SG178504A1 - Fused heterocyclic ring derivative and use thereof - Google Patents
Fused heterocyclic ring derivative and use thereof Download PDFInfo
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- SG178504A1 SG178504A1 SG2012011599A SG2012011599A SG178504A1 SG 178504 A1 SG178504 A1 SG 178504A1 SG 2012011599 A SG2012011599 A SG 2012011599A SG 2012011599 A SG2012011599 A SG 2012011599A SG 178504 A1 SG178504 A1 SG 178504A1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- 229940124513 senna glycoside Drugs 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N serine Chemical compound OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- FESBVLZDDCQLFY-UHFFFAOYSA-N sete Chemical compound [Te]=[Se] FESBVLZDDCQLFY-UHFFFAOYSA-N 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 210000003859 smegma Anatomy 0.000 description 1
- 210000004894 snout Anatomy 0.000 description 1
- 229950010372 sobuzoxane Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 1
- IYYIUOWKEMQYNV-UHFFFAOYSA-N sodium;ethoxy-oxido-oxophosphanium Chemical compound [Na+].CCO[P+]([O-])=O IYYIUOWKEMQYNV-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 1
- 229960003787 sorafenib Drugs 0.000 description 1
- 238000004677 spark ionization mass spectrometry Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- SETMGIIITGNLAS-UHFFFAOYSA-N spizofurone Chemical compound O=C1C2=CC(C(=O)C)=CC=C2OC21CC2 SETMGIIITGNLAS-UHFFFAOYSA-N 0.000 description 1
- 229950001870 spizofurone Drugs 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 235000013547 stew Nutrition 0.000 description 1
- 239000010907 stover Substances 0.000 description 1
- 229940021506 stye Drugs 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- 238000009120 supportive therapy Methods 0.000 description 1
- 238000004416 surface enhanced Raman spectroscopy Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 201000001872 syndromic X-linked intellectual disability Cabezas type Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229960003198 tamsulosin hydrochloride Drugs 0.000 description 1
- UXXQOJXBIDBUAC-UHFFFAOYSA-N tandutinib Chemical compound COC1=CC2=C(N3CCN(CC3)C(=O)NC=3C=CC(OC(C)C)=CC=3)N=CN=C2C=C1OCCCN1CCCCC1 UXXQOJXBIDBUAC-UHFFFAOYSA-N 0.000 description 1
- 229950009893 tandutinib Drugs 0.000 description 1
- DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 description 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 229960003433 thalidomide Drugs 0.000 description 1
- 238000000015 thermotherapy Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 101150014006 thrA gene Proteins 0.000 description 1
- 101150009089 tifa gene Proteins 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000004481 total suppression of sideband Methods 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 238000011830 transgenic mouse model Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000003652 trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 230000005747 tumor angiogenesis Effects 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 102000003298 tumor necrosis factor receptor Human genes 0.000 description 1
- 229940056345 tums Drugs 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- OOLLAFOLCSJHRE-ZHAKMVSLSA-N ulipristal acetate Chemical compound C1=CC(N(C)C)=CC=C1[C@@H]1C2=C3CCC(=O)C=C3CC[C@H]2[C@H](CC[C@]2(OC(C)=O)C(C)=O)[C@]2(C)C1 OOLLAFOLCSJHRE-ZHAKMVSLSA-N 0.000 description 1
- 210000000623 ulna Anatomy 0.000 description 1
- 210000000689 upper leg Anatomy 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 125000005289 uranyl group Chemical group 0.000 description 1
- 210000000626 ureter Anatomy 0.000 description 1
- 229960000241 vandetanib Drugs 0.000 description 1
- UHTHHESEBZOYNR-UHFFFAOYSA-N vandetanib Chemical compound COC1=CC(C(/N=CN2)=N/C=3C(=CC(Br)=CC=3)F)=C2C=C1OCC1CCN(C)CC1 UHTHHESEBZOYNR-UHFFFAOYSA-N 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 239000002435 venom Substances 0.000 description 1
- 210000001048 venom Anatomy 0.000 description 1
- 231100000611 venom Toxicity 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 210000002845 virion Anatomy 0.000 description 1
- 208000025247 virus-associated trichodysplasia spinulosa Diseases 0.000 description 1
- 229960004449 vismodegib Drugs 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 238000004329 water eliminated fourier transform Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 238000001786 wide angle neutron scattering Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
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- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009195770 | 2009-08-26 | ||
| JP2010015644 | 2010-01-27 | ||
| PCT/JP2010/064413 WO2011024872A1 (ja) | 2009-08-26 | 2010-08-25 | 縮合複素環誘導体およびその用途 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG178504A1 true SG178504A1 (en) | 2012-04-27 |
Family
ID=43627972
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2012011599A SG178504A1 (en) | 2009-08-26 | 2010-08-25 | Fused heterocyclic ring derivative and use thereof |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US8907089B2 (enExample) |
| EP (1) | EP2471790B1 (enExample) |
| JP (1) | JP5599802B2 (enExample) |
| KR (1) | KR20120078703A (enExample) |
| CN (1) | CN102574851A (enExample) |
| AU (1) | AU2010287492A1 (enExample) |
| BR (1) | BR112012004134A2 (enExample) |
| CA (1) | CA2771833A1 (enExample) |
| CL (1) | CL2012000461A1 (enExample) |
| CR (1) | CR20120095A (enExample) |
| DO (1) | DOP2012000048A (enExample) |
| EA (1) | EA201270311A1 (enExample) |
| EC (1) | ECSP12011747A (enExample) |
| GE (1) | GEP20146075B (enExample) |
| IL (1) | IL218323A0 (enExample) |
| IN (1) | IN2012DN02069A (enExample) |
| MA (1) | MA33589B1 (enExample) |
| MX (1) | MX2012002419A (enExample) |
| NZ (1) | NZ598749A (enExample) |
| PE (1) | PE20121326A1 (enExample) |
| SG (1) | SG178504A1 (enExample) |
| TN (1) | TN2012000084A1 (enExample) |
| WO (1) | WO2011024872A1 (enExample) |
| ZA (1) | ZA201201795B (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2471793B1 (en) * | 2009-08-26 | 2016-10-05 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
| WO2014140077A1 (en) * | 2013-03-14 | 2014-09-18 | Glaxosmithkline Intellectual Property (No.2) Limited | Furopyridines as bromodomain inhibitors |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6436965B1 (en) | 2000-03-02 | 2002-08-20 | Merck Frosst Canada & Co. | PDE IV inhibiting amides, compositions and methods of treatment |
| EP1310488A4 (en) | 2000-08-09 | 2005-08-10 | Mitsubishi Pharma Corp | CONDENSED BICYCLIC AMIDE COMPOUNDS AND MEDICAL USES THEREOF |
| CA2469435A1 (en) | 2001-12-21 | 2003-07-24 | X-Ceptor Therapeutics, Inc. | Modulators of lxr |
| US7482366B2 (en) | 2001-12-21 | 2009-01-27 | X-Ceptor Therapeutics, Inc. | Modulators of LXR |
| AU2003265853A1 (en) | 2002-08-29 | 2004-03-19 | Curis, Inc. | Hedgehog antagonists, methods and uses related thereto |
| WO2005033288A2 (en) * | 2003-09-29 | 2005-04-14 | The Johns Hopkins University | Hedgehog pathway antagonists |
| US20050203081A1 (en) | 2004-02-25 | 2005-09-15 | Jinbo Lee | Inhibitors of protein tyrosine phosphatase 1B |
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| WO2008057469A1 (en) * | 2006-11-02 | 2008-05-15 | Wyeth | Small organic molecule regulators of cell proliferation |
| US8273747B2 (en) | 2006-11-02 | 2012-09-25 | Curis, Inc. | Small organic molecule regulators of cell proliferation |
| LT2170860T (lt) | 2007-06-29 | 2017-01-10 | Pfizer Inc. | Benzimidazolo dariniai |
| RU2364597C1 (ru) | 2007-12-14 | 2009-08-20 | Андрей Александрович Иващенко | ГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ Hh-СИГНАЛЬНОГО КАСКАДА, ЛЕКАРСТВЕННЫЕ КОМПОЗИЦИИ НА ИХ ОСНОВЕ И СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЙ, СВЯЗАННЫХ С АББЕРАНТНОЙ АКТИВНОСТЬЮ Hh СИГНАЛЬНОЙ СИСТЕМЫ |
| JP4685891B2 (ja) | 2008-02-19 | 2011-05-18 | 株式会社ハネックス | 分離装置 |
| JO3259B1 (ar) | 2008-02-26 | 2018-09-16 | Takeda Pharmaceuticals Co | مشتق دائري مغاير ملتحم واستخدامه |
| JP2010015644A (ja) | 2008-07-04 | 2010-01-21 | Fujitsu Ltd | スピンドル機構、電磁変換特性評価機、および情報記憶装置 |
| GB0900484D0 (en) | 2009-01-13 | 2009-02-11 | Angeletti P Ist Richerche Bio | Therapeutic agent |
-
2010
- 2010-08-25 BR BR112012004134A patent/BR112012004134A2/pt not_active IP Right Cessation
- 2010-08-25 CA CA2771833A patent/CA2771833A1/en not_active Abandoned
- 2010-08-25 JP JP2011528831A patent/JP5599802B2/ja active Active
- 2010-08-25 US US13/391,791 patent/US8907089B2/en active Active
- 2010-08-25 SG SG2012011599A patent/SG178504A1/en unknown
- 2010-08-25 GE GEAP201012641A patent/GEP20146075B/en unknown
- 2010-08-25 IN IN2069DEN2012 patent/IN2012DN02069A/en unknown
- 2010-08-25 CN CN2010800469387A patent/CN102574851A/zh active Pending
- 2010-08-25 PE PE2012000255A patent/PE20121326A1/es not_active Application Discontinuation
- 2010-08-25 WO PCT/JP2010/064413 patent/WO2011024872A1/ja not_active Ceased
- 2010-08-25 AU AU2010287492A patent/AU2010287492A1/en not_active Abandoned
- 2010-08-25 EA EA201270311A patent/EA201270311A1/ru unknown
- 2010-08-25 KR KR1020127007793A patent/KR20120078703A/ko not_active Withdrawn
- 2010-08-25 MX MX2012002419A patent/MX2012002419A/es not_active Application Discontinuation
- 2010-08-25 EP EP10811921.5A patent/EP2471790B1/en active Active
- 2010-08-25 NZ NZ598749A patent/NZ598749A/xx not_active IP Right Cessation
-
2012
- 2012-02-21 TN TNP2012000084A patent/TN2012000084A1/en unknown
- 2012-02-22 DO DO2012000048A patent/DOP2012000048A/es unknown
- 2012-02-23 CL CL2012000461A patent/CL2012000461A1/es unknown
- 2012-02-24 CR CR20120095A patent/CR20120095A/es not_active Application Discontinuation
- 2012-02-26 IL IL218323A patent/IL218323A0/en unknown
- 2012-03-12 ZA ZA2012/01795A patent/ZA201201795B/en unknown
- 2012-03-16 MA MA34695A patent/MA33589B1/fr unknown
- 2012-03-26 EC ECSP12011747 patent/ECSP12011747A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2010287492A1 (en) | 2012-03-29 |
| IL218323A0 (en) | 2012-04-30 |
| CA2771833A1 (en) | 2011-03-03 |
| GEP20146075B (en) | 2014-04-10 |
| KR20120078703A (ko) | 2012-07-10 |
| JP5599802B2 (ja) | 2014-10-01 |
| TN2012000084A1 (en) | 2013-09-19 |
| ECSP12011747A (es) | 2012-05-30 |
| ZA201201795B (en) | 2013-05-29 |
| DOP2012000048A (es) | 2012-05-15 |
| EA201270311A1 (ru) | 2012-09-28 |
| PE20121326A1 (es) | 2012-10-11 |
| JPWO2011024872A1 (ja) | 2013-01-31 |
| MA33589B1 (fr) | 2012-09-01 |
| WO2011024872A1 (ja) | 2011-03-03 |
| CN102574851A (zh) | 2012-07-11 |
| EP2471790A1 (en) | 2012-07-04 |
| IN2012DN02069A (enExample) | 2015-08-21 |
| BR112012004134A2 (pt) | 2017-06-20 |
| EP2471790A4 (en) | 2013-07-31 |
| CL2012000461A1 (es) | 2012-10-05 |
| US8907089B2 (en) | 2014-12-09 |
| EP2471790B1 (en) | 2015-03-18 |
| CR20120095A (es) | 2012-06-26 |
| MX2012002419A (es) | 2012-04-19 |
| US20120220570A1 (en) | 2012-08-30 |
| NZ598749A (en) | 2013-01-25 |
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