphoinositol.
  • a pharmaceutical composition comprising, as an active ingredient, a compound herein, and a pharmaceutically acceptable carrier.
  • a method of treating or preventing an inflammation associated with an endogenous oxidized lipid comprising administering to a subject in need thereof a therapeutically effective amount of a compound described herein, thereby treating or preventing the inflammation associated with an endogenous oxidized lipid in the subject.
  • a method of decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 in a subject comprising administering to the subject an effective amount of a compound described herein.
  • a method of treating a disease or disorder in which decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 is beneficial comprising administering to a subject in need thereof an effective amount of a compound described herein.
  • a use of the compound described herein in the manufacture of a medicament for decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 in a subject is provided.
  • Ri is an alkyl chain 2-28 carbons in length.
  • the compound described herein is identified for use in a method of treating or preventing an inflammation associated with an endogenous oxidized lipid.
  • the compound described herein is identified for use in a method for decreasing of a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23.
  • the compound described herein is identified for use in a method of treating a disease or disorder in which decreasing of a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 is beneficial.
  • the pharmaceutical composition is packaged in a packaging material and identified in print, in or on the packaging material, for use in the treatment or prevention of an inflammation associated with an endogenous oxidized lipid.
  • the pharmaceutical composition is packaged in a packaging material and identified in print, in or on the packaging material, for decreasing of a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23.
  • the pharmaceutical composition is packaged in a packaging material and identified in print, in or on the packaging material, for use in the treatment of a disease or disorder in which decreasing of a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 is beneficial.
  • the inflammation is associated with a disease or disorder selected from the group consisting of an idiopathic inflammatory disease or disorder, a chronic inflammatory disease or disorder, an acute inflammatory disease or disorder, an autoimmune disease or disorder, an infectious disease or disorder, an inflammatory malignant disease or disorder, an inflammatory transplantation-related disease or disorder, an inflammatory degenerative disease or disorder, a disease or disorder associated with a hypersensitivity, an inflammatory cardiovascular disease or disorder, an inflammatory cerebrovascular disease or disorder, a peripheral vascular disease or disorder, an inflammatory glandular disease or disorder, an inflammatory gastrointestinal disease or disorder, an inflammatory cutaneous disease or disorder, an inflammatory hepatic disease or disorder, an inflammatory neurological disease or disorder, an inflammatory musculo-skeletal disease or disorder, an inflammatory renal disease or disorder, an inflammatory reproductive disease or disorder, an inflammatory systemic disease or disorder, an inflammatory connective tissue disease or disorder, an inflammatory tumor, necrosis, an inflammatory implant-related disease or disorder, an inflammatory aging process
  • a disease or disorder selected
  • FIG. 1 is a graph showing IL12/23 p40 production iii cells treated with various doses of CI-202 (each bar represents 3 samples); P ⁇ 0.004 for each dose in comparison with the control (0 ⁇ g/ml);
  • FIG. 2 is a graph showing IL12/23 p40 mRNA expression in cells treated with CI- 201, CI-202 and phosphatidyl choline (PC) at 2, 3 and 4 hours after treatment;
  • FIG. 3 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ g/ml (18.5 or 37 ⁇ ) CI-202, 10 or 20 (17 or 34 ⁇ ) CI-201, phosphatidyl choline (PC) and PBS/1 % ethanol (sol); ERK1/2 is shown as a control for protein loading;
  • FIGs. 4A and 4B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-202;
  • FIG. 5 is a graph showing the development of MOG-induced experimental autoimmune encephalomyelitis in mice treated with PBS or 4 mg/kg CI-202;
  • FIG. 6 is a graph showing development of collagen-induced arthritis in mice treated with CI-202 (ethanolamine analog of CI-201) and in control mice;
  • FIG. 7 is a graph showing IL12/23 p40 production in cells treated with various doses of CI-203 (each bar represents 6 samples) and P values in comparison with the control (0 ⁇ ?/ ⁇ ⁇ ⁇ );
  • FIG. 8 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 1 or 20 ⁇ g/ml (1.6 or 33 ⁇ ) of R) -CI-203 (R-CI-203), and racemic CI-203 (rac-CI-203), 1 or 20 ⁇ g/ml (1.7 or 34 ⁇ ) of R -CI-201 (R-CI-201) and (S)-Cl-201 (S-CI-201), and 1 or 20 ⁇ g/ml (1.3 or 26 ⁇ ) of phosphatidyl choline (Ph.Ch.); ERK1/2 is shown as a control for protein loading;
  • FIGs. 9A and 9B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-203;
  • FIG. 10 is a graph showing IL12/23 p40 production in cells treated with various doses of CI-209 (each bar represents 5 samples) and P values (P ⁇ 0.008 for doses of 10 and 20 ⁇ g/ml, and P ⁇ 0.016 for doses of 1, 2.5 and 5 in comparison with the control (0 ⁇ );
  • FIG. 11 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 20 ⁇ ⁇ (38 ⁇ ) CI-209, CI-201 or phosphatidyl choline (PC) or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIGs. 12A and 12B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-209;
  • FIG. 13 is a graph showing IL12/23 p40 production in cells treated with various doses of CI-210 (each bar represents 4 samples) and P values (P ⁇ 0.029 for doses of 10 and 20 ⁇ g/ml, and P ⁇ 0.057 for doses of 2.5 and 5 ⁇ g ml) in comparison with the control (0 g/ml);
  • FIG. 14 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 20 ⁇ (31 ⁇ ) CI-210, CI-201 or phosphatidyl choline (PC) or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIGs. 15A and 15B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-210;
  • FIG. 16 is a graph showing IL12/23 p40 production in cells treated with various doses of CI-216 (each bar represents 4 samples) and P values in comparison with the control (0 ⁇ ⁇ );
  • FIG. 17 presents a photograph of a Western blot showing phosphotyrosine (p-
  • Tyrosine in samples treated with 10 or 20 ⁇ g/ml (17 or 34 ⁇ ) CI-215, or with phosphatidyl choline (PC) or PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIG. 18 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ g/ml (15 or 30 ⁇ ) CI-216, 10 or 20 ⁇ g/ml (17 or 34 ⁇ ) CI-201, phosphatidyl choline (PC) or PBS/1 % ethanol (sol); ERKl/2 is shown as a control for protein loading;
  • FIG. 19 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 20 ⁇ g/ml (38 ⁇ ) of CI-206 or phosphatidyl choline (PC) or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIG. 20 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 20 ⁇ g/ml (35 ⁇ ) of CI-205, CI-201 or phosphatidyl choline (PC) or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIGs. 21A and 21B are each graphs showing results of an individual experiment testing toxicity of various doses of CI -206;
  • FIGs. 22A and 22B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-205;
  • FIG. 23 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 20 ⁇ g/ml (34 ⁇ ) of CI-208, CI-201 or phosphatidyl choline (PC); -tubulin (a-Tub) is shown as a control for protein loading;
  • FIGs. 24A and 24B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-208;
  • FIGs. 25A and 25B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-213;
  • FIGs. 26A and 26B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-214;
  • FIG. 27 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ g/ml (18 or 36 ⁇ ) CI-217, 10 or 20 ⁇ g/ml (17 or 34 ⁇ ) CI-201, phosphatidyl choline (PC) or PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIG. 28 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ g/ml (31 ⁇ ) of CI-219 and 20 ⁇ g/ml (34 ⁇ ) of CI-201 or phosphatidyl choline (PC), or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIG. 29 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ ⁇ (34 ⁇ ) of CI-220 and 20 ⁇ g/ml (34 ⁇ ) of CI-201 or phosphatidyl choline (PC), or with PBS/1 % ethanol (Sol); ERKl/2 is shown as a control for protein loading;
  • FIGs. 30A and 30B are each graphs showing results of an individual experiment testing toxicity of various doses of CI-201-PA;
  • FIG. 31 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ng ml (17 or 34 ⁇ ) l-S-CI-201 (CI-S-201), 10 or 20 ⁇ g/ml (17 or 34 ⁇ ) CI-201, phosphatidyl choline (PC) or PBS/1 % ethanol (Sol); E 1/2 is shown as a control for protein loading;
  • FIG. 32 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 10 or 20 ⁇ g/ml (18 or 36 ⁇ ) l-S-CI-202 (CI-S-202), 10 or 20 ⁇ g/ml (18.5 or 37 ⁇ ) CI-202, 10 or 20 ⁇ g/ml (17 or 34 ⁇ ) CI-201, phosphatidyl choline (PC) or PBS/1 % ethanol (sol); ERK1/2 is shown as a control for protein loading;
  • FIGs. 33A and 33B are each graphs showing results of an individual experiment testing toxicity of various doses of di-OH;
  • FIG. 34 is a graph showing the area of atherosclerotic lesions in mice treated with di-OH and in control mice;
  • FIG. 35 is a graph showing the area of atherosclerotic lesions in mice treated with diMeAc and in control mice;
  • FIGs. 36A and 36B are each graphs showing results of an individual experiment testing toxicity of various doses of diEtAc;
  • FIG. 37 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 1, 5, 10 or 20 aglxn[ (1.7, 8.3, 16.7 or 33.3 ⁇ ) VB-223 or PBS/1 % ethanol (Sol); ERK1/2 is shown as a control for protein loading;
  • FIG. 38 presents a photograph of a Western blot showing phosphotyrosine (p- Tyrosine) in samples treated with 1, 5, 10 or 20 ⁇ / ⁇ 1 (1.6, 8, 16 or 32 ⁇ ) VB-221 or PBS/1 % ethanol (Sol); ERK1/2 is shown as a control for protein loading; and
  • FIG. 39 presents a photograph of a Western blot showing phosphotyrosine (p-
  • the present invention in some embodiments thereof, relates to novel oxidized lipids and to methods employing oxidized lipids for treating or preventing an inflammation associated with endogenous oxidized lipids.
  • the oxidized lipids described herein can be utilized in treating or preventing inflammation associated diseases and disorders such as, for example, atherosclerosis and related disorders, autoimmune diseases or disorders, and proliferative diseases or disorders.
  • CI-201 (also referred to herein and in the art as VB-201) is a promising oxidized phospholipid which is currently in advanced clinical trials for treatment of inflammatory conditions such as atherosclerosis.
  • the present inventors have prepared novel oxidized phospholipids and structurally related compounds, which are designed to exhibit an improved anti-inflammatory effect and/or improved pharmacological performance.
  • Improved anti-inflammatory effect can be readily determined by known in vitro and in vivo models for inflammatory processes, and can be exhibited by improved therapeutic effect for a disease to be treated, as further detailed hereinbelow.
  • Improved pharmacological performance includes improved biostability, bioavailability, reduced toxicity and further, improved stability in production, formulation and/or storage. These features can also be determined by experimentations readily recognized by those skilled in the art, and as is further detailed hereinbelow.
  • the compounds described herein exhibit minor toxicity, and exhibit biological effects at doses at which the compounds are substantially non-toxic.
  • FIGs. 1 and 2 show inhibition by the exemplary compound CI-202 of production of the p40 subunit of the pro-inflammatory cytokines interleukin-12 and interleukin-23.
  • FIG. 3 shows tyrosine phosphorylation modulation by CI-202 as being similar to that exhibited by CI-201.
  • FIGs. 4A and 4B show toxicity profiles of CI-202.
  • FIG. 5 shows that CI-202 is therapeutically effective in a mouse autoimmune encephalomyelitis model (an experimental model of human multiple sclerosis and acute disseminated . encephalomyelitis).
  • FIG. 6 shows that CI-202 is therapeutically effective in a mouse arthritis model.
  • FIG. 7 shows inhibition by the exemplary compound CI-203 of production of the p40 subunit of the pro-inflammatory cytokines interleukin-12 and interleukin-23.
  • FIG. 8 shows tyrosine phosphorylation modulation by CI-203 as being similar to that exhibited by CI-201.
  • FIGs. 9A and 9B show toxicity profiles of CI-203.
  • FIG. 10 shows inhibition by the exemplary compound CI-209 of production of the p40 subunit of the pro-inflammatory cytokines interleukin-12 and interleukin-23.
  • FIG. 11 shows tyrosine phosphorylation modulation by CI-209.
  • FIGs. 12A and 12B show toxicity profiles of CI-209.
  • FIG. 13 shows inhibition by the exemplary compound CI-210 of production of the p40 subunit of the pro-inflammatory cytokines interleukin-12 and interleukin-23.
  • FIG. 14 shows tyrosine phosphorylation modulation by CI-210.
  • FIGs. 15A and 15B show toxicity profiles of CI-210.
  • FIG. 16 shows inhibition by the exemplary compound CI-216 of production of the p40 subunit of the pro-inflammatory cytokines interleukin-12 and interleukin-23.
  • FIG. 18 shows tyrosine phosphorylation modulation by CI-216 as being similar to that exhibited by CI-201.
  • FIG. 17 shows tyrosine phosphorylation modulation by CI-215.
  • FIG. 19 tyrosine phosphorylation modulation by the exemplary compound CI-206.
  • FIGs. 21A and 21B show toxicity profiles of CI-206.
  • FIG. 20 shows tyrosine phosphorylation modulation by the exemplary compound CI-205 as being similar to that exhibited by CI-201.
  • FIGs. 22A and 22B show toxicity profiles of CI-205.
  • FIG. 23 shows tyrosine, phosphorylation modulation by the exemplary compound
  • FIGs. 25A and 25B, and 26A and 26B show toxicity profiles of the exemplary compounds CI-213 and CI-214, respectively.
  • FIG. 27 shows tyrosine phosphorylation modulation by the exemplary compound CI-217 as being similar to that exhibited by CI-201.
  • FIG. 29 shows tyrosine phosphorylation modulation by the exemplary compound
  • FIGs. 30A and 30B show toxicity profiles of the exemplary compound CI-201-PA.
  • FIG. 31 shows tyrosine phosphorylation modulation by the exemplary compound l-S-CI-201 as being similar to that exhibited by CI-201.
  • FIG. 32 shows tyrosine phosphorylation modulation by the exemplary compound l-S-CI-202 as being similar to that exhibited by CI-201.
  • FIG. 34 shows that the exemplary compound di-OH is therapeutically effective an a mouse atherosclerosis model.
  • FIGs. 33A and 33B show toxicity profiles of di-OH.
  • FIG. 35 shows that the exemplary compound diMeAc is therapeutically effective an a mouse atherosclerosis model.
  • FIGs. 36A and 36B show toxicity profiles of diEtAc, a compound closely related to diMeAc.
  • FIGs. 37-39 shows tyrosine phosphorylation modulation by the exemplary compounds VB-223, VB-221 and VB-222, respectively.
  • exemplary compounds described herein have been shown to be biologically active by in vitro tests, and some of the compounds have been confirmed to be therapeutically effective in vivo.
  • the performance of the oxidized lipid which have not yet been tested in vivo can be further tested in suitable animal models such as, for example, those described in the Examples section hereinbelow, in International Patent Application No. PCT/IL2004/000453 (Publication No. WO 04/106486) and U.S. Patent Application No. 11/528,657 (Publication No. 2007-0099868), and in models designed as described, for example, in Singh et al., Clinical Chemistry 51:12, 2252-2256 (2005), which is incorporated by reference as if fully set forth herein.
  • the biostability of the oxidized lipids described herein is improved due to the presence of ether and/or sulfide bonds instead of the ester bonds present in most lipids. Biostability typically improves . the therapeutic effect of a compound.
  • the biostability of the oxidized lipids can be determined, for example, by assaying its enzymatic degradation by phospholipase-C, using ELISA or absorbance measurements.
  • oxidized lipids described herein can therefore be advantageously recognized as exhibiting an improved effect in treating or preventing inflammation associated with endogenous oxidized lipids, in terms of improved therapeutic and/or pharmacokinetic parameters.
  • novel oxidized lipids e.g., oxidized phospholipids as described herein.
  • the oxidized lipid is l-hexadecyl-2-(4- carboxy)butyl-glycero-3-phosphate (also referred to herein as "CI-201-PA").
  • the oxidized lipid is l-hexadecyl-2-(4-methylcarboxy)butyl- glycero-3-phosphoethanolamine.
  • the oxidized lipid is l-hexadecyl-2-(4-methylcarboxy)butyl-glycero-3-phosphocholine (also referred to herein as "CI-208").
  • the oxidized lipid is 1- hexadecyl-2-(4-carboxy)butyl-glycero-3-phosphoethanolamine (also referred to herein as "CI-202").
  • the oxidized lipid is l-hexadecyl-2- (3-carboxy)propyl-glycero-3-phosphoethanolamine (also referred to herein as "CI-206").
  • the oxidized lipid is l-hexadecyl-2-(3- carboxy)propyl-glycero-3-phosphocholine (also referred to herein as "CI-205").
  • the oxidized lipid is l-hexadecyl-2-(6-carboxy)hexanyl- glycero-3-phosphocholine (also referred to herein as "CI-203").
  • the oxidized lipid is l-dodecyl-2-(4-carboxy)butyl-glycero-3- phosphocholine (also referred to herein as "CI-209").
  • the oxidized lipid is l-hexadecyl-2-(4-carboxy)butyl-glycero-3- phosphoethanolamine-N-glutaric acid (also referred to herein as "CI-210").
  • the oxidized lipid is l-(15'-carboxy)pentadecyl-2-(4- carboxy)butyl-glycero-3-phosphocholine (also referred to herein as "CI-213").
  • the oxidized lipid is l-(15'-carboxy)pentadecyl-2-(4- carboxy)butyl-glycero-3-phosphoethanolamine (also referred to herein as "CI-214").
  • the oxidized lipid is l-octadecyl-2-(4- carboxy)butyl-glycero-3-phosphocholine (also referred to herein as "CI-215").
  • the oxidized lipid is l-octadecyl-2-(4-carboxy)butyl-glycero- 3-phosphoethanolamine (also referred to herein as "CI-216").
  • the oxidized lipid is l-hexadecyl-2-(2-carboxy)ethyl-glycero-3- phosphocholine (also referred to herein as "CI-217").
  • the oxidized lipid is l-S-hexadecyl-2-(4-carboxy)butyl-glycero-3- phosphocholine (also referred to herein as "l-S-CI-201").
  • the oxidized lipid is l-S-hexadecyl-2-(4-carboxy)butyl-glycero-3- phosphoethanolamine (also referred to herein as "l-S-CI-202").
  • the oxidized lipid is l-hexadecyl-2-(5,6-dihydroxy)hexanyl- glycero-3-phosphocholine (also referred to herein as "di-OH").
  • the oxidized lipid is l-(cis-9-hexadecenyl)-2-(4-carboxy)butyl-glycero-3- phosphocholine.
  • the oxidized lipid is 1- hexadecyl-2-(4-carboxy)butyl-glycerol. According to an exemplary embodiment, the oxidized lipid is l-hexadecyl-2-(5',5'-diethoxypentyl)-glycero-3-phosphocholine (also referred to herein as "diEtAc"). According to an exemplary embodiment, the oxidized lipid is l-hexadecyl-2-(5',5'-dimethoxypentyl)-glycero-3-phosphocholine (also referred to herein as "diMeAc").
  • the oxidized lipid is 1- octyl-2-(4-carboxy)butyl-glycero-3-phosphocholine (also referred to herein as "CI-207").
  • the oxidized lipid is l-octyl-2-(4-carboxy)butyl- glycero-3-phosphoethanolamine.
  • the oxidized lipid is l-eicosanyl-2-(4-carboxy)butyl-glycero-3-phosphocholine (also referred to herein as "CI-219").
  • the oxidized lipid is l-eicosanyl-2- (4-carboxy)butyl-glycero-3-phosphoethanolamine (also referred to herein as "CI-220").
  • the oxidized lipid is l-(2-octyl)dodecyl-2-(4- carboxy)butyl-glycero-3-phosphocholine (also referred to herein as "VB-221").
  • the oxidized lipid is l-(2-octyl)dodecyl-2-(4-carboxy)butyl- glycero-3-phosphoethanolamine (also referred to herein as "VB-222").
  • the oxidized lipid is l-hexadecyl-2-(4-carboxy)butyl-glycero-3- phosphoserine (also referred to herein as "VB-223").
  • VB-223 l-hexadecyl-2-(4-carboxy)butyl-glycero-3- phosphoserine
  • 1-S- refers to a compound wherein the oxygen atom at the 1-position of the glycerol backbone (sn-l) is replaced by a sulfur atom, such that the compound is a derivative of 1-thioglycerol instead of a derivative of glycerol.
  • carbon atoms in each of the compounds described herein can be chiral or non-chiral.
  • the carbon atom at the 2-position of the glycerol backbone is chiral.
  • Any chiral carbon atom that is present in the compounds described herein can be either in an R- configuration, an S-configuration or as a racemate.
  • present embodiments encompass any combination of chiral and racemic carbon atoms, including all the possible stereoisomers, optical isomers, and enantiomers.
  • the compounds of embodiments of the present invention can be synthesized while retaining a configuration of the starting material.
  • the compounds of the present embodiments can be further selectively synthesized in terms of the stereochemistry of the oxidized group.
  • the optical purity e.g., the inclusion of chiral and/or racemic carbons
  • the obtained stereoisomers of the resulting compounds can be determined.
  • known techniques can be used to separate the optical or stereo- isomers. Such techniques are described, for example, in "Organic chemistry, fourth Edition by Paula Yurkanis Bruice, page 180-185 and page 214, Prentice Hall, Upper Sadde River, NJ 07458".
  • the above compounds may be characterized according to certain novel structural elements thereof.
  • some of the above oxidized lipids comprise a glycerol backbone to which an oxidized side chain is attached at the 2-position thereof, wherein the oxidized side chain is selected from the group consisting of (4-methylcarboxy)butyl, (3-carboxy)propyl, (6- carboxy)hexanyl, (2-carboxy)ethyl, 5,6-dihydroxyhexanyl, 5,5-diethoxypentyl and 5,5- dimethoxypentyl.
  • Ai, A 2 and A3 are each independently selected from the group consisting of O and S;
  • X is a C 1 .25 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is C1 alkyl
  • Ri is an alkyl chain 2-28 carbons in length.
  • oxidized lipids described hereinabove may be characterized in that they comprise a phosphoryl moiety at the 3-position . thereof selected from the group consisting of phosphate, phosphoethanolamine, phosphoethanolamine-N-glutaric acid and phosphoserine, or as being non-phosphorylated and non-substituted at the 3-position (i.e., a hydrogen atom is present at the 3-position).
  • At least one o f Ri and R 2 is wherein X is a C1-25 chain, Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is C1- alkyl
  • R 3 is selected from the group consisting of H, phosphate, phosphoethanolamine, phosphoethanolamine-N-glutaric acid and phosphoserine.
  • Ri is an alkyl chain 2-28 carbons in length. It is to be
  • R2 is
  • oxidized lipids described hereinabove may be characterized in that they comprise a side chain at the 1-position thereof selected from the group consisting of dodecyl, octadecyl, octyl, eicosanyl, cis-9-hexadecenyl, (2-octyl)dodecyl and (15- carboxy)pentadecyl.
  • Ai, A 2 and A 3 are each independently selected from the group consisting of O and S;
  • Ri is selected from the group consisting of dodecyl, octadecyl, octyl, eicosanyl, cis-9-hexadecenyl, (2-octyl)dodecyl and (15-carboxy)pentadecyl;
  • R 2 is selected from the group consisting of an alkyl chain 2-28 carbons in length and
  • X is a Ci -25 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is Ci ⁇ alkyl
  • R 3 is selected from the group consisting of H, acyl, alkyl, phosphate, phosphocholine, phosphoethanolamine, phpsphoethanolamine-N-glutaric acid, phosphoserine, and phosphoinositol. It is to be appreciated that a (15-carboxy)pentadecyl group described herein
  • X is a 13- carbon alkyl chain
  • Y is hydrogen
  • oxidized lipids described hereinabove may be characterized in that they comprise a sulfur atom at the 1-position thereof and oxygen atoms at the 2- and 3- positions thereof.
  • Ai is S and A 2 and A 3 are each O;
  • Ri and R 2 are each independently selected from the group consisting ' of an alkyl chain 2-28 carbons in length and provided that at least one o f Ri and R 2 is
  • X is a Ci -25 chain
  • Y is selected from the group consisting of:
  • Z is selected from the group consisting of:
  • R' is C 1-4 alkyl
  • R 3 is selected from the group consisting of H, acyl, alkyl, phosphate, phosphocholine, phosphoethanolamine, phosphoethanolamine -N-glutaric acid, phosphoserine, and phosphoinositol.
  • Ri is an alkyl chain 2-28 carbons in length.
  • variable Z described hereinabove is selected from the group consisting of:
  • variable Y is selected from the group consisting of H and -OH.
  • R' is a saturated, non-substituted Cm alkyl.
  • R' is selected from the group consisting of ethyl and methyl.
  • the alkyl chain 2-28 carbons in length described herein is saturated, unless specifically indicated otherwise.
  • the alkyl chain is non-substituted, unless specifically indicated otherwise.
  • variable X described herein a saturated alkyl chain 1 to 25 carbon atoms in length, unless specifically indicated otherwise.
  • the alkyl chain is non-substituted, unless specifically indicated otherwise.
  • alkyl refers to a saturated or unsaturated aliphatic hydrocarbon including straight chain and branched chain groups.
  • the alkyl group has 1 to 20 carbon atoms. Whenever a numerical range; e.g., "1-20", is stated herein, it implies that the group, in this case the alkyl group, may contain 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 20 carbon atoms. More preferably, the alkyl is a medium size alkyl having 1 to 10 carbon atoms. Most preferably, unless otherwise indicated, the alkyl is a lower alkyl having 1 to 4 carbon atoms.
  • the alkyl group may be substituted or non-substituted.
  • the substituent group can be, for example, cycloalkyl, aryl, heteroaryl, heteroalicyclic, halo, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azide, sulfonyl, sulfinyl, sulfonamide, phosphonyl, phosphinyl, oxo, carbonyl, thiocarbonyl, urea, thiourea, O-carbamyl, N- carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, C-carboxy, O-carboxy, and amino, as these terms are defined herein.
  • the alkyl is non- substituted.
  • a "cycloalkyl” group refers to an all-carbon monocyclic or fused ring (i.e., rings which share an adjacent pair of carbon atoms) group wherein one of more of the rings does not have a completely conjugated pi-electron system.
  • examples, without limitation, of cycloalkyl groups are cyclopropane, cyclobutane, cyclopentane, cyclopentene, cyclohexane, cyclohexadiene, cycloheptane, cycloheptatriene, and adamantane.
  • a cycloalkyl group may be substituted or unsubstituted.
  • the substituent group can be, for example, alkyl, aryl, heteroaryl, heteroalicyclic, halo, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azide, sulfonyl, sulfinyl, sulfonamide, phosphonyl, phosphinyl, oxo, carbonyl, thiocarbonyl, urea, thiourea, O- carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, C-carboxy, O-carboxy, and amino, as these terms are defined herein.
  • aryl group also referred to herein as "aromatic functional group” refers to an all-carbon monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of carbon atoms) groups having a completely conjugated pi-electron system. Examples, without limitation, of aryl groups are phenyl, naphthalenyl and anthracenyl. The aryl group may be substituted or unsubstituted.
  • the substituent group can be, for example, alkyl, cycloalkyl, aryl, heteroaryl, heteroalicyclic, halo, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azide, sulfonyl, sulfinyl, sulfonamide, phosphonyl, phosphinyl, oxo, carbonyl, thiocarbonyl, urea, thiourea, O-carbamyl, N- carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N-amido, C-carboxy, O-carboxy, and amino, as these terms are defined herein.
  • heteroaryl group refers to a monocyclic or fused ring (i.e., rings which share an adjacent pair of atoms) group having in the ring(s) one or more atoms, such as, for example, nitrogen, oxygen and sulfur and, in addition, having a completely conjugated pi- electron system.
  • heteroaryl groups include pyrrole, furane, thiophene, imidazole, oxazole, thiazole, pyrazole, pyridine, pyrimidine, quinoline, isoquinoline and purine.
  • the heteroaryl group may be substituted or unsubstituted.
  • the substituent group can be, for example, alkyl, cycloalkyl, aryl, heteroaryl, heteroalicyclic, halo, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azide, sulfonyl, sulfinyl, sulfonamide, phosphonyl, phosphinyl, oxo, carbonyl, thiocarbonyl, urea, thiourea, O-carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C- amido, N-amido, C-carboxy, O-carboxy, and amino, as these terms are defined herein.
  • heteroalicyclic group refers to a monocyclic or fused ring group having in the ring(s) one or more atoms such as nitrogen, oxygen and sulfur.
  • the rings may also have one or more double bonds. However, the rings do not have a completely conjugated pi- electron system.
  • the heteroalicyclic may be substituted or unsubstituted.
  • the substituted group can be, for example, lone pair electrons, alkyl, cycloalkyl, aryl, heteroaryl, heteroalicyclic, halo, hydroxy, alkoxy, aryloxy, thiohydroxy, thioalkoxy, thioaryloxy, cyano, nitro, azide, sulfonyl, sulfinyl, sulfonamide, phosphonyl, phosphinyl, oxo, carbonyl, thiocarbonyl, urea, thiourea, O-carbamyl, N-carbamyl, O-thiocarbamyl, N- thiocarbamyl, C-amido, N-amido, C-carboxy, O-carboxy, and amino, as these terms are defined herein.
  • Representative examples are piperidine, piperazine, tetrahydrofuran, tetrahydropyrane, morpholine and
  • a "hydroxy” group refers to an -OH group.
  • alkoxy refers to both an -O-alkyl and an -O-cycloalkyl group, as defined herein.
  • aryloxy refers to both an -O-aryl and an -O-heteroaryl group, as defined herein.
  • a "thiohydroxy” group refers to a -SH group.
  • a “thioalkoxy” group refers to both an -S-alkyl group, and an -S-cycloalkyl group, as defined herein.
  • aldehyde refers to a carbonyl group, where R is hydrogen.
  • a “carboxylic acid” group refers to a C-carboxyl group in which R is hydrogen.
  • a “halo” or “halogen” group refers to fluorine, chlorine, bromine or iodine.
  • amino group refers to an -NR 2 group where each of R is as defined herein.
  • a "nitro” group refers to an -N0 2 group.
  • phosphinyl describes a -PR 2 group, with each of R as defined hereinabove.
  • present embodiments further encompass any pharmaceutically acceptable salts, prodrugs, hydrates and solvates of the compounds described hereinabove.
  • prodrug refers to an agent, which is converted into the active compound (the active parent drug) in vivo.
  • Prodrugs are typically useful for facilitating the administration of the parent drug. They may, for instance, be bioavailable by oral administration whereas the parent drug is not.
  • the prodrug may also have improved solubility as compared with the parent drug in pharmaceutical compositions.
  • Prodrugs are also often used to achieve a sustained release of the active compound in vivo.
  • An example, without limitation, of a prodrug would be a compound as described herein, having one or more carboxylic acid moieties, which is administered as an ester (the "prodrug").
  • Such a prodrug is hydrolysed in vivo, to thereby provide the free compound (the parent drug).
  • the selected ester may affect both the solubility characteristics and the hydrolysis rate of the prodrug.
  • phrases "pharmaceutically acceptable salt” refers to a charged species of the parent compound and its counter ion, which is typically used to modify the solubility characteristics of the parent compound and/or to reduce any significant irritation to an organism by the parent compound, while not abrogating the biological activity and properties of the administered compound.
  • An example, without limitation, of a pharmaceutically acceptable salt would be a carboxylate anion and a cation such as, but not limited to, ammonium, sodium, potassium and the like.
  • solvate refers to a complex of variable stoichiometry (e.g., di-, tri-, tetra- , penta-, hexa-, and so on), which is formed by a solute (the compound of present embodiments) and a solvent, whereby the solvent does not interfere with the biological activity of the solute.
  • Suitable solvents include, for example, ethanol, acetic acid and the like.
  • hydrate refers to a solvate, as defined hereinabove, where the solvent is water.
  • the newly designed compounds of present embodiments exert a highly beneficial immunomodulation activity and therefore can be utilized in various therapeutic applications.
  • Utilizing these compounds in therapeutic application involves administration thereof either per se, or as a part of a pharmaceutical composition where it is mixed with suitable carriers or excipients.
  • a pharmaceutical composition which comprises, as an active ingredient, any of the compounds described herein, and a pharmaceutically acceptable carrier.
  • a pharmaceutical composition refers to a preparation of one or more of the active ingredients described herein with other chemical components such as physiologically suitable carriers and excipients. The purpose of a pharmaceutical composition is to facilitate administration of a compound to an organism.
  • active ingredient refers to the compounds (oxidized lipids) described hereinabove accountable for the biological effect.
  • physiologically acceptable carrier and “pharmaceutically acceptable carrier” which may be interchangeably used refer to a carrier or a diluent that does not cause significant irritation to an organism and does not abrogate the biological activity and properties of the administered compound.
  • An adjuvant is included under these phrases.
  • excipient refers to an inert substance added to a pharmaceutical composition to further facilitate administration of an active ingredient.
  • excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils and polyethylene glycols.
  • Suitable routes of administration may, for example, include oral, rectal, transmucosal, especially transnasal, intestinal or parenteral delivery, including intramuscular, subcutaneous and intramedullary injections as well as intrathecal, direct intraventricular, intravenous, intraperitoneal, intranasal, or intraocular injections.
  • the pharmaceutical compositions are designed for modulating an immune and/or inflammatory response via mucosal administration. In another optional embodiment of the present invention, the pharmaceutical compositions are designed for modulating an immune and/or inflammatory response via oral administration.
  • compositions of embodiments of the present invention are designed for nasal, or intraperitoneal administration, as is detailed hereinafter.
  • compositions of embodiments of the present invention may be manufactured by processes well known in the art, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.
  • compositions for use in accordance with present embodiments thus may be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the active ingredients into preparations which, can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen.
  • the active ingredients of the pharmaceutical composition may be formulated in aqueous solutions, for example, in physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological salt buffer.
  • physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological salt buffer.
  • penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art.
  • the pharmaceutical composition can be formulated readily by combining the active compounds with pharmaceutically acceptable carriers well known in the art.
  • Such carriers enable the pharmaceutical composition to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for oral ingestion by a patient.
  • Pharmacological preparations for oral use can be made using a solid excipient, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries if desired, to obtain tablets or dragee cores.
  • Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl-cellulose, sodium carboxymethylcellulose; and/or physiologically acceptable polymers such as polyvinylpyrrolidone (PVP).
  • disintegrating agents may be added, such as cross- linked polyvinyl pyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate.
  • Dragee cores are provided with suitable coatings.
  • suitable coatings For this purpose, concentrated sugar solutions may be used which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, titanium dioxide, lacquer solutions and suitable organic solvents or solvent mixtures.
  • Dyestuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses.
  • compositions which can be used Orally include push-fit capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol.
  • the push-fit capsules may contain the active ingredients in admixture with filler such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers.
  • the active ingredients may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols.
  • stabilizers may be added. All formulations for oral administration should be in dosages suitable for the chosen route of administration.
  • the active ingredients for use according to embodiments of the present invention are conveniently delivered in the form of an aerosol spray presentation from a pressurized pack or a nebulizer with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro- tetrafluoroethane or carbon dioxide.
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro- tetrafluoroethane or carbon dioxide.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • Capsules and cartridges of, e.g., gelatin for use in a dispenser may be formulated containing a powder mix of the compound and a suitable powder base such as lactose or starch.
  • compositions described herein may be formulated for parenteral administration, e.g., by bolus injection or continuous infusion.
  • Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multidose containers with optionally, an added preservative.
  • the compositions may be suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • compositions for parenteral administration include aqueous solutions of the active preparation in water-soluble form. Additionally, suspensions of the active ingredients may be prepared as appropriate oily or water based injection suspensions. Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acids esters such as ethyl oleate, triglycerides or liposomes. Aqueous injection suspensions may contain substances, which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol or dextran. Optionally, the suspension may also contain suitable stabilizers or agents which increase the solubility of the active ingredients to allow for the preparation of highly concentrated solutions.
  • the active ingredient may be in powder form for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water based solution, before use.
  • a suitable vehicle e.g., sterile, pyrogen-free water based solution
  • compositions of embodiments of the present invention may also be formulated in rectal compositions such as suppositories or retention enemas, using, e.g., conventional suppository bases such as cocoa butter or other glycerides.
  • compositions suitable for use in context of the present embodiments include compositions wherein the active ingredients are contained in an amount effective to achieve the intended purpose. More specifically, a therapeutically effective amount means an amount of active ingredients effective to prevent, alleviate or ameliorate symptoms of a disorder (e.g., atherosclerosis) or prolong the survival of the subject being treated.
  • a disorder e.g., atherosclerosis
  • the therapeutically effective amount or dose can be estimated initially from in vitro and cell culture assays.
  • a dose can be formulated in animal models to achieve a desired concentration or titer. Such information can be used to more accurately determine useful doses in humans.
  • Dosage amount and interval may be adjusted individually to provide plasma or brain levels of the active ingredient (minimal effective concentration, MEC) that are sufficient to induce or suppress an inflammation (e.g., angiogenesis).
  • MEC minimum effective concentration
  • the MEC will vary for each preparation, but can be estimated from in vitro data. Dosages necessary to achieve the MEC will depend on individual characteristics and route of administration. Detection assays can be used to determine plasma concentrations.
  • dosing can be of a single or a plurality of administrations, with course of treatment lasting from several days to several weeks or until cure is effected or diminution of the disease state is achieved.
  • compositions to be administered will, of course, be dependent on the subject being treated, the severity of the affliction, the manner of administration, the judgment of the prescribing physician, etc.
  • compositions of embodiments of the present invention may, if desired, be presented in a pack or dispenser device, such as an FDA approved kit, which may contain one or more unit dosage forms containing the active ingredient.
  • the pack may, for example, comprise metal or plastic foil, such as a blister pack.
  • the pack or dispenser device may be accompanied by instructions for administration.
  • the pack or dispenser may also be accommodated by a notice associated with the container in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the compositions or human or veterinary administration. Such notice, for example, may be of labeling approved by the U.S. Food and Drug Administration for prescription drugs or of an approved product insert.
  • Compositions comprising a preparation described herein formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition, as is further detailed hereinbelow.
  • the pharmaceutical composition is packaged in a packaging material and identified in print, on or in the packaging material, for use in the treatment or prevention of an inflammation associated with an endogenous oxidized lipid.
  • a packaging material and identified in print, on or in the packaging material, for use in the treatment or prevention of an inflammation associated with an endogenous oxidized lipid.
  • the pharmaceutical composition of present embodiments can further include an additional compound, which is useful in the treatment or prevention of the inflammation described herein.
  • an endogenous oxidized lipid refers to one or more oxidized lipids that are present or formed in vivo, as a result of inflammatory and other cell- or humoral-mediated processes.
  • treating or preventing includes abrogating, substantially inhibiting, slowing or reversing the progression of a disease, substantially ameliorating clinical symptoms of a disease or substantially preventing the appearance of clinical symptoms of a disease.
  • subjects suitable for such treatment include subjects suffering from a disease or disorder associated with an inflammation, as is detailed hereinbelow.
  • Suitable individual subjects according to present embodiments include mammals such as canines, felines, ovines, porcines, equines, and bovines.
  • the individual subjects according to the present embodiments are humans.
  • inflammation associated with an endogenous oxidized lipid describes an inflammation that is associated with the in vivo formation or presence of one or more oxidized lipids (e.g., oxidized LDL, oxidized membrane lipids, etc.).
  • oxidized lipids e.g., oxidized LDL, oxidized membrane lipids, etc.
  • Inflammation is a protective response of the body to an injury.
  • cytokines play key roles in mediating inflammatory reactions amongst which are interleukins 12 and 23 (IL-12 and IL-23). Excessive inflammation is oftentimes deleterious, involving or leading to a myriad of diseases and disorders. As is explained in detail hereinabove, excessive inflammatory response is typically associated with oxidized lipid epitopes.
  • a method of decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 in a subject is provided.
  • a method for treating a disease or disorder in which decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 is beneficial is provided.
  • the above methods are effected by administering to a subject in need thereof a therapeutically effective amount of one or more oxidized lipids as described herein.
  • a use of at least one oxidized lipid described herein in the manufacture of a medicament in the manufacture of a medicament.
  • Optional formulations for a medicament are described herein.
  • the medicament is for treating or preventing an inflammation associated with an endogenous oxidized lipid, as described in further detail herein.
  • the medicament is for decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 in a subject
  • the medicament is for treating a disease or disorder in which decreasing a level of a cytokine selected from the group consisting of interleukin-12 and interleukin-23 is beneficial. .
  • oxidized lipids described herein may be utilized in treating or preventing inflammation-associated disease or disorders in which endogenous oxidized LDL or any other endogenous oxidized lipid is implicated.
  • diseases and disorders include, for example, diseases or disorders associated with plaque formation, including but not limited to atherosclerosis, atherosclerotic cardiovascular disease, cerebrovascular disease, peripheral vascular disease, stenosis, restenosis and in-stent- stenosis, as well as autoimmune diseases or disorders, neurodegenerative diseases or disorders, proliferative disease or disorders and aging processes.
  • diseases or disorders associated with an inflammation which in turn is associated with an endogenous oxidized lipids, and are therefore treatable by the method of embodiments of the present invention include, for example, idiopathic inflammatory diseases or disorders, chronic inflammatory diseases or disorders, acute inflammatory diseases or disorders, autoimmune diseases or disorders, infectious diseases or disorders, inflammatory malignant diseases or disorders, inflammatory transplantation-related diseases or disorders, inflammatory degenerative diseases or disorders, diseases or disorders associated with a hypersensitivity, inflammatory cardiovascular diseases or disorders, inflammatory cerebrovascular diseases or disorders, peripheral vascular diseases or disorders, inflammatory glandular diseases or disorders, inflammatory gastrointestinal diseases or disorders, inflammatory cutaneous diseases or disorders, inflammatory hepatic diseases or disorders, inflammatory neurological diseases or disorders, inflammatory musculo-skeletal diseases or disorders, inflammatory renal diseases or disorders, inflammatory reproductive diseases or disorders, inflammatory systemic diseases or disorders, inflammatory connective tissue diseases or disorders, inflammatory tumors, necrosis, inflammatory implant-related diseases or disorders, inflammatory aging processes, immunode
  • hypersensitivities include Type I hypersensitivity, Type II hypersensitivity, Type III hypersensitivity, Type IV hypersensitivity, immediate hypersensitivity, antibody mediated hypersensitivity, immune complex mediated hypersensitivity, T lymphocyte mediated hypersensitivity, delayed type hypersensitivity, helper T lymphocyte mediated hypersensitivity, cytotoxic T lymphocyte mediated hypersensitivity, TH1 lymphocyte mediated hypersensitivity, and TH2 lymphocyte mediated hypersensitivity.
  • Non-limiting examples of inflammatory cardiovascular disease or disorder include occlusive diseases or disorders, atherosclerosis, a cardiac valvular disease, stenosis, restenosis, in-stent-stenosis, myocardial infarction, coronary arterial disease, acute coronary syndromes, congestive heart failure, angina pectoris, myocardial ischemia, thrombosis, Wegener's granulomatosis, Takayasu's arteritis, Kawasaki syndrome, anti-factor VIII autoimmune disease or disorder, necrotizing small vessel vasculitis, microscopic polyangiitis, Churg and Strauss syndrome, pauci-immune focal necrotizing glomerulonephritis, crescentic glomerulonephritis, antiphospholipid syndrome, antibody induced heart failure, thrombocytopenic purpura, autoimmune hemolytic anemia, cardiac autoimmunity, Chagas' disease or disorder, and anti-helper T lymphocyte autoimmunity.
  • Restenosis is the progressive re-occlusion often following reduction of occlusions in stenotic vasculature.
  • in-stent-stenosis may occur, re-occluding the treated vessel.
  • cerebrovascular diseases or disorders include stroke, cerebrovascular inflammation, cerebral hemorrhage and vertebral arterial insufficiency.
  • Non-limiting examples of peripheral vascular diseases or disorders include gangrene, diabetic vasculopathy, ischemic bowel disease, thrombosis, diabetic retinopathy and diabetic nephropathy.
  • Non-limiting examples of autoimmune diseases or disorders include all of the diseases caused by an immune response such as an autoantibody or cell-mediated immunity to an autoantigen and the like.
  • Representative examples are chronic rheumatoid arthritis, juvenile rheumatoid arthritis, systemic lupus erythematosus, scleroderma, mixed connective tissue disease, polyarteritis nodosa, polymyositis/dermatomyositis, Sjogren's syndrome, Bechet's disease, multiple sclerosis, autoimmune diabetes, Hashimoto's disease, psoriasis, primary myxedema, pernicious anemia, myasthenia gravis, chronic active hepatitis , autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura, uveitis, vasculitides and heparin induced thrombocytopenia.
  • Non-limiting examples of inflammatory glandular diseases or disorders include pancreatic diseases or disorders, Type I diabetes, thyroid diseases or disorders, Graves' disease, thyroiditis, spontaneous autoimmune thyroiditis, Hashimoto's thyroiditis, idiopathic myxedema, ovarian autoimmunity, autoimmune anti-sperm infertility, autoimmune prostatitis and Type I autoimmune polyglandular syndrome.
  • Non-limiting examples of inflammatory gastrointestinal diseases or disorders include colitis, ileitis, Crohn's disease, chronic inflammatory intestinal disease, inflammatory bowel syndrome, chronic inflammatory bowel disease, celiac disease, ulcerative colitis, an ulcer, a skin ulcer, a bed sore, a gastric ulcer, a peptic ulcer, a buccal ulcer, a nasopharyngeal ulcer, an esophageal ulcer, a duodenal ulcer and a gastrointestinal ulcer.
  • Non-limiting examples of inflammatory cutaneous diseases or disorders include acne, an autoimmune bullous skin disease, pemphigus vulgaris, bullous pemphigoid, pemphigus foliaceus, contact dermatitis and drug eruption.
  • Non-limiting examples of inflammatory hepatic diseases or disorders include autoimmune hepatitis, hepatic cirrhosis, and biliary cirrhosis.
  • Non-limiting examples of inflammatory neurological diseases or disorders include multiple sclerosis, Alzheimer's disease, Parkinson's disease, myasthenia gravis, motor neuropathy, Guillain-Barre syndrome, autoimmune neuropathy, Lambert-Eaton myasthenic syndrome, paraneoplastic neurological disease or disorder, paraneoplastic cerebellar atrophy, non-paraneoplastic stiff man syndrome, progressive cerebellar atrophy, Rasmussen's encephalitis, amyotrophic lateral sclerosis, Sydeham chorea, Gilles de la Tourette syndrome, autoimmune polyendocrinopathy, dysimmune neuropathy, acquired neuromyotonia, arthrogryposis multiplex, Huntington's disease, AIDS associated dementia, amyotrophic lateral sclerosis (AML), multiple sclerosis, stroke, an inflammatory retinal disease or disorder, an inflammatory ocular disease or disorder, optic neuritis, spongiform encephalopathy, migraine, headache, cluster headache, and stiff-man syndrome.
  • Non-limiting examples of inflammatory connective tissue diseases or disorders include autoimmune myositis, primary Sjogren's syndrome, smooth muscle autoimmune disease or disorder, myositis, tendinitis, a ligament inflammation, chondritis, a joint inflammation, a synovial inflammation, carpal tunnel syndrome, arthritis, rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, a skeletal inflammation, an autoimmune ear disease or disorder, and an autoimmune disease or disorder of the inner ear.
  • Non-limiting examples of inflammatory renal diseases or disorders include autoimmune interstitial nephritis and/or renal cancer.
  • Non-limiting examples of inflammatory reproductive diseases or disorders include repeated fetal loss, ovarian cyst, or a menstruation associated disease or disorder.
  • Non-limiting examples of inflammatory systemic diseases or disorders include systemic lupus erythematosus, systemic sclerosis, septic shock, toxic shock syndrome, and cachexia.
  • Non-limiting examples of infectious disease or disorder include chronic infectious diseases or disorders, a subacute infectious disease or disorder, an acute infectious disease or disorder, a viral disease or disorder, a bacterial disease or disorder, a protozoan disease or disorder, a parasitic disease or disorder, a fungal disease or disorder, a mycoplasma disease or disorder, gangrene, sepsis, a prion disease or disorder, influenza, tuberculosis, malaria, acquired immunodeficiency syndrome, and severe acute respiratory syndrome.
  • Non-limiting examples of inflammatory transplantation-related diseases or disorders include graft rejection, chronic graft rejection, subacute graft rejection, acute graft rejection hyperacute graft rejection, and graft versus host disease or disorder.
  • Exemplary implants include a prosthetic implant, a breast implant, a silicone implant, a dental implant, a penile implant, a cardiac implant, an artificial joint, a bone fracture repair device, a bone replacement implant, a drug delivery implant, a catheter, a pacemaker, an artificial heart, an artificial heart valve, a drug release implant, an electrode, and a respirator tube.
  • Non-limiting examples of inflammatory tumors include a malignant tumor, a benign tumor, a solid tumor, a metastatic tumor and a non-solid tumor.
  • Non-limiting examples of inflammatory pulmonary diseases or disorders include asthma, allergic asthma, emphysema, chronic obstructive pulmonary disease or disorder, sarcoidosis and bronchitis.
  • An example of a proliferative disease or disorder is cancer.
  • the oxidized lipids can be administered to a subject by various routes, including, for example, the oral, rectal, transmucosal, especially transnasal, intestinal or parenteral delivery, including intramuscular, subcutaneous and intramedullary injections as well as intrathecal, direct intraventricular, intravenous, intraperitoneal, intranasal, or intraocular routes.
  • routes of administration include the oral, mucosal, nasal, intradermal (subcutaneous) and intraperitoneal routes.
  • 0.1-100 mg/kg of an oxidized lipid as described herein is administered intraperitoneally, in a suitable carrier such as but not limited to PBS or glycerol, one to three times, every week, on a chronic or alternate regiment.
  • a suitable carrier such as but not limited to PBS or glycerol
  • 0.1-100 mg/kg of an oxidized lipid as described herein is administered nasally, in a suitable carrier such as but not limited to PBS or glycerol, one to three times, every week, on a chronic or alternate regiment.
  • a suitable carrier such as but not limited to PBS or glycerol
  • 0.1-100 mg/kg of an oxidized lipid as described herein is administered subcutaneously, in a suitable carrier such as but not limited to PBS or glycerol, one to three times, every week, on a chronic or alternate regiment.
  • a suitable carrier such as but not limited to PBS or glycerol
  • 0.1-100 mg kg of an oxidized lipid as described herein is administered orally, in a suitable carrier such as but not limited to PBS or glycerol, one to three times, every week, on a chronic or alternate regiment.
  • a suitable carrier such as but not limited to PBS or glycerol
  • compositions and the methods described herein may further involve the administration of one or more additional compounds that are capable of treating or preventing an inflammation associated with endogenous oxidized lipid as delineated hereinabove.
  • the methods according to embodiments of the present invention can therefore involve co-administering, prior to, concomitant with or after the administration of the oxidized lipids, a therapeutically effective amount of one or more of such additional compounds, while the pharmaceutical composition according to the present embodiments may include, in addition to the compounds as described herein, such additional compounds.
  • HMGCoA reductase inhibitors include, without limitation, HMGCoA reductase inhibitors (statins), mucosal adjuvants, corticosteroids, steroidal anti-inflammatory drugs, non-steroidal antiinflammatory drugs, analgesics, growth factors, toxins, cholesteryl ester transfer protein (CETP) inhibitors, peroxisomes, proliferative activated receptor (PPAR) agonists, anti- atherosclerosis drugs, anti-proliferative agents, ezetimide, nicotinic acid, squalene inhibitors, an ApoE Milano, HSPs, Beta-2-glycoprotein-I and any derivative and analog thereof.
  • statins HMGCoA reductase inhibitors
  • mucosal adjuvants corticosteroids
  • steroidal anti-inflammatory drugs include, without limitation, steroidal anti-inflammatory drugs, non-steroidal antiinflammatory drugs, analgesics, growth factors, toxins, cholesteryl ester transfer
  • statins HMGCoA reductase inhibitors
  • statins include Atorvastatin,
  • Ezetimibe is the first of a new class of cholesterol absorption inhibitors that potently and selectively inhibits dietary and biliary cholesterol absorption at the brush border of the intestinal epithelium, without affecting the absorption of triglyceride or fat-soluble vitamins. Ezetimibe thus reduces overall cholesterol delivery to the liver, secondarily inducing increased expression of LDL receptors, resulting in an increased removal of LDL-
  • Peroxisome is a single-membrane organelle present in nearly all eukaryotic cells.
  • One of the most important metabolic processes of the peroxisome is the ⁇ -oxidation of long and very long chain fatty acids; The peroxisome is also involved in bile acid synthesis, cholesterol synthesis, plasmalogen synthesis, amino acid metabolism, and purine metabolism.
  • Nicotinic acid is a known agent that lowers total cholesterol, LDL-cholesterol, and triglyceride levels, while raising HDL-cholesterol levels.
  • Squalene an isoprenoid compound structurally similar to beta-carotene, is an intermediate metabolite in the synthesis of cholesterol. In humans, about 60 percent of dietary squalene is absorbed. It is transported in serum generally in association with very low density lipoproteins and is distributed ubiquitously in human tissues, with the greatest concentration in the skin, where it is one of the major components of skin surface lipids. Squalene inhibitors (e.g., monooxygenase and synthase) serve as cholesterol biosynthesis inhibitors.
  • Proliferative Activated Receptor (PPAR) agonists are fatty acid- activated members of the nuclear receptor superfamily that play important roles in lipid and glucose metabolism, and have been implicated in obesity-related metabolic diseases such as hyperlipidemia, insulin resistance, and coronary artery disease. Fibrates are generally effective in lowering elevated plasma triglycerides and cholesterol and act as PPAR agonists. The most pronounced effect of fibrates includes a decrease in plasma triglyceride- rich lipoproteins (TRLs). Levels of LDL cholesterol (LDL-C) generally decrease in individuals with elevated baseline plasma concentrations, and HDL cholesterol (HDL-C) levels are usually increased when baseline plasma concentrations are low.
  • Non-limiting examples of commonly prescribed fibrates include bezafibrate, gemfibrozil and fenofibrate.
  • CETP inhibitors play a major role in atherogenesis, by reducing cholesteryl ester accumulation within macrophages and the arterial wall, and thus reducing foam cell formation and affecting the cholesterol absorption.
  • the most promising presently known CETP inhibitor is expimibe.
  • ApoA-I Milano is typically used as a recombinant complex with phospholipid (ETC-216) and produces significant regression of coronary atherosclerosis.
  • Non-limiting examples of steroidal anti-inflammatory drugs include, without limitation, corticosteroids such as hydrocortisone, hydroxyltriamcinolone, alpha-methyl dexamethasone, dexamethasone-phosphate, beclomethasone dipropionates, clobetasol valerate, desonide, desoxymethasone, desoxycorticosterone acetate, dexamethasone, dichlorisone, diflorasone diacetate, diflucortolone valerate, fluadrenolone, fluclorolone acetonide, fludrocortisone, flumethasone pivalate, fluosinolone acetonide, fluocinonide, flucoitine butylesters, fluocbrtolone, fluprednidene (fluprednylidene) acetate, flurandrenolone, halcinonide, hydrocortisone acetate, hydrocortis
  • Non-limiting examples of analgesics include aspirin and other salicylates (such as choline or magnesium salicylate), ibuprofen, ketoprofen, naproxen sodium, and acetaminophen.
  • Growth factors are hormones which have numerous functions, including regulation of adhesion molecule production, altering cellular proliferation, increasing vascularization, enhancing collagen synthesis, regulating bone metabolism and altering migration of cells into given area.
  • growth factors include insulin-like growth factor-1 (IGF-1), transforming growth factor- ⁇ (TGF- ⁇ ), a bone morphogenic protein (BMP) and the like.
  • Non-limiting examples of toxins include the cholera toxin, which also serves as an adjuvant.
  • Non-limiting examples of anti-proliferative agents include an alkylating agent such as a nitrogen mustard, an ethylenimine and a methylmelamine, an alkyl sulfonate, a nitrosourea, and a triazene; an antimetabolite such as a folic acid analog, a pyrimidine analog, and a purine analog; a natural product such as a vinca alkaloid, an epipodophyllotoxin, an antibiotic, an enzyme, a taxane, and a biological response modifier; miscellaneous agents such as a platinum coordination complex, an anthracenedione, an anthracycline, a substituted urea, a methyl hydrazine derivative, or an adrenocortical suppressant; or a hormone or an antagonist such as an adrenocorticosteroid, a progestin, an estrogen, an antiestrogen, an androgen, an antiandrogen, or a
  • chemotherapeutic agents include, for example, a nitrogen mustard, an epipodophyllotoxin, an antibiotic, a platinum coordination complex, bleomycin, doxorubicin, paclitaxel, etoposide, 4-OH cyclophosphamide, and cisplatinum.
  • HSP60 heat-shock protein 60
  • HSP has been implicated as a target autoantigen in several experimental autoimmune diseases (arthritis, type I diabetes).
  • Anti-HSP65 as well as anti- HSP60 antibodies have been demonstrably associated with atheromatous lesions in humans.
  • Studies conducted in rabbits and mice show that the generation of an HSP65- induced immune response by immunization with the recombinant protein or with an HSP65-rich preparation of Mycobacterium tuberculosis enhances atherogenesis.
  • Beta-2-glycoprotein I (beta2GPI) is a phospholipid binding protein shown to serve as a target for prothrombotic antiphospholipid antibodies. It has recently been demonstrated to drive an immune mediated reaction and enhance murine atherosclerosis. ⁇ -Antibodies to beta-2-GPI have the ability to activate monocytes and endothelial cells and can induce an immune response to beta2GPI in atherosclerosis-prone mice accelerated atherosclerosis. When beta2GPI-reactive lymph node and spleen cells were transferred to LDL-receptor- deficient mice they promoted fatty streak formation, proving a direct proatherogenic role for beta2GPI-specific lymphocytes.
  • beta2GPI is a candidate player in the atherosclerotic plaque, and can possibly be employed as an immunomodulator of plaque progression.
  • Oral feeding with of beta2GPI inhibited lymph node cell reactivity to beta2GPI in mice immunized against the human protein.
  • IL-4 and IL-10 production was upregulated in lymph node cells of beta2GPI-tolerant mice immunized against beta2GPI, upon priming with the respective protein.
  • oral administration of beta2GPI is an effective means of suppressing atherogenesis in mice (George et al. Suppression of early atherosclerosis in LDL-receptor deficient mice by oral tolerance with beta2-glycoprotein I. Cardiovasc Res. 2004;62(3):603-9).
  • oxidized lipids described herein may be prepared according to any suitable method know in the chemical arts.
  • phospholipids described herein may be prepared according to procedures described in International Patent Application No. PCT/IL05/000735 (Publication No. WO 06/006161) or U.S. Patent Application No. 11/650,973 (Publication No. 2007-0112211).
  • Acetic acid (glacial) was obtained from Bio-Lab;
  • DTT Dithiothreitol
  • Fetal bovine serum (heat inactivated) was obtained from Biological Industries (Israel);
  • MOG peptide 35-55 was obtained from Sigma-Aldrich;
  • Mouse GM-CSF (granulocyte-macrophage colony-stimulating factor) was obtained from Peprotech (Israel);
  • Penicillin/streptomycin solution was obtained from Biological Industries (Israel);
  • Red blood cell lysis buffer was obtained from Biological Industries (Israel).
  • RPMI-1640 medium with L-glutamine was obtained from Biological Industries (Israel).
  • COSTAR® Sterile 24-well tissue culture treated plates were obtained from Corning.
  • Phosphate buffered saline was prepared by diluting Dulbecco's phosphate buffered saline lOx concentrate without calcium or magnesium (Biological Industries, Israel) with double-distilled water.
  • Spectrometric measurements were performed using a Tecan SUNRISE plate reader and Magellan Version 6.3 data acquisition software. Absorption at 595 nm was determined using a Tecan SpectraFluor 595 nm band-pass filter.
  • the tested compounds were dissolved in ethanol to a concentration of 100 mg/ml and then diluted in PBS to a concentration of 1 mg/ml.
  • BMDCs bone marrow-derived cells
  • Mouse primary macrophages were isolated from the peritoneum of 7-8 week old C57BL/6 female mice following thioglycollate stimulation. Cells were pre-starved with 0.5 % fetal bovine serum (FBS) in RPMI-1640 medium overnight. Mouse primary bone marrow-derived cells were isolated by flushing bone marrow out of the femur and tibia of female SJL mice using cold RPMI-1640.
  • FBS fetal bovine serum
  • a cell suspension was prepared and erythrocytes were removed using red blood cell lysis buffer, and incubated at 4 °C for 15 minutes in a buffer containing phosphate buffered saline (PBS) and 0.5 % bovine serum albumin (BSA) with mouse B220 and CD90 microbeads (Miltenyi Biotech). Cells were then washed, resuspended in the same buffer and depleted of B and T cells on a Midi-Macs separation unit through a LD or LS column (Miltenyi Biotech).
  • PBS phosphate buffered saline
  • BSA bovine serum albumin
  • the depleted bone marrow cells were counted, washed and seeded at a concentration of 10 6 cells per ml in RPMI-1640 medium with L-glutamine, ⁇ -mercaptoethanol, 10 % fetal bovine serum, antibiotics (penicillin/streptomycin) and 2 ng/ml of mouse granulocyte-macrophage colony- stimulating factor (GM-CSF).
  • the medium was replaced every other day.
  • the cells were collected, counted and seeded (10 6 cells/ml) in the medium for 24 hours, followed by starvation with 0.5 % fetal bovine serum (FBS) in RPMI-1640 medium overnight.
  • FBS % fetal bovine serum
  • the macrophages or BMDCs were then treated for 10 minutes with 1, 10 or 20 ⁇ & ⁇ of the tested compound in phosphate buffered saline (PBS) with 1 % ethanol.
  • PBS phosphate buffered saline
  • Treatment with either 1 or 20 ⁇ g ml of phosphatidylcholine or solvent (PBS with 1 % ethanol) was used as a negative control.
  • Treatment with 1, 10 or 20 ⁇ g/ml CI-201 (1- hexadecyl-2-(4-carboxy)butyl-src-glycero-3-phosphocholine) was used as a positive control.
  • Proteins with phosphorylated tyrosine were then observed by Western blot, using a monoclonal anti-phosphotyrosine antibody.
  • Western blotting for ERKl/2 or a-tubulin was performed as a control for protein loading.
  • Thioglycollate-elicited mouse peritoneal macrophages were washed, counted and seeded (2xl0 5 to 3xl0 5 cells per well in 24-welI plates) in triplicate wells in medium containing RPMI-1640, L-glutamine, 10% FBS and antibiotics (penicillin/streptomycin). After a recovery period of 24 hours, the tested compound (or controls) was added to the cell medium at doses of 2, 10, 20, 50, 100 or 150 g/ml, keeping the added volume equal in all treatments by complementing the volume with solvent.
  • the cells were incubated for an additional 24 hours, after which the cells were washed, fixed with a solution of 10 % methanol/10 % acetic acid and stained with crystal violet (0.4 % in 20 % ethanol). Cell numbers were measured by determining optical density at 595 nm. Cells incubated with vehicle (PBS with 1 % ethanol) were used as a control, to which cell numbers in treated samples were normalized.
  • Bone marrow derived cells were obtained from the femur and tibia of female C57BL mice, cultured, and seeded at a concentration of 10 6 cells/ml 5-6 days post- culturing, as described hereinabove for the tyrosine phosphorylation assay.
  • the tested compound was then added to the cells for 1 hour at a concentration of 1, 2.5, 5, 10 or 20 ⁇ 3 ⁇ 41 ⁇ 21.
  • the cells were activated for IL12/23p40 production by incubation for 24 hours with 10 ⁇ g/ml peptidoglycan (PGN). Cytokine production from the supernatant was measured by ELISA. Activated cells without the tested compound were used as the control.
  • Bone marrow-derived cell cultures were prepared as described hereinabove. On days 5-6 post culturing, the cell cultures were enriched for CDllc+ dendritic cells (> 90 ) with mouse CDllc microbeads over MS or LS columns (Miltenyi Biotech). CDllc+ dendritic cells were stimulated for 1, 2 and 3 hours with 10 ⁇ g/ml peptidoglycan alone or in the presence of 20 ⁇ of the tested compound added 1 hour before activation. RNA was extracted from cells using RNeasy mini kit (Qiagen, Valencia, CA). For cDNA preparation, 1 ⁇ g of RNA was combined with Oligo dT for 10 minutes at 70 °C, 1 st strand buffer.
  • Dithiothreitol and dNTP and super-script reverse transcriptase (SS-II) were added for 50 minutes at 42 °C and the reaction was ended by incubation for an additional 15 minutes at 70 °C. All real time PGR reactions were performed using LightCycler Taqman master (Roche Diagnostics, Mannheim, Germany) and run on the LightCycler machine (Roche). Ready sets of probe with primers were used for IL12/23 p40 and GAPDH assays (Applied Biosystems, assays #Mm01288992_ml and Mm99999915_gl, respectively) with the latter served to normalize RNA levels. 20 g/ml CI-201 and phosphatidylcholine (PC) were used as positive and negative controls respectively.
  • SS-II super-script reverse transcriptase
  • C57BL/6 mice were orally administered with the indicated amount of the tested compound in a final volume of 200 ⁇ for 5 consecutive days starting 5 days before immunization.
  • mice were immunized subcutaneously with an emulsion containing 1.5 mg/ml MOG peptide 35-55 (MEVGWYRSPFSRVVHLYRNGK) and 2.5 mg/ml CFA (complete Freund's adjuvant), 100 ⁇ emulsion being injected into each flank.
  • Pertussis toxin 500 ng in 500 ⁇ PBS was administered intraperitoneally immediately and 48 hours after the immunization.
  • Onset of EAE was evaluated by a mean clinical score.
  • mice were immunized to induce arthritis by a collagen injection containing complete Freund's adjuvant (CFA) in the base of the tail (day 0) and a booster shot in the flank (day 21). Mice were followed for arthritis development until day 36. Administration by gavage of the tested compound and control substances began on day 22 and was carried out on a daily basis (6 times per week).
  • CFA complete Freund's adjuvant
  • 12-16-week old LDL-RD male mice were orally administered with 0.2 ml of PBS or PBS with an indicated amount of the tested compound, once a day, every other day, for 5 treatments.
  • the mice were challenged with western diet for 5 weeks and then sacrificed.
  • 14-16-week old ApoE KO mouse were orally administered with 0.2 ml of PBS or PBS with an indicated amount of the tested compound, once a day, every other day, for 5 treatments, and sacrificed by the end of 8 weeks.
  • the quantification of atherosclerotic lesions was done by calculating the lesion size in the aortic sinus as previously described [Paigen et al., Quantitative assessment of atherosclerotic lesions in mice. Atherosclerosis 1987; 68:231-240] with a few modifications. Briefly, the heart and the aorta were removed from the animals, and the peripheral fat was cleaned carefully. The hearts were embedded in Optimal Cutting Temperature (OCT) gel and frozen. Aortic sinus lesion was determined from 3-8 Oil red O-stained serial sections (10 ⁇ thick), throughout the aortic sinus (400 ⁇ ). The lesion area was calculated using a computer analyzing method (Image Pro Plus software [version 4.5.1.29], Medical Cybernetics Corporation).
  • the organic phase was washed consecutively with 200 ml water, twice with 200 ml dilute (1.5 %) sulfuric acid, 200 ml water, 200 ml saturated aqueous sodium bicarbonate, and again with 200 ml water.
  • the organic phase was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to give 36.86 grams of crude product as a residue. This residue was dissolved in hot hexane (200 ml) and the resulting solution was cooled at 4 °C overnight. The precipitated product was filtered, yielding 30.71 grams of (i?)-l-hexadecyl-3-trityl-glycerol.
  • the reaction mixture was cooled to room temperature, transferred to a separation funnel and extracted with 200 ml hexane.
  • the organic phase was washed with a solution of 15 grams Na 2 S 2 0 5 in 100 ml water.
  • Dilute hydrochloric acid (0.65 ml concentrated HC1 in 13 ml water) was added to the organic phase and 200 ml of the solvent was distilled under reduced pressure.
  • the remaining clear solution was heated to a temperature of 80 °C for 6 hours, and an additional volume of 250 ml of solvent was distilled off.
  • the residue was treated with 100 ml water and 10 ml of a 30 % NaOH solution, giving a pH of 12.
  • the precipitated triphenylmethanol was filter off and washed 4 times with 10 ml water.
  • the filtrate was extracted with a mixture of 50 ml hexane and 50 ml ethyl acetate to remove remaining triphenylmethanol and other impurities.
  • the sodium salt of l-hexadecyl-2-(4-carboxy)butyl-sra-glycerol was protonated with 8.45 ml (101.4 mmol) concentrated hydrochloric acid.
  • the resulting free carboxylic acid was extracted with 100 ml hexane.
  • reaction mixture was ice- cooled and a solution of 1.21 ml ethanolamine and 5.6 ml triethylamine in 50 ml THF was added dropwise over the course of 20 minutes. The stirring was continued for 10 minutes with cooling and at room temperature overnight. The reaction mixture was filtered and the solvent was removed under reduced pressure. The obtained residue was dissolved in a mixture of 24 ml acetic acid and 10 ml water and heated to 70 °C for 1 hour.
  • CI-202 inhibited production of IL12/23 p40 by bone marrow- derived cells in a dose-dependent manner. 1049
  • CI-202 inhibited IL12/23 p40 mRNA expression during the whole tested time period (2-4 hours following administration of CI-202), and the inhibition by CI-202 was comparable to the inhibition by CI-201.
  • CI-203 inhibited production of IL12/23 p40 by bone marrow- derived cells in a dose-dependent manner.
  • CI-203 The toxicity of CI-203 was evaluated as described hereinabove in the Materials and Methods section.
  • reaction mixture was then extracted thrice with 150 ml methyl tert-butyl ether (MTBE), the combined organic phase was washed with 100 ml water, and the solvent was then removed under reduced pressure, yielding 29.71 grams of a light brown oil. This residue was dissolved in 100 ml methanol. 6 ml of concentrated hydrochloric acid was added, and the resulting solution was refluxed until a clear solution was obtained, followed by cooling to room temperature and addition of 100 ml water. The product was extracted with 150 ml chloroform, washed consecutively with 150 ml water, 150 ml of a saturated aqueous solution of sodium bicarbonate, and again with 150 ml water.
  • MTBE methyl tert-butyl ether
  • the solution was extracted four times with 50 ml diethyl ether and the solvent from the combined organic phase was removed under reduced pressure, yielding 19.31 grams of a residue.
  • the residue was dissolved in 100 ml methanol and 6ml of concentrated HC1 (37 ) was then added.
  • the reaction mixture was refluxed for 4 hours, cooled to room temperature and stirred at this temperature for over 96 hours.
  • the reaction mixture was concentrated to about 50 ml by removal of the solvent under reduced pressure, and 50 ml water was added.
  • the solution was transferred to a separatory funnel and extracted twice with 100 ml MTBE. The solvent was then removed under reduced pressure.
  • reaction mixture was then cooled in an ice-bath, and a solution of 1.3 ml ethanolamine and 3.3 ml triethylamine in 30 ml THF was then added dropwise over the course of 15 minutes. The stirring was continued for 30 minutes in the ice-bath and then at room temperature overnight. The reaction mixture was filtered, and the solvent from the filtrate was removed under reduced pressure. The residue was dissolved in a mixture of 36 ml acetic acid and 15 ml water, heated to 70 °C for 1 hour, and cooled to room temperature.
  • the reaction mixture was stirred at room temperature overnight.
  • the pH of the reaction was adjusted to approximately 4 by addition of 20 grams of sodium dihydrogen phosphate and then 3 ml of 80 % phosphoric acid.
  • the reaction mixture was extracted thrice with 50 ml of a 2:1 mixture of chloroform: methanol, and the solvent from the organic phase was removed under reduced pressure. The residue was dissolved in chloroform and washed with water. The organic solution was dried over anhydrous Na 2 S0 4 and the solvent was removed under reduced pressure, yielding 4.89 grams of the crude product.
  • the crude product was purified by chromatography over silica gel (58.2 grams).
  • the solution was transferred to a separatory funnel and extracted with diethyl ether (3x 150 ml).
  • the combined organic phase was washed with water (3x 150 ml) and then the solvent removed under reduced pressure.
  • the residue (78 grams) was dissolved in acetic acid (200 ml) and the solution was cooled in an ice bath.
  • a mixture of 40 ml acetic anhydride (40 ml) and 1 ml 70 % perchloric acid were added.
  • the reaction mixture was allowed to reach room temperature and was then stirred at room temperature overnight. Ice was added, and then diethyl ether (400 ml) and water (400 ml) were added.
  • the organic phase was separated and the solvent was removed under reduced pressure.
  • the solution was extracted with hexane (3x 100 ml).
  • the combined organic phase was washed twice with aqueous sodium bisulfite (15 grams in 100 ml water) and then with water (100 ml).
  • the solvent was concentrated under reduced pressure and treated with 100 ml water and 10ml of 30 % NaOH to reach a pH of 12.
  • the mixture was stirred at room temperature overnight.
  • the mixture was extracted with an 8:2 (v/v) mixture of hexane: MTBE (200ml) in order to remove remaining impurities.
  • aqueous basic solution was acidified with HC1 (6 ml) to pH 1 and then extracted with a 7:3 (v/v) mixture of hexane: ethyl acetate (3 x 100 ml).
  • the combined organic phase was dried over sodium sulfate and the solvent was removed under reduced pressure.
  • the residue (30 grams of a yellow oil) was purified by chromatography on a silica gel column (500 grams).
  • reaction mixture was then cooled in an ice-bath, and a solution of ethanolamine (22 ml) and triethylamine (7.2 ml) in 50 ml THF was then added dropwise over the course of 60 minutes while stirring. The stirring was continued for 30 minutes in the ice-bath and then at room temperature overnight. The reaction mixture was filtered, and the solvent from the filtrate was removed under reduced pressure. The residue (14 grams of a yellow oil) was dissolved in a mixture of acetic acid (120 ml) and water (50 ml), heated to 70 °C for 1 hour, and cooled to room temperature.
  • CI-209 inhibited production of IL12/23 p40 by bone marrow- derived cells in a dose-dependent manner.
  • CI-209 The toxicity of CI-209 was evaluated as described hereinabove in the Materials and Methods section.
  • reaction mixture was transferred to a separatory funnel, the phases separated, and the aqueous phase was extracted twice with 100 ml chloroform.
  • the combined organic phase was dried over anhydrous Na 2 S0 4 and the solvent was removed under reduced pressure. 1.16 gram of the crude product was obtained, which was purified over silica gel (60 grams).
  • the product was eluted from the column with 200 ml of chloroform followed by mixtures of chloroform: methanol at ratios of 9:1, 8:2 and 7:3 (v/v), and then 200 ml of chloroform: methanol (1:1 by volumetric ratio).
  • CI-210 inhibited production of IL12/23 p40 by bone marrow- derived cells in a dose-dependent manner.
  • treatment with 20 ⁇ g/ml of CI-210 induced an increase in phosphotyrosine levels
  • treatment with 20 ⁇ g/ml of CI-201 caused a decrease in phosphotyrosine levels.
  • CI-210 The toxicity of CI-210 was evaluated as described hereinabove in the Materials and Methods section.
  • the obtained residue was dissolved in 100 ml of a mixture of 90:10:5 (v/v) methanol: water: concentrated hydrochloric acid, and the resulting solution was refluxed for 1 hour, followed by cooling to room temperature and addition of 200 ml water.
  • the product was extracted twice with 200 ml chloroform, washed consecutively with 200 ml water, 200 ml of a saturated aqueous solution of sodium carbonate, and again with 200 ml water.
  • reaction mixture was cooled to room temperature and 200 ml water was added.
  • the mixture was extracted thrice with 200 ml diethyl ether, the combined organic phase was washed thrice with 200 ml water, and the solvent was removed under reduced pressure, yielding 50 grams of (7?)-l-octadecyl-2-(5'-hexenyl)-3- trityl-glycerol as an orange oil.
  • the reaction mixture was cooled to room temperature, 100 ml diethyl ether was added, and the mixture was washed with water (3 x 50 ml) and dried over sodium sulfate. The solvent was removed under reduced pressure. The obtained residue (7.8 grams) was dissolved in 20 ml hexane and cooled to 4 °C overnight. The precipitated byproduct was filtered off, and the solvent was removed under reduced pressure to give 7.75 grams of the product as a yellow oil.
  • the combined organic phase was washed with 50 ml water, twice with 20 ml of a solution of sodium bisulfite (prepared from 5 grams sodium bisulfite in 20 ml water), and twice with 50 ml water, then dried over sodium sulfate, filtered and evaporated under reduced pressure to give 11 grams of the product as a yellow wax.
  • the basic solution was acidified with sodium dihydrogen phosphate until a pH in the range of 4-5 was obtained.
  • 100 ml diethyl ether and 100 ml water were added, the phases were separated, and the aqueous phase was washed twice with 100 ml diethyl ether.
  • the combined organic phase was then washed with 100 ml water and 100 ml brine, dried over sodium sulfate, filtered, and the solvent was removed under reduced . pressure to give 8 grams of the product.
  • the product was crystallized from a 1:9 mixture of acetone: hexane to give 2.4 grams of (S)-l ⁇ hexadecyl-2-(3-carboxy)propyl-glycerol.
  • treatment with 20 ⁇ / ⁇ of CI-205 causes reduction in phosphotyrosine levels, as did treatment with 20 ⁇ 1 of the positive control, CI-201.
  • the reaction mixture was then extracted thrice with 150 ml diethyl ether, the combined organic phase was washed with 100 ml water, and the solvent was then removed under reduced pressure.
  • the obtained residue was dissolved in 100 ml of a 90:10:5 (v/v) mixture of methanol: water: concentrated hydrochloric acid, and the resulting solution was refluxed for 2 hours, followed by cooling to room temperature and addition of 100 ml water.
  • the product was extracted thrice with 150 ml chloroform, washed consecutively with 150 ml water, 150 ml of saturated aqueous solution of sodium bicarbonate, and again with 100 ml water.
  • the solvent was dried over anhydrous Na 2 S0 4 , filtered, and removed under reduced pressure, yielding 34 grams of (iS -l-octyl-glycerol.
  • the organic phase was washed consecutively with 150 ml water, twice with 100 ml dilute (1.5 %) H 2 S0 4 , 200 ml water, 200 ml concentrated aqueous sodium bicarbonate, and again with 200 ml water.
  • the solution was then dried over anhydrous Na 2 S0 4 and the solvent was removed under reduced pressure.
  • the obtained residue 80 grams of a brown oil, was dissolved in 500 ml hot hexane and kept at a temperature of 4 °C overnight.
  • the precipitate was filtered off and the solvent from the filtrate was removed under reduced pressure.
  • the obtained residue was purified by chromatography on silica gel. The resulting pure f ?
  • the reaction mixture was cooled to room temperature and stirred at room temperature overnight. 100 ml water was added, and the solution was extracted twice with 100 ml diethyl ether. The combined organic phase was washed with 100 ml water, 100 ml saturated aqueous sodium bicarbonate solution, and again with 100 ml water. The solvent was removed under reduced pressure. The obtained residue (20.1 grams) was dissolved in 250 ml hexane, and the obtained solution was stored at a temperature of 4 °C for 96 hours, causing most of the triphenyl carbinol to precipitate. After filtration and removal of the solvent from the filtrate, the remaining product (12 grams) was purified by chromatography over silica gel (91.4 grams).
  • the reaction mixture was then cooled in an ice-bath, and a solution of 1.1 ml ethanolamine and 2.8 ml triethylamine in 30 ml THF was then added dropwise over the course of 15 minutes while stirring. The stirring was continued for 35 minutes in the ice-bath and then at room temperature overnight.
  • the reaction mixture was filtered, the solid washed twice with 15 ml THF, and the solvent from the filtrate was removed under reduced pressure.
  • the obtained residue (5.6 grams) was dissolved in a mixture of 36 ml acetic acid and 15 ml water and heated to a temperature of 70 °C for 1 hour.
  • the reaction mixture was cooled to room temperature, filtered via celite, and the celite was washed with tert-butanol. 100 ml of 10 % sulfuric acid solution was added dropwise, and the solution was transferred to a separatory funnel and extracted thrice with 200 ml hexane.
  • the organic phase was washed with a solution of 20 grams of Na 2 S 2 0 5 in 100ml water and then with 200 ml water.
  • the organic phase was concentrated by removal of solvent under reduced pressure until the volume was reduced to about 150 ml. 15 ml of water and 2 ml concentrated HCl were added to the remaining solution and the obtained mixture was refluxed for 6 hours, then cooled to room temperature and concentrated again by removal of solvent under reduced pressure.
  • the pH of the residue was adjusted to 12 by addition of 100 ml water and 10 ml 30 % NaOH solution.
  • the precipitate was filtered off and washed with four times with 20 ml water.
  • the filtrate was extracted with 100 ml of a 1:1 (v/v) mixture of hexane: ethyl acetate.
  • the aqueous phase was acidified to a pH of 1 by addition of 10 ml concentrated HCl and extracted thrice with 100 ml hexane. Drying over anhydrous NaS0 4 and removal of the solvent under reduced pressure gave 7.4 grams of crude product as a yellow oil.
  • the crude product was purified by chromatography over silica gel (100 grams).
  • reaction mixture was then cooled in an ice-bath, and a solution of 0.154 ml ethanolamine and 0.885 ml triethylamine in 50 ml THF was then added dropwise over the course of 15 minutes while stirring. The stirring was continued for 15 minutes in the ice-bath, and then at room temperature overnight.
  • the reaction mixture was filtered and the solvent was removed under reduced pressure. The obtained residue was dissolved in a mixture of 24 ml acetic acid and 10 ml water and heated to 70 °C for 1 hour. The mixture was extracted thrice with 80 ml chloroform and washed twice with 50 ml water. Removal of the solvent under reduced pressure resulted in 1.12 gram of (R)- l-octyl-2-(4-benzhydrylcarboxy)butyl-sn-glycero-3-phosphoethanolamine as a yellow oil.
  • a solution of 50 grams of potassium carbonate in 100 ml water was added so as to obtain a pH above 11.
  • the solution was kept at a temperature in the range of 35-40 °C during the dropwise addition of 11.15 grams methyltosylate in 100ml isopropanol during a time period of 45 minutes.
  • the mixture was acidified with hydrochloric acid.
  • 100 ml water and 550 ml dichloromethane were added and the phases were separated.
  • the organic phase was washed with 100 ml water and the solvent was removed under reduced pressure.
  • the crude product was purified by chromatography on a silica gel column.
  • the calculated mass for l-hexadecyl-2-(4-methylcarboxy)butyl-glycero-3- phosphocholine (C 3 oH 62 N0 8 P) was 595.79.
  • the MS spectrum is in agreement with the chemical structure of l-hexadecyl-2-(4- methylcarboxy)butyl-glycero-3-phosphocholine.
  • treatment with 20 ⁇ ⁇ CI-208 causes a reduction in phosphotyrosine levels, which is stronger than the reduction caused by treatment with 20 ⁇ g/ml of the CI-201 control.
  • CI-208 The toxicity of CI-208 was evaluated as described hereinabove in the Materials and Methods section.
  • toxicity of CI-208 was detected at doses of 50 g/ml or higher, with toxicity at a dose of 20 ⁇ g/ml being detected in only one of two experiments.
  • the LD 50 of CI-208 appeared to lie between 50 and 100 ⁇ g/m ⁇ .
  • the organic phase was washed consecutively with 100 ml water, twice with 100 ml dilute (1.5 %) sulfuric acid, 100 ml water, 100 ml concentrated sodium bicarbonate solution, and again with 100 ml water.
  • the organic phase was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure, yielding 11 grams of l-trityl-3-benzyl-sra-glycerol as a yellow oil. The yield was 94 %.
  • the volume of the solvent was gradually reduced to about 20 ml.
  • the reaction mixture was cooled to room temperature, 100 ml water and 100 ml ieri-butanol were added.
  • the pH of the reaction mixture was adjusted to approximately 1 by adding concentrated HC1.
  • the mixture was stirred at room temperature for 2 hours and extracted thrice with 100 ml diethyl ether.
  • the combined organic phase was washed with 100 ml portions of water until the pH was neutral. Drying over anhydrous Na 2 S0 4 and removal of solvent under reduced pressure yielded 6 grams of a brown oil. This oil was dissolved in 100 ml of a 1:1 (v/v) mixture of hexane: ethyl acetate.
  • the solution was extracted twice with 100 ml of an 8:2 (v/v) mixture of methanol: aqueous 10 % NaOH.
  • the basic solution was acidified to a pH of 4-5 by adding NaH 2 P0 4 .
  • 100 ml diethyl ether and 100 ml water were added and the phases were then separated.
  • the aqueous phase was extracted twice with 100 ml diethyl ether and combined with the organic phase.
  • the organic phase was washed with 100 ml water and 100 ml brine.
  • the washing solutions were combined with the filtrate and the solvent from the filtrate was removed under reduced pressure.
  • the residue (5 grams) was dissolved in a mixture of 10 ml of 10 % aqueous sodium hydroxide solution and 40 ml methanol, and the obtained mixture was stirred at room temperature for 2 hours.
  • the reaction mixture was washed with 50 ml of a 1:1 (v/v) mixture of hexane: toluene.
  • the pH of the reaction mixture was adjusted to 5 by addition of sodium dihydrogen phosphate, and the mixture was then extracted thrice with 50 ml chloroform.
  • the organic phase was washed with 50 ml brine and dried over anhydrous Na 2 S0 4 , and the solvent was removed under reduced pressure.
  • the elution was performed with 100 ml chloroform, followed by 100 ml of chloroform: methanol mixtures (9:1 and 8:2 by volumetric ratio), and then 200 ml of chloroform: methanol: water mixtures (70:26:4, and 60:35:5 by volumetric ratio).
  • the solvent from fractions containing the desired product was removed under reduced pressure, the residue was dissolved in chloroform and dried over anhydrous Na 2 S0 4 , and the solvent was removed by reduced pressure to give 88 mg of pure ( ⁇ ?)-1-(15'- carboxy)pentadecyl-2-(4-carboxy)butyl-s/i-glycero-3-phosphoethanolamine (CI-214) as a yellow wax.
  • the sample was dissolved in deuterated chloroform (CDC1 3 ) with a few drops of deuterated methanol. The spectra were then measured at 300 MHz.
  • the elution was performed with 100 ml chloroform, followed by 100 ml of chloroform: methanol mixtures (9:1 and 8:2 by volumetric ratio), and then 200 ml of chloroform: methanol: water mixtures (70:26:4, and 60:35:5 by volumetric ratio).
  • the solvent from fractions containing the desired product was removed under reduced pressure, the residue was dissolved in chloroform and dried over anhydrous Na 2 S0 4 , and the solvent was removed under reduced pressure to yield 105 mg of pure ( ?J-l-(15'-carboxy)pentadecyl-2-(4-carboxy)butyl-sn- glycero-3-phosphocholine (CI-213) as a yellow wax.
  • the sample was dissolved in deuterated chloroform (CDC1 3 ) with a few drops of deuterated methanol.
  • the spectra were measured at 300 MHz.
  • CI-213 did not clearly exhibit significant toxicity within the range of tested doses (i.e., up to 150 ⁇ g ml ) 245.2 ⁇ ). A statistically significant decrease in cell number was detected in only one experiment, at a dose of 100igl ⁇ (163.5 ⁇ ).
  • CI-214 did not clearly exhibit significant toxicity within the range of tested doses (i.e., up to 150 ⁇ g/ml, 263.3 ⁇ ). A statistically significant decrease in cell number was detected in only one experiment, at a dose of 100 ⁇ g/ml (175.5 ⁇ ).
  • 5 ⁇ -l-Hexadecyl-2-(2-carboxy)ethyl-glycero-3-phosphocholine is synthesized using the same procedures, but with (5)-(+)-2,2-dimethyl-l,3-dioxolane-4-methanol as the starting material.
  • the organic phase was washed consecutively with 200 ml water, twice with 200 ml dilute (1.5 ) sulfuric acid, 200 ml water, 200 ml saturated aqueous sodium bicarbonate, and again with 200 ml water.
  • the organic phase was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to yield 41.79 grams of crude product as a residue.
  • This residue was dissolved in 300 ml ethyl acetate and cooled at -20 °C overnight.
  • the mixture was centrifuged (3,500 rotations per minute) at -10 °C, and the mother liquid was poured of.
  • the obtained solid melted and was dissolved in hexane and refrigerated (5 ⁇ 3 °C) overnight. Filtration of the precipitate yielded 18.97 grams of pure (i?)-l-hexadecyl-3-trityl-.s/i-glycerol as an off white solid.
  • the organic phase was washed with 50 ml water, 50 ml 10 % aqueous sulfuric acid, 50 ml water, 50 ml 10 % aqueous sodium bicarbonate, and then twice with 50 ml water.
  • the solvent was dried over anhydrous Na 2 S0 4 and removed under reduced pressure.
  • the obtained residue (34.90 grams) was purified by chromatography over silica gel (85.37 grams). 18.83 grams of 3-hexenyl-l-methane sulfonate was obtained by elution with a 1:1 (v/v) mixture of chloroform and hexane.
  • the stirring was continued for an additional 10 minutes with cooling and for an additional 45 minutes at room temperature.
  • the reaction mixture was then cooled in an ice bath, and a solution of 0.55 ml ethanolamine and 2.0 ml triethylamine in 15 ml THF was then added dropwise over the course of 25 minutes.
  • the stirring was continued for 30 minutes in the ice bath and then at room temperature overnight.
  • An additional 0.18 nl ethanolamine was added, and the reaction mixture was stirred at room temperature for 2 hours.
  • the reaction mixture was filtered and the solvent from the filtrate was removed under reduced pressure. The obtained residue was dissolved in a mixture of 48 ml acetic acid and 20 ml water, heated to 77 °C for 1 hour, and cooled to room temperature.
  • the sample was dissolved in deuterated chloroform (CDCI 3 ) with a few drops of deuterated methanol.
  • the spectra were measured at 600 MHz.
  • the reaction mixture was then extracted thrice with 150 ml diethyl ether, the combined organic phase was washed with 100 ml water, and the solvent was then removed under reduced pressure.
  • the obtained residue was dissolved in 105 ml of a 90:10:5 (v/v) methanol: water: concentrated hydrochloric acid mixture, and the resulting solution was refluxed until the solution became clear.
  • the solution was then cooled to room temperature and 100 ml water was added.
  • the product was extracted with 150 ml chloroform, washed consecutively with 150 ml water, 150 ml saturated aqueous solution of sodium carbonate, and again with 150 ml water.
  • the mixture was extracted thrice with 150 ml diethyl ether, the combined organic phase was washed thrice with 150 ml water, and the solvent was removed under reduced pressure.
  • the obtained residue 28 grams of a brown oil, was purified over a silica gel column (200 grams). 28 grams of the product was eluted with chloroform as a light yellow oil. The yield was 87.5 %.
  • the reaction mixture was cooled to room temperature, filtered via celite, and the celite washed then with 50 ml teri-butanol. 100 ml of 10 % sulfuric acid solution was added dropwise, and the solution was transferred to separator funnel and extracted thrice with 200 ml hexane.
  • the organic phase was washed with a solution of 20 grams a 2 S 2 05 in 100ml water and then with 100 ml water.
  • the organic phase was concentrated by removal of about 400 ml solvent under reduced pressure. To the remained solution, 15 ml of water and 2 ml concentrated HC1 were added, and the obtained mixture was refluxed for 6 hours. The mixture was then cooled to room temperature and concentrated again by removal of solvent under reduced pressure.
  • the pH of the residue was adjusted to 12 by addition of 100 ml water and 10 ml of 30 % NaOH solution.
  • the precipitate was filtered off and washed four times with 20 ml water.
  • the filtrate was extracted with 100 ml of a 1:1 (v/v) mixture of hexane: ethyl acetate.
  • the aqueous phase was acidified to a pH of 1 by adding 10 ml concentrated HC1 and was then extracted thrice with 100 ml hexane.
  • This solution was added dropwise during the course of 30 minutes to an ice-cooled solution of 5.36 ml POCI3 in 40 ml THF while stirring. The stirring was continued for an additional 30 minutes with cooling and for an additional 45 minutes at room temperature. The reaction mixture was then cooled in an ice bath, and a solution of 3.5 ml ethanolamine and 16 ml triethylamine in 50 ml THF was then added dropwise over the course of 30 minutes while stirring. The stirring was continued for 30 minutes in the ice bath, and then at room temperature overnight. The reaction mixture was filtered and the solvent was removed under reduced pressure.

Abstract

L'invention porte sur de nouveaux lipides oxydés, ainsi que sur des procédés pour les produire, et sur leurs utilisations pour le traitement ou la prévention d'une inflammation associée à des lipides oxydés endogènes et des pathologies apparentées.
PCT/IL2009/001049 2008-11-06 2009-11-05 Composés lipidiques oxydés et leurs utilisations WO2010052718A1 (fr)

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RU2011122729/04A RU2532546C2 (ru) 2008-11-06 2009-11-05 Окисленные соединения липидов и их применение
EP09824498.1A EP2348866B1 (fr) 2008-11-06 2009-11-05 Composés lipidiques oxydés et leurs utilisations
AU2009312355A AU2009312355C1 (en) 2008-11-06 2009-11-05 Oxidized lipid compounds and uses thereof
NZ592357A NZ592357A (en) 2008-11-06 2009-11-05 Oxidized lipid compounds and uses thereof
ES09824498.1T ES2534044T3 (es) 2008-11-06 2009-11-05 Compuestos de lípidos oxidados y usos de los mismos
CA2740726A CA2740726A1 (fr) 2008-11-06 2009-11-05 Composes lipidiques oxydes et leurs utilisations
JP2011535207A JP5752599B2 (ja) 2008-11-06 2009-11-05 酸化脂質化合物およびその使用
CN200980153378.2A CN102271517B (zh) 2008-11-06 2009-11-05 氧化的脂质化合物和其用途
US13/127,717 US9206206B2 (en) 2008-11-06 2009-11-05 Oxidized lipid compounds and uses thereof
MX2011004773A MX2011004773A (es) 2008-11-06 2009-11-05 Compuestos de lipido oxidados y sus usos.
ZA2011/02872A ZA201102872B (en) 2008-11-06 2011-04-18 Oxidized lipid compounds and uses thereof
IL212721A IL212721A (en) 2008-11-06 2011-05-05 Oxidized fatty substances and uses
HK11109192.4A HK1155906A1 (en) 2008-11-06 2011-08-31 Oxidized lipid compounds and uses thereof
US13/828,883 US20130203707A1 (en) 2008-11-06 2013-03-14 Oxidized Lipid Compounds and Uses Thereof

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US8569529B2 (en) 2007-01-09 2013-10-29 Vascular Biogenics Ltd. High-purity phospholipids
WO2010041242A2 (fr) * 2008-10-08 2010-04-15 Vascular Biogenics Ltd. Composés de thiophospholipides oxydés et leurs utilisations
JP5752599B2 (ja) * 2008-11-06 2015-07-22 ヴァスキュラー バイオジェニックス リミテッド 酸化脂質化合物およびその使用
WO2012119781A2 (fr) * 2011-03-10 2012-09-13 University Of Geneva Nouveaux lipides, phospholipides, compositions de phospholipides et de lipides et leur utilisation
SG11201400208PA (en) * 2011-09-01 2014-03-28 Vascular Biogenics Ltd Formulations and dosage forms of oxidized phospholipids
WO2013088245A1 (fr) * 2011-12-12 2013-06-20 Vascular Biogenics Ltd. Traitement de l'inflammation
JP6717825B2 (ja) 2014-11-26 2020-07-08 バスキュラー バイオジェニックス リミテッド 酸化脂質、および線維症の処置または予防方法
US9771385B2 (en) * 2014-11-26 2017-09-26 Vascular Biogenics Ltd. Oxidized lipids
ES2839456T3 (es) 2015-07-31 2021-07-05 Vascular Biogenics Ltd Proteína 2 que contiene el dominio del esperma móvil y del cáncer
JP6755530B2 (ja) * 2016-09-02 2020-09-16 国立大学法人岩手大学 皮膚炎の予防又は治療用医薬組成物
WO2021199003A1 (fr) * 2020-04-02 2021-10-07 Vascular Biogenics Ltd. Lipides oxydés et traitement ou prévention d'une inflammation ou d'une maladie infectieuse provoquée par une infection à coronavirus
IL300412A (en) 2020-08-24 2023-04-01 Gilead Sciences Inc Phospholipid compounds and their uses
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AU2009312355C1 (en) 2016-02-18
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ES2534044T3 (es) 2015-04-16
EP2826369A2 (fr) 2015-01-21
US20130203707A1 (en) 2013-08-08
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MX2011004773A (es) 2011-06-21
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US20110207703A1 (en) 2011-08-25
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JP2015129157A (ja) 2015-07-16
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US9206206B2 (en) 2015-12-08
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