HRP20201769T1 - Spojevi 1-fenilpropanona i njihove uporabe - Google Patents
Spojevi 1-fenilpropanona i njihove uporabe Download PDFInfo
- Publication number
- HRP20201769T1 HRP20201769T1 HRP20201769TT HRP20201769T HRP20201769T1 HR P20201769 T1 HRP20201769 T1 HR P20201769T1 HR P20201769T T HRP20201769T T HR P20201769TT HR P20201769 T HRP20201769 T HR P20201769T HR P20201769 T1 HRP20201769 T1 HR P20201769T1
- Authority
- HR
- Croatia
- Prior art keywords
- compound
- phenyl
- propan
- methylpiperazin
- piperidin
- Prior art date
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- QCCDLTOVEPVEJK-UHFFFAOYSA-N phenylacetone Chemical class CC(=O)CC1=CC=CC=C1 QCCDLTOVEPVEJK-UHFFFAOYSA-N 0.000 title claims 4
- 150000001875 compounds Chemical class 0.000 claims 33
- -1 4-morpholyl Chemical group 0.000 claims 21
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 10
- 229910052717 sulfur Inorganic materials 0.000 claims 9
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 7
- 229910052711 selenium Inorganic materials 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 5
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 claims 4
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 claims 4
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 claims 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 4
- NLIRCCPCCRFQQB-UHFFFAOYSA-N 1-(4-heptoxyphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCCC)OC1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O NLIRCCPCCRFQQB-UHFFFAOYSA-N 0.000 claims 4
- OJBZYLXALQSOCF-UHFFFAOYSA-N 1-(4-heptylphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCCC)C1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O OJBZYLXALQSOCF-UHFFFAOYSA-N 0.000 claims 4
- NZVIPIOEHZCUPC-UHFFFAOYSA-N 1-(4-heptylphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C(CCCCCC)C1=CC=C(C=C1)C(CCN1CCOCC1)=O NZVIPIOEHZCUPC-UHFFFAOYSA-N 0.000 claims 4
- DYKACALDGQXIQC-UHFFFAOYSA-N 1-(4-heptylselanylphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCCC)[Se]C1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O DYKACALDGQXIQC-UHFFFAOYSA-N 0.000 claims 4
- OXJWQNHWZFNERF-UHFFFAOYSA-N 1-(4-heptylselanylphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C(CCCCCC)[Se]C1=CC=C(C=C1)C(CCN1CCOCC1)=O OXJWQNHWZFNERF-UHFFFAOYSA-N 0.000 claims 4
- PJQKKHOHAOAJKV-UHFFFAOYSA-N 1-(4-heptylselanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C(CCCCCC)[Se]C1=CC=C(C=C1)C(CCN1CCCCC1)=O PJQKKHOHAOAJKV-UHFFFAOYSA-N 0.000 claims 4
- SHNQCTQKJYTOTL-UHFFFAOYSA-N 1-(4-heptylsulfanylphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCCC)SC1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O SHNQCTQKJYTOTL-UHFFFAOYSA-N 0.000 claims 4
- NIFWAIYELZWMOM-UHFFFAOYSA-N 1-(4-heptylsulfanylphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C(CCCCCC)SC1=CC=C(C=C1)C(CCN1CCOCC1)=O NIFWAIYELZWMOM-UHFFFAOYSA-N 0.000 claims 4
- IKVQHWQLXZLIDS-UHFFFAOYSA-N 1-(4-heptylsulfanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C(CCCCCC)SC1=CC=C(C=C1)C(CCN1CCCCC1)=O IKVQHWQLXZLIDS-UHFFFAOYSA-N 0.000 claims 4
- JWTFTGVGPNLKIM-UHFFFAOYSA-N 1-(4-hexylsulfanylphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCC)SC1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O JWTFTGVGPNLKIM-UHFFFAOYSA-N 0.000 claims 4
- RYSHHRGWRYZJMC-UHFFFAOYSA-N 1-(4-pentylsulfanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C(CCCC)SC1=CC=C(C=C1)C(CCN1CCCCC1)=O RYSHHRGWRYZJMC-UHFFFAOYSA-N 0.000 claims 4
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 claims 4
- YSUIQYOGTINQIN-UZFYAQMZSA-N 2-amino-9-[(1S,6R,8R,9S,10R,15R,17R,18R)-8-(6-aminopurin-9-yl)-9,18-difluoro-3,12-dihydroxy-3,12-bis(sulfanylidene)-2,4,7,11,13,16-hexaoxa-3lambda5,12lambda5-diphosphatricyclo[13.2.1.06,10]octadecan-17-yl]-1H-purin-6-one Chemical compound NC1=NC2=C(N=CN2[C@@H]2O[C@@H]3COP(S)(=O)O[C@@H]4[C@@H](COP(S)(=O)O[C@@H]2[C@@H]3F)O[C@H]([C@H]4F)N2C=NC3=C2N=CN=C3N)C(=O)N1 YSUIQYOGTINQIN-UZFYAQMZSA-N 0.000 claims 4
- 229940126657 Compound 17 Drugs 0.000 claims 4
- XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 claims 4
- KGNDCEVUMONOKF-UGPLYTSKSA-N benzyl n-[(2r)-1-[(2s,4r)-2-[[(2s)-6-amino-1-(1,3-benzoxazol-2-yl)-1,1-dihydroxyhexan-2-yl]carbamoyl]-4-[(4-methylphenyl)methoxy]pyrrolidin-1-yl]-1-oxo-4-phenylbutan-2-yl]carbamate Chemical compound C1=CC(C)=CC=C1CO[C@H]1CN(C(=O)[C@@H](CCC=2C=CC=CC=2)NC(=O)OCC=2C=CC=CC=2)[C@H](C(=O)N[C@@H](CCCCN)C(O)(O)C=2OC3=CC=CC=C3N=2)C1 KGNDCEVUMONOKF-UGPLYTSKSA-N 0.000 claims 4
- 229940126543 compound 14 Drugs 0.000 claims 4
- 229940125810 compound 20 Drugs 0.000 claims 4
- 229940125833 compound 23 Drugs 0.000 claims 4
- 229940125961 compound 24 Drugs 0.000 claims 4
- 229940125898 compound 5 Drugs 0.000 claims 4
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 claims 3
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 claims 3
- WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 claims 3
- LILYNRBMVRCYOX-UHFFFAOYSA-N 1-(4-hexylselanylphenyl)-3-(4-methylpiperazin-1-yl)propan-1-one Chemical compound C(CCCCC)[Se]C1=CC=C(C=C1)C(CCN1CCN(CC1)C)=O LILYNRBMVRCYOX-UHFFFAOYSA-N 0.000 claims 3
- YWTBLUBXRRJDEQ-UHFFFAOYSA-N 1-(4-hexylselanylphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C(CCCCC)[Se]C1=CC=C(C=C1)C(CCN1CCOCC1)=O YWTBLUBXRRJDEQ-UHFFFAOYSA-N 0.000 claims 3
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 claims 3
- GXXQFLLZTNUSLD-UHFFFAOYSA-N 3-(4-methylpiperazin-1-yl)-1-(4-pentylselanylphenyl)propan-1-one Chemical compound CN1CCN(CC1)CCC(=O)C1=CC=C(C=C1)[Se]CCCCC GXXQFLLZTNUSLD-UHFFFAOYSA-N 0.000 claims 3
- YFNJVZDFFGTZIR-UHFFFAOYSA-N 3-(4-methylpiperazin-1-yl)-1-(4-pentylsulfanylphenyl)propan-1-one Chemical compound CN1CCN(CC1)CCC(=O)C1=CC=C(C=C1)SCCCCC YFNJVZDFFGTZIR-UHFFFAOYSA-N 0.000 claims 3
- FECOIOFQIQOMNN-UHFFFAOYSA-N 3-morpholin-4-yl-1-(4-pentylselanylphenyl)propan-1-one Chemical compound O1CCN(CC1)CCC(=O)C1=CC=C(C=C1)[Se]CCCCC FECOIOFQIQOMNN-UHFFFAOYSA-N 0.000 claims 3
- KAYLAACFSGZSCT-UHFFFAOYSA-N 3-morpholin-4-yl-1-(4-pentylsulfanylphenyl)propan-1-one Chemical compound O1CCN(CC1)CCC(=O)C1=CC=C(C=C1)SCCCCC KAYLAACFSGZSCT-UHFFFAOYSA-N 0.000 claims 3
- OPFJDXRVMFKJJO-ZHHKINOHSA-N N-{[3-(2-benzamido-4-methyl-1,3-thiazol-5-yl)-pyrazol-5-yl]carbonyl}-G-dR-G-dD-dD-dD-NH2 Chemical compound S1C(C=2NN=C(C=2)C(=O)NCC(=O)N[C@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(O)=O)C(N)=O)=C(C)N=C1NC(=O)C1=CC=CC=C1 OPFJDXRVMFKJJO-ZHHKINOHSA-N 0.000 claims 3
- 229940125797 compound 12 Drugs 0.000 claims 3
- 229940125758 compound 15 Drugs 0.000 claims 3
- 229940126142 compound 16 Drugs 0.000 claims 3
- 229940126086 compound 21 Drugs 0.000 claims 3
- 229940126208 compound 22 Drugs 0.000 claims 3
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 claims 2
- MGBSEAVFZLXRPF-UHFFFAOYSA-N 1-(4-heptoxyphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C1=CC(OCCCCCCC)=CC=C1C(=O)CCN1CCCCC1 MGBSEAVFZLXRPF-UHFFFAOYSA-N 0.000 claims 2
- TYZVDSJPWONVCP-UHFFFAOYSA-N 1-(4-heptylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C1=CC(CCCCCCC)=CC=C1C(=O)CCN1CCCCC1 TYZVDSJPWONVCP-UHFFFAOYSA-N 0.000 claims 2
- ZGFOUPARLAVRJX-UHFFFAOYSA-N 1-(4-hexylselanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C1=CC([Se]CCCCCC)=CC=C1C(=O)CCN1CCCCC1 ZGFOUPARLAVRJX-UHFFFAOYSA-N 0.000 claims 2
- GLKNBGOKXZJIAF-UHFFFAOYSA-N 1-(4-hexylsulfanylphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C(CCCCC)SC1=CC=C(C=C1)C(CCN1CCOCC1)=O GLKNBGOKXZJIAF-UHFFFAOYSA-N 0.000 claims 2
- SPPTXAJILJYJLY-UHFFFAOYSA-N 1-(4-hexylsulfanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C(CCCCC)SC1=CC=C(C=C1)C(CCN1CCCCC1)=O SPPTXAJILJYJLY-UHFFFAOYSA-N 0.000 claims 2
- DLICCFGCIMONFN-UHFFFAOYSA-N 1-(4-pentylselanylphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C1=CC([Se]CCCCC)=CC=C1C(=O)CCN1CCCCC1 DLICCFGCIMONFN-UHFFFAOYSA-N 0.000 claims 2
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 claims 2
- 208000010839 B-cell chronic lymphocytic leukemia Diseases 0.000 claims 2
- 206010006187 Breast cancer Diseases 0.000 claims 2
- 208000026310 Breast neoplasm Diseases 0.000 claims 2
- 208000031422 Lymphocytic Chronic B-Cell Leukemia Diseases 0.000 claims 2
- 206010029260 Neuroblastoma Diseases 0.000 claims 2
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 claims 2
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 208000032852 chronic lymphocytic leukemia Diseases 0.000 claims 2
- 229940125773 compound 10 Drugs 0.000 claims 2
- 229940125846 compound 25 Drugs 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 claims 2
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 claims 2
- FQBHGHZOLYJZGY-UHFFFAOYSA-N 1-(4-heptoxyphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C1=CC(OCCCCCCC)=CC=C1C(=O)CCN1CCOCC1 FQBHGHZOLYJZGY-UHFFFAOYSA-N 0.000 claims 1
- VJZCZCUEZMGVCL-UHFFFAOYSA-N 1-(4-hexoxyphenyl)-3-morpholin-4-ylpropan-1-one Chemical compound C1=CC(OCCCCCC)=CC=C1C(=O)CCN1CCOCC1 VJZCZCUEZMGVCL-UHFFFAOYSA-N 0.000 claims 1
- WXYWMSOSIIBMMM-UHFFFAOYSA-N 1-(4-hexoxyphenyl)-3-piperidin-1-ylpropan-1-one Chemical compound C1=CC(OCCCCCC)=CC=C1C(=O)CCN1CCCCC1 WXYWMSOSIIBMMM-UHFFFAOYSA-N 0.000 claims 1
- 230000000259 anti-tumor effect Effects 0.000 claims 1
- 229940125904 compound 1 Drugs 0.000 claims 1
- 229940125782 compound 2 Drugs 0.000 claims 1
- 229940126214 compound 3 Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
Classifications
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4453—Non condensed piperidines, e.g. piperocaine only substituted in position 1, e.g. propipocaine, diperodon
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/4965—Non-condensed pyrazines
-
- 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
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- A—HUMAN NECESSITIES
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Claims (15)
1. Spoj 1-fenilpropanona formule (I)
[image]
ili njegova farmaceutski prihvatljiva sol
pri čemu:
X je metilen skupina (-CH2-) ili atom odabran od skupine koja se sastoji od O, S i Se,
n je cijeli broj od 4 do 6,
A je supstituent odabran od skupine koja se sastoji od 4-morfolila, 1-piperidinila i 4-metil-1-piperazinila, te je izborno supstituiran s (C1-C3)alkilom ili (C1-C3)acil radikalom,
uz uvjet da kad X je CH2, n je jednak 5,
za uporabu kao antitumorski agens u liječenju raka dojke, kronične limfocitne leukemije ili neuroblastoma.
2. Spoj za uporabu prema zahtjevu 1, pri čemu X je S, Se ili CH2, poželjno S.
3. Spoj za uporabu prema zahtjevu 1 ili 2, pri čemu n je 5 ili 6.
4. Spoj za uporabu prema zahtjevu 1, pri čemu je spomenuti spoj odabran od skupine koja se sastoji od:
Spoj 1 (AF08), 1-(4-(heksiloksi)fenil)-3-morfolinopropan-1-on,
Spoj 2 (CC11) 1-(4-(heptiloksi)fenil)-3-morfolinopropan-1-on
Spoj 3 (AF07), 1-(4-(heksiloksi)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 4 (CC12), 1-(4-(heptiloksi)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 5 (AI01), 1-(4-(heptiloksi)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 6 (MD63), 3-morfolino-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 7 (VP158), 1-(4-(heksiltio)fenil)-3-morfolinopropan-1-on,
Spoj 8 (FT017), 1-(4-(heptiltio)fenil)-3-morfolinopropan-1-on,
Spoj 9 (MC12), 1-(4-(pentiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 10 (VP157), 1-(4-(heksiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 11 (FT018), 1-(4-(heptiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 12 (FT013), 3-(4-metilpiperazin-1-il)-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 13 (FT016), 1-(4-(heksiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 14 (FT019), 1-(4-(heptiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 15 (GR376), 3-morfolino-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 16 (GR377), 1-(4-(heksilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 17 (GR386), 1-(4-(heptilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 18 (GR378), 1-(4-(pentilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 19 (GR381), 1-(4-(heksilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 20 (GR387), 1-(4-(heptilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 21 (GR379), 3-(4-metilpiperazin-1-il)-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 22 (GR383), 1-(4-(heksilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 23 (GR388), 1-(4-(heptilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 24 (GR390), 1-(4-heptilfenil)-3-morfolinopropan-1-on,
Spoj 25 (GR391), 1-(4-heptilfenil)-3-(piperidin-1-il)propan-1-on, te
Spoj 26 (GR392), 1-(4-heptilfenil)-3-(4-metilpiperazin-1-il)propan-1-on.
5. Spoj 1-fenilpropanona formule (I)
[image]
ili njegova farmaceutski prihvatljiva sol
pri čemu:
X je metilen skupina (-CH2-) ili atom odabran od skupine koja se sastoji od O, S i Se,
n je cijeli broj od 4 do 6,
A je supstituent odabran od skupine koja se sastoji od 4-morfolila, 1-piperidinila i 4-metil-1-piperazinila, te je izborno supstituiran s (C1-C3)alkilom ili (C1-C3)acil radikalom,
uz uvjet da
kad X je O, A je 4-metil-1-piperazinil, te n je jednak 6,
kad X je S i n je 5, tad A je 4-metil-1-piperazinil,
kad X je Se i A je 1-piperidinil, tad n je 6,
kad X je CH2, n je jednak 5, te A je 4-metil-1-piperazinil ili 4-morfolil.
6. Spoj za uporabu prema zahtjevu 5, pri čemu X je odabran od skupine koja se sastoji od S, Se ili CH2, poželjno S.
7. Spoj za uporabu prema zahtjevu 5 ili 6, pri čemu n je 5 ili 6.
8. Spoj prema zahtjevu 6, pri čemu je spomenuti spoj odabran od skupine koja se sastoji od:
Spoj 5 (AI01), 1-(4-(heptiloksi)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 6 (MD63), 3-morfolino-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 8 (FT017), 1-(4-(heptiltio)fenil)-3-morfolinopropan-1-on,
Spoj 9 (MC12), 1-(4-(pentiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 11 (FT018), 1-(4-(heptiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 12 (FT013), 3-(4-metilpiperazin-1-il)-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 13 (FT016), 1-(4-(heksiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 14 (FT019), 1-(4-(heptiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 15 (GR376), 3-morfolino-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 16 (GR377), 1-(4-(heksilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 17 (GR386), 1-(4-(heptilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 20 (GR387), 1-(4-(heptilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 21 (GR379), 3-(4-metilpiperazin-1-il)-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 22 (GR383), 1-(4-(heksilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 23 (GR388), 1-(4-(heptilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 24 (GR390), 1-(4-heptilfenil)-3-morfolinopropan-1-on, te
Spoj 26 (GR392), 1-(4-heptilfenil)-3-(4-metilpiperazin-1-il)propan-1-on.
9. Spoj prema zahtjevu 8, pri čemu je spomenuti spoj odabran od skupine koja se sastoji od:
Spoj 5 (AI01), 1-(4-(heptiloksi)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 8 (FT017), 1-(4-(heptiltio)fenil)-3-morfolinopropan-1-on,
Spoj 9 (MC12), 1-(4-(pentiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 11 (FT018), 1-(4-(heptiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 13 (FT016), 1-(4-(heksiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 14 (FT019), 1-(4-(heptiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 17 (GR386), 1-(4-(heptilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 20 (GR387), 1-(4-(heptilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 23 (GR388), 1-(4-(heptilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 24 (GR390), 1-(4-heptilfenil)-3-morfolinopropan-1-on, te
Spoj 26 (GR392), 1-(4-heptilfenil)-3-(4-metilpiperazin-1-il)propan-1-on.
10. Spoj formule (I)
[image]
ili njegova farmaceutski prihvatljiva sol
pri čemu:
X je metilen skupina (-CH2-) ili atom odabran od skupine koja se sastoji od O, S i Se,
n je cijeli broj od 4 do 6,
A je supstituent odabran od skupine koja se sastoji od 4-morfolila, 1-piperidinila i 4-metil-1-piperazinila, te je izborno supstituiran s (C1-C3)alkilom ili (C1-C3)acil radikalom,
uz uvjet da
kad X je O, A je 4-metil-1-piperazinil, te n je jednak 6,
kad X je S i n je 5, tad A je 4-metil-1-piperazinil ili 4-morfolil, 5 kad X je Se i A je 1-piperidinil,
tad n je 6,
kad X je CH2, n je jednak 5, te A je 4-metil-1-piperazinil ili 4-morfolil, za uporabu kao lijek.
11. Farmaceutski sastav koji sadrži spoj prema formuli iz zahtjeva 10 ili njegovu farmaceutski prihvatljivu sol i farmaceutski prihvatljivi nosač za uporabu kao lijek.
12. Spoj formule (I)
[image]
ili njegova farmaceutski prihvatljiva sol
pri čemu:
X je metilen skupina (-CH2-) ili atom odabran od skupine koja se sastoji od O, S i Se,
n je cijeli broj od 4 do 6,
A je supstituent odabran od skupine koja se sastoji od 4-morfolila, 1-piperidinila i 4-metil-1-piperazinila, te je izborno supstituiran s (C1-C3)alkilom ili (C1-C3)acil radikalom,
uz uvjet da
kad X je O, A je 4-metil-1-piperazinil ili 1-piperidinil, te n je jednak 6,
kad X je CH2, n je 5
za uporabu kao antitumorski agens.
13. Spoj za uporabu prema zahtjevu 12, pri čemu je antitumorsko liječenje protiv raka dojke, hepatokarcinoma, kronične limfocitne leukemije ili neuroblastoma.
14. Spoj za uporabu prema zahtjevu 12 ili 13, pri čemu je X odabran od skupine koja se sastoji od S, Se ili CH2, poželjno S.
15. Spoj za uporabu prema zahtjevu 12, pri čemu je spoj 1-fenilpropanona odabran od skupine koja se sastoji od:
Spoj 4 (CC12), 1-(4-(heptiloksi)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 5 (AI01), 1-(4-(heptiloksi)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 6 (MD63), 3-morfolino-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 7 (VP158), 1-(4-(heksiltio)fenil)-3-morfolinopropan-1-on,
Spoj 8 (FT017), 1-(4-(heptiltio)fenil)-3-morfolinopropan-1-on,
Spoj 9 (MC12), 1-(4-(pentiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 10 (VP157), 1-(4-(heksiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 11 (FT018), 1-(4-(heptiltio)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 12 (FT013), 3-(4-metilpiperazin-1-il)-1-(4-(pentiltio)fenil)propan-1-on,
Spoj 13 (FT016), 1-(4-(heksiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 14 (FT019), 1-(4-(heptiltio)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 15 (GR376), 3-morfolino-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 16 (GR377), 1-(4-(heksilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 17 (GR386), 1-(4-(heptilselenil)fenil)-3-morfolinopropan-1-on,
Spoj 18 (GR378), 1-(4-(pentilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 19 (GR381), 1-(4-(heksilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 20 (GR387), 1-(4-(heptilselenil)fenil)-3-(piperidin-1-il)propan-1-on,
Spoj 21 (GR379), 3-(4-metilpiperazin-1-il)-1-(4-(pentilselenil)fenil)propan-1-on,
Spoj 22 (GR383), 1-(4-(heksilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 23 (GR388), 1-(4-(heptilselenil)fenil)-3-(4-metilpiperazin-1-il)propan-1-on,
Spoj 24 (GR390), 1-(4-heptilfenil)-3-morfolinopropan-1-on,
Spoj 25 (GR391), 1-(4-heptilfenil)-3-(piperidin-1-il)propan-1-on, te
Spoj 26 (GR392), 1-(4-heptilfenil)-3-(4-metilpiperazin-1-il)propan-1-on.
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IT102016000098338A IT201600098338A1 (it) | 2016-09-30 | 2016-09-30 | Composti 1-fenilpropanone e loro impiego |
EP17791160.9A EP3518927B9 (en) | 2016-09-30 | 2017-09-29 | 1-phenylpropanone compounds and use thereof |
PCT/IB2017/056010 WO2018060947A1 (en) | 2016-09-30 | 2017-09-29 | 1-phenylpropanone compounds and use thereof |
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JPS54125630A (en) * | 1978-02-22 | 1979-09-29 | Nippon Zoki Pharmaceutical Co | Novel propanone derivative*its manufacture and medical composition containing it as active component |
DE2842091A1 (de) * | 1978-09-27 | 1980-04-10 | Dow Chemical Co | Verfahren zur inaktivierung behuellter viren |
JPS5549317A (en) * | 1978-10-02 | 1980-04-09 | Dow Chemical Co | Control of virus surrounded with phenylketones |
US4931473A (en) * | 1989-02-15 | 1990-06-05 | Richardson-Vicks Inc. | Anesthetic oral compositions |
AU7847800A (en) | 1999-10-15 | 2001-04-30 | Mayo Foundation For Medical Education And Research | Topical anesthetics useful for treating cancer, autoimmune diseases and ischemia |
ES2414205T3 (es) * | 2006-06-02 | 2013-07-18 | The Ohio State University Research Foundation | Agentes terapéuticos para el tratamiento de linfoma de células del manto |
FR2902789A1 (fr) * | 2006-06-21 | 2007-12-28 | Genfit Sa | Derives de 1,3-diphenylpropane substitues, preparations et utilisations |
US20100285001A1 (en) * | 2007-10-02 | 2010-11-11 | University Of Rochester | Method and Compositions Related to Synergistic Responses to Oncogenic Mutations |
US8309768B2 (en) * | 2010-11-29 | 2012-11-13 | The Ohio State University Research Foundation | FTY720-derived anticancer agents |
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ES2830749T3 (es) | 2021-06-04 |
HUE052039T2 (hu) | 2021-04-28 |
US11345673B2 (en) | 2022-05-31 |
RU2019113064A (ru) | 2020-10-30 |
SI3518927T1 (sl) | 2021-01-29 |
RU2765102C2 (ru) | 2022-01-25 |
CA3038008A1 (en) | 2018-04-05 |
IT201600098338A1 (it) | 2018-03-30 |
BR112019006565A2 (pt) | 2019-07-02 |
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