AR100975A1 - Inhibidores de fosfatidilinositol 3-quinasa - Google Patents
Inhibidores de fosfatidilinositol 3-quinasaInfo
- Publication number
- AR100975A1 AR100975A1 ARP150102013A ARP150102013A AR100975A1 AR 100975 A1 AR100975 A1 AR 100975A1 AR P150102013 A ARP150102013 A AR P150102013A AR P150102013 A ARP150102013 A AR P150102013A AR 100975 A1 AR100975 A1 AR 100975A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkylene
- alkyl
- aryl
- or1x
- Prior art date
Links
Classifications
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- 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
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
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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
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D405/14—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 three or more hetero rings
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la estructura de la fórmula (1), A es N o CH; n es 0, 1, 2, 3, ó 4; m es 0, 1, 2, 3, ó 4; cada R¹ se selecciona independientemente de alquilo opcionalmente sustituido, haloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, halo, ciano, NHC(=O)alquileno-N(R¹ˣ)₂, NO₂, OR¹ˣ, N(R¹ˣ)₂, OC(=O)R¹ˣ, C(=O)R¹ˣ, C(=O)OR¹ˣ, aril-OR¹ʸ, cicloalquilo opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido, NR¹ˣC(=O)alquileno-C(=O)OR¹ˣ, aril-O-alquileno-N(R¹ˣ)₂, aril-O-C(=O)R¹ˣ, alquileno-C(=O)OR¹ˣ, alquileno-C(=O)N(R¹ˣ)₂, alquileno-C(=O)-Het, O-alquileno-C(=O)OR¹ˣ, alquileno-O-alquileno-C(=O)OR¹ˣ, C(=O)NR¹ˣSO₂R¹ˣ, alquileno-N(R¹ˣ)₂, alquenileno-N(R¹ˣ)₂, C(=O)NR¹ˣ-alquileno-OR¹ˣ, C(=O)NR¹ˣ-alquileno-Het, O-alquileno-N(R¹ˣ)₂, O-alquileno-CH(OR¹ʸ)CH₂N(R¹ˣ)₂, O-alquileno-Het, O-alquileno-C(=O)OR¹ˣ, O-alquileno-C(=O)-Het, S-alquileno-OR¹ˣ, O-alquileno-OR¹ˣ, O-alquenileno C₁₋₆-CH(OR¹ʸ)alquenileno C₁₋₆-OR¹ˣ, O-alquileno-NR¹ˣC(=O)OR¹ˣ, NR¹ˣ-alquileno-N(R¹ˣ)₂, NR¹ˣC(=O)R¹ˣ, NR¹ˣC(=O)N(R¹ˣ)₂, N(SO₂-alquilo)₂, NR¹ˣ(SO₂-alquilo), SO₂R¹ᶻ, SO₂N(R¹ˣ)₂, alquileno-arilo, alquileno-Het, alquileno-OR¹ʸ, alquileno-N(R¹ˣ)₂, C(=O)N(R¹ˣ)₂, NHC(=O)alquileno-arilo, aril-O-alquileno-N(R¹ˣ)₂, aril-OC(=O)R¹ʸ, NHC(=O)alquileno-heterocicloalquilo, NHC(=O)alquileno-Het, O-alquileno-O-alquileno-C(=O)OR¹ʸ, C(=O)alquileno-Het, y NHC(=O)halo-alquilo, en donde Het es heteroarilo opcionalmente sustituido o heterocicloalquilo opcionalmente sustituido, en donde R¹ˣ es independientemente hidrógeno, alquilo opcionalmente sustituido, haloalquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido, y arilo opcionalmente sustituido, en donde Rʸ es independientemente hidrógeno, alquilo opcionalmente sustituido, haloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, y heteroarilo opcionalmente sustituido, y en donde R¹ᶻ es independientemente alquilo opcionalmente sustituido, haloalquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido, y arilo opcionalmente sustituido; cada R² se selecciona independientemente de halo, ciano, alquilo opcionalmente sustituido, haloalquilo, SO₂N(R²ˣ)₂, y alcoxi opcionalmente sustituido, en donde R²ˣ es hidrógeno, alquilo opcionalmente sustituido, o haloalquilo opcionalmente sustituido; R³ es hidrógeno, alquilo opcionalmente sustituido, haloalquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, o heterocicloalquilo opcionalmente sustituido; R⁵ es hidrógeno o alquilo, o R⁵ y R³ junto con los átomos a los cuales se unen opcionalmente forman un anillo heterocíclico de cuatro, cinco o seis miembros opcionalmente sustituido; R⁴ es ciano, C(=O)NR⁴ˣR⁴ʸ, SO₂-alquilo, halo, haloalquilo, o C(=O)R⁴ˣ, en donde cada R⁴ˣ y R⁴ʸ es independientemente hidrógeno, alquilo opcionalmente sustituido, y haloalquilo opcionalmente sustituido; R⁶ es NH₂, halo, alquilo opcionalmente sustituido, o haloalquilo opcionalmente sustituido; y R⁷ es NH₂, halo, alquilo opcionalmente sustituido, o haloalquilo opcionalmente sustituido; con la condición de que cuando R⁵ y R³ forman un anillo heterocíclico de 5 miembros que se sustituye opcionalmente con hidroxilo, halo, o metoxi, R⁴ es ciano, R⁶ es amino, y R⁷ es amino; o una sal farmacéuticamente aceptable, isómero, o una mezcla de los mismos.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462016194P | 2014-06-24 | 2014-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR100975A1 true AR100975A1 (es) | 2016-11-16 |
Family
ID=53674285
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150102013A AR100975A1 (es) | 2014-06-24 | 2015-06-23 | Inhibidores de fosfatidilinositol 3-quinasa |
Country Status (19)
Country | Link |
---|---|
US (2) | US9765060B2 (es) |
EP (1) | EP3160960B1 (es) |
JP (2) | JP6391718B2 (es) |
KR (1) | KR20170015521A (es) |
CN (1) | CN106459008A (es) |
AR (1) | AR100975A1 (es) |
AU (1) | AU2015280138B2 (es) |
BR (1) | BR112016029846A2 (es) |
CA (1) | CA2953820A1 (es) |
EA (1) | EA201692487A1 (es) |
ES (1) | ES2900812T3 (es) |
HK (1) | HK1231474A1 (es) |
IL (1) | IL249404A0 (es) |
MA (1) | MA40045A (es) |
MX (1) | MX2016017110A (es) |
NZ (1) | NZ727185A (es) |
SG (1) | SG11201610341PA (es) |
TW (1) | TW201625558A (es) |
WO (1) | WO2015200352A1 (es) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2952012A1 (en) | 2014-06-13 | 2015-12-17 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
KR20170010063A (ko) | 2014-06-13 | 2017-01-25 | 길리애드 사이언시즈, 인코포레이티드 | 포스파티딜이노시톨 3-키나제 억제제 |
NZ726055A (en) | 2014-06-13 | 2018-04-27 | Gilead Sciences Inc | Quinazolinone derivatives as phosphatidylinositol 3-kinase inhibitors |
SG11201610095SA (en) | 2014-06-13 | 2016-12-29 | Gilead Sciences Inc | Phosphatidylinositol 3-kinase inhibitors |
EP3164400A1 (en) | 2014-07-04 | 2017-05-10 | Lupin Limited | Quinolizinone derivatives as pi3k inhibitors |
TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
TW201813963A (zh) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201815787A (zh) * | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
TW201825465A (zh) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | 磷脂醯肌醇3-激酶抑制劑 |
CN106632077B (zh) * | 2016-10-10 | 2019-01-22 | 上海再启生物技术有限公司 | 一种2-氨基-4-溴嘧啶的制备方法 |
US10396145B2 (en) * | 2017-01-12 | 2019-08-27 | Micron Technology, Inc. | Memory cells comprising ferroelectric material and including current leakage paths having different total resistances |
US20200165257A1 (en) * | 2017-06-22 | 2020-05-28 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Servic | Inhibitors of phosphoinositide 3-kinase and histone deacetylase for treatment of cancer |
SG11202000523PA (en) * | 2017-07-31 | 2020-02-27 | The Trustees Of Columbia Univeristy In The City Of New York | Compounds, compositions, and methods for treating t-cell acute lymphoblastic leukemia |
US10751339B2 (en) | 2018-01-20 | 2020-08-25 | Sunshine Lake Pharma Co., Ltd. | Substituted aminopyrimidine compounds and methods of use |
CA3114260A1 (en) * | 2018-09-27 | 2020-04-02 | Shanghai Yingli Pharmaceutical Co., Ltd | Crystal form of morpholino quinazoline compound, preparation method therefor and use thereof |
CN110590681B (zh) * | 2019-09-30 | 2021-06-01 | 中山大学 | 一种新型喹唑啉酮类化合物及其制备方法和应用 |
WO2021086966A1 (en) * | 2019-10-29 | 2021-05-06 | Biogen Ma Inc. | Spirocyclic o-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors |
CN113512042A (zh) * | 2020-04-09 | 2021-10-19 | 成都赜灵生物医药科技有限公司 | 取代喹唑啉-4-酮类化合物及其制备方法和用途 |
WO2024064024A1 (en) * | 2022-09-19 | 2024-03-28 | Onkure, Inc. | ((4-oxo-3,4-dihydroquinazolin-8-yl)methyl)amine derivatives as p13k inhibitors for the treatment of cancer |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6667300B2 (en) * | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
DK1939203T3 (en) | 2000-04-25 | 2015-02-23 | Icos Corp | INHIBITORS OF HUMAN phosphatidyl-inositol 3-kinase DELTA ISOFORM |
US8193182B2 (en) * | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
SG10201605472WA (en) * | 2008-01-04 | 2016-09-29 | Intellikine Llc | Certain Chemical Entities, Compositions And Methods |
WO2011146882A1 (en) * | 2010-05-21 | 2011-11-24 | Intellikine, Inc. | Chemical compounds, compositions and methods for kinase modulation |
RU2014111823A (ru) * | 2011-08-29 | 2015-10-10 | Инфинити Фармасьютикалз, Инк. | Гетероциклические соединения и их применения |
WO2014100767A1 (en) * | 2012-12-21 | 2014-06-26 | Gilead Calistoga Llc | Isoquinolinone or quinazolinone phosphatidylinositol 3-kinase inhibitors |
WO2014128612A1 (en) * | 2013-02-20 | 2014-08-28 | Novartis Ag | Quinazolin-4-one derivatives |
UY35675A (es) | 2013-07-24 | 2015-02-27 | Novartis Ag | Derivados sustituidos de quinazolin-4-ona |
US20150148345A1 (en) * | 2013-11-26 | 2015-05-28 | Gilead Sciences, Inc. | Therapies for treating myeloproliferative disorders |
WO2015168079A1 (en) | 2014-04-29 | 2015-11-05 | Infinity Pharmaceuticals, Inc. | Pyrimidine or pyridine derivatives useful as pi3k inhibitors |
CA2952012A1 (en) * | 2014-06-13 | 2015-12-17 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
KR20170010063A (ko) * | 2014-06-13 | 2017-01-25 | 길리애드 사이언시즈, 인코포레이티드 | 포스파티딜이노시톨 3-키나제 억제제 |
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2015
- 2015-06-23 SG SG11201610341PA patent/SG11201610341PA/en unknown
- 2015-06-23 BR BR112016029846A patent/BR112016029846A2/pt not_active IP Right Cessation
- 2015-06-23 AR ARP150102013A patent/AR100975A1/es unknown
- 2015-06-23 EP EP15739079.0A patent/EP3160960B1/en active Active
- 2015-06-23 CN CN201580034671.2A patent/CN106459008A/zh active Pending
- 2015-06-23 JP JP2016574424A patent/JP6391718B2/ja not_active Expired - Fee Related
- 2015-06-23 AU AU2015280138A patent/AU2015280138B2/en not_active Ceased
- 2015-06-23 NZ NZ727185A patent/NZ727185A/en not_active IP Right Cessation
- 2015-06-23 EA EA201692487A patent/EA201692487A1/ru unknown
- 2015-06-23 KR KR1020177001682A patent/KR20170015521A/ko active IP Right Grant
- 2015-06-23 WO PCT/US2015/037234 patent/WO2015200352A1/en active Application Filing
- 2015-06-23 US US14/747,931 patent/US9765060B2/en active Active
- 2015-06-23 CA CA2953820A patent/CA2953820A1/en not_active Abandoned
- 2015-06-23 MA MA040045A patent/MA40045A/fr unknown
- 2015-06-23 MX MX2016017110A patent/MX2016017110A/es unknown
- 2015-06-23 ES ES15739079T patent/ES2900812T3/es active Active
- 2015-06-24 TW TW104120373A patent/TW201625558A/zh unknown
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2016
- 2016-12-06 IL IL249404A patent/IL249404A0/en unknown
-
2017
- 2017-05-22 HK HK17105165.9A patent/HK1231474A1/zh unknown
- 2017-08-17 US US15/680,045 patent/US20180065953A1/en not_active Abandoned
-
2018
- 2018-03-19 JP JP2018051249A patent/JP2018090644A/ja active Pending
Also Published As
Publication number | Publication date |
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AU2015280138A1 (en) | 2016-12-22 |
JP6391718B2 (ja) | 2018-09-19 |
EP3160960A1 (en) | 2017-05-03 |
US20180065953A1 (en) | 2018-03-08 |
JP2017519021A (ja) | 2017-07-13 |
AU2015280138B2 (en) | 2018-06-14 |
NZ727185A (en) | 2018-04-27 |
KR20170015521A (ko) | 2017-02-08 |
JP2018090644A (ja) | 2018-06-14 |
EP3160960B1 (en) | 2021-10-13 |
WO2015200352A1 (en) | 2015-12-30 |
US9765060B2 (en) | 2017-09-19 |
IL249404A0 (en) | 2017-02-28 |
MA40045A (fr) | 2021-06-02 |
CA2953820A1 (en) | 2015-12-30 |
US20160024054A1 (en) | 2016-01-28 |
CN106459008A (zh) | 2017-02-22 |
TW201625558A (zh) | 2016-07-16 |
SG11201610341PA (en) | 2017-01-27 |
ES2900812T3 (es) | 2022-03-18 |
MX2016017110A (es) | 2017-05-01 |
HK1231474A1 (zh) | 2017-12-22 |
BR112016029846A2 (pt) | 2017-08-22 |
EA201692487A1 (ru) | 2017-06-30 |
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