CA1291990C - Antiatherosclerotic tetrasubstituted ureas and thioureas - Google Patents
Antiatherosclerotic tetrasubstituted ureas and thioureasInfo
- Publication number
- CA1291990C CA1291990C CA000416765A CA416765A CA1291990C CA 1291990 C CA1291990 C CA 1291990C CA 000416765 A CA000416765 A CA 000416765A CA 416765 A CA416765 A CA 416765A CA 1291990 C CA1291990 C CA 1291990C
- Authority
- CA
- Canada
- Prior art keywords
- benzyl
- butyl
- compound
- phenylurea
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 150000003585 thioureas Chemical class 0.000 title abstract description 18
- 150000003672 ureas Chemical class 0.000 title abstract description 16
- 230000000879 anti-atherosclerotic effect Effects 0.000 title abstract description 10
- 235000013877 carbamide Nutrition 0.000 title description 22
- 150000001875 compounds Chemical class 0.000 claims description 56
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 40
- -1 phenoxy, mercapto Chemical class 0.000 claims description 34
- 241000124008 Mammalia Species 0.000 claims description 19
- 235000012000 cholesterol Nutrition 0.000 claims description 17
- 230000003902 lesion Effects 0.000 claims description 14
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 10
- 125000001424 substituent group Chemical group 0.000 claims description 10
- 230000003143 atherosclerotic effect Effects 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- 208000031226 Hyperlipidaemia Diseases 0.000 claims description 8
- 150000004982 aromatic amines Chemical class 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 150000003335 secondary amines Chemical class 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 7
- 239000003937 drug carrier Substances 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 4
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- ARYSHHMZECOUSD-UHFFFAOYSA-N 1,1-dibutyl-3,3-bis(3-chloro-4-methylphenyl)urea Chemical compound C=1C=C(C)C(Cl)=CC=1N(C(=O)N(CCCC)CCCC)C1=CC=C(C)C(Cl)=C1 ARYSHHMZECOUSD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000006277 halobenzyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 5
- 231100000252 nontoxic Toxicity 0.000 claims 4
- 230000003000 nontoxic effect Effects 0.000 claims 4
- 150000001840 cholesterol esters Chemical class 0.000 claims 3
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims 1
- GGASLBIKCHDXIR-UHFFFAOYSA-N 1,1-dibenzyl-3,3-bis(2,4-dimethylphenyl)urea Chemical compound CC1=CC(C)=CC=C1N(C=1C(=CC(C)=CC=1)C)C(=O)N(CC=1C=CC=CC=1)CC1=CC=CC=C1 GGASLBIKCHDXIR-UHFFFAOYSA-N 0.000 claims 1
- OGYFEVHYAAMGOC-UHFFFAOYSA-N 1,1-dibenzyl-3,3-bis(3-chloro-4-methylphenyl)urea Chemical compound C1=C(Cl)C(C)=CC=C1N(C=1C=C(Cl)C(C)=CC=1)C(=O)N(CC=1C=CC=CC=1)CC1=CC=CC=C1 OGYFEVHYAAMGOC-UHFFFAOYSA-N 0.000 claims 1
- PMTJFNCBHGLANZ-UHFFFAOYSA-N 1,1-dibenzyl-3-(2,4-dimethylphenyl)-3-phenylurea Chemical compound CC1=CC(C)=CC=C1N(C=1C=CC=CC=1)C(=O)N(CC=1C=CC=CC=1)CC1=CC=CC=C1 PMTJFNCBHGLANZ-UHFFFAOYSA-N 0.000 claims 1
- YRDCXMXKLCKKAB-UHFFFAOYSA-N 1,1-dibenzyl-3-(3-chloro-4-methylphenyl)-3-phenylurea Chemical compound C1=C(Cl)C(C)=CC=C1N(C=1C=CC=CC=1)C(=O)N(CC=1C=CC=CC=1)CC1=CC=CC=C1 YRDCXMXKLCKKAB-UHFFFAOYSA-N 0.000 claims 1
- CAUZWNSDXRQLNI-UHFFFAOYSA-N 1,1-dibutyl-3,3-bis(2,4-dimethylphenyl)urea Chemical compound C=1C=C(C)C=C(C)C=1N(C(=O)N(CCCC)CCCC)C1=CC=C(C)C=C1C CAUZWNSDXRQLNI-UHFFFAOYSA-N 0.000 claims 1
- FSPCLMBAJQVIKB-UHFFFAOYSA-N 1,1-dibutyl-3-(2,4-dimethylphenyl)-3-phenylurea Chemical compound C=1C=C(C)C=C(C)C=1N(C(=O)N(CCCC)CCCC)C1=CC=CC=C1 FSPCLMBAJQVIKB-UHFFFAOYSA-N 0.000 claims 1
- NQEMGGCWHYRERK-UHFFFAOYSA-N 1,1-dibutyl-3-(3-chloro-4-methylphenyl)-3-phenylurea Chemical compound C=1C=C(C)C(Cl)=CC=1N(C(=O)N(CCCC)CCCC)C1=CC=CC=C1 NQEMGGCWHYRERK-UHFFFAOYSA-N 0.000 claims 1
- WHHRTWFORQAQNP-UHFFFAOYSA-N 1,3-dibenzyl-1-butyl-3-phenylurea Chemical compound C=1C=CC=CC=1CN(C=1C=CC=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 WHHRTWFORQAQNP-UHFFFAOYSA-N 0.000 claims 1
- KIUHMQOWQPDOHS-UHFFFAOYSA-N 1-benzyl-1-butyl-3,3-bis(2,4-dimethylphenyl)urea Chemical compound C=1C=C(C)C=C(C)C=1N(C=1C(=CC(C)=CC=1)C)C(=O)N(CCCC)CC1=CC=CC=C1 KIUHMQOWQPDOHS-UHFFFAOYSA-N 0.000 claims 1
- NZKMENOYGWGDHX-UHFFFAOYSA-N 1-benzyl-1-butyl-3,3-bis(3-chloro-4-methylphenyl)urea Chemical compound C=1C=C(C)C(Cl)=CC=1N(C=1C=C(Cl)C(C)=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 NZKMENOYGWGDHX-UHFFFAOYSA-N 0.000 claims 1
- ZSUBZLUMQRVHST-UHFFFAOYSA-N 1-benzyl-1-butyl-3,3-diphenylurea Chemical compound C=1C=CC=CC=1N(C=1C=CC=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 ZSUBZLUMQRVHST-UHFFFAOYSA-N 0.000 claims 1
- IUFVSMIQRNBCNL-UHFFFAOYSA-N 1-benzyl-1-butyl-3-(2,4-dimethylphenyl)-3-phenylurea Chemical compound C=1C=CC=CC=1N(C=1C(=CC(C)=CC=1)C)C(=O)N(CCCC)CC1=CC=CC=C1 IUFVSMIQRNBCNL-UHFFFAOYSA-N 0.000 claims 1
- ALSBVGNFMVSOAJ-UHFFFAOYSA-N 1-benzyl-1-butyl-3-(3-chloro-4-methylphenyl)-3-phenylurea Chemical compound C=1C=CC=CC=1N(C=1C=C(Cl)C(C)=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 ALSBVGNFMVSOAJ-UHFFFAOYSA-N 0.000 claims 1
- JKXLTTZJKQMKLA-UHFFFAOYSA-N 1-benzyl-1-butyl-3-(3-chlorophenyl)-3-phenylurea Chemical compound C=1C=CC=CC=1N(C=1C=C(Cl)C=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 JKXLTTZJKQMKLA-UHFFFAOYSA-N 0.000 claims 1
- YQHFTXOCCGHGMT-UHFFFAOYSA-N 1-benzyl-1-butyl-3-(4-chlorophenyl)-3-phenylurea Chemical compound C=1C=CC=CC=1N(C=1C=CC(Cl)=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 YQHFTXOCCGHGMT-UHFFFAOYSA-N 0.000 claims 1
- ZPZXGIWDJQEXKE-UHFFFAOYSA-N 1-benzyl-1-butyl-3-naphthalen-1-yl-3-phenylurea Chemical compound C=1C=CC=CC=1N(C=1C2=CC=CC=C2C=CC=1)C(=O)N(CCCC)CC1=CC=CC=C1 ZPZXGIWDJQEXKE-UHFFFAOYSA-N 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 16
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- 238000002360 preparation method Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
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- 229940107161 cholesterol Drugs 0.000 description 16
- 239000000543 intermediate Substances 0.000 description 15
- 201000001320 Atherosclerosis Diseases 0.000 description 12
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 description 11
- 239000004202 carbamide Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
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- 230000015572 biosynthetic process Effects 0.000 description 8
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 150000002632 lipids Chemical class 0.000 description 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 6
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- 125000005843 halogen group Chemical group 0.000 description 4
- DGWIPMVOWWLJMU-UHFFFAOYSA-N n-(2,4-dichlorophenyl)-1-(2,4-dimethylphenyl)methanimine Chemical compound CC1=CC(C)=CC=C1C=NC1=CC=C(Cl)C=C1Cl DGWIPMVOWWLJMU-UHFFFAOYSA-N 0.000 description 4
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- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
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- BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 description 1
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- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
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- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
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- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
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- VVUAADACTIQHDR-UHFFFAOYSA-N n-(3-chlorophenyl)-n-phenylcarbamoyl chloride Chemical compound C=1C=CC(Cl)=CC=1N(C(=O)Cl)C1=CC=CC=C1 VVUAADACTIQHDR-UHFFFAOYSA-N 0.000 description 1
- 230000004903 negative regulation of intestinal cholesterol absorption Effects 0.000 description 1
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- 239000012299 nitrogen atmosphere Substances 0.000 description 1
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- 235000019198 oils Nutrition 0.000 description 1
- XDUHQPOXLUAVEE-BPMMELMSSA-N oleoyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CCCCCCC\C=C/CCCCCCCC)O[C@H]1N1C2=NC=NC(N)=C2N=C1 XDUHQPOXLUAVEE-BPMMELMSSA-N 0.000 description 1
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- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
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- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
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- 239000008159 sesame oil Substances 0.000 description 1
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- 239000000741 silica gel Substances 0.000 description 1
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000013222 sprague-dawley male rat Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 230000000948 sympatholitic effect Effects 0.000 description 1
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- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000004797 therapeutic response Effects 0.000 description 1
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- 235000019165 vitamin E Nutrition 0.000 description 1
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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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US342,693 | 1982-01-26 | ||
| US06/342,693 US4473579A (en) | 1982-01-26 | 1982-01-26 | Antiatherosclerotic tetrasubstituted ureas and thioureas |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1291990C true CA1291990C (en) | 1991-11-12 |
Family
ID=23342884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000416765A Expired - Fee Related CA1291990C (en) | 1982-01-26 | 1982-12-01 | Antiatherosclerotic tetrasubstituted ureas and thioureas |
Country Status (6)
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4623662A (en) | 1985-05-23 | 1986-11-18 | American Cyanamid Company | Antiatherosclerotic ureas and thioureas |
| US5003106A (en) * | 1983-07-19 | 1991-03-26 | American Cyanamid Company | Antiatherosclerotic ureas and thioureas |
| DE3636190A1 (de) * | 1986-10-24 | 1988-04-28 | Bayer Ag | Verfahren zur herstellung von n,n-diaryl-harnstoffen |
| US4782071A (en) * | 1986-11-03 | 1988-11-01 | Warner-Lambert Company | Tetrasubstituted urea cholinergic agents |
| ES2037768T3 (es) * | 1987-07-02 | 1993-07-01 | Warner-Lambert Company | Procedimiento para preparar n-(fenil(2,6-disustituido))-ureas y carbamatos inhibidores de acil-coa: colesterol acil-transferasa. |
| CN1021819C (zh) * | 1988-01-20 | 1993-08-18 | 山之内制药株式会社 | 作为药物有用的双脲衍生物的制备方法 |
| US5116848A (en) * | 1988-03-30 | 1992-05-26 | Warner-Lambert Company | N-(((2,6-disubstituted)phenyl)-n-diarylalkyl)ureas as antihyperlipidemic and antiatherosclerotic agents |
| US4999373A (en) * | 1988-03-30 | 1991-03-12 | Warner-Lambert Company | Antihyperlipidemic and antiatherosclerotic compounds and compositions |
| US4868210A (en) * | 1988-03-30 | 1989-09-19 | Warner-Lambert Company | Antihyperlipidemic and antiatherosclerotic compounds and compositions |
| US5290814A (en) * | 1988-11-21 | 1994-03-01 | Burroughs Wellcome Co. | Anti-atherosclerotic diaryl compounds |
| DE3920616A1 (de) * | 1989-06-23 | 1991-01-03 | Boehringer Mannheim Gmbh | Arzneimittel, enthaltend di-tert.-butylhydroxyphenyl-derivate sowie neue derivate |
| JPH05310678A (ja) * | 1990-01-22 | 1993-11-22 | Mitsubishi Kasei Corp | １−フェニルアルキル−３−フェニル尿素誘導体 |
| ATE115558T1 (de) * | 1990-03-12 | 1994-12-15 | Yamanouchi Pharma Co Ltd | Harnstoffderivate, deren herstellung sowie diese enthaltende pharmazeutische zusammensetzungen. |
| US5106873A (en) * | 1990-06-26 | 1992-04-21 | Warner-Lambert Company | ACAT inhibitors |
| US5362878A (en) * | 1991-03-21 | 1994-11-08 | Pfizer Inc. | Intermediates for making N-aryl and N-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme A: cholesterol acyl transferase (ACAT) |
| US5401825A (en) * | 1993-05-05 | 1995-03-28 | Gould Inc. | Styrene type monomers containing substituents thereon, e.g. urea, and polymers and copolymers thereof |
| US6187799B1 (en) * | 1997-05-23 | 2001-02-13 | Onyx Pharmaceuticals | Inhibition of raf kinase activity using aryl ureas |
| US6344476B1 (en) | 1997-05-23 | 2002-02-05 | Bayer Corporation | Inhibition of p38 kinase activity by aryl ureas |
| US7329670B1 (en) * | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| US20080300281A1 (en) * | 1997-12-22 | 2008-12-04 | Jacques Dumas | Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas |
| US20080269265A1 (en) * | 1998-12-22 | 2008-10-30 | Scott Miller | Inhibition Of Raf Kinase Using Symmetrical And Unsymmetrical Substituted Diphenyl Ureas |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| ATE556713T1 (de) | 1999-01-13 | 2012-05-15 | Bayer Healthcare Llc | Omega-carboxyarylsubstituierte-diphenyl- harnstoffe als p38-kinasehemmer |
| US7928239B2 (en) | 1999-01-13 | 2011-04-19 | Bayer Healthcare Llc | Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas |
| RU2319693C9 (ru) * | 1999-01-13 | 2008-08-20 | Байер Копэрейшн | Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты) |
| MXPA02002578A (es) | 1999-09-08 | 2002-10-23 | Guilford Pharm Inc | Compuestos de union a ciclofilina no peptidicos, y su uso. |
| US7235576B1 (en) | 2001-01-12 | 2007-06-26 | Bayer Pharmaceuticals Corporation | Omega-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US6656971B2 (en) | 2001-01-25 | 2003-12-02 | Guilford Pharmaceuticals Inc. | Trisubstituted carbocyclic cyclophilin binding compounds and their use |
| US7371763B2 (en) * | 2001-04-20 | 2008-05-13 | Bayer Pharmaceuticals Corporation | Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas |
| ES2426938T3 (es) * | 2001-12-03 | 2013-10-25 | Bayer Healthcare Llc | Compuestos de aril urea en combinación con otros agentes citostáticos o citotóxicos para tratar cánceres humanos |
| SI1580188T1 (sl) * | 2002-02-11 | 2012-02-29 | Bayer Healthcare Llc | Aril sečnine kot kinazni inhibitorji |
| AU2003209116A1 (en) | 2002-02-11 | 2003-09-04 | Bayer Pharmaceuticals Corporation | Aryl ureas with angiogenesis inhibiting activity |
| US20030216396A1 (en) | 2002-02-11 | 2003-11-20 | Bayer Corporation | Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors |
| CN1289467C (zh) * | 2002-08-30 | 2006-12-13 | 日本烟草产业株式会社 | 二苄胺化合物及其药物用途 |
| US7557129B2 (en) | 2003-02-28 | 2009-07-07 | Bayer Healthcare Llc | Cyanopyridine derivatives useful in the treatment of cancer and other disorders |
| US8796250B2 (en) | 2003-05-20 | 2014-08-05 | Bayer Healthcare Llc | Diaryl ureas for diseases mediated by PDGFR |
| BRPI0412219B8 (pt) | 2003-07-23 | 2021-07-27 | Bayer Healthcare Llc | compostos ômega-carboxi aril difenil uréia fluoro substituídos e composições farmacêuticas compreendendo os referidos compostos |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL92838C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1949-12-06 | |||
| US2867520A (en) * | 1956-11-23 | 1959-01-06 | Monsanto Chemicals | 1-(chloraryl) 3-alkyl 3-alkynyl urea |
| US2993930A (en) * | 1958-03-18 | 1961-07-25 | Midwest Research Inst | Tetra-substituted ureas |
| US3277061A (en) * | 1963-07-01 | 1966-10-04 | Union Oil Co | Carbonylation of amines and substituted ureas derived therefrom |
| US3326663A (en) * | 1964-09-25 | 1967-06-20 | Shell Oil Co | Herbicidal phenylureas |
| GB1143802A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1965-03-25 | |||
| US3897493A (en) * | 1971-09-13 | 1975-07-29 | Stauffer Chemical Co | Meta-anilide urea compositions and their utility as herbicides |
| JPS5224104B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1974-10-07 | 1977-06-29 | ||
| JPS5312844A (en) * | 1976-07-20 | 1978-02-04 | Nippon Tokushu Noyaku Seizo Kk | Nn44halogenobenzyllnnmethyl*or nonsubstitutedd*cycloalkylln**phenylurea or thiourea compounds* their preparation and fungicides containing the same as active constituents |
| DE3027253C2 (de) * | 1980-07-18 | 1982-11-04 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von Wasserstoffperoxid |
| JPS6032447A (ja) * | 1983-08-03 | 1985-02-19 | Nec Corp | 群別２線式搬送回線の折返し回路 |
-
1982
- 1982-01-26 US US06/342,693 patent/US4473579A/en not_active Expired - Fee Related
- 1982-12-01 CA CA000416765A patent/CA1291990C/en not_active Expired - Fee Related
-
1983
- 1983-01-21 PH PH28412A patent/PH18706A/en unknown
- 1983-01-25 JP JP58009484A patent/JPS58134070A/ja active Granted
- 1983-01-25 ZA ZA83484A patent/ZA83484B/xx unknown
- 1983-01-26 BE BE0/209971A patent/BE895708A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58134070A (ja) | 1983-08-10 |
| JPH0254821B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-11-22 |
| US4473579A (en) | 1984-09-25 |
| BE895708A (fr) | 1983-07-26 |
| PH18706A (en) | 1985-09-05 |
| ZA83484B (en) | 1983-10-26 |
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| Publication | Publication Date | Title |
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