JP2018521056A - インドールアミン2,3−ジオキシゲナーゼの阻害剤 - Google Patents
インドールアミン2,3−ジオキシゲナーゼの阻害剤 Download PDFInfo
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- JP2018521056A JP2018521056A JP2017568056A JP2017568056A JP2018521056A JP 2018521056 A JP2018521056 A JP 2018521056A JP 2017568056 A JP2017568056 A JP 2017568056A JP 2017568056 A JP2017568056 A JP 2017568056A JP 2018521056 A JP2018521056 A JP 2018521056A
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- mmol
- acid
- oxadiazol
- bromo
- compound
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- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- RRFLKIOOOVMCBE-UHFFFAOYSA-N methyl 1-hydroxy-3,4-dihydro-2,1-benzoxaborinine-8-carboxylate Chemical compound OB1OCCC2=C1C(=CC=C2)C(=O)OC RRFLKIOOOVMCBE-UHFFFAOYSA-N 0.000 description 1
- MASRAGFWFYHMFI-UHFFFAOYSA-N methyl 3-bromo-4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C(Br)=C1 MASRAGFWFYHMFI-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 210000001616 monocyte Anatomy 0.000 description 1
- ACTNHJDHMQSOGL-UHFFFAOYSA-N n',n'-dibenzylethane-1,2-diamine Chemical compound C=1C=CC=CC=1CN(CCN)CC1=CC=CC=C1 ACTNHJDHMQSOGL-UHFFFAOYSA-N 0.000 description 1
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- KBMUEQGVDODCPL-UHFFFAOYSA-N n-[4-[4-(3-bromo-4-fluorophenyl)-5-oxo-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl]-2,2,2-trifluoroacetamide Chemical compound C1=C(Br)C(F)=CC=C1N1C(=O)ON=C1C1=NON=C1NC(=O)C(F)(F)F KBMUEQGVDODCPL-UHFFFAOYSA-N 0.000 description 1
- 229960000884 nelfinavir Drugs 0.000 description 1
- QAGYKUNXZHXKMR-HKWSIXNMSA-N nelfinavir Chemical compound CC1=C(O)C=CC=C1C(=O)N[C@H]([C@H](O)CN1[C@@H](C[C@@H]2CCCC[C@@H]2C1)C(=O)NC(C)(C)C)CSC1=CC=CC=C1 QAGYKUNXZHXKMR-HKWSIXNMSA-N 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 239000002581 neurotoxin Substances 0.000 description 1
- 229960000689 nevirapine Drugs 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229960002969 oleic acid Drugs 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- KHPXUQMNIQBQEV-UHFFFAOYSA-N oxaloacetic acid Chemical compound OC(=O)CC(=O)C(O)=O KHPXUQMNIQBQEV-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000003544 oxime group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000006179 pH buffering agent Substances 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 230000009038 pharmacological inhibition Effects 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 238000011533 pre-incubation Methods 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 229960004742 raltegravir Drugs 0.000 description 1
- CZFFBEXEKNGXKS-UHFFFAOYSA-N raltegravir Chemical compound O1C(C)=NN=C1C(=O)NC(C)(C)C1=NC(C(=O)NCC=2C=CC(F)=CC=2)=C(O)C(=O)N1C CZFFBEXEKNGXKS-UHFFFAOYSA-N 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- YIBOMRUWOWDFLG-ONEGZZNKSA-N rilpivirine Chemical compound CC1=CC(\C=C\C#N)=CC(C)=C1NC1=CC=NC(NC=2C=CC(=CC=2)C#N)=N1 YIBOMRUWOWDFLG-ONEGZZNKSA-N 0.000 description 1
- 229960001852 saquinavir Drugs 0.000 description 1
- QWAXKHKRTORLEM-UGJKXSETSA-N saquinavir Chemical compound C([C@@H]([C@H](O)CN1C[C@H]2CCCC[C@H]2C[C@H]1C(=O)NC(C)(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)C=1N=C2C=CC=CC2=CC=1)C1=CC=CC=C1 QWAXKHKRTORLEM-UGJKXSETSA-N 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical class O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- PODWXQQNRWNDGD-UHFFFAOYSA-L sodium thiosulfate pentahydrate Chemical compound O.O.O.O.O.[Na+].[Na+].[O-]S([S-])(=O)=O PODWXQQNRWNDGD-UHFFFAOYSA-L 0.000 description 1
- 239000007909 solid dosage form Substances 0.000 description 1
- 239000012439 solid excipient Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229960001203 stavudine Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229940032330 sulfuric acid Drugs 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- WINGEFIITRDOLJ-UHFFFAOYSA-N tert-butyl 2-hydroxyacetate Chemical compound CC(C)(C)OC(=O)CO WINGEFIITRDOLJ-UHFFFAOYSA-N 0.000 description 1
- BEUUJDAEPJZWHM-COROXYKFSA-N tert-butyl n-[(2s,3s,5r)-3-hydroxy-6-[[(2s)-1-(2-methoxyethylamino)-3-methyl-1-oxobutan-2-yl]amino]-6-oxo-1-phenyl-5-[(2,3,4-trimethoxyphenyl)methyl]hexan-2-yl]carbamate Chemical compound C([C@@H]([C@@H](O)C[C@H](C(=O)N[C@H](C(=O)NCCOC)C(C)C)CC=1C(=C(OC)C(OC)=CC=1)OC)NC(=O)OC(C)(C)C)C1=CC=CC=C1 BEUUJDAEPJZWHM-COROXYKFSA-N 0.000 description 1
- JHLVEBNWCCKSGY-UHFFFAOYSA-N tert-butyl n-methylcarbamate Chemical compound CNC(=O)OC(C)(C)C JHLVEBNWCCKSGY-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229960004559 theobromine Drugs 0.000 description 1
- 238000011285 therapeutic regimen Methods 0.000 description 1
- ODBLHEXUDAPZAU-UHFFFAOYSA-N threo-D-isocitric acid Natural products OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 description 1
- ZFEAMMNVDPDEGE-LGRGJMMZSA-N tifuvirtide Chemical compound C([C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(C)=O)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)C1=CC=C(O)C=C1 ZFEAMMNVDPDEGE-LGRGJMMZSA-N 0.000 description 1
- 229960000838 tipranavir Drugs 0.000 description 1
- SUJUHGSWHZTSEU-FYBSXPHGSA-N tipranavir Chemical compound C([C@@]1(CCC)OC(=O)C([C@H](CC)C=2C=C(NS(=O)(=O)C=3N=CC(=CC=3)C(F)(F)F)C=CC=2)=C(O)C1)CC1=CC=CC=C1 SUJUHGSWHZTSEU-FYBSXPHGSA-N 0.000 description 1
- 230000000451 tissue damage Effects 0.000 description 1
- 231100000827 tissue damage Toxicity 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- UPCXAARSWVHVLY-UHFFFAOYSA-N tris(2-hydroxyethyl)azanium;acetate Chemical compound CC(O)=O.OCCN(CCO)CCO UPCXAARSWVHVLY-UHFFFAOYSA-N 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000029812 viral genome replication Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229960000523 zalcitabine Drugs 0.000 description 1
- 229960002555 zidovudine Drugs 0.000 description 1
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 description 1
Classifications
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/22—Boron compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Transplantation (AREA)
- Virology (AREA)
- Inorganic Chemistry (AREA)
- Epidemiology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Xは、CH2又はC(O)であり;
R1は、-NR2R3であり;
R2は、-H又は-CH3であり;
R3は、
を有する、IDOのモジュレーターである化合物、又はその薬学的に許容される塩を提供する。
Xは、CH2又はC(O)であり;
R1は、-NR2R3であり;
R2は、-H又は-CH3であり;
R3は、
の構造を有する化合物、又はその薬学的に許容される塩が提供される。
創傷、うつ病、神経変性障害、心的外傷、加齢性白内障、臓器移植拒絶、自己免疫疾患、などを処置する方法を提供する。
ヌクレオチド逆転写酵素阻害剤、例えば、ジドブジン、ジダノシン、ラミブジン、ザルシタビン、アバカビル、スタブジン、アデフォビル、アデフォビルジピボキシル、フォジブジン、トドキシル、エムトリシタビン、アロブジン、アムドキソビル、エルブシタビン、及び同様の作用剤;
非ヌクレオチド逆転写酵素阻害剤(抗酸化活性を有する作用剤、例えば、イムノカル、オルチプラズ、などを含む)、例えば、ネビラピン、デラビルジン、エファビレンツ、ロビリデ、イムノカル、オルチプラズ、カプラビリン、レルシビリン、GSK2248761、TMC-278、TMC-125、エトラビリン、及び同様の作用剤;
プロテアーゼ阻害剤、例えば、サキナビル、リトナビル、インジナビル、ネルフィナビル、アンプレナビル、フォサムプレナビル、ブレカナビル、ダルナビル(darunavir)、アタザナビル、チプラナビル、パリナビル、ラシナビル、及び同様の作用剤:
侵入、付着及び融合阻害剤、例えば、エンフビルチド(T-20)、T-1249、PRO-542、PRD-140、TNX-355、BMS-806、BMS-663068及びBMS-626529、5-ヘリックス、並びに同様の作用剤;
インテグラーゼ阻害剤、例えば、ラルテグラビル、エルビテグラビル、GSK1349572、GSK1265744、及び同様の作用剤;
変異阻害剤、例えば、PA-344及びPA-457、並びに同様の作用剤;並びに
CXCR4及び/又はCCR5阻害剤、例えば、ビクリビロク(Sch-C)、Sch-D、TAK779、マラビロク(UK427、857)、TAK449、並びに国際公開第02/74769号、PCT/US03/39644、PCT/US03/39975、PCT/US03/39619、PCT/US03/39618、PCT/US03/39740、及びPCT/US03/39732に開示されたもの、並びに同様の作用剤。
以下の実施例は、上記発明を製造及び使用する方法についてより十分に説明するために役立つ。これらの実施例は、本発明の真の範囲を限定するためには決して役立たず、むしろ、例証的目的のために提示されると理解されたい。以下の実施例及び合成スキームにおいて、以下の略語は、以下の意味を有する。略語が定義されない場合、それはその一般に受け入れられた意味を有する。
3-(4-((2-アミノエチル)アミノ)-1,2,5-オキサジアゾール-3-イル)-4-(3-ブロモ-4-フルオロフェニル)-1,2,4-オキサジアゾール-5(4H)-オン塩酸塩
4-アミノ-N'-ヒドロキシ-1,2,5-オキサジアゾール-3-カルボキシイミダミド
4-アミノ-N-ヒドロキシ-1,2,5-オキサジアゾール-3-カルビミドイルクロリド
4-アミノ-N'-ヒドロキシ-N-(2-メトキシエチル)-1,2,5-オキサジアゾール-3-カルボキシイミダミド
N'-ヒドロキシ4-((2-メトキシエチル)アミノ)-1,2,5-オキサジアゾール-3-カルボキシイミダミド
N-ヒドロキシ-4-((2-メトキシエチル)アミノ)-1,2,5-オキサジアゾール-3-カルビミドイルクロリド
N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシ-4-((2-メトキシエチル)アミノ)-1,2,5-オキサジアゾール-3-カルボキシイミダミド
4-(3-ブロモ-4-フルオロフェニル)-3-(4-((2-メトキシエチル)アミノ)-1,2,5-オキサジアゾール-3-イル)-1,2,4-オキサジアゾール-5(4H)-オン
4-(3-ブロモ-4-フルオロフェニル)-3-(4-((2-ヒドロキシエチル)アミノ)-1,2,5-オキサジアゾール-3-イル)-1,2,4-オキサジサゾール-5(4H)-オン
2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチルメタンスルホネート
3-(4-((2-アジドエチル)アミノ)-1,2,5-オキサジアゾール-3-イル)-4-(3-ブロモ-4-フルオロフェニル)-1,2,4-オキサジアゾール-5(4H)-オン
tert-ブチル(2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)カルバメート
3-(4-((2-アミノエチル)アミノ)-1,2,5-オキサジアゾール-3-イル)-4-(3-ブロモ-4-フルオロフェニル)-1,2,4-オキサジアゾール-5(4H)-オン塩酸塩
メチル3-メチル-2-(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゾエート
メチル3-(ブロモメチル)-2-(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゾエート
1-ヒドロキシ-1,3-ジヒドロベンゾ[c][1,2]オキサボロール-7-カルボン酸
(3-ブロモ-1,2-フェニレン)ジメタノール
2,2'-(((3-ブロモ-1,2-フェニレン)ビス(メチレン))ビス(オキシ))ビス(テトラヒドロ-2H-ピラン)
4-(ヒドロキシメチル)ベンゾ[c][1,2]オキサボロール-1(3H)-オール
4-(ブロモメチル)ベンゾ[c][1,2]オキサボロール-1(3H)-オール
tert-ブチル((1-ヒドロキシ-1,3-ジヒドロベンゾ[c][1,2]オキサボロール-4-イル)メチル)(メチル)カルバメート
4-((メチルアミノ)メチル)ベンゾ[c][1,2]オキサボロール-1(3H)-オール
化合物1
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
メチル2-ブロモ-3-(ジブロモメチル)ベンゾエート
メチル2-ブロモ-3-ホルミルベンゾエート
メチル2-ブロモ-3-(2-メトキシビニル)ベンゾエート
メチル3-(2-メトキシビニル)-2-(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゾエート
メチル1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキシレート
メチル1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキシレート
N-(2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
化合物2
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
N-(2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
N-(2-((4-N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-8-カルボキサミド
化合物3
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボキサミド
メチル3-ブロモ-4-(ジブロモメチル)ベンゾエート
メチル3-ブロモ-4-ホルミルベンゾエート
メチル3-ブロモ-4-(2-メトキシビニル)ベンゾエート
メチル4-(2-メトキシビニル)-3-(4,4,5,5-テトラメチル-1,3,2-ジオキサボロラン-2-イル)ベンゾエート
メチル1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボキシレート
1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボン酸
N-(2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボキサミド
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボキサミド
化合物4
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-7カルボキサミド
メチル1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボキシレート
1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c][1,2]オキサボリニン-7-カルボン酸
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-3,4-ジヒドロ-1H-ベンゾ[c](1,2]オキサボリニン-7-カルボキサミド
化合物5
2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)-N-((1-ヒドロキシ-1,3-ジヒドロベンゾ[c][1,2]オキサボロール-4-イル)メチル)-N-メチルアセトアミド2,2,2-トリフルオロアセテート
N-(4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)-2,2,2-トリフルオロアセトアミド
tert-ブチル2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)アセテート
2-((4-(4-(3-ブロモ-4-フルオロフェニル)-5-オキソ-4,5-ジヒドロ-1,2,4-オキサジアゾール-3-イル)-1,2,5-オキサジアゾール-3-イル)アミノ)酢酸
2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)-N-((1-ヒドロキシ-1,3-ジヒドロベンゾ[c][1,2]オキサボロール-4-イル)メチル)-N-メチルアセトアミド2,2,2-トリフルオロアセテート
化合物6
N-(2-((4-(N-(3-ブロモ-4-フルオロフェニル)-N'-ヒドロキシカルバミミドイル)-1,2,5-オキサジアゾール-3-イル)アミノ)エチル)-1-ヒドロキシ-1,3-ジヒドロベンゾ[c][1,2]オキサボロール-7-カルボキサミド
別の実施形態において、薬学的に許容される希釈剤、及び治療有効量の式I〜式VIIの化合物又はその薬学的に許容される塩を含む、医薬組成物が提供される。
ヒトのインドールアミン2,3-ジオキシゲナーゼ(IDO)酵素及び細胞データ、並びにラット及びマウスのクリアランスデータを、以下の表2に提示する。グラフ1は、時間に対する薬物濃度としてラット経口薬物動態(PK)を示す。酵素及び細胞アッセイ、並びにラットのためのインビボ薬物動態方法の簡潔な記載は、以下に、表及びグラフに続く。
Lohse N, Hansen AB, Pedersen G, Kronborg G, Gerstoft J, Sorensen HT, Vaeth M, Obel N. Survival of persons with and without HIV infection in Denmark, 1995-2005. Ann Intern Med. 2007 Jan 16;146(2):87-95.
Deeks SG. HIV infection, inflammation, immunosenescence, and aging. Annu Rev Med. 2011;62:141-55.
Hunt PW, Sinclair E, Rodriguez B, Shive C, Clagett B, Funderburg N, Robinson J, Huang Y, Epling L, Martin JN, Deeks SG, Meinert CL, Van Natta ML, Jabs DA, Lederman MM. Gut epithelial barrier dysfunction and innate immune activation predict mortality in treated HIV infection. J Infect Dis. 2014 Oct 15; 210(8):1228-38.
Tenorio AR, Zheng Y, Bosch RJ, Krishnan S, Rodriguez B, Hunt PW, Plants J, Seth A, Wilson CC, Deeks SG, Lederman MM, Landay AL. Soluble markers of inflammation and coagulation but not T-cell activation predict non-AIDS-defining morbid events during suppressive antiretroviral treatment. J Infect Dis. 2014 Oct 15; 210(8):1248-59.
Byakwaga H, Boum Y 2nd, Huang Y, Muzoora C, Kembabazi A, Weiser SD, Bennett J, Cao H, Haberer JE, Deeks SG, Bangsberg DR, McCune JM, Martin JN, Hunt PW. The kynurenine pathway of tryptophan catabolism, CD4+ T-cell recovery, and mortality among HIV-infected Ugandans initiating antiretroviral therapy. J Infect Dis. 2014 Aug 1; 210(3):383-91.
Pearson JT, Siu S, Meininger DP, Wienkers LC, Rock DA. In vitro modulation of cytochrome P450 reductase supportedindoleamine 2,3-dioxygenase activity by allosteric effectors cytochrome b(5) and methylene blue. Biochemistry 49, 2647-2656 (2010)
Claims (8)
- 式(I):
Xは、CH2又はC(O)であり;
R1は、-NR2R3であり;
R2は、-H又は-CH3であり;
R3は、
の構造を有する化合物、又はその薬学的に許容される塩。 - 式(II):
- 式(III):
- 式(IV):
- 式(V):
- 式(VI):
- 式(VII):
- 対象におけるAIDS及び一般的免疫抑制の進行の予防を含む、HIVの予防及び/又は処置の方法であって、対象に請求項1〜7の化合物を投与することを含む方法。
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IL282535B2 (en) | 2018-10-31 | 2024-05-01 | Gilead Sciences Inc | Transformed 6-azabanzimidazole compounds as HPK1 inhibitors |
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JP2011527686A (ja) * | 2008-07-08 | 2011-11-04 | インサイト・コーポレイション | インドールアミン2,3−ジオキシゲナーゼの阻害剤としての1,2,5−オキサジアゾール |
WO2012067663A1 (en) * | 2010-11-18 | 2012-05-24 | Glaxo Group Limited | Compounds |
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