NZ739077B2 - Il-8 inhibitors for use in the treatment of certain urological disorders - Google Patents
Il-8 inhibitors for use in the treatment of certain urological disordersInfo
- Publication number
- NZ739077B2 NZ739077B2 NZ739077A NZ73907716A NZ739077B2 NZ 739077 B2 NZ739077 B2 NZ 739077B2 NZ 739077 A NZ739077 A NZ 739077A NZ 73907716 A NZ73907716 A NZ 73907716A NZ 739077 B2 NZ739077 B2 NZ 739077B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- inhibitor
- pbs
- oab
- alkyl
- treatment
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title claims abstract 19
- 208000014001 urinary system disease Diseases 0.000 title 1
- 102000004890 Interleukin-8 Human genes 0.000 claims abstract 12
- 108090001007 Interleukin-8 Proteins 0.000 claims abstract 12
- 206010020853 Hypertonic bladder Diseases 0.000 claims abstract 11
- 208000009722 Overactive Urinary Bladder Diseases 0.000 claims abstract 11
- 208000020629 overactive bladder Diseases 0.000 claims abstract 11
- 208000005615 Interstitial Cystitis Diseases 0.000 claims abstract 10
- 150000001875 compounds Chemical class 0.000 claims abstract 10
- 102100036166 C-X-C chemokine receptor type 1 Human genes 0.000 claims abstract 5
- 230000002265 prevention Effects 0.000 claims abstract 5
- 108010018951 Interleukin-8B Receptors Proteins 0.000 claims abstract 3
- 230000009977 dual effect Effects 0.000 claims abstract 3
- 238000011319 anticancer therapy Methods 0.000 claims abstract 2
- 101000947174 Homo sapiens C-X-C chemokine receptor type 1 Proteins 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 102100028989 C-X-C chemokine receptor type 2 Human genes 0.000 claims 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims 2
- NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical compound C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 159000000000 sodium salts Chemical class 0.000 claims 2
- GUHPRPJDBZHYCJ-SECBINFHSA-N (2s)-2-(5-benzoylthiophen-2-yl)propanoic acid Chemical compound S1C([C@H](C(O)=O)C)=CC=C1C(=O)C1=CC=CC=C1 GUHPRPJDBZHYCJ-SECBINFHSA-N 0.000 claims 1
- OUGCUPYREMACGK-ZETCQYMHSA-N (2s)-2-[4-[[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino]phenyl]propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1NC1=NC(C(F)(F)F)=CS1 OUGCUPYREMACGK-ZETCQYMHSA-N 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- -1 4-{[4-(trifluoromethyl)-1,3-thiazol yl]amino}phenyl Chemical group 0.000 claims 1
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 1
- PJAAESPGJOSQGZ-DZGBDDFRSA-N Isovelleral Chemical compound O=CC1=C[C@@H]2CC(C)(C)C[C@@H]2[C@@]2(C)C[C@]21C=O PJAAESPGJOSQGZ-DZGBDDFRSA-N 0.000 claims 1
- 229940126422 TRPV1 antagonist Drugs 0.000 claims 1
- 229940009456 adriamycin Drugs 0.000 claims 1
- 229960000190 bacillus calmette–guérin vaccine Drugs 0.000 claims 1
- 229960004397 cyclophosphamide Drugs 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 229960004857 mitomycin Drugs 0.000 claims 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 210000004197 pelvis Anatomy 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- 229940080818 propionamide Drugs 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- 238000001959 radiotherapy Methods 0.000 claims 1
- 150000003384 small molecules Chemical class 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 229960001312 tiaprofenic acid Drugs 0.000 claims 1
- 108010018976 Interleukin-8A Receptors Proteins 0.000 abstract 1
- 102000002791 Interleukin-8B Receptors Human genes 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4168—1,3-Diazoles having a nitrogen attached in position 2, e.g. clonidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/664—Amides of phosphorus acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
Abstract
The present invention relates to IL-8 inhibitor compounds, preferably dual CXCR1 /CXCR2 receptor inhibitors, useful in the treatment and/or prevention of interstitial cystitis / painful bladder syndrome (IC/PBS) and/or over active bladder (OAB), also including IC/PBS and/or OAB induced by anticancer therapy. Methods of treatment and/or prevention, combinations and kits comprising said IL-8 inhibitors are also covered therein.
Claims (16)
1. A use of an IL-8 inhibitor in the manufacture of a medicament for use in the treatment and/or prevention of interstitial cystitis/painful bladder syndrome (IC/PBS) and/or over active bladder (OAB), wherein the IL-8 inhibitor is a CXCR1 5 inhibitor or a dual CXCR1 and CXCR2 inhibitor.
2. The use as claimed in claim 1, wherein said IC/PBS and/or over active bladder (OAB) is induced by anticancer therapy or radiotherapy to the pelvis.
3. The use as claimed in claim 1 or 2, wherein the IL-8 inhibitor is selected from a small molecule, antibody or peptide. 10
4. The use as claimed in any one of claims 1 to 3, wherein the IL-8 inhibitor comprises a compound of formula (I) or pharmaceutically acceptable salts thereof, wherein 15 R1 is hydrogen; X is OH; R2 is hydrogen or linear C1-C4 alkyl; Y is a heteroatom selected from S, O and N; Z is selected from linear or branched C1-C4 alkyl, linear or branched C1-C4 alkoxy, 20 halo C1-C3 alkyl and halo C1-C3 alkoxy.
5. The use as claimed in any one of claims 1 to 4, wherein said IL-8 inhibitor is selected from (R,S)(4-{[4-(trifluoromethyl)-1,3-thiazol yl]amino}phenyl)propanoic acid and (2S)(4-{[4-(trifluoromethyl)-1,3-thiazolyl] amino} phenyl) propanoic acid.
6. The use as claimed in claim 5, wherein the IL-8 inhibitor comprises a sodium salt of said compounds.
7. The use as claimed in any one of claims 1 to 3, wherein the IL-8 inhibitor comprises a compound of formula (II) 5 (II) or pharmaceutically acceptable salts thereof, wherein R’ is hydrogen; R is a residue of formula SO Ra wherein Ra is linear or branched C -C alkyl or 2 1 4 10 halo C -C alkyl.
8. The use as claimed in any one of claims 1 to 3 and 7, wherein said IL-8 inhibitor is R(-)[(4’-trifluoromethanesulfonyloxy)phenyl]-N-methanesulfonyl propionamide.
9. The use as claimed in claim 8, wherein the IL-inhibitor is the sodium salt 15 thereof.
10. A use of a pharmaceutical composition comprising an IL-8 inhibitor in the manufacture of a medicament for use in the treatment and/or prevention of interstitial cystitis/painful bladder syndrome (IC/PBS) and/or over active bladder (OAB), wherein the IL-8 inhibitor is a CXCR1 inhibitor or a dual CXCR1 and 20 CXCR2 inhibitor.
11. A use as claimed in claim 10, wherein the medicament further comprises at least one further pharmaceutically active compound.
12. A use as claimed in claim 11, wherein said further pharmaceutically active compound is an active compound useful for the prevention and treatment of IC/PBS, an/or OAB.
13. A use as claimed in claim 12, wherein said further pharmaceutically active 5 compound is a TRPV1 antagonist.
14. A use as claimed in claim 11, wherein said further pharmaceutically active compound is a drug that induces, as an undesired effect, IC /PBS or OAB.
15. A use as claimed in claim 14, wherein said further pharmaceutically active compound is selected from cyclophosphamide, Bacillus Calmette-Guérin to be 10 instilled directly into the bladder, mitomycin C, Adriamycin or tiaprofenic acid.
16. A use as claimed in any one of claims 1-15 substantially as described herein and with reference to any example thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15176726.6A EP3117835A1 (en) | 2015-07-14 | 2015-07-14 | Il-8 inhibitors for use in the treatment of certain urological disorders |
| PCT/EP2016/066511 WO2017009323A1 (en) | 2015-07-14 | 2016-07-12 | Il-8 inhibitors for use in the treatment of certain urological disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ739077A NZ739077A (en) | 2023-12-22 |
| NZ739077B2 true NZ739077B2 (en) | 2024-03-26 |
Family
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