FR23C1017I1 - QUINOLINE-8-SULFONAMIDE DERIVATIVES WITH ANTICANCER ACTIVITY - Google Patents
QUINOLINE-8-SULFONAMIDE DERIVATIVES WITH ANTICANCER ACTIVITYInfo
- Publication number
- FR23C1017I1 FR23C1017I1 FR23C1017C FR23C1017C FR23C1017I1 FR 23C1017 I1 FR23C1017 I1 FR 23C1017I1 FR 23C1017 C FR23C1017 C FR 23C1017C FR 23C1017 C FR23C1017 C FR 23C1017C FR 23C1017 I1 FR23C1017 I1 FR 23C1017I1
- Authority
- FR
- France
- Prior art keywords
- quinoline
- anticancer activity
- sulfonamide derivatives
- sulfonamide
- derivatives
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/20—Nitrogen atoms
- C07D241/22—Benzenesulfonamido pyrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/36—Sulfur atoms
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/40—Nitrogen atoms attached in position 8
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/08—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/12—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
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- 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
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22143009P | 2009-06-29 | 2009-06-29 | |
US29236010P | 2010-01-05 | 2010-01-05 | |
PCT/US2010/040486 WO2011002817A1 (en) | 2009-06-29 | 2010-06-29 | Therapeutic compounds and compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
FR23C1017I1 true FR23C1017I1 (en) | 2023-06-23 |
FR23C1017I2 FR23C1017I2 (en) | 2024-03-22 |
Family
ID=43381412
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR23C1017C Active FR23C1017I2 (en) | 2009-06-29 | 2023-04-28 | QUINOLINE-8-SULFONAMIDE DERIVATIVES WITH ANTICANCER ACTIVITY |
Country Status (39)
Country | Link |
---|---|
US (7) | US8785450B2 (en) |
EP (3) | EP3708169A1 (en) |
JP (2) | JP5856052B2 (en) |
KR (2) | KR101712035B1 (en) |
CN (2) | CN104817498B (en) |
AR (1) | AR077292A1 (en) |
AU (1) | AU2010266386C1 (en) |
BR (1) | BRPI1011587B1 (en) |
CA (2) | CA2766882C (en) |
CL (1) | CL2011003350A1 (en) |
CO (1) | CO6480955A2 (en) |
CR (2) | CR20170071A (en) |
CY (1) | CY1119443T1 (en) |
DK (1) | DK2448582T3 (en) |
EC (1) | ECSP11011567A (en) |
ES (1) | ES2632954T3 (en) |
FI (1) | FIC20230017I1 (en) |
FR (1) | FR23C1017I2 (en) |
HR (1) | HRP20170955T1 (en) |
HU (2) | HUE032969T2 (en) |
IL (1) | IL217277A (en) |
IN (1) | IN2012DN00471A (en) |
LT (2) | LT2448582T (en) |
MX (1) | MX2012000256A (en) |
MY (1) | MY191825A (en) |
NI (1) | NI201200003A (en) |
NL (1) | NL301230I2 (en) |
NO (1) | NO2023017I1 (en) |
NZ (2) | NZ597379A (en) |
PE (1) | PE20120693A1 (en) |
PL (1) | PL2448582T3 (en) |
PT (1) | PT2448582T (en) |
RU (1) | RU2561132C2 (en) |
SG (3) | SG177434A1 (en) |
SI (1) | SI2448582T1 (en) |
TW (4) | TWI598337B (en) |
UA (1) | UA107667C2 (en) |
WO (1) | WO2011002817A1 (en) |
ZA (1) | ZA201200054B (en) |
Families Citing this family (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2010223919B2 (en) | 2009-03-13 | 2016-03-31 | Les Laboratoires Servier | Methods and compositions for cell-proliferation-related disorders |
AU2010234526B2 (en) | 2009-04-06 | 2016-07-21 | Agios Pharmaceuticals, Inc. | Pyruvate kinase M2 modulators, therapeutic compositions and related methods of use |
ES2619557T3 (en) | 2009-05-04 | 2017-06-26 | Agios Pharmaceuticals, Inc. | PKM2 activators for use in cancer treatment |
AR077280A1 (en) | 2009-06-29 | 2011-08-17 | Incyte Corp | PYRIMIDINONES AS PI3K INHIBITORS, AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM |
JP5764555B2 (en) | 2009-06-29 | 2015-08-19 | アジオス ファーマシューティカルズ, インコーポレイテッド | Therapeutic compositions and related methods of use |
UA107667C2 (en) | 2009-06-29 | 2015-02-10 | Аджиос Фармасьютікалз, Інк. | Medical compounds stimulating activity of pyruvate kinase m2, compositions on their basis and use in the treatment of cancer |
CA2793836C (en) | 2009-10-21 | 2020-03-24 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
WO2011050210A1 (en) | 2009-10-21 | 2011-04-28 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
ES2642109T3 (en) * | 2009-12-09 | 2017-11-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds for use in the treatment of cancer characterized by having an IDH mutation |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
EP2558463A1 (en) | 2010-04-14 | 2013-02-20 | Incyte Corporation | Fused derivatives as i3 inhibitors |
US9062055B2 (en) | 2010-06-21 | 2015-06-23 | Incyte Corporation | Fused pyrrole derivatives as PI3K inhibitors |
EP2632920A1 (en) | 2010-10-27 | 2013-09-04 | Dynamix Pharmaceuticals Ltd. | Sulfonamides for the modulation of pkm2 |
FR2967674B1 (en) | 2010-11-23 | 2012-12-14 | Pf Medicament | HETEROARYLSULFONAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN HUMAN THERAPEUTICS |
WO2012083246A1 (en) | 2010-12-17 | 2012-06-21 | Agios Pharmaceuticals, Inc. | Novel n- (4- (azetidine - 1 - carbonyl) phenyl) - (hetero - ) arylsulfonamide derivatives as pyruvate kinase m2 (pmk2) modulators |
TW201249844A (en) | 2010-12-20 | 2012-12-16 | Incyte Corp | N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines as PI3K inhibitors |
JP6092118B2 (en) | 2010-12-21 | 2017-03-08 | アジオス ファーマシューティカルズ, インコーポレイテッド | Bicyclic PKM2 activator |
TWI549947B (en) * | 2010-12-29 | 2016-09-21 | 阿吉歐斯製藥公司 | Therapeutic compounds and compositions |
WO2012125629A1 (en) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors |
WO2012135009A1 (en) | 2011-03-25 | 2012-10-04 | Incyte Corporation | Pyrimidine-4,6-diamine derivatives as pi3k inhibitors |
US9388164B2 (en) | 2011-05-03 | 2016-07-12 | Agios Pharmaceuticals, Inc | Methods of using pyruvate kinase activators |
BR112013028422B8 (en) * | 2011-05-03 | 2022-01-11 | Agios Pharmaceuticals Inc | Pyruvate kinase activators for use in therapy |
WO2012151452A1 (en) * | 2011-05-03 | 2012-11-08 | Agios Pharmaceuticals, Inc | Pyruvate kinase activators for use in therapy |
WO2012151440A1 (en) | 2011-05-03 | 2012-11-08 | Agios Pharmaceuticals, Inc. | Pyruvate kinase activators for use for increasing lifetime of the red blood cells and treating anemia |
CN102827170A (en) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Active treatment compositions and use method thereof |
CN102827073A (en) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Therapeutically active compositions and application methods thereof |
SI2751109T1 (en) | 2011-09-02 | 2017-03-31 | Incyte Holdings Corporation | Heterocyclylamines as pi3k inhibitors |
US20140249150A1 (en) * | 2011-10-13 | 2014-09-04 | Agios Pharmaceuticals, Inc | Activators of pyruvate kinase m2 and methods of treating disease |
US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
KR102083041B1 (en) | 2012-02-22 | 2020-05-27 | 샌포드 번햄 프레비즈 메디컬 디스커버리 인스티튜트 | Sulfonamide compounds and uses as tnap inhibitors |
AR090548A1 (en) | 2012-04-02 | 2014-11-19 | Incyte Corp | BICYCLIC AZAHETEROCICLOBENCILAMINS AS PI3K INHIBITORS |
US9605521B2 (en) | 2012-09-14 | 2017-03-28 | Weatherford Technology Holdings, Llc | Gas lift valve with mixed bellows and floating constant volume fluid chamber |
WO2014062511A1 (en) | 2012-10-15 | 2014-04-24 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
WO2014071512A1 (en) * | 2012-11-06 | 2014-05-15 | Universite Laval | Combination therapy and methods for the treatment of respiratory diseases |
KR20150080619A (en) * | 2012-11-08 | 2015-07-09 | 아지오스 파마슈티컬스 아이엔씨. | Therapeutic compounds and compositions and their use as pkm2 modulators |
CN103808929A (en) * | 2012-11-08 | 2014-05-21 | 中国科学院上海生命科学研究院 | GBSS1 specific enzyme activity determination method |
WO2014139144A1 (en) | 2013-03-15 | 2014-09-18 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
WO2015006591A1 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | 2,4- or 4,6-diaminopyrimidine compounds as idh2 mutants inhibitors for the treatment of cancer |
US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
AU2015229214B2 (en) | 2014-03-14 | 2019-07-11 | Les Laboratoires Servier | Pharmaceutical compositions of therapeutically active compounds |
WO2015191677A1 (en) | 2014-06-11 | 2015-12-17 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors |
GB201419579D0 (en) * | 2014-11-03 | 2014-12-17 | Iomet Pharma Ltd | Pharmaceutical compound |
WO2016115463A1 (en) * | 2015-01-15 | 2016-07-21 | Whitehead Institute For Biomedical Research | Inhibitors of phosphoglycerate dehydrogenase (phgdh) and uses thereof |
CN117800973A (en) | 2015-02-27 | 2024-04-02 | 因赛特控股公司 | Salts of PI3K inhibitors and methods of making the same |
CN104803923B (en) * | 2015-04-22 | 2017-09-05 | 江苏恩华药业股份有限公司 | A kind of preparation method of 1 (2 pyrimidine) piperazine hydrochloride |
WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
EP4344703A1 (en) * | 2015-06-11 | 2024-04-03 | Agios Pharmaceuticals, Inc. | Methods of using pyruvate kinase activators |
DK3362066T3 (en) | 2015-10-15 | 2021-11-22 | Les Laboratoires Servier Sas | COMBINATION THERAPY FOR THE TREATMENT OF MALIGNITIES |
SG11201803088PA (en) | 2015-10-15 | 2018-05-30 | Agios Pharmaceuticals Inc | Combination therapy for treating malignancies |
EA201992215A1 (en) | 2017-03-20 | 2020-02-06 | Форма Терапьютикс, Инк. | Pyrrolopyrrole Compositions as Pyruvate Kinase Activators (PKR) |
DK3668513T3 (en) | 2017-08-15 | 2022-01-10 | Agios Pharmaceuticals Inc | PYRUVAT CHINASE ACTIVITIES FOR USE IN THE TREATMENT OF BLOOD DISEASES |
WO2019099651A1 (en) * | 2017-11-16 | 2019-05-23 | Agios Pharmaceuticals, Inc. | Methods of using deuterated pyruvate kinase activators |
WO2019104134A1 (en) * | 2017-11-22 | 2019-05-31 | Agios Pharmaceuticals, Inc. | Crystalline forms of n-(4-(4-(cyclopropylmethyl) piperazine-1-carbonyl)phenyl)quinoline-8-sulfonamide |
CN108440505A (en) * | 2018-03-30 | 2018-08-24 | 中南大学 | The total synthesis method of eptapirone |
US10980788B2 (en) | 2018-06-08 | 2021-04-20 | Agios Pharmaceuticals, Inc. | Therapy for treating malignancies |
US20220031671A1 (en) | 2018-09-19 | 2022-02-03 | Forma Therapeutics, Inc. | Treating sickle cell disease with a pyruvate kinase r activating compound |
EP3852791A4 (en) | 2018-09-19 | 2022-06-15 | Forma Therapeutics, Inc. | Activating pyruvate kinase r |
US20220081412A1 (en) * | 2018-12-20 | 2022-03-17 | The Regents Of The University Of Michigan | Quinolinyl-pyrazine-carboxamide compounds and uses thereof |
EP3924056A1 (en) | 2019-02-13 | 2021-12-22 | Agios Pharmaceuticals, Inc. | Thieno[3,2-b] pyrrole[3,2-d]pyridazinone derivatives and their use as pkm2 derivatives for the treatment of cancer, obesity and diabetes related disorders |
MX2021014228A (en) | 2019-05-22 | 2022-02-21 | Agios Pharmaceuticals Inc | Crystalline salt forms of n-(4-(4-(cyclopropylmethyl)piperazine-1 -carbonyl)phenyl)quinoline-8-sulfonamide. |
US11878049B1 (en) * | 2019-06-14 | 2024-01-23 | Agios Pharmaceuticals, Inc. | Mitapivat therapy and modulators of cytochrome P450 |
JP2022553832A (en) * | 2019-11-07 | 2022-12-26 | クリネティックス ファーマシューティカルズ,インク. | Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof |
EP4097085A1 (en) | 2020-01-28 | 2022-12-07 | Teva Pharmaceuticals International GmbH | Solid state forms of mitapivat and process for preparation thereof |
TW202228691A (en) | 2020-09-25 | 2022-08-01 | 美商阿吉歐斯製藥公司 | Pharmaceutical formulation |
KR20240004620A (en) | 2021-04-30 | 2024-01-11 | 아지오스 파마슈티컬스 아이엔씨. | How to Titrate Mitapivat |
WO2022231627A1 (en) | 2021-04-30 | 2022-11-03 | Agios Pharmaceuticals, Inc. | Methods for titrating mitapivat for use in treating thalassemia |
WO2023154036A1 (en) | 2022-02-08 | 2023-08-17 | Agios Pharmaceuticals, Inc. | Methods for titrating mitapivat |
WO2023091414A1 (en) | 2021-11-16 | 2023-05-25 | Agios Pharmaceuticals, Inc. | Compounds for treating mds-associated anemias and other conditions |
DE202022106287U1 (en) | 2022-11-09 | 2022-11-21 | Ahmad Salawi | A method for the synthesis and biological evaluation of new sulfonamide analogues |
Family Cites Families (266)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2390529A (en) | 1942-02-03 | 1945-12-11 | Ernst A H Friedheim | Hydrazino-1,3,5-triazino derivatives of substituted phenylarsenic compounds |
DE879203C (en) * | 1949-07-23 | 1953-04-23 | Kalle & Co Ag | Process for the production of copies, especially printing forms, with the aid of diazo compounds |
GB935538A (en) * | 1959-04-06 | 1963-08-28 | Stop Motion Devices Corp | Stop-motion head for use on knitting machines |
GB1274436A (en) | 1970-06-09 | 1972-05-17 | Wolfen Filmfab Veb | Process for the sensitization of photographic silver chloride and silver chlorobromide emulsions that may contain colour couplers |
BE754242A (en) | 1970-07-15 | 1971-02-01 | Geigy Ag J R | DIAMINO-S-TRIAZINES AND DINITRO-S-TRIAZINES |
US3867383A (en) | 1971-03-29 | 1975-02-18 | Ciba Geigy Corp | Monoanthranilatoanilino-s-triazines |
CH606334A5 (en) | 1974-06-21 | 1978-10-31 | Ciba Geigy Ag | |
US3998828A (en) * | 1975-01-31 | 1976-12-21 | Pfizer Inc. | 4-[2-(1,3-Dialkyl-1,2,3,4-tetra-hydropyrimidine-2,4-dione-5-carboxamido)ethyl]-1-piperidine sulfonamide |
US4235871A (en) * | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
DE2928485A1 (en) | 1979-07-14 | 1981-01-29 | Bayer Ag | USE OF UREA DERIVATIVES AS A MEDICINAL PRODUCT IN THE TREATMENT OF FATTY METABOLISM DISORDERS |
DE2948434A1 (en) * | 1979-12-01 | 1981-06-11 | Hoechst Ag, 6000 Frankfurt | 1-PIPERIDINSULFONYL UREA AND METHOD FOR THE PRODUCTION THEREOF |
JPS58186682A (en) | 1982-04-27 | 1983-10-31 | 日本化薬株式会社 | Dyeing of cellulose or cellulose containing fiber material |
US4474599A (en) | 1982-07-14 | 1984-10-02 | The Dow Chemical Company | 1-(Pyridyl)-1H-1,2,3-triazole derivatives, and use as herbicidal agents |
US4501728A (en) * | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
GB8325370D0 (en) | 1983-09-22 | 1983-10-26 | Fujisawa Pharmaceutical Co | Benzoxazoline and benzothiazoline derivatives |
US4593102A (en) * | 1984-04-10 | 1986-06-03 | A. H. Robins Company, Inc. | N-[(amino)alkyl]-1-pyrrolidine, 1-piperidine and 1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked substitution in the 2, 3 or 4-position |
US4643759A (en) | 1984-07-13 | 1987-02-17 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
IT1196195B (en) | 1984-07-20 | 1988-11-10 | Minnesota Mining & Mfg | CUL DYE FORMING COPULANTS AND PHOTOGRAPHIC ELEMENTS AND PROCEDURES |
US5019369A (en) * | 1984-10-22 | 1991-05-28 | Vestar, Inc. | Method of targeting tumors in humans |
JPS61129129A (en) | 1984-11-28 | 1986-06-17 | Kureha Chem Ind Co Ltd | Antitumor agent |
FI855180A (en) | 1985-01-18 | 1986-07-19 | Nissan Chemical Ind Ltd | PYRAZOLESULFONAMIDDERIVAT, FOERFARANDE FOER DESS FRAMSTAELLANDE OCH DET INNEHAOLLANDE OGRAESGIFT. |
DE3512630A1 (en) | 1985-04-06 | 1986-10-23 | Hoechst Ag, 6230 Frankfurt | METHOD FOR COLORING OR PRINTING CELLULOSE FIBERS OR CELLULOSE MIXED FIBERS |
EP0246749A3 (en) * | 1986-05-17 | 1988-08-31 | AgrEvo UK Limited | Triazole herbicides |
JPS6339875A (en) | 1986-08-05 | 1988-02-20 | Nissin Food Prod Co Ltd | Pyrimidine derivative |
US4837028A (en) * | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
US4775762A (en) * | 1987-05-11 | 1988-10-04 | The Dow Chemical Company | Novel (1H-1,2,3-triazol-1-yl)pyridines |
US5962490A (en) * | 1987-09-25 | 1999-10-05 | Texas Biotechnology Corporation | Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
DE3813886A1 (en) | 1988-04-20 | 1989-11-02 | Schering Ag | 1-Triazinyl-1H-1,2,4-triazole-3-sulphonamides, processes for their preparation, and their use as herbicides, fungicides and plant growth regulators |
DE3813885A1 (en) | 1988-04-20 | 1989-11-02 | Schering Ag | 1-CHLORPYRIMIDINYL-1H-1,2,4-TRIAZOL-3-SULPHONIC ACID AMIDE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS AGENT WITH HERBICIDES, FUNGICIDES AND PLANT GROWTH REGULATING EFFECT |
US5220028A (en) * | 1988-10-27 | 1993-06-15 | Nissan Chemical Industries, Ltd. | Halogeno-4-methylpyrazoles |
US5041443A (en) | 1989-02-21 | 1991-08-20 | Dainippon Pharmaceutical Co., Ltd. | Medicament for treating cerebral insufficiency diseases, novel 2-(1-piperazinyl)-4-phenylcycloalkanopyrimidine derivatives, and process for the production thereof |
US5021421A (en) | 1989-03-03 | 1991-06-04 | Dainippon Pharmaceutical Co., Ltd. | 2-(1-Piperazinyl)-4-phenylcycloalkanopyridine derivatives, processes for the production thereof, and pharmaceutical composition containing the same |
KR910021381A (en) * | 1990-02-20 | 1991-12-20 | 모리 히데오 | 4-tert-butylimidazole derivatives, and preparation method and use thereof |
CA2036148A1 (en) * | 1990-06-29 | 1991-12-30 | Hiroki Tomioka | A 1-phenylimidazole derivative and its production and use |
JPH0499768A (en) | 1990-08-17 | 1992-03-31 | Dainippon Pharmaceut Co Ltd | 4-(4-phenylpyridin-2-yl)piperazine-1-oxide derivative |
HUT65077A (en) | 1990-12-31 | 1994-04-28 | Monsanto Co | Antidoted herbicides and process for combatting the phytotoxic action of herbicidal compounds |
AU644297B2 (en) * | 1991-06-28 | 1993-12-02 | Sumitomo Chemical Company, Limited | A 1-pyridylimidazole derivative and its production and use |
IT1252567B (en) | 1991-12-20 | 1995-06-19 | Italfarmaco Spa | DERIVATIVES OF 5-ISOKINOLINSULPHONAMIDS INHIBITORS OF PROTEIN-KINASES |
DE69322076D1 (en) | 1992-02-28 | 1998-12-17 | Zenyaku Kogyo Kk | S-TRIAZINE DERIVATIVES AND THESE ACTIVE INGREDIENTS AGAINST OSTROGEN-DEPENDENT DISEASES |
JPH0625177A (en) | 1992-07-09 | 1994-02-01 | Nissan Chem Ind Ltd | Pyrazole derivative and herbicide |
JP3409165B2 (en) * | 1993-04-28 | 2003-05-26 | 株式会社林原生物化学研究所 | Hair restorer and its production method |
JP3719612B2 (en) | 1993-06-14 | 2005-11-24 | 塩野義製薬株式会社 | Urea derivatives containing heterocycles |
JP3545461B2 (en) | 1993-09-10 | 2004-07-21 | エーザイ株式会社 | Bicyclic heterocycle-containing sulfonamide derivatives |
IL115420A0 (en) * | 1994-09-26 | 1995-12-31 | Zeneca Ltd | Aminoheterocyclic derivatives |
CN1164232A (en) * | 1994-09-26 | 1997-11-05 | 曾尼卡有限公司 | Aminoheterocyclic derivatives as antithrombotic or anticoagulant agents |
RU2126001C1 (en) * | 1995-01-10 | 1999-02-10 | Самдзин Фармасьютикал Ко., Лтд | Piperazine derivatives and pharmaceutical composition on their basis |
EP0804428B1 (en) | 1995-01-20 | 2007-12-26 | G.D. Searle LLC. | Bis-sulfonamide hydroxyethylamino retroviral protease inhibitors |
IL117580A0 (en) | 1995-03-29 | 1996-07-23 | Merck & Co Inc | Inhibitors of farnesyl-protein transferase and pharmaceutical compositions containing them |
WO1998021191A1 (en) | 1995-05-16 | 1998-05-22 | Nissan Chemical Industries, Ltd. | Cyanoethylmelamine derivatives and process for producing the same |
FR2735127B1 (en) | 1995-06-09 | 1997-08-22 | Pf Medicament | NEW HETEROAROMATIC PIPERAZINES USEFUL AS MEDICAMENTS. |
ES2100129B1 (en) | 1995-10-11 | 1998-02-16 | Medichem Sa | NEW POLYCLIC AMINOPYRIDINE COMPOUNDS ACETYLCHOLINESTERASE INHIBITORS, PROCEDURE FOR THE PREPARATION AND USE. |
DE19541146A1 (en) | 1995-10-25 | 1997-04-30 | Schering Ag | Imidazole derivatives and their use as nitric oxide synthase inhibitors |
GB9602166D0 (en) * | 1996-02-02 | 1996-04-03 | Zeneca Ltd | Aminoheterocyclic derivatives |
WO1997028128A1 (en) * | 1996-02-02 | 1997-08-07 | Zeneca Limited | Heterocyclic compounds useful as pharmaceutical agents |
FR2744449B1 (en) | 1996-02-02 | 1998-04-24 | Pf Medicament | NOVEL AROMATIC PIPERAZINES DERIVED FROM SUBSTITUTED CYCLOAZANES, AS WELL AS THEIR PREPARATION METHOD, PHARMACEUTICAL COMPOSITIONS AND THEIR USE AS MEDICAMENTS |
US5807876A (en) | 1996-04-23 | 1998-09-15 | Vertex Pharmaceuticals Incorporated | Inhibitors of IMPDH enzyme |
JPH09291034A (en) | 1996-02-27 | 1997-11-11 | Yoshitomi Pharmaceut Ind Ltd | Condensed pyridine compound and its use as medicine |
US6262113B1 (en) | 1996-03-20 | 2001-07-17 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
US5834485A (en) * | 1996-05-20 | 1998-11-10 | Chiroscience Limited | Quinoline sulfonamides and their therapeutic use |
US5843485A (en) * | 1996-06-28 | 1998-12-01 | Incoe Corporation | Valve-gate bushing for gas-assisted injection molding |
ES2186908T3 (en) | 1996-07-13 | 2003-05-16 | Glaxo Group Ltd | HETEROCICICLES CONDENSED COMPOUNDS AS INHIBITORS OF PPROTEINA-TIROSINA-QUINASAS. |
DE19629335A1 (en) | 1996-07-20 | 1998-01-22 | Golden Records Ass Internation | Plastic card |
US5984882A (en) | 1996-08-19 | 1999-11-16 | Angiosonics Inc. | Methods for prevention and treatment of cancer and other proliferative diseases with ultrasonic energy |
US6020357A (en) * | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
DE19702988A1 (en) * | 1997-01-28 | 1998-07-30 | Hoechst Ag | Isoxazole and crotonic acid amide derivatives and their use as pharmaceuticals and diagnostics |
EP0970072A1 (en) * | 1997-03-11 | 2000-01-12 | E.I. Dupont De Nemours And Company | Heteroaryl azole herbicides |
US7863444B2 (en) * | 1997-03-19 | 2011-01-04 | Abbott Laboratories | 4-aminopyrrolopyrimidines as kinase inhibitors |
US6399358B1 (en) | 1997-03-31 | 2002-06-04 | Thomas Jefferson University | Human gene encoding human chondroitin 6-sulfotransferase |
WO1998054164A1 (en) * | 1997-05-30 | 1998-12-03 | Takeda Chemical Industries, Ltd. | Sulfonamide derivatives, their production and use |
JPH1158073A (en) | 1997-08-12 | 1999-03-02 | Ishikawajima Harima Heavy Ind Co Ltd | Device for welding hanging piece |
JPH11158073A (en) | 1997-09-26 | 1999-06-15 | Takeda Chem Ind Ltd | Adenosine a3 antagonist |
DE19743435A1 (en) | 1997-10-01 | 1999-04-08 | Merck Patent Gmbh | Benzamidine derivatives |
ATE297383T1 (en) | 1997-12-22 | 2005-06-15 | Bayer Pharmaceuticals Corp | INHIBITION OF P38 KINASE USING SYMMETRIC AND ASYMMETRIC DIPHENYL UREASES |
US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
US6106849A (en) * | 1998-01-21 | 2000-08-22 | Dragoco Gerberding & Co. Ag | Water soluble dry foam personal care product |
GB9805520D0 (en) | 1998-03-17 | 1998-05-13 | Zeneca Ltd | Chemical compounds |
US6214879B1 (en) | 1998-03-24 | 2001-04-10 | Virginia Commonwealth University | Allosteric inhibitors of pyruvate kinase |
GB9811427D0 (en) * | 1998-05-29 | 1998-07-22 | Zeneca Ltd | Chemical compounds |
AU754204B2 (en) * | 1998-09-01 | 2002-11-07 | Bristol-Myers Squibb Company | Potassium channel inhibitors and method |
DE19841985A1 (en) | 1998-09-03 | 2000-03-09 | Schering Ag | New heterocyclic alkanesulfonic and alkane carboxylic acid derivatives are VEGF receptor blockers useful in treatment of e.g. psoriasis, rheumatoid arthritis, stroke, tumors and endometriosis |
CZ2001959A3 (en) | 1998-09-18 | 2001-12-12 | Basf Aktiengesellschaft | 4-Aminopyrrolopyrimidines functioning as kinase inhibitors |
UY25842A1 (en) | 1998-12-16 | 2001-04-30 | Smithkline Beecham Corp | IL-8 RECEPTOR ANTAGONISTS |
US6211182B1 (en) | 1999-03-08 | 2001-04-03 | Schering Corporation | Imidazole compounds substituted with a six or seven membered heterocyclic ring containing two nitrogen atoms |
WO2000075129A1 (en) | 1999-06-07 | 2000-12-14 | Shire Biochem Inc. | Thiophene integrin inhibitors |
US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
DE60023920T2 (en) | 1999-08-27 | 2006-07-20 | Sugen, Inc., South San Francisco | Phosphate mimetics and methods of treatment with phosphatase inhibitors HIBITORS |
MX226123B (en) | 1999-09-17 | 2005-02-07 | Millennium Pharm Inc | BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa. |
IL148698A0 (en) | 1999-09-17 | 2002-09-12 | Cor Therapeutics Inc | INHIBITORS OF FACTOR Xa |
US6376515B2 (en) | 2000-02-29 | 2002-04-23 | Cor Therapeutics, Inc. | Benzamides and related inhibitors of factor Xa |
US20010037689A1 (en) * | 2000-03-08 | 2001-11-08 | Krouth Terrance F. | Hydraulic actuator piston measurement apparatus and method |
US6515013B2 (en) | 2000-07-13 | 2003-02-04 | Abbott Laboratories | 1,3-disubstituted and 1,3,3-trisubstituted pyrrolidines as histamine-3 receptor ligands and their therapeutic applications |
US6723730B2 (en) | 2000-07-20 | 2004-04-20 | Neurogen Corporation | Capsaicin receptor ligands |
FR2817349B1 (en) * | 2000-11-28 | 2003-06-20 | Centre Nat Rech Scient | NEW METHOD FOR SCREENING MODULATORS OF THE BACTERIAL TRANSCRIPTION |
JP2002193710A (en) | 2000-12-25 | 2002-07-10 | Kumiai Chem Ind Co Ltd | Pyrimidine or triazine derivative and fungicide for agriculture and horticulture |
US6525091B2 (en) | 2001-03-07 | 2003-02-25 | Telik, Inc. | Substituted diarylureas as stimulators for Fas-mediated apoptosis |
DE10112926B4 (en) * | 2001-03-13 | 2005-11-10 | Schebo Biotech Ag | Use of aminooxyacetate for tumor treatment |
WO2002088101A2 (en) | 2001-04-27 | 2002-11-07 | Vertex Pharmaceuticals Incorporated | Inhibitors of bace |
EP1387679A4 (en) * | 2001-05-07 | 2004-08-11 | Smithkline Beecham Corp | Sulfonamides |
US20040152648A1 (en) * | 2001-05-23 | 2004-08-05 | Axel Ullrich | Pyruvate-kinase as a novel target molecule |
US6967212B2 (en) * | 2001-05-30 | 2005-11-22 | Bristol-Myers Squibb Company | Substituted azole acid derivatives useful as antidiabetic and antiobesity agents and method |
EP1412325A1 (en) | 2001-06-11 | 2004-04-28 | Biovitrum Ab | Substituted sulfonamide compounds, process for their use as medicament for the treatment of cns disorders, obesity and type ii diabetes |
DE10128331A1 (en) * | 2001-06-12 | 2002-12-19 | Aventis Pharma Gmbh | New 2-(heteroarylsulfonyl-amino)-benzamide derivatives, which are potassium ion channel blocking antiarrhythmic agents, useful for e.g. treating atrial fibrillation or flutter |
JP4083397B2 (en) * | 2001-06-18 | 2008-04-30 | 株式会社ルネサステクノロジ | Semiconductor integrated circuit device |
JP2005500294A (en) | 2001-06-19 | 2005-01-06 | ブリストル−マイヤーズ スクイブ カンパニー | Pyrimidine inhibitors for phosphodiesterase 7 |
CN1865258A (en) * | 2001-08-15 | 2006-11-22 | 纳幕尔杜邦公司 | Ortho-substituted aryl amides for controlling invertebrate pests |
DE60238066D1 (en) | 2001-08-17 | 2010-12-02 | Basf Se | TRIAZINE DERIVATIVES AND THEIR USE AS SUN PROTECTION AGENTS |
JP4753336B2 (en) | 2001-09-04 | 2011-08-24 | 日本化薬株式会社 | Novel allyl compound and process for producing the same |
JP2003081937A (en) | 2001-09-07 | 2003-03-19 | Bayer Ag | Benzenesulfonamide derivative |
US7169788B2 (en) | 2001-10-30 | 2007-01-30 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
US6878196B2 (en) | 2002-01-15 | 2005-04-12 | Fuji Photo Film Co., Ltd. | Ink, ink jet recording method and azo compound |
US7148236B2 (en) | 2002-01-17 | 2006-12-12 | Merck & Co., Inc. | Modulators of acetylcholine receptors |
CA2473181A1 (en) * | 2002-02-04 | 2003-08-14 | F. Hoffmann-La Roche Ag | Quinoline derivatives as npy antagonists |
US20040180889A1 (en) | 2002-03-01 | 2004-09-16 | Pintex Pharmaceuticals, Inc. | Pin1-modulating compounds and methods of use thereof |
PL212089B1 (en) * | 2002-03-13 | 2012-08-31 | Janssen Pharmaceutica Nv | New inhibitors of histone deacetylase |
EP1485365B1 (en) | 2002-03-13 | 2008-05-14 | Janssen Pharmaceutica N.V. | Sulfonyl-derivatives as novel inhibitors of histone deacetylase |
KR101020399B1 (en) * | 2002-03-27 | 2011-03-08 | 글락소 그룹 리미티드 | Quinolin Derivatives and Their Use as 5-HT6 Ligands |
CA2484209C (en) | 2002-05-03 | 2013-06-11 | Exelixis, Inc. | Protein kinase modulators and methods of use |
GB0215775D0 (en) | 2002-07-06 | 2002-08-14 | Astex Technology Ltd | Pharmaceutical compounds |
US20040067234A1 (en) | 2002-07-11 | 2004-04-08 | Paz Einat | Isocitrate dehydrogenase and uses thereof |
SI2256108T1 (en) | 2002-07-18 | 2016-05-31 | Janssen Pharmaceutica N.V. | Substituted triazine kinase inhibitors |
AU2003261415C1 (en) | 2002-08-09 | 2010-01-14 | Merck Sharp & Dohme Corp. | Tyrosine kinase inhibitors |
JP2004107220A (en) | 2002-09-13 | 2004-04-08 | Mitsubishi Pharma Corp | TNF-alpha PRODUCTION INHIBITOR |
EP1556040A1 (en) | 2002-10-24 | 2005-07-27 | Sterix Limited | Inhibitors of 11-beta-hydroxy steroid dehydrogenase type 1 and type 2 |
AR042052A1 (en) | 2002-11-15 | 2005-06-08 | Vertex Pharma | USEFUL DIAMINOTRIAZOLS AS INHIBITORS OF PROTEINQUINASES |
AU2003293333A1 (en) | 2002-12-02 | 2004-06-23 | Arqule, Inc. | Method of treating cancers |
EP1590364B1 (en) | 2002-12-16 | 2011-10-05 | Genmab A/S | Human monoclonal antibodies against interleukin 8 (il-8) |
MXPA05007382A (en) | 2003-01-10 | 2005-11-23 | Threshold Pharmaceuticals Inc | Treatment of cancer with 2-deoxyglucose. |
US7358262B2 (en) | 2003-01-29 | 2008-04-15 | Whitehead Institute For Biomedical Research | Identification of genotype-selective anti-tumor agents |
WO2004073619A2 (en) | 2003-02-14 | 2004-09-02 | Smithkline Beecham Corporation | Ccr8 antagonists |
WO2004074438A2 (en) | 2003-02-14 | 2004-09-02 | Smithkline Beecham Corporation | Ccr8 antagonists |
KR100728425B1 (en) | 2003-02-19 | 2007-06-13 | 에프. 호프만-라 로슈 아게 | Sulfonamide substituted xanthine derivatives for use as pepck inhibitors |
WO2004076640A2 (en) * | 2003-02-25 | 2004-09-10 | Ambion, Inc. | Small-molecule inhibitors of angiogenin and rnases and in vivo and in vitro methods of using same |
ATE524452T1 (en) * | 2003-03-27 | 2011-09-15 | Cytokinetics Inc | SULFONAMIDES FOR TREATING CONGESTIVE HEART FAILURE, COMPOSITIONS AND USES THEREOF. |
RS20050733A (en) * | 2003-03-28 | 2007-06-04 | Janssen Pharmaceutica N.V., | Benzo/1,2,5/thiadiazole compounds |
EP1615698B1 (en) | 2003-04-11 | 2010-09-29 | High Point Pharmaceuticals, LLC | New amide derivatives and pharmaceutical use thereof |
EP1635832A2 (en) | 2003-06-06 | 2006-03-22 | Merck & Co., Inc. | Combination therapy for the treatment of diabetes |
ES2222827B1 (en) * | 2003-07-30 | 2006-03-01 | Laboratorios Del Dr. Esteve, S.A. | DERIVATIVES OF 5-INDOLILSULFONAMIDS, ITS PREPARATION AND ITS APPLICATION AS MEDICINES. |
US6818631B1 (en) * | 2003-08-15 | 2004-11-16 | Nippon Soda Co. Ltd. | Fungicidal pyrimidine derivatives |
EP1689722A2 (en) | 2003-10-10 | 2006-08-16 | Bayer Pharmaceuticals Corporation | 4-aminopyrimidine derivatives for treatment of hyperproliferative disorders |
US20080051414A1 (en) * | 2003-10-14 | 2008-02-28 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Protein Kinase Inhibitors |
JP4099768B2 (en) | 2003-11-10 | 2008-06-11 | 富士電機デバイステクノロジー株式会社 | Electrophotographic photosensitive member and method for determining presence or absence of interference fringes resulting from electrophotographic photosensitive member |
US20070196395A1 (en) | 2003-12-12 | 2007-08-23 | Mackerell Alexander | Immunomodulatory compounds that target and inhibit the py'binding site of tyrosene kinase p56 lck sh2 domain |
TW200522944A (en) * | 2003-12-23 | 2005-07-16 | Lilly Co Eli | CB1 modulator compounds |
CA2551524A1 (en) | 2003-12-24 | 2005-07-21 | Scios, Inc. | Treatment of malignant gliomas with tgf-beta inhibitors |
US20050170316A1 (en) | 2004-01-29 | 2005-08-04 | Russell Bruce M. | Toothbrush for detecting the presence of plaque |
WO2005074946A1 (en) * | 2004-02-10 | 2005-08-18 | Adenobio N.V. | Stable and active complexes of adenosine and adenosine phosphates with aminoalcohols for the treatment of pulmonary artery hypertension, cardiac failure and other diseases |
CN1980929A (en) * | 2004-02-24 | 2007-06-13 | 比奥阿克松医疗技术股份有限公司 | 4-substituted piperidine derivatives |
US7588779B2 (en) | 2004-05-28 | 2009-09-15 | Andrx Labs, Llc | Pharmaceutical formulation containing a biguanide and an angiotensin antagonist |
GB0412526D0 (en) | 2004-06-05 | 2004-07-14 | Leuven K U Res & Dev | Type 2 diabetes |
CA2577309C (en) * | 2004-06-24 | 2013-10-22 | Temple University - Of The Commonwealth System Of Higher Education | Alpha, beta-unsaturated sulfones, sulfoxides, sulfonimides, sulfinimides, acylsulfonamides and acylsulfinamides and therapeutic uses thereof |
TW200606152A (en) | 2004-07-02 | 2006-02-16 | Tanabe Seiyaku Co | Piperidine compound and process for preparing the same |
FR2872704B1 (en) | 2004-07-12 | 2007-11-02 | Laurent Schwartz | PLURITHERAPY AGAINST CANCER |
CA2580845A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
AU2005286593A1 (en) | 2004-09-23 | 2006-03-30 | Reddy Us Therapeutics, Inc. | Novel pyridine compounds, process for their preparation and compositions containing them |
WO2006033628A1 (en) | 2004-09-24 | 2006-03-30 | Astrazeneca Ab | Benzimidazole derivatives, compositions containing them, preparation thereof and uses thereof |
WO2006038594A1 (en) * | 2004-10-04 | 2006-04-13 | Ono Pharmaceutical Co., Ltd. | N-type calcium channel inhibitor |
WO2006043950A1 (en) | 2004-10-20 | 2006-04-27 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
EP1807417A2 (en) * | 2004-11-04 | 2007-07-18 | Neurogen Corporation | Pyrazolylmethyl heteroaryl derivatives |
SE0402762D0 (en) | 2004-11-11 | 2004-11-11 | Astrazeneca Ab | Indazole sulphonamide derivatives |
WO2006055880A2 (en) * | 2004-11-16 | 2006-05-26 | Genzyme Corporation | Diagnostic pkm2 methods and compositions |
US20080194681A1 (en) * | 2004-12-09 | 2008-08-14 | Kalypsys, Inc. | Novel Inhibitors of Histone Deacetylase for the Treatment of Disease |
US20100160324A1 (en) | 2004-12-30 | 2010-06-24 | Astex Therapeutics Limited | Pyrazole derivatives as that modulate the activity of cdk, gsk and aurora kinases |
JPWO2006077821A1 (en) | 2005-01-19 | 2008-06-19 | 大日本住友製薬株式会社 | Aromatic sulfone compounds as aldosterone receptor modulators |
BRPI0606930A2 (en) | 2005-01-25 | 2009-12-01 | Astrazeneca Ab | compound or a pharmaceutically acceptable salt thereof, process for preparing a compound or a pharmaceutically acceptable salt thereof, pharmaceutical composition, use of a compound or a pharmaceutically acceptable salt thereof, and methods for producing a drug inhibiting effect. b-raf in a warm-blooded animal, for producing an anti-cancer effect on a warm-blooded animal and for treating diseases of an animal in a warm-blooded animal |
NZ561613A (en) * | 2005-02-18 | 2010-12-24 | Astrazeneca Ab | Antibacterial piperidine derivatives |
SI1879877T1 (en) | 2005-05-03 | 2013-02-28 | Ranbaxy Laboratories Limited | Antimicrobial agents |
JP2008540586A (en) | 2005-05-18 | 2008-11-20 | フォルシュングスフェアブント ベルリン エー ファウ | Non-peptide inhibitors of AKAP-PKA interaction |
WO2006133420A2 (en) | 2005-06-08 | 2006-12-14 | Millennium Pharmaceuticals, Inc. | Treatment of patients with cancer therapy |
GB0513702D0 (en) | 2005-07-04 | 2005-08-10 | Sterix Ltd | Compound |
AR054529A1 (en) * | 2005-07-05 | 2007-06-27 | Astrazeneca Ab | BENZAZEPIN DERIVATIVES AS 5-HYDROXY-TRIPTAMINE 6 RECEPTOR MODULATORS |
WO2007008143A1 (en) | 2005-07-08 | 2007-01-18 | Astrazeneca Ab | Heterocyclic sulfonamide derivatives as inhibitors of factor xa |
BRPI0615233A2 (en) * | 2005-08-26 | 2011-05-10 | Serono Lab | pyrazine derivatives and their use as p13k inhibitors |
US8133900B2 (en) | 2005-11-01 | 2012-03-13 | Targegen, Inc. | Use of bi-aryl meta-pyrimidine inhibitors of kinases |
FI20055644A0 (en) * | 2005-12-02 | 2005-12-02 | Nokia Corp | group Communications |
AU2006331963A1 (en) * | 2005-12-22 | 2007-07-05 | Merck & Co., Inc. | Substituted piperidines as calcium channel blockers |
US20090069302A1 (en) | 2006-01-20 | 2009-03-12 | Smithkline Beecham Corporation | Chemical compounds |
JP2007238458A (en) | 2006-03-06 | 2007-09-20 | D Western Therapeutics Institute Inc | Novel isoquinoline derivative and medicine containing the same |
US20090054453A1 (en) * | 2006-03-17 | 2009-02-26 | Lilian Alcaraz | Novel Tetralins as 5-HT6 Modulators |
EP2004619A1 (en) * | 2006-03-23 | 2008-12-24 | Amgen Inc. | 1-phenylsulfonyl-diaza heterocyclic amide compounds and their uses as modulators of hydroxsteroid dehydrogenases |
MX2008012482A (en) | 2006-03-31 | 2008-10-10 | Abbott Lab | Indazole compounds. |
TW200815426A (en) | 2006-06-28 | 2008-04-01 | Astrazeneca Ab | New pyridine analogues II 333 |
ES2614931T3 (en) | 2006-08-04 | 2017-06-02 | Beth Israel Deaconess Medical Center | Pyruvate kinase inhibitors and disease treatment methods |
US20090247499A1 (en) * | 2006-08-21 | 2009-10-01 | Fletcher Joan M | Sulfonylated piperazines as cannabinoid-1 receptor modulators |
EP2059809B1 (en) | 2006-08-30 | 2014-07-23 | Metanomics GmbH | Means and method for diagnosing hemolytic anemia |
JP5121717B2 (en) | 2006-09-01 | 2013-01-16 | 大塚アグリテクノ株式会社 | N-pyridylpiperidine compound, production method thereof and pest control agent |
EP2074345B1 (en) | 2006-10-12 | 2011-01-05 | Fluid Automation Systems S.A. | Rocker valve mechanism and rocker valve |
MX2009003157A (en) | 2006-10-16 | 2009-04-03 | Pfizer Prod Inc | Therapeutic pyrazolyl thienopyridines. |
JP2010508300A (en) | 2006-10-26 | 2010-03-18 | フライン、ギャリー・エー. | Aquaporin modifiers and methods for their use for the treatment of edema and fluid balance abnormalities |
HUP0600810A3 (en) | 2006-10-27 | 2008-09-29 | Richter Gedeon Nyrt | New sulfonamide derivatives as bradykinin antagonists, process and intermediates for their preparation and pharmaceutical compositions containing them |
CN101679371A (en) | 2006-12-04 | 2010-03-24 | 艾美罗股份公司 | Substituted pyrimidines as adenosine receptor antagonists |
WO2008073670A2 (en) | 2006-12-08 | 2008-06-19 | Millennium Pharmaceuticals, Inc. | Unit dose formulations and methods of treating thrombosis with an oral factor xa inhibitor |
US7858782B2 (en) | 2006-12-15 | 2010-12-28 | Abraxis Bioscience, Llc | Triazine derivatives and their therapeutical applications |
US7897776B2 (en) * | 2007-04-23 | 2011-03-01 | Salutria Pharmaceuticals Llc | Sulfonamide containing compounds for treatment of inflammatory disorders |
WO2008131547A1 (en) | 2007-04-30 | 2008-11-06 | Prometic Biosciences Inc. | 'triazine derivatives, compositions containing such derivatives, and methods of treatment of cancer and autoimmune diseases using such derivatives' |
US20090029992A1 (en) | 2007-06-11 | 2009-01-29 | Agoston Gregory E | Substituted pyrazole compounds |
WO2009012430A1 (en) | 2007-07-18 | 2009-01-22 | Janssen Pharmaceutica N.V. | Sulfonamides as trpm8 modulators |
CN103923072B (en) | 2007-07-20 | 2017-05-31 | 内尔维阿诺医学科学有限公司 | As the substituted indazole derivative with kinase inhibitory activity |
TW200906818A (en) | 2007-07-31 | 2009-02-16 | Astrazeneca Ab | Chemical compounds |
WO2009025781A1 (en) | 2007-08-16 | 2009-02-26 | Beth Israel Deaconess Medical Center | Activators of pyruvate kinase m2 and methods of treating disease |
TW200924778A (en) | 2007-10-10 | 2009-06-16 | Takeda Pharmaceutical | Amide compound |
EP2053045A1 (en) | 2007-10-26 | 2009-04-29 | Syngenta Participations AG | Novel imidazole derivatives |
GT200800229A (en) * | 2007-10-26 | 2010-04-20 | NEWS DERIVED FROM IMIDAZOL | |
WO2009086303A2 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
GB0805477D0 (en) | 2008-03-26 | 2008-04-30 | Univ Nottingham | Pyrimidines triazines and their use as pharmaceutical agents |
JP5277685B2 (en) | 2008-03-26 | 2013-08-28 | 富士ゼロックス株式会社 | Electrophotographic photosensitive member, image forming apparatus, process cartridge, and image forming method |
US20090281089A1 (en) | 2008-04-11 | 2009-11-12 | Genentech, Inc. | Pyridyl inhibitors of hedgehog signalling |
CN101575408B (en) | 2008-05-09 | 2013-10-30 | Mca技术有限公司 | Polytriazinyl compounds as flame retardants and light stabilizers |
FR2932483A1 (en) | 2008-06-13 | 2009-12-18 | Cytomics Systems | COMPOUNDS USEFUL FOR THE TREATMENT OF CANCERS. |
TW201028381A (en) | 2008-07-14 | 2010-08-01 | Shionogi & Co | Pyridine derivative having ttk inhibition activity |
GB0815781D0 (en) | 2008-08-29 | 2008-10-08 | Xention Ltd | Novel potassium channel blockers |
WO2010028099A1 (en) | 2008-09-03 | 2010-03-11 | The Johns Hopkins University | Genetic alterations in isocitrate dehydrogenase and other genes in malignant glioma |
US20100144722A1 (en) | 2008-09-03 | 2010-06-10 | Dr. Reddy's Laboratories Ltd. | Novel heterocyclic compounds as gata modulators |
JP2010079130A (en) | 2008-09-29 | 2010-04-08 | Fuji Xerox Co Ltd | Electrophotographic photoreceptor, process cartridge, and image forming apparatus |
US8841305B2 (en) | 2008-10-09 | 2014-09-23 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Activators of the human pyruvate kinase M2 receptor |
EP2370417A2 (en) | 2008-11-21 | 2011-10-05 | Millennium Pharmaceuticals, Inc. | Lactate salt of 4-[6-methoxy-7-(3-piperidin-1-yl-propoxy)quinazolin-4-yl]piperazine-1-carboxylic acid(4-isopropoxyphenyl)-amide and pharmaceutical compositions thereof for the treatment of cancer and other diseases or disorders |
JP2010181540A (en) | 2009-02-04 | 2010-08-19 | Fuji Xerox Co Ltd | Electrophotographic photoreceptor, process cartridge and image forming apparatus |
AU2010211672B2 (en) | 2009-02-06 | 2016-08-04 | Nippon Shinyaku Co., Ltd. | Aminopyrazine derivative and medicine |
AU2010223919B2 (en) | 2009-03-13 | 2016-03-31 | Les Laboratoires Servier | Methods and compositions for cell-proliferation-related disorders |
AU2010234526B2 (en) | 2009-04-06 | 2016-07-21 | Agios Pharmaceuticals, Inc. | Pyruvate kinase M2 modulators, therapeutic compositions and related methods of use |
ES2619557T3 (en) | 2009-05-04 | 2017-06-26 | Agios Pharmaceuticals, Inc. | PKM2 activators for use in cancer treatment |
WO2010130638A1 (en) | 2009-05-14 | 2010-11-18 | Evotec Ag | Sulfonamide compounds, pharmaceutical compositions and uses thereof |
WO2010144338A1 (en) | 2009-06-08 | 2010-12-16 | Abraxis Bioscience, Llc | Triazine derivatives and their therapeutical applications |
AU2010258974A1 (en) | 2009-06-09 | 2012-01-12 | California Capital Equity, Llc | Pyridil-triazine inhibitors of hedgehog signaling |
WO2010144522A1 (en) | 2009-06-09 | 2010-12-16 | Abraxis Bioscience, Llc | Ureidophenyl substituted triazine derivatives and their therapeutical applications |
JP5764555B2 (en) | 2009-06-29 | 2015-08-19 | アジオス ファーマシューティカルズ, インコーポレイテッド | Therapeutic compositions and related methods of use |
UA107667C2 (en) | 2009-06-29 | 2015-02-10 | Аджиос Фармасьютікалз, Інк. | Medical compounds stimulating activity of pyruvate kinase m2, compositions on their basis and use in the treatment of cancer |
WO2011032169A2 (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 |
JP5473851B2 (en) | 2009-09-30 | 2014-04-16 | 富士フイルム株式会社 | Polymer film, retardation film, polarizing plate and liquid crystal display device |
US8652534B2 (en) | 2009-10-14 | 2014-02-18 | Berry Pharmaceuticals, LLC | Compositions and methods for treatment of mammalian skin |
WO2011050210A1 (en) | 2009-10-21 | 2011-04-28 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
CA2793836C (en) | 2009-10-21 | 2020-03-24 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
US9062076B2 (en) | 2009-10-22 | 2015-06-23 | Fibrotech Therapeutics Pty Ltd | Fused ring analogues of anti-fibrotic agents |
ES2642109T3 (en) | 2009-12-09 | 2017-11-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds for use in the treatment of cancer characterized by having an IDH mutation |
KR20130044382A (en) | 2010-03-01 | 2013-05-02 | 마이렉시스 인코포레이티드 | Compounds and therapeutic uses thereof |
WO2011108724A1 (en) * | 2010-03-04 | 2011-09-09 | 味の素株式会社 | Prophylactic or therapeutic agent for diabetes or obesity |
WO2011123618A1 (en) | 2010-04-01 | 2011-10-06 | Agios Pharmaceuticals, Inc. | Methods of identifying a candidate compound |
EP2563761A1 (en) | 2010-04-29 | 2013-03-06 | The U.S.A. As Represented By The Secretary, Department Of Health And Human Services | Activators of human pyruvate kinase |
US20130109643A1 (en) | 2010-05-10 | 2013-05-02 | The Johns Hopkins University | Metabolic inhibitor against tumors having an idh mutation |
NZ604035A (en) * | 2010-06-04 | 2015-02-27 | Albany Molecular Res Inc | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
ES2704862T3 (en) | 2010-07-16 | 2019-03-20 | Agios Pharmaceuticals Inc | Therapeutically active compositions and their method of use |
JP2014502070A (en) | 2010-10-20 | 2014-01-23 | ヨタ デバイセズ アイピーアール リミテッド | Portable device having input means |
PT2630146T (en) | 2010-10-21 | 2020-07-20 | Medivation Tech Llc | Crystaline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phtalazin-3(7h)-one tosylate salt |
FR2967674B1 (en) | 2010-11-23 | 2012-12-14 | Pf Medicament | HETEROARYLSULFONAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION IN HUMAN THERAPEUTICS |
KR20140049961A (en) | 2010-11-29 | 2014-04-28 | 갈레온 파마슈티칼스, 인코포레이티드 | Novel compounds as respiratory stimulants for treatment of breathing control disorders or diseases |
WO2012083246A1 (en) | 2010-12-17 | 2012-06-21 | Agios Pharmaceuticals, Inc. | Novel n- (4- (azetidine - 1 - carbonyl) phenyl) - (hetero - ) arylsulfonamide derivatives as pyruvate kinase m2 (pmk2) modulators |
JP6092118B2 (en) | 2010-12-21 | 2017-03-08 | アジオス ファーマシューティカルズ, インコーポレイテッド | Bicyclic PKM2 activator |
TWI549947B (en) | 2010-12-29 | 2016-09-21 | 阿吉歐斯製藥公司 | Therapeutic compounds and compositions |
JP5854050B2 (en) | 2011-02-04 | 2016-02-09 | 日本電気株式会社 | Radio communication system, base station apparatus, radio resource control method, and program |
WO2012151452A1 (en) | 2011-05-03 | 2012-11-08 | Agios Pharmaceuticals, Inc | Pyruvate kinase activators for use in therapy |
BR112013028422B8 (en) | 2011-05-03 | 2022-01-11 | Agios Pharmaceuticals Inc | Pyruvate kinase activators for use in therapy |
TWI555737B (en) | 2011-05-24 | 2016-11-01 | 拜耳知識產權公司 | 4-aryl-n-phenyl-1,3,5-triazin-2-amines containing a sulfoximine group |
CN102827073A (en) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Therapeutically active compositions and application methods thereof |
CN102827170A (en) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | Active treatment compositions and use method thereof |
US20140249150A1 (en) | 2011-10-13 | 2014-09-04 | Agios Pharmaceuticals, Inc | Activators of pyruvate kinase m2 and methods of treating disease |
CN102659765B (en) | 2011-12-31 | 2014-09-10 | 沈阳药科大学 | Pyrimidine and triazine compound preparation method and application |
KR101893112B1 (en) | 2012-01-06 | 2018-08-30 | 아지오스 파마슈티컬스 아이엔씨. | Therapeutically active compounds and their methods of use |
US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
EP2804850B1 (en) | 2012-01-19 | 2018-08-29 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
EP2634259A1 (en) | 2012-03-01 | 2013-09-04 | Deutsches Krebsforschungszentrum | Means and methods for the determination of (D)-2-hydroxyglutarate (D2HG) |
CN104169260A (en) | 2012-03-09 | 2014-11-26 | 卡尔那生物科学株式会社 | Novel triazone derivative |
WO2014015422A1 (en) | 2012-07-27 | 2014-01-30 | Ontario Institute For Cancer Research | Cellulose-based nanoparticles for drug delivery |
WO2014062511A1 (en) | 2012-10-15 | 2014-04-24 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
EP4344703A1 (en) | 2015-06-11 | 2024-04-03 | Agios Pharmaceuticals, Inc. | Methods of using pyruvate kinase activators |
WO2019104134A1 (en) * | 2017-11-22 | 2019-05-31 | Agios Pharmaceuticals, Inc. | Crystalline forms of n-(4-(4-(cyclopropylmethyl) piperazine-1-carbonyl)phenyl)quinoline-8-sulfonamide |
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- 2014-11-04 JP JP2014224372A patent/JP2015028083A/en not_active Withdrawn
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2017
- 2017-01-23 US US15/412,976 patent/US10029987B2/en active Active
- 2017-06-23 HR HRP20170955TT patent/HRP20170955T1/en unknown
- 2017-06-28 CY CY20171100682T patent/CY1119443T1/en unknown
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2018
- 2018-06-18 US US16/010,717 patent/US20190241523A1/en not_active Abandoned
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2019
- 2019-01-09 US US16/243,247 patent/US10988448B2/en active Active
-
2020
- 2020-12-22 US US17/131,562 patent/USRE49582E1/en active Active
-
2021
- 2021-03-08 US US17/195,243 patent/US11866411B2/en active Active
-
2023
- 2023-04-27 NO NO2023017C patent/NO2023017I1/en unknown
- 2023-04-27 LT LTPA2023513C patent/LTPA2023513I1/lt unknown
- 2023-04-28 FR FR23C1017C patent/FR23C1017I2/en active Active
- 2023-05-02 HU HUS2300018C patent/HUS2300018I1/en unknown
- 2023-05-02 FI FIC20230017C patent/FIC20230017I1/en unknown
- 2023-05-02 NL NL301230C patent/NL301230I2/en unknown
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