EA022459B1 - Производные транилципромина в качестве ингибиторов гистон деметилаз lsd1 и/или lsd2 - Google Patents
Производные транилципромина в качестве ингибиторов гистон деметилаз lsd1 и/или lsd2 Download PDFInfo
- Publication number
- EA022459B1 EA022459B1 EA201291073A EA201291073A EA022459B1 EA 022459 B1 EA022459 B1 EA 022459B1 EA 201291073 A EA201291073 A EA 201291073A EA 201291073 A EA201291073 A EA 201291073A EA 022459 B1 EA022459 B1 EA 022459B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- aminocyclopropyl
- trans
- benzyl
- phenylamino
- ylcarbamate
- Prior art date
Links
- 102000008157 Histone Demethylases Human genes 0.000 title claims description 4
- 108010074870 Histone Demethylases Proteins 0.000 title claims description 4
- 239000003112 inhibitor Substances 0.000 title claims 2
- IGLYMJRIWWIQQE-QUOODJBBSA-N (1S,2R)-2-phenylcyclopropan-1-amine (1R,2S)-2-phenylcyclopropan-1-amine Chemical class N[C@H]1C[C@@H]1C1=CC=CC=C1.N[C@@H]1C[C@H]1C1=CC=CC=C1 IGLYMJRIWWIQQE-QUOODJBBSA-N 0.000 title abstract description 3
- 101100334370 Schizosaccharomyces pombe (strain 972 / ATCC 24843) fas2 gene Proteins 0.000 title 1
- 101100455527 Schizosaccharomyces pombe (strain 972 / ATCC 24843) lsd2 gene Proteins 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 29
- 201000010099 disease Diseases 0.000 claims abstract description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 8
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 4
- 230000002265 prevention Effects 0.000 claims abstract description 4
- 208000036142 Viral infection Diseases 0.000 claims abstract description 3
- 239000003814 drug Substances 0.000 claims abstract description 3
- 230000000694 effects Effects 0.000 claims abstract description 3
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 3
- 238000013518 transcription Methods 0.000 claims abstract description 3
- 230000035897 transcription Effects 0.000 claims abstract description 3
- 230000009385 viral infection Effects 0.000 claims abstract description 3
- 230000004069 differentiation Effects 0.000 claims description 2
- 230000008482 dysregulation Effects 0.000 claims description 2
- -1 benzyloxy, benzyl Chemical group 0.000 claims 11
- 238000000034 method Methods 0.000 claims 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 125000001246 bromo group Chemical group Br* 0.000 claims 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 4
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 125000006239 protecting group Chemical group 0.000 claims 3
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 2
- 206010005003 Bladder cancer Diseases 0.000 claims 2
- 206010006187 Breast cancer Diseases 0.000 claims 2
- 208000026310 Breast neoplasm Diseases 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 2
- 208000009889 Herpes Simplex Diseases 0.000 claims 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 2
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 2
- 206010029260 Neuroblastoma Diseases 0.000 claims 2
- 206010060862 Prostate cancer Diseases 0.000 claims 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 2
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 2
- 239000002246 antineoplastic agent Substances 0.000 claims 2
- 239000003443 antiviral agent Substances 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 2
- 239000004305 biphenyl Chemical group 0.000 claims 2
- 235000010290 biphenyl Nutrition 0.000 claims 2
- 210000004027 cell Anatomy 0.000 claims 2
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000006301 indolyl methyl group Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 201000005202 lung cancer Diseases 0.000 claims 2
- 208000020816 lung neoplasm Diseases 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 1
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 1
- 208000009052 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 1
- 208000029052 T-cell acute lymphoblastic leukemia Diseases 0.000 claims 1
- BBFSSGWGPSUYCK-XAGPSQNTSA-N [1-[4-[(1S,2R)-2-aminocyclopropyl]anilino]-1-oxo-3-phenylpropan-2-yl]-[(4-bromophenyl)methyl]carbamic acid Chemical compound N[C@@H]1C[C@H]1c1ccc(NC(=O)C(Cc2ccccc2)N(Cc2ccc(Br)cc2)C(O)=O)cc1 BBFSSGWGPSUYCK-XAGPSQNTSA-N 0.000 claims 1
- 230000001154 acute effect Effects 0.000 claims 1
- WHQIXYSISIAXMR-ZXABPTRBSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]-n-methylanilino]-1-oxo-3-phenylpropan-2-yl]carbamate Chemical compound C=1C=C([C@H]2[C@@H](C2)N)C=CC=1N(C)C(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WHQIXYSISIAXMR-ZXABPTRBSA-N 0.000 claims 1
- ASLBWLIVSCJXGE-VXLAJHQFSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-1-oxo-3,3-diphenylpropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(C(C=1C=CC=CC=1)C=1C=CC=CC=1)NC(=O)OCC1=CC=CC=C1 ASLBWLIVSCJXGE-VXLAJHQFSA-N 0.000 claims 1
- HDVDLEPVLVTECB-XAGPSQNTSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-1-oxo-3-phenylpropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 HDVDLEPVLVTECB-XAGPSQNTSA-N 0.000 claims 1
- QLBXSMSHSPUCHK-ZXABPTRBSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-1-oxo-4-phenylbutan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CCC1=CC=CC=C1 QLBXSMSHSPUCHK-ZXABPTRBSA-N 0.000 claims 1
- MTRYTBUOCQFRLH-XAGPSQNTSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-(4-bromophenyl)-1-oxopropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1=CC=C(Br)C=C1 MTRYTBUOCQFRLH-XAGPSQNTSA-N 0.000 claims 1
- PBWBVFCDMWLZOQ-ZXABPTRBSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-(4-methoxyphenyl)-1-oxopropan-2-yl]carbamate Chemical compound C1=CC(OC)=CC=C1CC(C(=O)NC=1C=CC(=CC=1)[C@H]1[C@@H](C1)N)NC(=O)OCC1=CC=CC=C1 PBWBVFCDMWLZOQ-ZXABPTRBSA-N 0.000 claims 1
- MXXUWNXLDQSFIG-XAGPSQNTSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-cyclohexyl-1-oxopropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1CCCCC1 MXXUWNXLDQSFIG-XAGPSQNTSA-N 0.000 claims 1
- DDNLQJBLMBTXLP-ABZYKWASSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C=1C=C([C@H]2[C@@H](C2)N)C=CC=1NC(=O)C(C(C)C)NC(=O)OCC1=CC=CC=C1 DDNLQJBLMBTXLP-ABZYKWASSA-N 0.000 claims 1
- MXIJEHVOYGTOKM-MDEZFMAYSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-naphthalen-1-yl-1-oxopropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC2=CC=CC=C12 MXIJEHVOYGTOKM-MDEZFMAYSA-N 0.000 claims 1
- QGICAEAHSKDUIT-MDEZFMAYSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-3-naphthalen-2-yl-1-oxopropan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CC1=CC=C(C=CC=C2)C2=C1 QGICAEAHSKDUIT-MDEZFMAYSA-N 0.000 claims 1
- MEUKJABSFDBHKI-LHJLODMPSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-4-(1-benzothiophen-3-yl)-1-oxobutan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CCC1=CSC2=CC=CC=C12 MEUKJABSFDBHKI-LHJLODMPSA-N 0.000 claims 1
- ZODMCOGPPKFWDE-QDSWCARHSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-4-(1h-indol-3-yl)-1-oxobutan-2-yl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(NC(=O)OCC=1C=CC=CC=1)CCC1=CNC2=CC=CC=C12 ZODMCOGPPKFWDE-QDSWCARHSA-N 0.000 claims 1
- DSONMQMFFYCVKT-MCOCGALXSA-N benzyl n-[1-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-4-methyl-1-oxopentan-2-yl]carbamate Chemical compound C=1C=C([C@H]2[C@@H](C2)N)C=CC=1NC(=O)C(CC(C)C)NC(=O)OCC1=CC=CC=C1 DSONMQMFFYCVKT-MCOCGALXSA-N 0.000 claims 1
- PQSQVGJMIYHPAM-ZVTBYLAHSA-N benzyl n-[2-[4-[(1s,2r)-2-aminocyclopropyl]anilino]-2-oxo-1-phenylethyl]carbamate Chemical compound N[C@@H]1C[C@H]1C(C=C1)=CC=C1NC(=O)C(C=1C=CC=CC=1)NC(=O)OCC1=CC=CC=C1 PQSQVGJMIYHPAM-ZVTBYLAHSA-N 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 208000003747 lymphoid leukemia Diseases 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- FFYGOYSNGFPHEN-UHFFFAOYSA-N n-[4-(2-aminocyclopropyl)phenyl]benzamide Chemical compound NC1CC1C(C=C1)=CC=C1NC(=O)C1=CC=CC=C1 FFYGOYSNGFPHEN-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 230000000861 pro-apoptotic effect Effects 0.000 claims 1
- 230000035755 proliferation Effects 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 230000004663 cell proliferation Effects 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 229940124597 therapeutic agent Drugs 0.000 abstract description 2
- 230000001225 therapeutic effect Effects 0.000 abstract description 2
- 101000619676 Drosophila melanogaster Lipid storage droplets surface-binding protein 2 Proteins 0.000 abstract 1
- 101001050886 Homo sapiens Lysine-specific histone demethylase 1A Proteins 0.000 abstract 1
- 101000613960 Homo sapiens Lysine-specific histone demethylase 1B Proteins 0.000 abstract 1
- 102100040596 Lysine-specific histone demethylase 1B Human genes 0.000 abstract 1
- 230000024245 cell differentiation Effects 0.000 abstract 1
- 230000003831 deregulation Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
-
- 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
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/44—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a carbon atom of an unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/77—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/80—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/20—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
- C07C275/24—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/54—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D333/60—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Hematology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32595210P | 2010-04-20 | 2010-04-20 | |
| PCT/EP2011/055990 WO2011131576A1 (en) | 2010-04-20 | 2011-04-15 | Tranylcypromine derivatives as inhibitors of histone demethylase lsd1 and/or lsd2 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA201291073A1 EA201291073A1 (ru) | 2013-10-30 |
| EA022459B1 true EA022459B1 (ru) | 2016-01-29 |
Family
ID=43929076
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201291073A EA022459B1 (ru) | 2010-04-20 | 2011-04-15 | Производные транилципромина в качестве ингибиторов гистон деметилаз lsd1 и/или lsd2 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8765820B2 (enExample) |
| EP (1) | EP2560949B1 (enExample) |
| JP (1) | JP5934184B2 (enExample) |
| CN (1) | CN102985402B (enExample) |
| AU (1) | AU2011244478B2 (enExample) |
| BR (1) | BR112012027062B8 (enExample) |
| CA (1) | CA2797011C (enExample) |
| EA (1) | EA022459B1 (enExample) |
| ES (1) | ES2564352T3 (enExample) |
| PL (1) | PL2560949T3 (enExample) |
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| CN102985402B (zh) | 2015-04-29 |
| CA2797011C (en) | 2018-10-02 |
| US20130035377A1 (en) | 2013-02-07 |
| ZA201207856B (en) | 2013-06-29 |
| WO2011131576A1 (en) | 2011-10-27 |
| EP2560949B1 (en) | 2015-12-02 |
| BR112012027062A2 (pt) | 2017-03-14 |
| CA2797011A1 (en) | 2011-10-27 |
| BR112012027062B8 (pt) | 2021-05-25 |
| PL2560949T3 (pl) | 2017-01-31 |
| CN102985402A (zh) | 2013-03-20 |
| ES2564352T3 (es) | 2016-03-22 |
| JP5934184B2 (ja) | 2016-06-15 |
| US8765820B2 (en) | 2014-07-01 |
| JP2013525318A (ja) | 2013-06-20 |
| BR112012027062B1 (pt) | 2021-04-20 |
| EP2560949A1 (en) | 2013-02-27 |
| AU2011244478B2 (en) | 2014-07-17 |
| AU2011244478A1 (en) | 2012-11-01 |
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