ME02439B - Odredjeni amino-pirimidini, njihove kompozicije, i metode njihove upotrebe - Google Patents
Odredjeni amino-pirimidini, njihove kompozicije, i metode njihove upotrebeInfo
- Publication number
- ME02439B ME02439B MEP-2016-137A MEP13716A ME02439B ME 02439 B ME02439 B ME 02439B ME P13716 A MEP13716 A ME P13716A ME 02439 B ME02439 B ME 02439B
- Authority
- ME
- Montenegro
- Prior art keywords
- fluoro
- pyrimidin
- cyclobutyl
- pharmaceutically acceptable
- acceptable salt
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 2
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 41
- 150000003839 salts Chemical class 0.000 claims 24
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 14
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 8
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 8
- 201000010099 disease Diseases 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- 208000005764 Peripheral Arterial Disease Diseases 0.000 claims 4
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 claims 4
- 208000018262 Peripheral vascular disease Diseases 0.000 claims 4
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 4
- 208000002320 spinal muscular atrophy Diseases 0.000 claims 4
- 206010028289 Muscle atrophy Diseases 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 210000003205 muscle Anatomy 0.000 claims 3
- 201000000585 muscular atrophy Diseases 0.000 claims 3
- KDUMOALBWXOBGD-UHFFFAOYSA-N 1-[2-[[3-fluoro-1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]pyrazole-4-carboxamide Chemical compound C1=C(C(=O)N)C=NN1C(C=N1)=CN=C1NCC1(C=2C(=CC=CN=2)F)CC(F)C1 KDUMOALBWXOBGD-UHFFFAOYSA-N 0.000 claims 2
- ZVXKYWHJBYIYNI-UHFFFAOYSA-N 1h-pyrazole-4-carboxamide Chemical compound NC(=O)C=1C=NNC=1 ZVXKYWHJBYIYNI-UHFFFAOYSA-N 0.000 claims 2
- VTTRAIDITYVAOB-UHFFFAOYSA-N 2-[2-[[1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]-1,3-thiazole-5-carboxamide Chemical compound S1C(C(=O)N)=CN=C1C(C=N1)=CN=C1NCC1(C=2C(=CC=CN=2)F)CCC1 VTTRAIDITYVAOB-UHFFFAOYSA-N 0.000 claims 2
- WLKVZKYMKDRMTG-UHFFFAOYSA-N 4-[2-[[1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]pyridine-2-carboxamide Chemical compound C1=NC(C(=O)N)=CC(C=2C=NC(NCC3(CCC3)C=3C(=CC=CN=3)F)=NC=2)=C1 WLKVZKYMKDRMTG-UHFFFAOYSA-N 0.000 claims 2
- DGJHHMDCUBNXAA-UHFFFAOYSA-N 4-[2-[[3-fluoro-1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]pyridine-2-carboxamide Chemical compound C1=NC(C(=O)N)=CC(C=2C=NC(NCC3(CC(F)C3)C=3C(=CC=CN=3)F)=NC=2)=C1 DGJHHMDCUBNXAA-UHFFFAOYSA-N 0.000 claims 2
- GVALDHCSWANPJG-UHFFFAOYSA-N 4-fluoro-3-[2-[[1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]benzamide Chemical compound NC(=O)C1=CC=C(F)C(C=2C=NC(NCC3(CCC3)C=3C(=CC=CN=3)F)=NC=2)=C1 GVALDHCSWANPJG-UHFFFAOYSA-N 0.000 claims 2
- JKSLDPJHCPGXNE-UHFFFAOYSA-N 4-fluoro-3-[2-[[3-fluoro-1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]-n-methylbenzamide Chemical compound CNC(=O)C1=CC=C(F)C(C=2C=NC(NCC3(CC(F)C3)C=3C(=CC=CN=3)F)=NC=2)=C1 JKSLDPJHCPGXNE-UHFFFAOYSA-N 0.000 claims 2
- NJVMEJNDGULDBP-UHFFFAOYSA-N 4-fluoro-3-[2-[[3-fluoro-1-(3-fluoropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]benzamide Chemical compound NC(=O)C1=CC=C(F)C(C=2C=NC(NCC3(CC(F)C3)C=3C(=CC=CN=3)F)=NC=2)=C1 NJVMEJNDGULDBP-UHFFFAOYSA-N 0.000 claims 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 2
- 206010008874 Chronic Fatigue Syndrome Diseases 0.000 claims 2
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 2
- 206010049565 Muscle fatigue Diseases 0.000 claims 2
- 208000021642 Muscular disease Diseases 0.000 claims 2
- 201000009623 Myopathy Diseases 0.000 claims 2
- 208000008589 Obesity Diseases 0.000 claims 2
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 2
- 230000006735 deficit Effects 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 230000020763 muscle atrophy Effects 0.000 claims 2
- 208000029766 myalgic encephalomeyelitis/chronic fatigue syndrome Diseases 0.000 claims 2
- 206010028417 myasthenia gravis Diseases 0.000 claims 2
- 208000018360 neuromuscular disease Diseases 0.000 claims 2
- 235000020824 obesity Nutrition 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- MQXWPWOCXGARRK-UHFFFAOYSA-N reldesemtiv Chemical compound C1=C(C(=O)N)C=CN1C(C=N1)=CN=C1NCC1(C=2C(=CC=CN=2)F)CC(F)C1 MQXWPWOCXGARRK-UHFFFAOYSA-N 0.000 claims 2
- 229960000581 salicylamide Drugs 0.000 claims 2
- SCONBEUHDLCWPD-UHFFFAOYSA-N 2-[2-[2-[[1-(3-chloropyridin-2-yl)cyclobutyl]methylamino]pyrimidin-5-yl]-1,3-thiazol-5-yl]acetamide Chemical compound S1C(CC(=O)N)=CN=C1C(C=N1)=CN=C1NCC1(C=2C(=CC=CN=2)Cl)CCC1 SCONBEUHDLCWPD-UHFFFAOYSA-N 0.000 claims 1
- LOCNMZAIQWCGOY-UHFFFAOYSA-N 4-fluoro-3-[2-[[2-(3-fluoropyridin-2-yl)-2-methylpropyl]amino]pyrimidin-5-yl]benzamide Chemical compound N=1C=CC=C(F)C=1C(C)(C)CNC(N=C1)=NC=C1C1=CC(C(N)=O)=CC=C1F LOCNMZAIQWCGOY-UHFFFAOYSA-N 0.000 claims 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 1
- 238000007918 intramuscular administration Methods 0.000 claims 1
- 238000007912 intraperitoneal administration Methods 0.000 claims 1
- 238000001990 intravenous administration Methods 0.000 claims 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims 1
- 238000007920 subcutaneous administration Methods 0.000 claims 1
- 230000000699 topical effect Effects 0.000 claims 1
Classifications
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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Claims (27)
1.Jedinjenje odаbrаno od sledećeg:4-fluoro-3-(2-{[2-(3-fluoro(2-piridil))-2-metilpropil]аmino}pirimidin-5-il)benzаmid; 4-fluoro-3-[2-({[(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]benzаmid; 4-fluoro-3-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]benzаmid; {4-fluoro-3-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]fenil}-N-metil kаrboksаmid; {4-fluor-3-[2-({[trаns-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]fenil}-N-metilkаrboksаmid; 4-fluoro-3-(2-((trans-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)-2-hidroksibenzamid; 3-(2-((trаns-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilаmino)pirimidin-5-il)-4-hidroksi-N-metil-benzаmid; 4-[2-({[(3-fluoro-2-piridil)ciklobutil]metil}аmino)pirimidin-5-il]piridin-2-kаrboksаmid; 4-[2-({[3-fluoro-1-(3-f!uoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]piridin-2-karboksamid; 4-[2-({[trаns-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]piridin-2-kаrboksаmid; 1-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]pirаzol-4-kаrboksаmid; 1-[2-({[trаns-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]pirаzol-4-kаrboksаmid; 1-(2-((3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilаmino)pirimidin-5-il)-1H-pirol-3-kаrboksаmid; 1-(2-(((trans)-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)-1H-pirol-3-karboksamid; 2-[2-({[(3-fluoro-2-piridil)ciklobutil]metil}аmino)pirimidin-5-il]-1,3-tiаzol-5-kаrboksаmid; 2-(2-(2-((1-(3-hloropiridin-2-il)ciklobutil)metilаmino)pirimidin-5-il)tiаzol-5-il) аcetаmid; i 2-(2-((trans-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)tiazol-5-karboksamid;ili njegovа fаrmаceutski prihvаtljivа so.
2.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-fluor-3-(2-{[2-(3-fluoro(2-piridil))-2-metilpropil]аmino}pirimidin-5-il)benzаmid; ili njegovа fаrmаceutski prihvаtljivа so.
3.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-fluor-3-[2-({[(3-fluoro (2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]benzаmid; ili njegovа fаrmаceutski prihvаtljivа so.
4.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-fluor-3-[2-({[3-fluoro-1- (3-fluoro (2-piridil))ciklobutil]metil}аmino)pirimidin-5-il]benzаmid; ili njegovа fаrmаceutski prihvаtljivа so.
5.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje {4-fluoro-3-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]fenil}-N-metilkarboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
6.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje {4-fluoro-3-[2-({[trans-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]fenil}-N-metilkarboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
7.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-fluoro-3-(2-((trans-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)-2-hidroksibenzamid; ili njegovа fаrmаceutski prihvаtljivа so.
8.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 3-(2-((trans-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)-4-hidroksi-N-metilbenzamid; ili njegovа fаrmаceutski prihvаtljivа so.
9.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-[2-({[(3-fluoro-2-piridil) ciklobutil]metil}аmino)pirimidin-5-il]piridin-2-kаrboksаmid; ili njegovа fаrmаceutski prihvаtljivа so.
10.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]piridin-2-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
11.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 4-[2-(([trans-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]piridin-2-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
12.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 1-[2-({[3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]pirazol-4-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
13.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 1-[2-({[trans-3-fluoro-1-(3-fluoro(2-piridil))ciklobutil]metil}amino)pirimidin-5-il]pirazol-4-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
14.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 1-(2-((3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)-1H-pirol-3-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
15.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 1-(2-(((trans)-3-fluoro-1-(3-fluoropiridin-2-il) ciklobutil) metilamino) pirimidin-5-il)-1H-pirol-3-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
16.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 2-[2-({[(3-fluoro-2-piridil) ciklobutil]metil}аmino)pirimidin-5-il]-1,3-tiаzol-5-kаrboksаmid; ili njegovа fаrmаceutski prihvаtljivа so.
17.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 2-(2-(2-((1-(3-hloropiridin-2-il)ciklobutil)metilаmino)pirimidin-5-il)tiаzol-5-il)аcetаmid; ili njegovа fаrmаceutski prihvаtljivа so.
18.Jedinjenje premа zаhtevu 1, naznačeno time što je pomenuto jedinjenje 2-(2-((trans-3-fluoro-1-(3-fluoropiridin-2-il)ciklobutil)metilamino)pirimidin-5-il)tiazol-5-karboksamid; ili njegovа fаrmаceutski prihvаtljivа so.
19.Fаrmаceutskа kompozicijа kojа sаdrži jedinjenje premа jednom od zаhtevа 1 do 18 ili njegovu fаrmаceutski prihvаtljivu so.
20.Fаrmаceutskа kompozicijа premа zаhtevu 19, naznačena time što je fаrmаceutskа kompozicijа formulisаnа zа orаlnu, sublingvаlnu, subkutаnu, pаrenterаlnu, intrаvenoznu, intrаnаzаlnu, topikаlnu, trаnsdermаlnu, intrаperitoneаlnu, intrаmuskulаrnu, intrаpulmonаrnu, vаginаlnu, rektаlnu, ili intrаokulаrnu primenu.
21.Fаrmаceutskа kompozicijа premа zаhtevu 20, naznačena time što je fаrmаceutskа kompozicijа formulisаnа zа orаlnu аdministrаciju.
22.Upotrebа jedinjenjа premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegove fаrmаceutski prihvаtljive soli, zа pripremanje lekа zа lečenje bolesti ili stаnjа izаbrаnog od neuromuskulаrnih poremećаjа, stаnjа gubitka mišićne mаse, mišićnih miopаtija, sa rehаbilitаcijom povezanih deficita, periferne vаskulаrne bolesti, periferne аrterijske bolesti, slabosti, mišićne аtrofije i umora, metаboličkog sindroma, sindroma hroničnog umorа, i gojаznosti.
23.Upotrebа jedinjenjа premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegove fаrmаceutski prihvаtljive soli, zа pripremanje lekа zа lečenje bolesti odаbrаne od Amiotrofne Lаterаlne Skleroze (ALS), Spinаlne Mišićne Atrofije (SMA) i mijаstenije grаvis.
24.Upotrebа jedinjenjа premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegove fаrmаceutski prihvаtljive soli, zа pripremanje lekа zа lečenje bolesti odаbrаne od periferne vаskulаrne bolesti i periferne аrterijske bolesti.
25.Jedinjenje premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegovа fаrmаceutski prihvаtljivа so, zа upotrebu u postupku lečenjа oboljenjа ili stаnjа odаbrаnog od neuromuskulаrnih poremećаjа, stanja gubitka mišićne mаse, mišićne miopаtije, sa rehаbilitаcijom povezаnih deficita, periferne vаskulаrne bolesti, periferne аrterijske bolesti, slаbosti, аtrofije mišićа i umora, metаboličkog sindroma, sindroma hroničnog umorа, i gojаznosti.
26.Jedinjenje premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegovа fаrmаceutski prihvаtljivа so, zа upotrebu u postupku lečenjа bolesti odаbrаne od Amiotrofne Lаterаlne Skleroze (ALS), Spinаlne Mišićne Atrofije (SMA) i miаstenije grаvis.
27.Jedinjenje premа bilo kojem od pаtentnih zаhtevа 1 do 18, ili njegovа fаrmаceutski prihvаtljivа so, zа upotrebu u postupku lečenjа bolesti odаbrаne od periferne vаskulаrne bolesti i periferne аrterijske bolesti. 1
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| EP11772782.6A EP2560653B1 (en) | 2010-04-23 | 2011-04-22 | Certain amino-pyrimidines, compositions thereof, and methods for their use |
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Families Citing this family (87)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8748623B2 (en) | 2009-02-17 | 2014-06-10 | Syntrix Biosystems, Inc. | Pyridinecarboxamides as CXCR2 modulators |
| WO2011133920A1 (en) | 2010-04-23 | 2011-10-27 | Cytokinetics, Inc. | Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use |
| AR081331A1 (es) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos |
| AR081626A1 (es) | 2010-04-23 | 2012-10-10 | Cytokinetics Inc | Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos |
| CA2811990C (en) * | 2010-08-23 | 2023-03-21 | Dean Y. Maeda | Aminopyridine- and aminopyrimidinecarboxamides as cxcr2 modulators |
| AR083797A1 (es) | 2010-11-10 | 2013-03-20 | Novartis Ag | Succinato de dimetil-amida del acido 7-ciclopentil-2-(5-piperazin-1-il-piridin-2-il-amino)-7h-pirrolo-[2,3-d]pirimidin-6-carboxilico, proceso para prepararla, intermediarios de dicha sintesis y proceso de preparacion de los mismos |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| PH12014500682A1 (en) | 2011-09-27 | 2014-05-12 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| JP5966014B2 (ja) * | 2011-11-28 | 2016-08-10 | ノバルティス アーゲー | 新規トリフルオロメチル−オキサジアゾール誘導体および疾患の処置におけるその使用 |
| UY34632A (es) | 2012-02-24 | 2013-05-31 | Novartis Ag | Compuestos de oxazolidin- 2- ona y usos de los mismos |
| KR20160046693A (ko) * | 2012-04-02 | 2016-04-29 | 싸이토키네틱스, 인코포레이티드 | 횡격막 기능을 향상시키는 방법들 |
| KR102163931B1 (ko) * | 2012-04-11 | 2020-10-12 | 싸이토키네틱스, 인코포레이티드 | 골격근 피로에 대한 저항을 개선 |
| RS61089B1 (sr) | 2012-06-13 | 2020-12-31 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| US9296733B2 (en) | 2012-11-12 | 2016-03-29 | Novartis Ag | Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| WO2014141104A1 (en) | 2013-03-14 | 2014-09-18 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| DK2986610T5 (en) | 2013-04-19 | 2018-12-10 | Incyte Holdings Corp | BICYCLIC HETEROCYCLES AS FGFR INHIBITORS |
| US8969365B2 (en) | 2013-08-02 | 2015-03-03 | Syntrix Biosystems, Inc. | Thiopyrimidinecarboxamides as CXCR1/2 modulators |
| US10046002B2 (en) | 2013-08-02 | 2018-08-14 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| US10561676B2 (en) | 2013-08-02 | 2020-02-18 | Syntrix Biosystems Inc. | Method for treating cancer using dual antagonists of CXCR1 and CXCR2 |
| WO2015163435A1 (ja) | 2014-04-24 | 2015-10-29 | 田辺三菱製薬株式会社 | 新規2-アミノ-ピリジン及び2-アミノ-ピリミジン誘導体及びその医薬用途 |
| HRP20220183T1 (hr) | 2014-04-29 | 2022-04-29 | Cytokinetics, Inc. | Postupci smanjivanja propadanja vitalnog kapaciteta |
| PT3192512T (pt) * | 2014-09-09 | 2019-10-29 | Cytokinetics Inc | Nova composição farmacêutica para prevenção e/ou tratamento de incontinência urinária |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| SG11201706287PA (en) | 2015-02-20 | 2017-09-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2016149160A1 (en) * | 2015-03-15 | 2016-09-22 | Sunshine Lake Pharma Co., Ltd. | Substituted aminopyrimidine compounds and methods of use |
| CN105111151B (zh) * | 2015-04-17 | 2018-09-28 | 成都理工大学 | 作为PPAR-γ调节剂的氨基嘧啶衍生物 |
| CA2987179C (en) * | 2015-05-29 | 2020-08-25 | Pfizer Inc. | Heterocyclic compounds as inhibitors of vanin-1 enzyme |
| DK3328844T3 (da) | 2015-07-27 | 2020-03-02 | Chong Kun Dang Pharmaceutical Corp | 1,3,4-oxadiazolsulfamidderivater som histondeacetylase-6-inhibitor og farmaceutisk sammensætning omfattende samme |
| JP6560436B2 (ja) | 2015-07-27 | 2019-08-14 | チョン クン ダン ファーマシューティカル コーポレーション | ヒストン脱アセチル化酵素6阻害剤としての1,3,4−オキサジアゾールスルホンアミド誘導体化合物及びこれを含有する薬剤学的組成物 |
| MX377262B (es) | 2015-07-27 | 2025-03-07 | Chong Kun Dang Pharmaceutical Corp | Compuesto derivado de amida de 1,3,4-oxadiazol como inhibidor de histona desacetilasa 6 y composición farmacéutica que lo contiene. |
| HUE057544T2 (hu) | 2015-08-04 | 2022-05-28 | Chong Kun Dang Pharmaceutical Corp | 1,3,4-oxadiazol-származék vegyületek mint hiszton deacetiláz 6 inhibitorok, és ezeket tartalmazó gyógyszerkészítmények |
| DK3362445T3 (da) * | 2015-10-12 | 2023-02-27 | Chong Kun Dang Pharmaceutical Corp | Oxadiazolaminderivatforbindelser som histondeacetylase 6-inhibitor, og den farmaceutiske sammensætning dermed |
| ES2913423T3 (es) | 2016-02-12 | 2022-06-02 | Cytokinetics Inc | Derivados de tetrahidroisoquinolina |
| AU2017296338A1 (en) * | 2016-07-14 | 2019-01-03 | Pfizer Inc. | Novel pyrimidine carboxamides as inhibitors of vanin-1 enzyme |
| US10660909B2 (en) | 2016-11-17 | 2020-05-26 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| US10357493B2 (en) | 2017-03-10 | 2019-07-23 | Selenity Therapeutics (Bermuda), Ltd. | Metalloenzyme inhibitor compounds |
| KR101798840B1 (ko) | 2017-05-17 | 2017-11-17 | 주식회사 레고켐 바이오사이언스 | 신규 오토탁신 저해 화합물 및 이를 함유하는 약제학적 조성물 |
| US10961242B2 (en) | 2017-05-17 | 2021-03-30 | Legochem Biosciences, Inc. | Compounds as autotaxin inhibitors and pharmaceutical compositions comprising the same |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| EP3661509A4 (en) | 2017-08-04 | 2021-01-13 | Skyhawk Therapeutics, Inc. | METHODS AND COMPOSITIONS FOR MODULATING THE SPLICE |
| US11547712B2 (en) | 2017-11-20 | 2023-01-10 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds and compositions and methods of use |
| US11142516B2 (en) * | 2017-12-26 | 2021-10-12 | Cytokinetics, Inc. | Process for the preparation of an amino-pyrimidine and intermediates thereof |
| WO2019134661A1 (zh) * | 2018-01-03 | 2019-07-11 | 南京明德新药研发股份有限公司 | 异吲哚啉酮及其衍生物作为csf-1r抑制剂 |
| WO2019136320A1 (en) | 2018-01-05 | 2019-07-11 | Icahn School Of Medicine At Mount Sinai | Method of increasing proliferation of pancreatic beta cells, treatment method, and composition |
| CN112135613A (zh) | 2018-03-20 | 2020-12-25 | 西奈山伊坎医学院 | 激酶抑制剂化合物和组合物及使用方法 |
| WO2019213544A2 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
| KR20210018264A (ko) | 2018-05-04 | 2021-02-17 | 인사이트 코포레이션 | Fgfr 억제제의 염 |
| CN110483440A (zh) * | 2018-06-11 | 2019-11-22 | 上海睿升化工科技有限公司 | 一种2-(2-溴-1,3-噻唑-5-基)乙腈的制备方法 |
| KR102316234B1 (ko) | 2018-07-26 | 2021-10-22 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| CN113272280B (zh) | 2018-11-06 | 2026-01-09 | 艾知怀斯治疗学公司 | 哒嗪酮化合物及其用途 |
| AU2019376647B2 (en) | 2018-11-06 | 2025-03-06 | Edgewise Therapeutics, Inc. | Pyridazinone compounds and uses thereof |
| HUE063586T2 (hu) | 2018-11-06 | 2024-01-28 | Edgewise Therapeutics Inc | Piridazinon-vegyületek és alkalmazásaik |
| CA3124353A1 (en) * | 2018-12-31 | 2020-07-09 | Icahn School Of Medicine At Mount Sinai | Kinase inhibitor compounds and compositions and methods of use |
| IL284510B2 (en) | 2019-01-23 | 2025-10-01 | Novartis Ag | Crystalline forms of succinate salt of 7-cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-h7-pyrrolo[3,2-d]pyrimidine-6-carboxylic acid dimethylamide |
| CN114007613A (zh) | 2019-02-05 | 2022-02-01 | 斯基霍克疗法公司 | 用于调节剪接的方法和组合物 |
| JP7551629B2 (ja) | 2019-02-05 | 2024-09-17 | スカイホーク・セラピューティクス・インコーポレーテッド | スプライシングを調節するための方法および組成物 |
| CN113677344A (zh) | 2019-02-06 | 2021-11-19 | 斯基霍克疗法公司 | 用于调节剪接的方法和组合物 |
| WO2020163647A1 (en) | 2019-02-06 | 2020-08-13 | Skyhawk Therapeutics, Inc. | Methods and compositions for modulating splicing |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| WO2020232424A1 (en) | 2019-05-16 | 2020-11-19 | Nexus Pharmaceuticals, Inc. | Compositions comprising ephedrine or an ephedrine salt and methods of making and using same |
| CA3136223C (en) | 2019-05-31 | 2023-09-12 | Chong Kun Dang Pharmaceutical Corp. | 1,3,4-oxadiazole homophthalimide derivative compounds as histone deacetylase 6 inhibitor, and the pharmaceutical composition comprising the same |
| JP2022538119A (ja) * | 2019-06-27 | 2022-08-31 | サイトキネティックス, インコーポレイテッド | 1-(2-((((trans)-3-フルオロ-1-(3-フルオロピリジン-2-イル)シクロブチル)メチル)アミノ)ピリミジン-5-イル)-1H-ピロール-3-カルボキサミドの多形 |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| EP4003319A4 (en) | 2019-07-30 | 2023-11-08 | Eikonizo Therapeutics, Inc. | HDAC6 INHIBITORS AND THEIR USES |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| EP4045151A1 (en) | 2019-10-14 | 2022-08-24 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021113479A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| IL293001A (en) | 2019-12-04 | 2022-07-01 | Incyte Corp | Derivatives of fgfr repressors |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| JP7606537B2 (ja) * | 2020-05-13 | 2024-12-25 | エッジワイズ セラピューティクス, インコーポレイテッド | 神経筋疾患の処置のためのピリダジノン化合物 |
| WO2021231572A1 (en) * | 2020-05-13 | 2021-11-18 | Edgewise Therapeutics, Inc. | Pyridazinone compounds for the treatment of neuromuscular diseases |
| EP4182030A1 (en) * | 2020-07-15 | 2023-05-24 | IFM Due, Inc. | Compounds and compositions for treating conditions associated with sting activity |
| GB2598768B (en) * | 2020-09-11 | 2024-09-11 | Moa Tech Limited | Herbicidal heterocyclic derivatives |
| TW202233602A (zh) * | 2020-10-27 | 2022-09-01 | 美商艾尼納製藥公司 | 可用於治療5-ht2a血清素受體相關疾病之作為5-ht2a血清素受體調節劑之嘧啶衍生物 |
| CA3176635A1 (en) | 2020-11-06 | 2022-05-12 | Cytokinetics, Inc. | Bicyclic 1,4-diazepanones and therapeutic uses thereof |
| TW202235073A (zh) | 2021-01-08 | 2022-09-16 | 美商Ifm Due有限公司 | 用於治療與sting活性相關的病狀之化合物及組合物 |
| JP2024513575A (ja) | 2021-04-12 | 2024-03-26 | インサイト・コーポレイション | Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法 |
| TW202313610A (zh) | 2021-06-09 | 2023-04-01 | 美商英塞特公司 | 作為fgfr抑制劑之三環雜環 |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| MX2024001817A (es) | 2021-08-10 | 2024-05-03 | Ifm Due Inc | Compuestos y composiciones para tratar condiciones asociadas con actividad de sting. |
| WO2023107705A1 (en) | 2021-12-10 | 2023-06-15 | Incyte Corporation | Bicyclic amines as cdk12 inhibitors |
| WO2024064745A1 (en) | 2022-09-21 | 2024-03-28 | Cytokinetics, Incorporated | Synthesis of reldesemtiv |
Family Cites Families (264)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB284425A (en) | 1926-11-22 | 1928-02-02 | James Last | Improvements in and relating to sand or like moulds for making castings |
| CH361573A (de) * | 1957-07-12 | 1962-04-30 | Cilag Chemie Aktiengesellschaf | Verfahren zur Herstellung neuer 5-Aminomethyl-pyrimidine |
| US3239345A (en) | 1965-02-15 | 1966-03-08 | Estrogenic compounds and animal growth promoters | |
| JPS5416487B1 (me) | 1970-03-17 | 1979-06-22 | ||
| US4411890A (en) | 1981-04-14 | 1983-10-25 | Beckman Instruments, Inc. | Synthetic peptides having pituitary growth hormone releasing activity |
| GB1345880A (en) | 1971-06-18 | 1974-02-06 | Cepbepe | Pyridazine derivatives |
| US4036979A (en) | 1974-01-25 | 1977-07-19 | American Cyanamid Company | Compositions containing 4,5,6,7-tetrahydrobenz[b]thien-4-yl-ureas or derivatives and methods of enhancing growth rate |
| US4157392A (en) | 1977-05-17 | 1979-06-05 | Diamond Shamrock Corporation | Pharmacologically active substituted 1,2,4-triazines |
| HU175471B (hu) | 1977-06-13 | 1980-08-28 | Gyogyszerkutato Intezet | Sposob poluchenija novykh proizvodnykh 3-skobka-1-pirazolil-skobka zakryta-piridazina |
| DE2730467A1 (de) | 1977-07-06 | 1979-01-18 | Basf Ag | Benzylpyrimidine, verfahren zu ihrer herstellung und diese enthaltende arzneimittel |
| FR2510997A1 (fr) | 1981-08-10 | 1983-02-11 | Sanofi Sa | Nouveaux derives de la methyl-4 phenyl-6 pyridazine, procede pour leur preparation et medicaments actifs sur le systeme nerveux central en contenant |
| CA1218655A (en) | 1983-01-28 | 1987-03-03 | Kathleen Biziere | Process for the preparation of pyridazine derivatives having a psychotropic action |
| FR2540115B1 (fr) | 1983-01-28 | 1985-06-07 | Sanofi Sa | Derive de la pyridazine ayant une action psychotrope, son mode de preparation et les medicaments en contenant |
| US4868183A (en) | 1986-07-21 | 1989-09-19 | Otsuka Pharmaceutical Factory, Inc. | N-pyrazinyl substituted P-aminophenols |
| JPS63165376A (ja) | 1986-12-27 | 1988-07-08 | Nippon Soda Co Ltd | オキサ(チア)ジアゾ−ル誘導体その製造方法及び殺ダニ剤 |
| ATE94538T1 (de) | 1987-06-25 | 1993-10-15 | Dowelanco | Verfahren zur herstellung von harnstoffen. |
| EP0400051B1 (en) | 1988-01-28 | 1995-05-10 | Polygen Holding Corporation | Polypeptide compounds having growth hormone releasing activity |
| EP0398961B1 (en) | 1988-01-28 | 1994-11-02 | Polygen Holding Corporation | Polypeptide compounds having growth hormone releasing activity |
| JPH01261381A (ja) | 1988-04-12 | 1989-10-18 | Nippon Soda Co Ltd | オキサ(チア)ジアゾール誘導体、その製造方法及び殺ダニ剤 |
| FR2636628B1 (fr) | 1988-08-25 | 1990-12-28 | Sanofi Sa | Derives du thiadiazole-1,3,4, leur procede d'obtention et compositions pharmaceutiques en contenant |
| JPH02164863A (ja) | 1988-12-15 | 1990-06-25 | Otsuka Pharmaceut Co Ltd | p−アミノフェノール誘導体の製造方法 |
| US5461053A (en) | 1989-02-07 | 1995-10-24 | Sanofi | Pyridazine derivatives |
| FR2663326B2 (fr) | 1989-11-17 | 1992-10-16 | Sanofi Sa | Derives de la pyridazine, procede de preparation et compositions pharmaceutiques en contenant. |
| US5656631A (en) | 1989-02-07 | 1997-08-12 | Sanofi | Pyridazine derivatives |
| GR900100380A (el) | 1989-05-20 | 1991-10-10 | Fisons Plc | Μέ?οδος παρασκευής αντι-φλεγμονωδών παραγώγων αμινοφενόλης. |
| IL96891A0 (en) | 1990-01-17 | 1992-03-29 | Merck Sharp & Dohme | Indole-substituted five-membered heteroaromatic compounds,their preparation and pharmaceutical compositions containing them |
| GB9008123D0 (en) | 1990-04-10 | 1990-06-06 | Lilly Industries Ltd | Pharmaceutical compounds |
| US5208248A (en) | 1991-01-11 | 1993-05-04 | Merck Sharpe & Dohme, Ltd. | Indazole-substituted five-membered heteroaromatic compounds |
| US5317103A (en) | 1991-01-15 | 1994-05-31 | Merck Sharp & Dohme Limited | Indole-substituted five-membered heteroaromatic compounds as 5-HT1 agonists |
| JP2651755B2 (ja) | 1991-03-01 | 1997-09-10 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
| WO1992016527A1 (fr) | 1991-03-22 | 1992-10-01 | Nippon Soda Co., Ltd. | Derive de pyridine substitue en position 2, sa production, et bactericide d'agrohorticulture |
| US5114958A (en) | 1991-05-09 | 1992-05-19 | Warner-Lambert Company | 1,2,4-oxadiazole and 1,2,4-thiadiazole derivatives of fenamates as antiinflammatory agents |
| FR2676444B1 (fr) | 1991-05-16 | 1995-03-10 | Sanofi Elf | Nouveaux derives d'amino-3 pyridazines actifs sur le systeme nerveux central, procede de preparation et compositions pharmaceutiques en contenant. |
| EP0596933A1 (en) | 1991-08-03 | 1994-05-18 | Smithkline Beecham Plc | 5-ht4 receptor antagonists |
| US5663146A (en) | 1991-08-22 | 1997-09-02 | Administrators Of The Tulane Educational Fund | Polypeptide analogues having growth hormone releasing activity |
| JPH05117255A (ja) | 1991-10-25 | 1993-05-14 | Nippon Soda Co Ltd | オキサジアゾール及びチアジアゾール誘導体、その製法 |
| BR9305466A (pt) | 1992-03-26 | 1994-12-20 | Dowelanco | Nitroanilinas n-heterocíclicas usadas como fungicidas |
| US5654322A (en) | 1992-08-11 | 1997-08-05 | Wakunaga Seiyaku Kabushiki Kaisha | Biphenylmethane derivatives and pharmaceuticals containing the same |
| CA2165344A1 (en) | 1993-06-15 | 1994-12-22 | Peter C. Canning | Immune stimulants in bacterial infections |
| ZW8594A1 (en) | 1993-08-11 | 1994-10-12 | Bayer Ag | Substituted azadioxacycbalkenes |
| DE4331178A1 (de) * | 1993-09-14 | 1995-03-16 | Hoechst Schering Agrevo Gmbh | Substituierte Pyridine und Pyrimidine, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel und Fungizide |
| US5776983A (en) | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
| DE4424788A1 (de) | 1993-12-22 | 1995-06-29 | Bayer Ag | Arylessigsäurederivate |
| US6008257A (en) | 1994-01-28 | 1999-12-28 | Bayer Aktiengesellschaft | Hydroxamic-acid derivatives, method of preparing them and their use as fungicides |
| GB9405347D0 (en) | 1994-03-18 | 1994-05-04 | Agrevo Uk Ltd | Fungicides |
| CA2186371A1 (en) | 1994-03-25 | 1995-10-05 | Robert T. Foster | Enhancement of the efficacy of dihydropyridines by deuteration |
| US6334997B1 (en) | 1994-03-25 | 2002-01-01 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| US5488064A (en) | 1994-05-02 | 1996-01-30 | Bristol-Myers Squibb Company | Benzo 1,3 dioxole derivatives |
| US5922751A (en) | 1994-06-24 | 1999-07-13 | Euro-Celtique, S.A. | Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same |
| WO1996007636A1 (de) | 1994-09-09 | 1996-03-14 | Bayer Aktiengesellschaft | Imidsäurederivate und ihre verwendung als schädlingsbekämpfungsmittel |
| US5491134A (en) | 1994-09-16 | 1996-02-13 | Bristol-Myers Squibb Company | Sulfonic, phosphonic or phosphiniic acid β3 agonist derivatives |
| US5541204A (en) | 1994-12-02 | 1996-07-30 | Bristol-Myers Squibb Company | Aryloxypropanolamine β 3 adrenergic agonists |
| US6096895A (en) | 1995-05-17 | 2000-08-01 | E. I. Du Pont De Nemours And Company | Heterocyclic dihydrazole compounds and their use for controlling fungal plant diseases |
| TW502026B (en) | 1995-06-20 | 2002-09-11 | Zeneca Ltd | Aromatic compounds useful as antagonists of e-type prostaglandins, processes for the preparation thereof, pharmaceutical compositions comprising the compounds, and intermediates |
| TW434240B (en) | 1995-06-20 | 2001-05-16 | Zeneca Ltd | Aromatic compounds, preparation thereof and pharmaceutical composition comprising same |
| JPH11508257A (ja) | 1995-06-20 | 1999-07-21 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 殺節足動物性及び殺菌・殺カビ性環式アミド |
| US5834468A (en) | 1995-07-07 | 1998-11-10 | Zeneca Limited | Substituted aryl and heteroaryl compounds as E-type prostaglandin antagonists |
| DE19525969A1 (de) | 1995-07-17 | 1997-01-23 | Bayer Ag | Etherderivate |
| US20070173465A9 (en) | 1995-10-11 | 2007-07-26 | Monahan Sean D | Expression of zeta negative and zeta positive nucleic acids using a dystrophin gene |
| CN1056370C (zh) | 1995-10-17 | 2000-09-13 | 化学工业部沈阳化工研究院 | 具有除草活性的4-芳氧(硫或氨)基嘧啶衍生物及其制备 |
| US5729399A (en) | 1995-12-13 | 1998-03-17 | International Business Machines Corporation | Contact start/stop disk drive with minimized head-disk wear in textured landing zone |
| WO1997021993A2 (en) | 1995-12-13 | 1997-06-19 | The Regents Of The University Of California | Nuclear receptor ligands and ligand binding domains |
| US6114537A (en) | 1996-02-26 | 2000-09-05 | Apotex Inc. | Process for scavenging thiols |
| US5874452A (en) | 1996-04-03 | 1999-02-23 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
| US5854265A (en) | 1996-04-03 | 1998-12-29 | Merck & Co., Inc. | Biheteroaryl inhibitors of farnesyl-protein transferase |
| JP2000507956A (ja) | 1996-04-03 | 2000-06-27 | メルク エンド カンパニー インコーポレーテッド | ファルネシル−タンパク質トランスフェラーゼ阻害剤 |
| JP2000507595A (ja) | 1996-04-03 | 2000-06-20 | メルク エンド カンパニー インコーポレーテッド | ファルネシルプロテイントランスフェラーゼの阻害剤 |
| WO1997036897A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| JP2000509371A (ja) | 1996-04-03 | 2000-07-25 | メルク エンド カンパニー インコーポレーテッド | ファルネシル―タンパク質トランスフェラーゼ阻害剤 |
| US5883105A (en) | 1996-04-03 | 1999-03-16 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| US5859035A (en) | 1996-04-03 | 1999-01-12 | Merck & Co., Inc. | Arylheteroaryl inhibitors of farnesyl-protein transferase |
| US5770615A (en) | 1996-04-04 | 1998-06-23 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
| TW414795B (en) | 1996-07-01 | 2000-12-11 | Yamanouchi Pharma Co Ltd | A thiophene derivative and the pharmaceutical composition |
| EP0934283A2 (en) | 1996-08-01 | 1999-08-11 | E.I. Du Pont De Nemours And Company | Arthropodicidal and fungicidal cyclic amides |
| WO1998023155A1 (en) | 1996-11-26 | 1998-06-04 | E.I. Du Pont De Nemours And Company | Arthropodicidal and fungicidal cyclic amides |
| US6187797B1 (en) | 1996-12-23 | 2001-02-13 | Dupont Pharmaceuticals Company | Phenyl-isoxazoles as factor XA Inhibitors |
| US5939439A (en) | 1996-12-30 | 1999-08-17 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| HRP980093A2 (en) | 1997-02-28 | 1998-12-31 | Lilly Co Eli | Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting "beta"-amyloid peptide release and/or its synthesis by use of such compounds |
| DE19725450A1 (de) | 1997-06-16 | 1998-12-17 | Hoechst Schering Agrevo Gmbh | 4-Haloalkyl-3-heterocyclylpyridine und 4-Haloalkyl-5-heterocyclylpyrimidine, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
| US6699853B2 (en) | 1997-06-16 | 2004-03-02 | Hoechst Schering Agrevo Gmbh | 4-haloalkyl-3-heterocyclylpyridines, 4-haloalkyl-5-heterocyclyl-pyrimidines and 4-trifluoromethyl-3-oxadiazolylpyridines, processes for their preparation, compositions comprising them, and their use as pesticides |
| GB9713739D0 (en) | 1997-06-27 | 1997-09-03 | Karobio Ab | Thyroid receptor ligands |
| GB9716446D0 (en) | 1997-08-05 | 1997-10-08 | Agrevo Uk Ltd | Fungicides |
| AU3289299A (en) | 1998-02-19 | 1999-09-06 | Tularik Inc. | Antiviral agents |
| US6506782B1 (en) | 1998-02-27 | 2003-01-14 | Athena Neurosciences, Inc. | Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds |
| DE19824175A1 (de) | 1998-05-29 | 1999-12-02 | Novartis Ag | Amino-azol-Verbindungen |
| PL346247A1 (en) | 1998-08-18 | 2002-01-28 | Ucb Sa | Muscarinic agonists and antagonists |
| AU1324300A (en) | 1998-10-26 | 2000-05-15 | Vertex Pharmaceuticals Incorporated | Pentacyclic compounds useful as inhibitors of hepatitis c virus ns3 helicase |
| AU1455500A (en) | 1998-10-29 | 2000-05-22 | Trega Biosciences, Inc. | Oxadiazole, thiadiazole and triazole derivatives and combinatorial libraries thereof |
| US20040053900A1 (en) | 1998-12-23 | 2004-03-18 | Pharmacia Corporation | Method of using a COX-2 inhibitor and an aromatase inhibitor as a combination therapy |
| GB9828442D0 (en) | 1998-12-24 | 1999-02-17 | Karobio Ab | Novel thyroid receptor ligands and method II |
| ES2359235T3 (es) | 1999-02-24 | 2011-05-19 | F. Hoffmann-La Roche Ag | Derivados de 4-fenilpiridina y su empleo como antagonistas del receptor nk-1. |
| JP2000281579A (ja) | 1999-03-29 | 2000-10-10 | Sumitomo Pharmaceut Co Ltd | オキサジアゾリル−1,4−ジヒドロピリジン誘導体を含有するプロテオグリカン生成促進剤 |
| US6548529B1 (en) | 1999-04-05 | 2003-04-15 | Bristol-Myers Squibb Company | Heterocyclic containing biphenyl aP2 inhibitors and method |
| US6410254B1 (en) | 1999-05-18 | 2002-06-25 | Cytokinetics | Compositions and assays utilizing ADP or phosphate for detecting protein modulators |
| US6743599B1 (en) | 1999-05-18 | 2004-06-01 | Cytokinetics, Inc. | Compositions and assays utilizing ADP or phosphate for detecting protein modulators |
| US7202051B1 (en) | 1999-05-18 | 2007-04-10 | Cytokinetics, Inc. | Compositions and assays utilizing ADP or phosphate for detecting protein modulators |
| TR200200099T2 (tr) | 1999-07-23 | 2002-06-21 | Shionogi &Co., Ltd. | Th2 farklılaşma inhibitörleri |
| AU6994600A (en) | 1999-08-12 | 2001-03-13 | Basf Aktiengesellschaft | Substituted benzoxazoles |
| EP1078632A1 (en) | 1999-08-16 | 2001-02-28 | Sanofi-Synthelabo | Use of monoamine oxydase inhibitors for the manufacture of drugs intended for the treatment of obesity |
| JP4144978B2 (ja) | 1999-09-09 | 2008-09-03 | 富士フイルム株式会社 | 1,2,4−チアジアゾール誘導体の合成法 |
| US6632815B2 (en) | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| US6844367B1 (en) | 1999-09-17 | 2005-01-18 | Millennium Pharmaceuticals, Inc. | Benzamides and related inhibitors of factor Xa |
| WO2001021160A2 (en) | 1999-09-23 | 2001-03-29 | Axxima Pharmaceuticals Aktiengesellschaft | Carboxymide and aniline derivatives as selective inhibitors of pathogens |
| GB9927844D0 (en) * | 1999-11-26 | 2000-01-26 | Glaxo Group Ltd | Chemical compounds |
| CA2388529A1 (en) | 1999-11-29 | 2001-06-07 | Pierre Ducray | Pesticidal n-heteroaryl alpha-alkoximino-carboxamides |
| DE60013910T2 (de) | 1999-12-02 | 2005-09-29 | Novartis Ag | Aminoheterocyclylamide als pestizide und antiparasitisch wirksame wirkstoffe |
| US6602872B1 (en) | 1999-12-13 | 2003-08-05 | Merck & Co., Inc. | Substituted pyridazines having cytokine inhibitory activity |
| WO2001046165A2 (en) | 1999-12-16 | 2001-06-28 | Novartis Ag | N-heteroaryl-amides and their use as parasiticides |
| TWI284639B (en) | 2000-01-24 | 2007-08-01 | Shionogi & Co | A compound having thrombopoietin receptor agonistic effect |
| AU2001233044A1 (en) | 2000-01-28 | 2001-08-07 | Akkadix Corporation | Methods for killing nematodes and nematode eggs using bis-amino-1,2,4-thiadiazoles |
| DE10006453A1 (de) | 2000-02-14 | 2001-08-16 | Bayer Ag | Piperidylcarbonsäuren als Integrinantagonisten |
| US7078536B2 (en) | 2001-03-14 | 2006-07-18 | Genesoft Pharmaceuticals, Inc. | Charged compounds comprising a nucleic acid binding moiety and uses therefor |
| EP1273287A1 (en) | 2000-04-04 | 2003-01-08 | Shionogi & Co., Ltd. | Oily compositions containing highly fat-soluble drugs |
| AU2001244610A1 (en) | 2000-04-05 | 2001-10-23 | Shionogi And Co., Ltd. | Oil-in-water microemulsions containing tricyclic compounds or preconcentrates thereof |
| US6552033B1 (en) | 2000-05-16 | 2003-04-22 | The Procter & Gamble Co. | Imidazo-containing heterocyclic compounds, their compositions and uses |
| GB0012671D0 (en) * | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
| WO2002000647A1 (en) | 2000-06-23 | 2002-01-03 | Bristol-Myers Squibb Pharma Company | Heteroaryl-phenyl substituted factor xa inhibitors |
| ES2290150T3 (es) | 2000-06-23 | 2008-02-16 | Bristol-Myers Squibb Pharma Company | Derivados de pirazol condensados con 1-(heteroaril-fenilo) como inhibidores del factor xa. |
| PE20020384A1 (es) | 2000-07-21 | 2002-05-28 | Schering Corp | PEPTIDOS COMO INHIBIDORES DE LA PROTEASA SERINA NS3/NS4a DEL VIRUS DE LA HEPATITIS C |
| EP1178036A1 (en) | 2000-08-04 | 2002-02-06 | Aventis Cropscience S.A. | Fungicidal phenylimidate derivatives |
| EP1178035B1 (en) | 2000-08-04 | 2008-07-30 | Bayer CropScience S.A. | Fungicidal phenylimine derivatives |
| EP1180512A1 (en) | 2000-08-04 | 2002-02-20 | Aventis Cropscience S.A. | Fungicidal phenylimine derivatives |
| FR2812633A1 (fr) | 2000-08-04 | 2002-02-08 | Aventis Cropscience Sa | Derives de phenyl(thio)urees et phenyl(thio)carbamates fongicides |
| WO2002026712A2 (en) | 2000-09-29 | 2002-04-04 | Millennium Pharmaceuticals, Inc. | Quaternary amines and related inhibitors of factor xa |
| US6667326B1 (en) | 2000-11-16 | 2003-12-23 | Novartis Animal Health Us, Inc. | Pesticidal aminoheterocyclamide compounds |
| AUPR213700A0 (en) | 2000-12-18 | 2001-01-25 | Biota Scientific Management Pty Ltd | Antiviral agents |
| JP2002212169A (ja) | 2001-01-12 | 2002-07-31 | Sumitomo Pharmaceut Co Ltd | 5員複素芳香環化合物 |
| WO2002059100A1 (en) | 2001-01-26 | 2002-08-01 | Shionogi & Co., Ltd. | Halogen compounds having thrombopoietin receptor agonism |
| JP4145654B2 (ja) | 2001-01-26 | 2008-09-03 | 塩野義製薬株式会社 | トロンボポエチン受容体アゴニスト作用を有する環状化合物 |
| CA2440374A1 (en) | 2001-03-14 | 2002-09-19 | Takayuki Maruyama | A pharmaceutical composition for the treatment of depression comprising the ep1 antagonist as active ingredient |
| US6960595B2 (en) | 2001-03-23 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | 5-6 to 5-7 Heterobicycles as factor Xa inhibitors |
| JP2002305083A (ja) | 2001-04-04 | 2002-10-18 | Mitsubishi Chemicals Corp | 有機電界発光素子 |
| AU2002313633B2 (en) | 2001-06-08 | 2007-03-01 | Cytovia, Inc. | Substituted 3-aryl-5-aryl-[1,2,4]-oxadiazoles and analogs |
| TWI320039B (en) | 2001-09-21 | 2010-02-01 | Lactam-containing compounds and derivatives thereof as factor xa inhibitors | |
| US6825221B2 (en) | 2001-10-18 | 2004-11-30 | Allergan, Inc. | Arylsulfanyl and heteroarylsulfanyl derivatives for treating pain |
| US6921762B2 (en) * | 2001-11-16 | 2005-07-26 | Amgen Inc. | Substituted indolizine-like compounds and methods of use |
| JPWO2003043655A1 (ja) | 2001-11-19 | 2005-03-10 | 小野薬品工業株式会社 | 頻尿の治療剤 |
| US20050113283A1 (en) | 2002-01-18 | 2005-05-26 | David Solow-Cordero | Methods of treating conditions associated with an EDG-4 receptor |
| US6995144B2 (en) | 2002-03-14 | 2006-02-07 | Eisai Co., Ltd. | Nitrogen containing heterocyclic compounds and medicines containing the same |
| US20040110757A1 (en) | 2002-03-21 | 2004-06-10 | Thomas Arrhenius | Flt-1 ligands and their uses in the treatment of diseases regulatable by angiogenesis |
| AU2003222648A1 (en) | 2002-05-13 | 2003-12-02 | Eli Lilly And Company | Multicyclic compounds for use as melanin concentrating hormone antagonists in the treatment of obesity and diabetes |
| US7119111B2 (en) | 2002-05-29 | 2006-10-10 | Amgen, Inc. | 2-oxo-1,3,4-trihydroquinazolinyl derivatives and methods of use |
| US7232616B2 (en) | 2002-06-13 | 2007-06-19 | Tsinghua University | Organic electroluminescent materials and devices made from such materials |
| EP1515964A1 (en) * | 2002-06-14 | 2005-03-23 | ALTANA Pharma AG | Substituted diaminopyrimidines |
| JP4529685B2 (ja) * | 2002-06-28 | 2010-08-25 | アステラス製薬株式会社 | ジアミノピリミジンカルボキサミド誘導体 |
| EP1539724B1 (en) | 2002-08-07 | 2007-10-10 | Neuraxon Inc. | Amino benzothiazole compounds with nos inhibitory activity |
| WO2004014881A2 (en) | 2002-08-09 | 2004-02-19 | Astra Zeneca Ab | '1,2,4'oxadiazoles as modulators of metabotropic glutamate receptor-5 |
| CA2497440C (en) * | 2002-09-04 | 2011-03-22 | Schering Corporation | Pyrazolopyrimidines as cyclin-dependent kinase inhibitors |
| AU2003266668A1 (en) | 2002-09-30 | 2004-04-23 | Banyu Pharmaceutical Co., Ltd. | 2-aminobenzimidazole derivative |
| US7259161B2 (en) | 2002-11-04 | 2007-08-21 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of JAK and other protein kinases |
| KR20050074571A (ko) | 2002-11-11 | 2005-07-18 | 바이엘 헬스케어 아게 | Ip 수용체 길항제로서의 페닐 또는 헤테로아릴 아미노알칸 유도체 |
| US20050043344A1 (en) | 2002-12-20 | 2005-02-24 | Pharmacia Corporation | Heteroarylalkanoic acids as integrin receptor antagonists derivatives |
| US20040147561A1 (en) | 2002-12-27 | 2004-07-29 | Wenge Zhong | Pyrid-2-one derivatives and methods of use |
| US7202257B2 (en) | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
| TW200418835A (en) | 2003-01-24 | 2004-10-01 | Tanabe Seiyaku Co | A pyrazolopyrimidine compound and a process for preparing the same |
| CN100345853C (zh) | 2003-01-24 | 2007-10-31 | 田边制药株式会社 | 吡唑并嘧啶化合物及其制备方法 |
| AR042956A1 (es) * | 2003-01-31 | 2005-07-13 | Vertex Pharma | Inhibidores de girasa y usos de los mismos |
| US7157455B2 (en) * | 2003-02-10 | 2007-01-02 | Hoffmann-La Roche Inc. | 4-Aminopyrimidine-5-one derivatives |
| US7223788B2 (en) | 2003-02-14 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Substituted N-aryl heterocycles, process for their preparation and their use as medicaments |
| JP2006523184A (ja) | 2003-02-22 | 2006-10-12 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフトング | 液晶としてのシアノピリドン誘導体 |
| US20050187266A1 (en) | 2003-04-15 | 2005-08-25 | Pfizer Inc | Alpha substituted carboxylic acids |
| PL1635824T3 (pl) | 2003-06-03 | 2010-01-29 | Novartis Ag | 5-Członowe heterocykliczne inhibitory P-38 |
| WO2004108133A2 (en) | 2003-06-05 | 2004-12-16 | Vertex Pharmaceuticals Incorporated | Modulators of vr1 receptor |
| EP1354876B1 (fr) | 2003-06-13 | 2005-04-27 | Les Laboratoires Servier | Nouveau procédé de synthèse de l'acide (2S, 3aS, 7aS)-perhydroindole-2-carboxylique et de ses esters, et application à la synthèse du perindopril |
| WO2005000309A2 (en) | 2003-06-27 | 2005-01-06 | Ionix Pharmaceuticals Limited | Chemical compounds |
| AU2004259012C1 (en) * | 2003-07-23 | 2012-08-02 | Exelixis, Inc. | Anaplastic lymphoma kinase modulators and methods of use |
| ATE536353T1 (de) | 2003-08-20 | 2011-12-15 | Vertex Pharma | 2-(4-amino-1,2,5-oxadiazol-4-yl)-imidazol- verbindungen als protein kinase inhibitoren |
| US7378409B2 (en) | 2003-08-21 | 2008-05-27 | Bristol-Myers Squibb Company | Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity |
| EP2210607B1 (en) | 2003-09-26 | 2011-08-17 | Exelixis Inc. | N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide for the treatment of cancer |
| TWI316955B (en) | 2003-11-19 | 2009-11-11 | Chisso Corp | Photo-polymerization liquid composition,polymer or polymer co mposition and optical compensation device thereof |
| WO2005051932A1 (ja) | 2003-11-28 | 2005-06-09 | Nippon Soda Co., Ltd. | アリール複素環誘導体および農園芸用殺菌剤および殺虫剤 |
| GB0328295D0 (en) | 2003-12-05 | 2004-01-07 | Muscagen Ltd | Therapeutic compounds |
| US20070191336A1 (en) | 2003-12-24 | 2007-08-16 | Flynn Daniel L | Anti-inflammatory medicaments |
| US7319108B2 (en) | 2004-01-25 | 2008-01-15 | Sanofi-Aventis Deutschland Gmbh | Aryl-substituted heterocycles, process for their preparation and their use as medicaments |
| WO2005077368A2 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
| WO2005077345A1 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Compounds for the treatment of gastro-esophageal reflux disease |
| WO2005077373A2 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
| UA83416C2 (en) | 2004-02-13 | 2008-07-10 | Баниу Фармасьютикал Ко., Лтд. | Fused ring 4-oxopyrimidine derivative |
| US7585881B2 (en) | 2004-02-18 | 2009-09-08 | Astrazeneca Ab | Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
| DE102004008141A1 (de) | 2004-02-19 | 2005-09-01 | Abbott Gmbh & Co. Kg | Guanidinverbindungen und ihre Verwendung als Bindungspartner für 5-HT5-Rezeptoren |
| JP5319113B2 (ja) * | 2004-03-26 | 2013-10-16 | メチルジーン インコーポレイテッド | ヒストンデアセチラーゼの阻害剤 |
| EP1731513A4 (en) | 2004-03-30 | 2007-10-31 | Daiichi Seiyaku Co | PHENOXYACETIC ACID DERIVATIVE AND MEDICAMENT CONTAINING THE SAME |
| EP1749827A4 (en) | 2004-03-30 | 2010-04-21 | Kyowa Hakko Kirin Co Ltd | ANTITUMOR AGENTS |
| EP1761496A2 (en) | 2004-03-31 | 2007-03-14 | Janssen Pharmaceutica N.V. | Non-imidazole heterocyclic compounds as histamine h3-receptor ligands |
| CN1960981A (zh) | 2004-03-31 | 2007-05-09 | 詹森药业有限公司 | 作为组胺h3受体调节剂的非咪唑杂环化合物 |
| RU2006138621A (ru) | 2004-04-02 | 2008-05-10 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Азаиндолы, полезные в качестве ингибиторов rock и других протеинкиназ |
| US7439369B2 (en) | 2004-06-22 | 2008-10-21 | Loa Alamos National Security, Llc | Method and system for hydrogen evolution and storage |
| US7705025B2 (en) | 2004-08-23 | 2010-04-27 | Eli Lilly And Company | Histamine H3 receptor agents, preparation and therapeutic uses |
| AU2005278292B2 (en) | 2004-08-31 | 2011-09-08 | Msd K.K. | Novel substituted imidazole derivatives |
| BRPI0517947A (pt) * | 2004-11-02 | 2008-10-21 | Univ Northwestern | composto de piridazina, composições e métodos |
| WO2006050476A2 (en) * | 2004-11-03 | 2006-05-11 | Vertex Pharmaceuticals Incorporated | Pyrimidine derivatives as ion channel modulators and methods of use |
| AU2005309566A1 (en) | 2004-11-22 | 2006-06-01 | Vertex Pharmaceuticals Incorporated | Bicyclic inhibitors or Rho kinase |
| CA2587642C (en) * | 2004-11-30 | 2013-04-09 | Amgen Inc. | Substituted heterocycles and methods of use |
| US20070123572A1 (en) | 2005-11-28 | 2007-05-31 | Kalypsys, Inc. | Novel method of preparation of 5-chloro-3-imidazol-1-yl-[1,2,4]thiadiazole and (3-imidazol-1-yl-[1,2,4]thiadiazol-5yl)-dialkyl-amines |
| MX2007007032A (es) * | 2004-12-17 | 2007-07-04 | Amgen Inc | Compuestos de aminopirimidina y metodos de uso. |
| US20060160869A1 (en) | 2005-01-05 | 2006-07-20 | Rigel Pharmaceuticals, Inc. | Ubiquitin ligase inhibitors |
| MX2007008434A (es) | 2005-01-19 | 2007-07-25 | Squibb Bristol Myers Co | Derivados de 2-fenoxi-n-(1,3,4-tiadizol-2il)piridin-3-amina y compuestos relacionados como inhibidores del receptor p2y1 para el tratamiento de trastornos tromboembolicos. |
| CN101232885A (zh) | 2005-01-25 | 2008-07-30 | 神经能质公司 | 经取代的哒嗪基喹啉-4-基胺和嘧啶基喹啉-4-基胺类似物 |
| WO2006081230A2 (en) | 2005-01-26 | 2006-08-03 | Schering Corporation | 3-(indazol-5-yl)-(1,2, 4) triazine derivatives and related compounds as protein kinase inhibitors for the treatment of cancer |
| MY158077A (en) | 2005-02-04 | 2016-08-30 | Senomyx Inc | Compounds comprising linked heteroaryl moieties and their use as novel umami flavor modifiers tastants and taste enhancers for comestible compositions |
| MX2007009843A (es) * | 2005-02-16 | 2007-08-23 | Astrazeneca Ab | Compuestos quimicos. |
| JP2006274133A (ja) | 2005-03-30 | 2006-10-12 | Fuji Photo Film Co Ltd | 液晶組成物、位相差板及び楕円偏光板 |
| US20080161305A1 (en) | 2005-04-06 | 2008-07-03 | Exelixis, Inc. | C-Met Modulators and Methods of Use |
| MX2007015427A (es) | 2005-06-07 | 2008-04-16 | Pharmacopeia Inc | Inhibidores de azinona y diazinona v3 para depresion y trastornos de estres. |
| EP2386554A1 (en) | 2005-07-04 | 2011-11-16 | High Point Pharmaceuticals, LLC | Compounds active at the histamine H3 receptor |
| WO2007012642A1 (de) | 2005-07-29 | 2007-02-01 | Basf Aktiengesellschaft | 7-amino-6-thiadiazolyl- und -oxadiazolyl- 1 , 2 , 4-triazolo [1 , 5 -a] pyrimidin- verbindungen und ihre verwendung zur bekämpfung von schadpilzen |
| US8093401B2 (en) | 2005-08-04 | 2012-01-10 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
| DK1910384T3 (da) | 2005-08-04 | 2012-12-17 | Sirtris Pharmaceuticals Inc | Imidazo [2,1-b] thiazol-derivater som sirtuinmodulerende forbindelser |
| RU2008110949A (ru) | 2005-08-23 | 2009-09-27 | Айрм Ллк (Bm) | Соединения и композиции-иммуносупрессанты |
| JP2007093918A (ja) | 2005-09-28 | 2007-04-12 | Fujifilm Corp | 光学ローパスフィルター、およびその製造方法 |
| JP2007093919A (ja) | 2005-09-28 | 2007-04-12 | Fujifilm Corp | 光学ローパスフィルター、およびその製造方法 |
| WO2007037010A1 (ja) | 2005-09-29 | 2007-04-05 | Daiichi Pharmaceutical Co., Ltd. | フェノキシ酢酸誘導体及びそれを用いた医薬 |
| US7531482B2 (en) | 2005-10-21 | 2009-05-12 | Dow Agrosciences Llc | Thieno-pyrimidine compounds having fungicidal activity |
| EP2078721B1 (en) | 2005-10-21 | 2014-01-22 | Dow AgroSciences LLC | Thieno-pyrimidine compounds having fungicidal activity |
| RU2008120619A (ru) | 2005-10-26 | 2009-12-10 | БЕРИНГЕР ИНГЕЛЬХАЙМ ИНТЕРНАЦИОНАЛЬ ГмбХ (DE) | (гетеро)арилы, обладающие антагонистической активностью по отношению к меланинконцентрирующему гормону |
| DK1945632T3 (da) | 2005-11-08 | 2013-12-16 | Vertex Pharma | Heterocycliske modulatorer af ATP-bindende kassettetransportører |
| SI1966202T1 (sl) | 2005-12-13 | 2012-01-31 | Incyte Corp | S heteroarilom substituirani pirolo (2,3-b)piridini in pirolo (2,3-b)pirimidini kot zaviralci janus kinaze |
| WO2007075377A2 (en) | 2005-12-15 | 2007-07-05 | Cytokinetics, Inc. | Certain chemical entities, compositions and methods |
| US7825120B2 (en) | 2005-12-15 | 2010-11-02 | Cytokinetics, Inc. | Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas |
| EP1959962A2 (en) | 2005-12-16 | 2008-08-27 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| WO2007075896A2 (en) | 2005-12-22 | 2007-07-05 | Kemia, Inc. | Heterocyclic cytokine inhibitors |
| WO2007076460A2 (en) | 2005-12-23 | 2007-07-05 | Kalypsys, Inc. | Substituted thiazole ureas useful as inhibitors of protein kinases |
| BRPI0709007A2 (pt) | 2006-03-09 | 2011-06-21 | Pharmacopeia Inc | inibidores de 8-heteroarilpurina mnk2 para tratamento de distúrbios metabólicos |
| JP5243696B2 (ja) | 2006-03-17 | 2013-07-24 | 田辺三菱製薬株式会社 | ベンゼン誘導体 |
| EA016264B1 (ru) * | 2006-03-31 | 2012-03-30 | Янссен Фармацевтика Н.В. | Бензоимидазол-2-илпиримидины и пиразины в качестве модуляторов рецептора гистамина н |
| CN101426766B (zh) | 2006-04-19 | 2014-03-26 | 默克雪兰诺有限公司 | 用作mek抑制剂的杂芳基取代的芳基氨基吡啶衍生物 |
| EP2010528B1 (en) | 2006-04-19 | 2017-10-04 | Novartis AG | 6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling |
| BRPI0710950A2 (pt) | 2006-04-28 | 2012-06-26 | Shionogi & Co | derivado de amina tendo atividade antagonìstica de receptor y5 de npi 53 a61p 3/04 a61p 9/04 a61p 9/12 a61p 15/00 a61p 25/08 a61p 25/20 a61p 25/24 a61p 43/00 c07c 311/07 c07c 317/36 c07d 207/325 c07d 211/14 c07d 213/38 c07d 213/74 c07d 213/82 c07d 215/38 c07d 217/04 c07d 217/14 c07d 217/22 c07d 219/10 c07d 231/38 c07d 233/61 c07d 235/30 c07d 237/20 c07d 237/22 c07d 237/34 c07d 239/42 c07d 241/20 c07d 261/14 c07d 261/20 c07d 263/58 c07d 265/30 c07d 265/36 c07d 267/14 c07d 275/02 c07d 277/28 c07d 277/62 c07d 277/82 c07d 295/12 c07d 295/18 c07d 333/36 c07d 333/40 c07d 333/66 c07d 333/72 c07d 403/04 c07d 409/04 c07d 413/04 c07d 417/12 c07d 498/04 c07d 513/04 |
| WO2007127475A2 (en) | 2006-04-28 | 2007-11-08 | Northwestern University | Pyridazines for demyelinating diseases and neuropathic pain |
| WO2007130383A2 (en) | 2006-04-28 | 2007-11-15 | Northwestern University | Compositions and treatments using pyridazine compounds and secretases |
| WO2007146712A2 (en) | 2006-06-09 | 2007-12-21 | Kemia, Inc. | Therapy using cytokine inhibitors |
| US8435774B2 (en) | 2006-06-28 | 2013-05-07 | Qiagen Gmbh | Enhancing reactivation of thermostable reversibly inactivated enzymes |
| BRPI0712795A2 (pt) | 2006-07-07 | 2012-09-04 | Boehringer Ingelheim Int | derivados de heteroarila substituìdos com fenila e uso dos mesmos como agentes antitumorais |
| WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| US8227603B2 (en) | 2006-08-01 | 2012-07-24 | Cytokinetics, Inc. | Modulating skeletal muscle |
| EP2059516A1 (en) | 2006-08-30 | 2009-05-20 | BIOVITRUM AB (publ) | Pyridine compounds for treating gpr119 related disorders |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| US20100197908A1 (en) | 2006-12-11 | 2010-08-05 | Boehringer Ingelheim International Gmbh | Pyridazine Derivatives with MCH Antagonistic Activity and Medicaments Comprising These Compounds |
| DE102007002717A1 (de) | 2007-01-18 | 2008-07-24 | Merck Patent Gmbh | Heterocyclische Indazolderivate |
| WO2009011285A1 (ja) * | 2007-07-13 | 2009-01-22 | Taisho Pharmaceutical Co., Ltd. | ヘテロアリールベンゼン化合物 |
| GB0720444D0 (en) | 2007-10-18 | 2007-11-28 | Glaxo Group Ltd | Novel compounds |
| US7943619B2 (en) | 2007-12-04 | 2011-05-17 | Hoffmann-La Roche Inc. | Isoxazolo-pyridazine derivatives |
| TW200940537A (en) | 2008-02-26 | 2009-10-01 | Astrazeneca Ab | Heterocyclic urea derivatives and methods of use thereof |
| US20090270398A1 (en) | 2008-04-21 | 2009-10-29 | Institute For Oneworld Health | Compounds, Compositions and Methods Comprising Pyridazine Derivatives |
| WO2009131958A2 (en) | 2008-04-21 | 2009-10-29 | Institute For Oneworld Health | Compounds, compositions and methods comprising triazine derivatives |
| WO2009143018A2 (en) * | 2008-05-19 | 2009-11-26 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
| CL2009001345A1 (es) | 2008-06-04 | 2010-06-11 | Astrazeneca Ab | Compuestos derivados de 1-piridin-2-il-urea y 1-pirimidin-2-il-urea sustituidos, inhibidores de adn girasa y topoisomerasa iv; composicion farmaceutica; y su uso en tratamiento de infecciones bacterianas como neumonia adquirida intrahospitalariamente, infecciones a la piel, bronquitis, sinusitis, entre otras enfermedades. |
| WO2009152168A2 (en) | 2008-06-09 | 2009-12-17 | Awd. Pharma Gmbh & Co. Kg | Carboxylic acid salts of 2-amino-3-carbethoxyamino-6-(4-fluoro-benzylamino)-pyridine |
| SG192446A1 (en) | 2008-06-30 | 2013-08-30 | Janssen Pharmaceutica Nv | Process for the preparation of benzoimidazol-2-yl pyrimidine derivatives |
| US20100025641A1 (en) | 2008-08-04 | 2010-02-04 | Fujifilm Corporation | Infrared region selective reflection coat and infrared region selective reflection film |
| TWI409265B (zh) * | 2008-08-20 | 2013-09-21 | Merck Sharp & Dohme | 經取代之吡啶及嘧啶衍生物及彼等於治療病毒感染之用途 |
| JP2010132590A (ja) | 2008-12-03 | 2010-06-17 | Astellas Pharma Inc | オキサジアゾール化合物 |
| MX2011010396A (es) * | 2009-03-30 | 2011-10-24 | Astellas Pharma Inc | Compuesto de pirimidina. |
| CA2773561A1 (en) | 2009-09-14 | 2011-03-17 | Phusis Therapeutics Inc. | Pharmaceutical compositions and formulations including inhibitors of the pleckstrin homology domain and methods for using same |
| WO2011133920A1 (en) | 2010-04-23 | 2011-10-27 | Cytokinetics, Inc. | Certain amino-pyridines and amino-triazines, compositions thereof, and methods for their use |
| AR081626A1 (es) | 2010-04-23 | 2012-10-10 | Cytokinetics Inc | Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos |
| AR081331A1 (es) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos |
| SG191040A1 (en) | 2010-12-23 | 2013-08-30 | Pfizer | Glucagon receptor modulators |
| MX2013010771A (es) | 2011-03-22 | 2014-01-31 | Amgen Inc | Compuestos de azoles como inhibidores. |
| US8759380B2 (en) | 2011-04-22 | 2014-06-24 | Cytokinetics, Inc. | Certain heterocycles, compositions thereof, and methods for their use |
| KR20160046693A (ko) | 2012-04-02 | 2016-04-29 | 싸이토키네틱스, 인코포레이티드 | 횡격막 기능을 향상시키는 방법들 |
| KR102163931B1 (ko) | 2012-04-11 | 2020-10-12 | 싸이토키네틱스, 인코포레이티드 | 골격근 피로에 대한 저항을 개선 |
| HRP20220183T1 (hr) | 2014-04-29 | 2022-04-29 | Cytokinetics, Inc. | Postupci smanjivanja propadanja vitalnog kapaciteta |
| PT3192512T (pt) * | 2014-09-09 | 2019-10-29 | Cytokinetics Inc | Nova composição farmacêutica para prevenção e/ou tratamento de incontinência urinária |
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