WO2021246868A1 - Chromanol, quinone or hydroquinone compounds for treatment of sepsis - Google Patents

Chromanol, quinone or hydroquinone compounds for treatment of sepsis Download PDF

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Publication number
WO2021246868A1
WO2021246868A1 PCT/NL2021/050351 NL2021050351W WO2021246868A1 WO 2021246868 A1 WO2021246868 A1 WO 2021246868A1 NL 2021050351 W NL2021050351 W NL 2021050351W WO 2021246868 A1 WO2021246868 A1 WO 2021246868A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
sul
use according
formula
sepsis
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/NL2021/050351
Other languages
English (en)
French (fr)
Inventor
Hjalmar Roland BOUMA
Guido Krenning
Robert Henk Henning
Adrianus Cornelis Van Der Graaf
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rijksuniversiteit Groningen
Sulfateq BV
Original Assignee
Rijksuniversiteit Groningen
Sulfateq BV
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.)
Filing date
Publication date
Application filed by Rijksuniversiteit Groningen, Sulfateq BV filed Critical Rijksuniversiteit Groningen
Priority to CA3185054A priority Critical patent/CA3185054A1/en
Priority to US17/928,645 priority patent/US20230202997A1/en
Priority to AU2021284148A priority patent/AU2021284148A1/en
Priority to EP21730995.4A priority patent/EP4157261A1/en
Priority to JP2022574167A priority patent/JP2023529612A/ja
Publication of WO2021246868A1 publication Critical patent/WO2021246868A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/66Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/453Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • R2 and R3 together with the N atom to which they are attached form a saturated or unsaturated, non-aromatic, optionally substituted, 5-8 membered ring, having one to four N, O, or S atoms, wherein R2 and R3 together contain 3-12 carbon atoms; ii.
  • the compound either according to formula (I) or according to formula (II) has a molecular weight lower than 500 Da, more preferably lower than 450 Da, and even most preferred, less than 400 Da (as the free base).
  • the compound either according to formula (I) or according to formula (II) is for use for treating or prophylaxis of sepsis in an organ system, wherein the organ is lung, heart and blood vessels, liver, kidney, brain, or intestines.
  • the compound contains more than one chiral center, these amounts apply.
  • the compounds are preferably used in effective amounts, to achieve treatment or prophylaxis of sepsis.
  • the wording treatment or prophylaxis includes amelioration of the symptoms of sepsis and/or reduction in progress of sepsis, including improvement of organ function.
  • the compounds according to the invention are for use of treatment or prophylaxis of sepsis in organs in mammals, wherein the mammal is preferably human.
  • the compound the compound either according to formula (I) or according to formula (II) is for use for treating or prophylaxis of organ dysfunction caused by a dysregulated host response to infection.
  • solid, oral dosage forms contain as a maximum about 500 mg compound, preferably about 450 mg or less, to allow for excipients.
  • parenteral administration such as for example i.v., or with other liquid forms of administration
  • larger amounts can be administered.
  • dosages which can be used are an effective amount of the compounds of the invention of a dosage of 0.2 mg/kg or higher, such as preferably within the range of about 1 mg /kg to about 100 mg/kg, or within about 2 mg /kg to about 40 mg/kg body weight, or within about 3 mg/kg to about 30 mg/kg body weight, or within about 4 mg/kg to about 15mg/kg body weight.
  • NGAL and urea are biomarkers for renal function in mice.
  • Figure 3 shows that CLP-induced kidney dysfunction in mice is precluded, or at least substantially reduced by treatment with SUL-138.
  • RNA expression of IL-6, TNF- ⁇ , IL-1 ⁇ and ICAM in the kidney were increased after induction of CLP, indicating a local inflammatory response in the kidney.
  • Treatment with Sul-138 significantly reduced expression of IL-6, while other markers were lowered by treatment with SUL-138.
  • Example 2 Drosophila Melanogaster Experimental W1118 flies were bred and housed at 25 °C with a 12h:12h light/dark-cycle. Flies were kept in vials containing approximately 5 mL of standard yeast-cornmeal medium.
  • flies Male flies (three to five days old) were anesthetized on a CO 2 pad just prior to injection. A tungsten needle (0.25mm diameter, Fine Science Tools, 10130-10) was dipped into the bacterial suspension and flies were pinpricked in the lateral side of the thorax (the presutural scutum of the thorax). Sham flies were administered PBS only, control flies were not operated and only anesthetized on the CO 2 pad. Sham flies were injected first to ensure a haemolymph coating on the needle and to prevent accidental bacterial injection of sham flies. Subgroups of flies were treated with antibiotics.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
PCT/NL2021/050351 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis Ceased WO2021246868A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA3185054A CA3185054A1 (en) 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis
US17/928,645 US20230202997A1 (en) 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis
AU2021284148A AU2021284148A1 (en) 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis
EP21730995.4A EP4157261A1 (en) 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis
JP2022574167A JP2023529612A (ja) 2020-06-02 2021-06-02 敗血症の治療のためのクロマノール、キノン又はヒドロキノン化合物

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NL2025730A NL2025730B1 (en) 2020-06-02 2020-06-02 Compounds for treatment of sepsis
NL2025730 2020-06-02

Publications (1)

Publication Number Publication Date
WO2021246868A1 true WO2021246868A1 (en) 2021-12-09

Family

ID=72659292

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/NL2021/050351 Ceased WO2021246868A1 (en) 2020-06-02 2021-06-02 Chromanol, quinone or hydroquinone compounds for treatment of sepsis

Country Status (7)

Country Link
US (1) US20230202997A1 (https=)
EP (1) EP4157261A1 (https=)
JP (1) JP2023529612A (https=)
AU (1) AU2021284148A1 (https=)
CA (1) CA3185054A1 (https=)
NL (1) NL2025730B1 (https=)
WO (1) WO2021246868A1 (https=)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL2010010C2 (en) * 2012-12-19 2014-06-23 Sulfateq B V Compounds for protection of cells.

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6231894B1 (en) 1999-10-21 2001-05-15 Duke University Treatments based on discovery that nitric oxide synthase is a paraquat diaphorase
WO2014011047A1 (en) 2012-07-12 2014-01-16 Khondrion B.V. Chromanyl derivatives for treating mitochondrial disease
WO2014098586A1 (en) 2012-12-19 2014-06-26 Sulfateq B.V. Compounds for protection of cells
WO2017060432A1 (en) 2015-10-08 2017-04-13 Khondrion Ip B.V. Novel compounds for treating mitochondrial disease
WO2017220810A1 (en) 2016-06-24 2017-12-28 Fundación Para La Investigación Biomédica Del Hospital Gregorio Marañón Cilastatin for use in the treatment of sepsis
WO2019172766A1 (en) 2018-03-08 2019-09-12 Am-Pharma B.V. Recombinant alkaline phosphatase for use in treating sepsis-associated acute kidney injury

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004045534A2 (en) * 2002-11-15 2004-06-03 Galileo Pharmaceuticals, Inc. Chroman derivatives for the reduction of inflammation symptoms
MX388654B (es) * 2015-05-22 2025-03-20 Sulfateq Bv Derivados de cromano y uso de los mismos en el tratamiento de daño en un órgano diabético, tal como un riñón.
SG11202003743SA (en) * 2017-11-22 2020-06-29 Khondrion Ip B V Compounds as mpges-1 inhibitors

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6231894B1 (en) 1999-10-21 2001-05-15 Duke University Treatments based on discovery that nitric oxide synthase is a paraquat diaphorase
WO2014011047A1 (en) 2012-07-12 2014-01-16 Khondrion B.V. Chromanyl derivatives for treating mitochondrial disease
WO2014098586A1 (en) 2012-12-19 2014-06-26 Sulfateq B.V. Compounds for protection of cells
WO2017060432A1 (en) 2015-10-08 2017-04-13 Khondrion Ip B.V. Novel compounds for treating mitochondrial disease
WO2017220810A1 (en) 2016-06-24 2017-12-28 Fundación Para La Investigación Biomédica Del Hospital Gregorio Marañón Cilastatin for use in the treatment of sepsis
WO2019172766A1 (en) 2018-03-08 2019-09-12 Am-Pharma B.V. Recombinant alkaline phosphatase for use in treating sepsis-associated acute kidney injury

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
FLEISCHMANN-STRUZEK, INTENSIVE CARE MED, 2018, Retrieved from the Internet <URL:https://doi.org/10.1007/s00134-018-5377-4>
RUDD ET AL., LANCET, vol. 395, 2020, pages 200 - 211
SEYMOUR ET AL., N. ENGL. J. MED., vol. 376, 2017, pages 2235 - 2244

Also Published As

Publication number Publication date
NL2025730B1 (en) 2022-01-20
EP4157261A1 (en) 2023-04-05
US20230202997A1 (en) 2023-06-29
CA3185054A1 (en) 2021-12-09
JP2023529612A (ja) 2023-07-11
AU2021284148A1 (en) 2022-12-08

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