DK2794627T3 - Substituerede nukleosider, nukleotider og analoger deraf - Google Patents
Substituerede nukleosider, nukleotider og analoger deraf Download PDFInfo
- Publication number
- DK2794627T3 DK2794627T3 DK12860391.7T DK12860391T DK2794627T3 DK 2794627 T3 DK2794627 T3 DK 2794627T3 DK 12860391 T DK12860391 T DK 12860391T DK 2794627 T3 DK2794627 T3 DK 2794627T3
- Authority
- DK
- Denmark
- Prior art keywords
- optionally substituted
- alkyl
- compound
- group
- hydrogen
- Prior art date
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000955 prescription drug Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical compound [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229940061374 relenza Drugs 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 208000020029 respiratory tract infectious disease Diseases 0.000 description 1
- 239000002342 ribonucleoside Substances 0.000 description 1
- 125000000548 ribosyl group Chemical group C1([C@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 229920002477 rna polymer Polymers 0.000 description 1
- 201000005404 rubella Diseases 0.000 description 1
- 229960002052 salbutamol Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 201000009890 sinusitis Diseases 0.000 description 1
- 206010041232 sneezing Diseases 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 229940036185 synagis Drugs 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
- DVFXLNFDWATPMW-IWOKLKJTSA-N tert-butyldiphenylsilyl Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)C(C)(C)C)[C@@H](OP(O)(=O)OC[C@@H]2[C@H](C[C@@H](O2)N2C3=C(C(NC(N)=N3)=O)N=C2)OP(O)(=O)OC[C@@H]2[C@H](C[C@@H](O2)N2C3=C(C(NC(N)=N3)=O)N=C2)OP(O)(=O)OC[C@@H]2[C@H](C[C@@H](O2)N2C3=C(C(NC(N)=N3)=O)N=C2)OP(O)(=O)OC[C@@H]2[C@H](CC(O2)N2C3=NC=NC(N)=C3N=C2)OP(O)(=O)OC[C@@H]2[C@H](C[C@@H](O2)N2C3=C(C(NC(N)=N3)=O)N=C2)O)C1 DVFXLNFDWATPMW-IWOKLKJTSA-N 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229960004559 theobromine Drugs 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- CBDKQYKMCICBOF-UHFFFAOYSA-N thiazoline Chemical compound C1CN=CS1 CBDKQYKMCICBOF-UHFFFAOYSA-N 0.000 description 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 231100000041 toxicology testing Toxicity 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- VTHOKNTVYKTUPI-UHFFFAOYSA-N triethoxy-[3-(3-triethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCSSSSCCC[Si](OCC)(OCC)OCC VTHOKNTVYKTUPI-UHFFFAOYSA-N 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000004952 trihaloalkoxy group Chemical group 0.000 description 1
- 125000004385 trihaloalkyl group Chemical group 0.000 description 1
- HYWCXWRMUZYRPH-UHFFFAOYSA-N trimethyl(prop-2-enyl)silane Chemical compound C[Si](C)(C)CC=C HYWCXWRMUZYRPH-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- JQSHBVHOMNKWFT-DTORHVGOSA-N varenicline Chemical compound C12=CC3=NC=CN=C3C=C2[C@H]2C[C@@H]1CNC2 JQSHBVHOMNKWFT-DTORHVGOSA-N 0.000 description 1
- 230000005727 virus proliferation Effects 0.000 description 1
- 210000001260 vocal cord Anatomy 0.000 description 1
- 230000036642 wellbeing Effects 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
Classifications
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
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- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/073—Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical
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- C07D405/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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Claims (48)
1. Forbindelse med formlen (I) eller et farmaceutisk acceptabelt salt deraf:
hvor: B1A er valgt fra gruppen bestående af:
hvor: RA2 er valgt fra gruppen bestående af hydrogen, halogen og NHRJ2, hvor RJ2 er valgt fra gruppen bestående af hydrogen, C(=O)RK2 og -C(=O)ORL2; RB2 er halogen eller NHRW2, hvor Rw2 er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C2-6-alkenyl, en eventuelt substitueret C3-8-cycloalkyl, -C(=O)RM2 og -C(=O)ORN2; Rc2 er hydrogen eller NHR02, hvor R02 er valgt fra gruppen bestående af hydrogen, -C(=O)RP2 og -C(=O)ORQ2; RD2 er valgt fra gruppen bestående af hydrogen, halogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C2-6-alkenyl og en eventuelt substitueret C2-6-alkynyl; RE2 er valgt fra gruppen bestående af hydrogen, hydroxy, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C3-8-cycloalkyl, -C(=O)RR2 og -C(=O)ORS2; RF2 er valgt fra gruppen bestående af hydrogen, halogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C2-
6-alkenyl og en eventuelt substitueret C2-6-alkynyl ; Y2 og Y3 er uafhængigt N eller CR12, hvor R12 er valgt fra gruppen bestående af hydrogen, halogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C2-6-alkenyl og en eventuelt substitueret C2-6-alkynyl; RG2 er en eventuelt substitueret Ci-6-alkyl; RH2 er hydrogen eller NHRT2, hvor RT2 er valgt fra gruppen bestående af hydrogen, -C(=O)RU2 og -C(=O)ORV2; og RK2, RL2, RM2, RN2, Rp2, RQ2, RR2, Rs2, Ru2 og Rv2 er uafhængigt valgt fra gruppen bestående af Ci-6-alkyl, C2-6-alkenyl, C2-6- alkynyl, C3-6-cycloalkyl, C3-6-cycloalkenyl, C6-io-aryl, heteroaryl, heteroalicyklyl, aryl (Ci-6-alkyl) , heteroaryl (C1-6-alkyl) og heteroalicyklyl (Ci-6-alkyl) ; R1A er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret acyl, en eventuelt substitueret O-bundet aminosyre,
den stiplede linje (------) f formel (I) er fraværende; R2A er valgt fra gruppen bestående af en ikke-substitueret C1-6-alkyl, en halogen-substitueret Ci-6-alkyl, en hydroxy-substitueret Ci-6-alkyl, en alkoxy-substitueret Ci-6-alkyl og en sulfenyl-subs ti tueret Ci-6-alkyl ; R3A er valgt fra gruppen bestående af OH, -OC(=O)R"A og en eventuelt substitueret O-bundet aminosyre; R4A er fluor; R5A er hydrogen; r6a, r7a og r8a er uafhængigt valgt fra gruppen bestående af fraværende, hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C3-6-cycloalkenyl, en eventuelt substitueret aryl, en eventuelt substitueret heteroaryl, en eventuelt substitueret aryl(Ci-6-alkyl), en eventuelt substitueret * - (CR15AR16A) p-O-Ci-24-alkyl, en eventuelt substitueret *- (CR17AR18A) q-O-Ci-24-alkenyl,
eller R6A er
og R7A er fraværende eller hydrogen; eller R6A og R7A er taget sammen for at danne en del valgt fra gruppen bestående af en eventuelt substitueret
og en eventuelt substitueret
hvor oxygenatomerne, der er forbundet med R6A og R7A, phosphor og delen danner et seks- til ti-leddet ringsystem;. R9A er valgt fra gruppen bestående af en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C3-6-cycloalkenyl, NR30AR31A, en eventuelt substitueret N-bundet aminosyre og et eventuelt substitueret N-bundet aminosyre-esterderivat; R10A og R11A er uafhængigt en eventuelt substitueret N-bundet aminosyre eller et eventuelt substitueret N-bundet aminosyre-esterderivat ; R12A, R13A og R14A er uafhængigt fraværende eller hydrogen;
hver R15A, hver R16A, hver R17A og hver R18A er uafhængigt hydrogen, en eventuelt substitueret Ci-24-alkyl eller alkoxy; R19A, R20A, R22A og R23A er uafhængigt valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl og en eventuelt substitueret aryl; R21A og R24A er uafhængigt valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret aryl, en eventuelt substitueret -O-Ci-24-alkyl og en eventuelt substitueret -O-aryl; R25A og r29a er uafhængigt valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl og en eventuelt substitueret aryl; R26A og R27A er uafhængigt -C^N eller en eventuelt substitueret substituent valgt fra gruppen bestående af C2-8-organylcarbonyl, C2-8-alkoxycarbonyl og C2-8- organylaminocarbonyl; R28A er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl og en eventuelt substitueret C3-6-cycloalkenyl ; R30A og R31A er uafhængigt valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl og en eventuelt substitueret C3-6-cycloalkenyl; R"A er en eventuelt substitueret Ci-24-alkyl; m er 0 eller 1; p og q er uafhængigt valgt fra gruppen bestående af 1, 2 og 3; r er 1 eller 2; og Z1A, Z2A, Z3A og Z4A er uafhængigt 0 eller S.
2. Forbindelse ifølge krav 1, hvor R1A er
eller
hvor Z1A, Z2A og Z3A hver er 0.
3. Forbindelse ifølge krav 2, hvor den ene af R6A og R7A er hydrogen, og den anden af R6A og R7A er valgt fra gruppen bestående af en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C3-6-cycloalkenyl, en eventuelt substitueret aryl, en eventuelt substitueret heteroaryl og en eventuelt substitueret aryl (Ci-6-alkyl) , den anden af R6A og R7A fortrinsvis er en eventuelt substitueret Ci-24-alkyl; eller R6A og R7A begge er uafhængigt valgt fra gruppen bestående af en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C3-6-cycloalkenyl, en eventuelt substitueret aryl, en eventuelt substitueret heteroaryl og en eventuelt substitueret aryl (Ci-6-alkyl) , R6A og R7A fortrinsvis begge er en eventuelt substitueret Ci-24-alkyl; eller den ene af R6A og R7A er valgt fra gruppen bestående af og den anden af
R6A og R7A er valgt fra gruppen bestående af fraværende, hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24-alkynyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C3-6-cycloalkenyl, en eventuelt substitueret aryl, en eventuelt substitueret heteroaryl og en eventuelt substitueret aryl (Ci-6-alkyl) , R6A og R7A fortrinsvis
begge er uafhænqiqt
valqt fra gruppen bestående af R6A og R7A fortrinsvis begge er
R6A og R7A fortrinsvis begge er
R6A og R7A fortrinsvis begge er
eller R6A og R7A begge er en eventuelt substitueret Ci-24-alkyl; eller R6A og R7A begge er en eventuelt substitueret C2-24- alkenyl; eller R6A og R7A begge er *-(CR15AR16A) p-O-Ci-24-alkyl; eller R6A og R7A begge er *-(CR17AR19A) q-O-C2-24-alkenyl; eller R6A og R7A begge er en eventuelt substitueret aryl; eller R6A og R7A begge er en eventuelt substitueret aryl (Ci-6-alkyl) ; eller R6A og R7A begge er
eller R6A og R7A begge er
eller R6A og R7A er taget sammen for at danne en del valgt fra
gruppen bestående af en eventuelt substitueret
og en eventuelt substitueret
hvor oxygenatomerne, der er forbundet med R6A og R7A, phosphor og delen danner et seks- til ti-leddet ringsystem, R6A og R7A fortrinsvis er taget sammen for at danne en del valgt fra gruppen bestående af
hvor R32A er en eventuelt substitueret aryl, en eventuelt substitueret heteroaryl eller en eventuelt substitueret heterocyclyl.
4. Forbindelse ifølge krav 2, hvor R8A er valgt fra gruppen bestående af fraværende, hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24~alkynyl, en eventuelt substitueret C3-6-cycloalkyl og en eventuelt substitueret C3-6-cycloalkenyl, og R9A er valgt fra gruppen bestående af en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-24~alkynyl, en eventuelt substitueret C3-6-cycloalkyl og en eventuelt substitueret C3-6-cycloalkenyl, R8A fortrinsvis er hydrogen, og R9A er en
eventuelt substitueret Ci-6-alkyl; eller R8A er hydrogen, og R9A er NR30AR31A, hvor R30A og R31A er uafhængigt valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-24-alkyl, en eventuelt substitueret C2-24-alkenyl, en eventuelt substitueret C2-2-alkynyl, en eventuelt substitueret C3-6-cycloalkyl og en eventuelt substitueret C3-6-cycloalkenyl; eller R8A er fraværende eller hydrogen, og R9A er en eventuelt substitueret N-bundet aminosyre eller et eventuelt substitueret N-bundet aminosyre-esterderivat; eller R8A er en eventuelt substitueret aryl, og R9A er en eventuelt substitueret N-bundet aminosyre eller et eventuelt substitueret N-bundet aminosyre-esterderivat .
5. Forbindelse ifølge krav 2, hvor R10A og R11A begge er en eventuelt substitueret N-bundet aminosyre eller et eventuelt substitueret N-bundet aminosyre-esterderivat, R10A og R11A fortrinsvis er uafhængigt valgt fra gruppen bestående af alanin, asparagin, aspartat, cystein, glutamat, glutamin, glycin, prolin, serin, tyrosin, arginin, histidin, isoleucin, leucin, lysin, methionin, phenylalanin, threonin, tryptophan, valin og esterderivater deraf, R10A og R11A fortrinsvis er uafhængigt valgt fra gruppen bestående af alanin-isopropylester, alanin-cyclohexylester, alanin-neopentylester, valin-isopropylester og leucin-isopropylester; eller R10A og R11A uafhængigt har strukturen
hvor r36a er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret aryl, en eventuelt substitueret aryl(Ci-6-alkyl) og en eventuelt substitueret halogenalkyl, R37A er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret Ci-6-halogenalkyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C6-aryl, en eventuelt substitueret C10-aryl og en eventuelt substitueret aryl (Ci-6-alkyl) , og R38A er hydrogen eller en eventuelt substitueret Ci-4-alkyl; eller
R37A og R38A er taget sammen for at danne en eventuelt substitueret C3-6-cycloalkyl, R37A fortrinsvis er en eventuelt substitueret Ci-6-alkyl, R37A fortrinsvis er methyl, R38A fortrinsvis er hydrogen, r36a fortrinsvis er en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret C3-6-cycloalkyl eller en eventuelt substitueret benzyl.
6. Forbindelse ifølge krav 1, hvor R1A er hvor R6A og R7A begge er hydrogen, eller R6A og R7A begge er fraværende; eller R1A er
hvor R6A er
m fortrinsvis er 0, og R7A, R12A og R13A uafhængigt er fraværende eller hydrogen, eller m fortrinsvis er 1, og R7A, R12A, R13A og R14A uafhængigt er fraværende eller hydrogen.
7. Forbindelse ifølge krav 1, hvor R1A er H.
8. Forbindelse ifølge krav 1, hvor R1A er en eventuelt substitueret acyl.
9. Forbindelse ifølge krav 8, hvor den eventuelt substituerede acyl er -C(=O)R39A, hvor R39A er valgt fra gruppen bestående af en eventuelt substitueret Ci-12-alkyl, en eventuelt substitueret C2-i2-alkenyl, en eventuelt substitueret C2-12-alkynyl, en eventuelt substitueret C3-8-cycloalkyl, en eventuelt substitueret Cs-8-cycloalkenyl, en eventuelt substitueret C6-io-aryl, en eventuelt substitueret heteroaryl, en eventuelt substitueret heterocyclyl, en eventuelt
substitueret aryl(Ci-6-alkyl), en eventuelt substitueret heteroaryl(Ci-6-alkyl) og en eventuelt substitueret heterocyclyl (Ci-6-alkyl) , R39A fortrinsvis er substitueret eller ikke-substitueret Ci-12-alkyl.
10. Forbindelse ifølge krav 9, hvor R39A er en ikke-substitueret Ci-12-alkyl.
11. Forbindelse ifølge krav 1, hvor R1A er en eventuelt substitueret O-bundet aminosyre, eller R1A er
hvor r4oa er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret Ci-6-halogenalkyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C6-aryl, en eventuelt substitueret C10-aryl og en eventuelt substitueret aryl (Ci-6-alkyl) , og R41A er hydrogen eller en eventuelt substitueret Ci-4-alkyl, eller R40A og R41A er taget sammen for at danne en eventuelt substitueret C3-6-cycloalkyl, R40A fortrinsvis er en eventuelt substitueret Ci-6-alkyl, r4oa fortrinsvis er methyl, R41A fortrinsvis er hydrogen.
12. Forbindelse ifølge krav 1, hvor B1A er
eller
13. Forbindelse ifølge krav 1, hvor B1A er
eller
14. Forbindelse ifølge et hvilket som helst af kravene 1-13, hvor R2A er en halogen-substitueret Ci-6-alkyl eller en sulfenyl-substitueret Ci-6-alkyl.
15. Forbindelse ifølge et hvilket som helst af kravene 1-13, hvor R2A er en halogen-substitueret Ci-6-alkyl.
16. Forbindelse ifølge et hvilket som helst af kravene 1-15, hvor R3A er OH.
17. Forbindelse ifølge et hvilket som helst af kravene 1-15, hvor R3A er -OC(=O)R"A, R3A fortrinsvis er -OC(=O)R"A, hvor R"A er en eventuelt substitueret Ci-8-alkyl.
18. Forbindelse ifølge krav 17, hvor R"A er en ikke-substitueret Ci-s-alkyl.
19. Forbindelse ifølge et hvilket som helst af kravene 1-15, hvor R3A er en eventuelt substitueret O-bundet aminosyre, den O-bundne aminosyre fortrinsvis er valgt fra gruppen bestående af alanin, asparagin, aspartat, cystein, glutamat, glutamin, glycin, prolin, serin, tyrosin, arginin, histidin, isoleucin, leucin, lysin, methionin, phenylalanin, threonin, tryptophan, valin, ornithin, hypusin, 2-aminoisosmørsyre, dehydroalanin, gamma-aminosmørsyre, citrullin, beta-alanin, alfa-ethylglycin, alfa-propylglycin og norleucin; eller R3A er
hvor R42A er valgt fra gruppen bestående af hydrogen, en eventuelt substitueret Ci-6-alkyl, en eventuelt substitueret Ci-6-halogenalkyl, en eventuelt substitueret C3-6-cycloalkyl, en eventuelt substitueret C6~aryl, en eventuelt substitueret Cio-aryl og en eventuelt substitueret aryl (Ci-6-alkyl) , og R43A er hydrogen eller en eventuelt substitueret Ci-4-alkyl, eller R42A og R43A er taget sammen for at danne en eventuelt substitueret C3-6-cycloalkyl, R42A fortrinsvis er en eventuelt substitueret Ci-6-alkyl, R42A fortrinsvis er methyl, R43A fortrinsvis er hydrogen.
20. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er valgt fra gruppen bestående af:
eller et farmaceutisk acceptabelt salt af en hvilket som helst af de foregående forbindelser.
21. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er valgt fra gruppen bestående af:
eller et farmaceutisk acceptabelt salt af en hvilket som helst af de foregående forbindelser.
22. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er valgt fra gruppen bestående af:
eller et farmaceutisk acceptabelt salt af en hvilket som helst af de foregående forbindelser.
23. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er valgt fra gruppen bestående af:
eller et farmaceutisk acceptabelt salt af en hvilket som helst af de foregående forbindelser.
24. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
25. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
26. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
27. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
28. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
29. Forbindelse ifølge et hvilket som helst af kravene 24-28, hvor B1A er cytosin.
30. Forbindelse ifølge et hvilket som helst af kravene 24-28, hvor R1A er hydrogen, et monophosphat, et diphosphat eller et triphosphat.
31. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
32. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
33. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
34. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
35. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
36. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
37. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
38. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
39. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
40. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
41. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
42. Forbindelse ifølge krav 1, hvor forbindelsen med formlen (I) er
eller et farmaceutisk acceptabelt salt deraf.
43. Forbindelse, der har en struktur valgt fra gruppen bestående af:
eller et farmaceutisk acceptabelt salt af en hvilket som helst af de foregående forbindelser.
44. Farmaceutisk sammensætning, der omfatter en effektiv mængde af en forbindelse ifølge et hvilket som helst af kravene 1-43 eller et farmaceutisk acceptabelt salt deraf, og en farmaceutisk acceptabelt bærer, diluent, excipiens eller kombination deraf.
45. Forbindelse ifølge et hvilket som helst af kravene 1-43 til anvendelse til forbedring eller behandling af en viral infektion med paramyxovirus, fortrinsvis en pneumoviral infektion, fortrinsvis en human respiratorisk syncytialvirusinfektion.
46. Forbindelse ifølge et hvilket som helst af kravene 1-43 til anvendelse til hæmning af replikationen af en paramyxovirus, fortrinsvis en pneumoviral infektion, fortrinsvis en human respiratorisk syncytialvirusinfektion.
47. Forbindelse til anvendelse ifølge krav 45 eller 46 i kombination med et eller flere anti-RSV-midler.
48. Forbindelse til anvendelse ifølge krav 47, hvor det ene eller flere RSV-midler er valgt fra gruppen bestående af ribavirin, palivizumab, RSV-IGIV, ALN-RSV01, BMS-433771, RFI-641, RSV604, MDT-637, BTA9881, TMC-353121, MBX-300, YM-53403 og en RSV-F-partikelvaccine.
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