[go: up one dir, main page]

SG11201609033TA - Inhibitors of lysine specific demethylase-1 - Google Patents

Inhibitors of lysine specific demethylase-1

Info

Publication number
SG11201609033TA
SG11201609033TA SG11201609033TA SG11201609033TA SG11201609033TA SG 11201609033T A SG11201609033T A SG 11201609033TA SG 11201609033T A SG11201609033T A SG 11201609033TA SG 11201609033T A SG11201609033T A SG 11201609033TA SG 11201609033T A SG11201609033T A SG 11201609033TA
Authority
SG
Singapore
Prior art keywords
inhibitors
specific demethylase
lysine specific
lysine
demethylase
Prior art date
Application number
SG11201609033TA
Inventor
Young K Chen
Toufike Kanouni
Stephen W Kaldor
Jefrey Alan Stafford
James Marvin Veal
Original Assignee
Celgene Quanticel Res Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Celgene Quanticel Res Inc filed Critical Celgene Quanticel Res Inc
Publication of SG11201609033TA publication Critical patent/SG11201609033TA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/002Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/34One oxygen atom
    • C07D239/36One oxygen atom as doubly bound oxygen atom or as unsubstituted hydroxy radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05Isotopically modified compounds, e.g. labelled

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Polyamides (AREA)
SG11201609033TA 2014-05-01 2015-04-30 Inhibitors of lysine specific demethylase-1 SG11201609033TA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201461987354P 2014-05-01 2014-05-01
PCT/US2015/028635 WO2015168466A1 (en) 2014-05-01 2015-04-30 Inhibitors of lysine specific demethylase-1

Publications (1)

Publication Number Publication Date
SG11201609033TA true SG11201609033TA (en) 2016-11-29

Family

ID=54354743

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201609033TA SG11201609033TA (en) 2014-05-01 2015-04-30 Inhibitors of lysine specific demethylase-1

Country Status (32)

Country Link
US (9) US9255097B2 (en)
EP (1) EP3137169B1 (en)
JP (1) JP6493890B2 (en)
KR (1) KR102400920B1 (en)
CN (1) CN106659914B (en)
AR (1) AR100251A1 (en)
AU (1) AU2015253040B2 (en)
BR (1) BR112016025248B1 (en)
CA (1) CA2947283C (en)
CL (1) CL2016002736A1 (en)
CY (1) CY1124959T1 (en)
DK (1) DK3137169T3 (en)
EA (1) EA036672B8 (en)
ES (1) ES2903423T3 (en)
HR (1) HRP20220096T1 (en)
HU (1) HUE057895T2 (en)
IL (1) IL248505B (en)
LT (1) LT3137169T (en)
MX (1) MX373373B (en)
NI (1) NI201600165A (en)
PE (1) PE20161438A1 (en)
PH (1) PH12016502179A1 (en)
PL (1) PL3137169T3 (en)
PT (1) PT3137169T (en)
RS (1) RS62874B1 (en)
SA (2) SA516380201B1 (en)
SG (1) SG11201609033TA (en)
SI (1) SI3137169T1 (en)
SM (1) SMT202200066T1 (en)
TW (1) TWI676620B (en)
WO (1) WO2015168466A1 (en)
ZA (1) ZA201607613B (en)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3094629B1 (en) 2014-01-17 2018-08-22 Novartis AG 1-(triazin-3-yl/pyridazin-3-yl)-piper(-azine)idine derivatives and compositions thereof for inhibiting the activity of shp2
EP3094627B1 (en) 2014-01-17 2018-08-22 Novartis AG 1-pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and and compositions thereof for inhibiting the activity of shp2
JO3517B1 (en) 2014-01-17 2020-07-05 Novartis Ag N-azaspirocycloalkane substituted n-heteroaryl compounds and compositions for inhibiting the activity of shp2
SI3137169T1 (en) * 2014-05-01 2022-04-29 Celgene Quanticel Research, Inc. Inhibitors of lysine specific demethylase-1
LT3160956T (en) * 2014-06-27 2020-09-10 Celgene Quanticel Research, Inc. LYSINE-SPECIFIC DEMETYLASE-1 INHIBITORS
MX395534B (en) * 2014-07-03 2025-03-25 Celgene Quanticel Res Inc LYSINE-SPECIFIC DEMETHYLASE-1 INHIBITORS.
CA2987876A1 (en) 2015-06-12 2016-12-15 Oryzon Genomics, S.A. Biomarkers associated with lsd1 inhibitors and uses thereof
US10308660B2 (en) 2015-06-19 2019-06-04 Novartis Ag Compounds and compositions for inhibiting the activity of SHP2
WO2016203404A1 (en) 2015-06-19 2016-12-22 Novartis Ag Compounds and compositions for inhibiting the activity of shp2
EP3310774B1 (en) 2015-06-19 2020-04-29 Novartis AG Compounds and compositions for inhibiting the activity of shp2
WO2017013061A1 (en) 2015-07-17 2017-01-26 Oryzon Genomics, S.A. Biomarkers associated with lsd1 inhibitors and uses thereof
PT3371152T (en) * 2015-11-05 2021-02-01 Celgene Quanticel Res Inc Compositions comprising an inhibitor of lysine specific demethylase-1
US10059668B2 (en) 2015-11-05 2018-08-28 Mirati Therapeutics, Inc. LSD1 inhibitors
PL3381896T3 (en) * 2015-11-27 2023-05-08 Taiho Pharmaceutical Co., Ltd. Biphenyl compound or salt thereof
SG11201805645QA (en) 2015-12-29 2018-07-30 Mirati Therapeutics Inc Lsd1 inhibitors
EA201892075A1 (en) 2016-03-15 2019-04-30 Оризон Дженомикс, С.А. COMBINATION OF LSD1 INHIBITORS FOR USE FOR THE TREATMENT OF SOLID TUMORS
US11034991B2 (en) 2016-03-16 2021-06-15 Oryzon Genomics S.A. Methods to determine KDM1A target engagement and chemoprobes useful therefor
US10150754B2 (en) 2016-04-19 2018-12-11 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
RU2744988C2 (en) 2016-06-14 2021-03-17 Новартис Аг Compounds and compositions for suppressing shp2 activity
MX381059B (en) 2016-08-10 2025-04-01 Celgene Quanticel Res Inc Treatment of relapsed and/or refractory solid tumors and non-hodgkin's lymphomas
WO2018059549A1 (en) * 2016-09-30 2018-04-05 Novartis Ag Immune effector cell therapies with enhanced efficacy
EP3535414A1 (en) 2016-11-03 2019-09-11 Oryzon Genomics, S.A. Pharmacodynamic biomarkers for personalized cancer care using epigenetic modifying agents
WO2018083189A1 (en) 2016-11-03 2018-05-11 Oryzon Genomics, S.A. Biomarkers for determining responsiveness to lsd1 inhibitors
ES2964956T3 (en) 2017-01-10 2024-04-10 Novartis Ag Pharmaceutical combination comprising an ALK inhibitor and a SHP2 inhibitor
ES2991090T3 (en) 2017-03-30 2024-12-02 Univ Freiburg Albert Ludwigs KDM4 inhibitors
CA3065077C (en) 2017-05-26 2022-09-20 Taiho Pharmaceutical Co., Ltd. Novel biphenyl compound or salt thereof
MA50467A (en) 2017-05-26 2020-09-02 Taiho Pharmaceutical Co Ltd ANTITUMOR EFFECT POTENTIALIZER USING A NEW BIPHENYL COMPOUND
US12435128B2 (en) 2017-05-31 2025-10-07 Taiho Pharmaceutical Co., Ltd. Method for predicting therapeutic effect of LSD1 inhibitor based on expression of INSM1
LT3661510T (en) 2017-08-03 2025-01-27 Oryzon Genomics, S.A. Methods of treating behavior alterations
CN112368272B (en) * 2018-03-21 2023-04-21 苏州浦合医药科技有限公司 SHP2 inhibitors and uses thereof
CN109668987A (en) * 2019-02-27 2019-04-23 浙江华贝药业有限责任公司 A kind of 3- amino piperidine dihydrochloride enantiomter measurement analysis method
SG11202109159VA (en) 2019-03-20 2021-10-28 Oryzon Genomics Sa Methods of treating borderline personality disorder
CN120837494A (en) 2019-03-20 2025-10-28 奥莱松基因组股份有限公司 Methods of treating attention deficit hyperactivity disorder using KDM1A inhibitors such as the compound vafidustat
MX2021015447A (en) 2019-06-13 2022-04-06 Celgene Corp CANCER TREATMENT METHODS DIRECTED AT COLD TUMORS.
US20220249528A1 (en) 2019-06-20 2022-08-11 Celgene Corporation Azacitidine in combination with venetoclax, gilteritinib, midostaurin or other compounds for treating leukemia or myelodysplastic syndrome
WO2021004610A1 (en) 2019-07-05 2021-01-14 Oryzon Genomics, S.A. Biomarkers and methods for personalized treatment of small cell lung cancer using kdm1a inhibitors
WO2021063821A1 (en) * 2019-10-01 2021-04-08 Bayer Aktiengesellschaft Pyrimidinedione derivatives
BR112022008020A2 (en) 2019-11-13 2022-07-12 Taiho Pharmaceutical Co Ltd METHODS OF TREATMENT OF LSD1-RELATED DISEASES AND DISORDERS WITH LSD1 INHIBITORS
JP2023516745A (en) * 2020-03-06 2023-04-20 セルジーン・クオンティセル・リサーチ・インコーポレイテッド Methods of treating small cell lung cancer and/or squamous non-small cell lung cancer
CN116056707A (en) 2020-06-05 2023-05-02 赛尔基因昆蒂赛尔研究公司 Methods of treating prostate cancer
EP4306520A4 (en) * 2021-03-11 2025-05-07 Medshine Discovery Inc. THIOPHENE COMPOUND AND APPLICATION THEREOF
CN117062813A (en) * 2021-03-24 2023-11-14 四川汇宇制药股份有限公司 Polycyclic compound and application thereof
KR20230167102A (en) 2021-04-08 2023-12-07 오리존 지노믹스 에스.에이. Combination of LSD1 inhibitors for the treatment of myeloid cancer
JP2025516648A (en) 2022-05-09 2025-05-30 オリゾン・ゲノミクス・ソシエダッド・アノニマ Treatment of NF1-mutated tumors using LSD1 inhibitors
WO2023217758A1 (en) 2022-05-09 2023-11-16 Oryzon Genomics, S.A. Methods of treating malignant peripheral nerve sheath tumor (mpnst) using lsd1 inhibitors
WO2024110649A1 (en) 2022-11-24 2024-05-30 Oryzon Genomics, S.A. Combinations of lsd1 inhibitors and menin inhibitors for treating cancer
KR20250110929A (en) 2022-12-02 2025-07-21 뉴모라 테라퓨틱스, 인코포레이티드 How to treat neurological disorders

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5550147A (en) * 1992-02-05 1996-08-27 Fujisawa Pharmaceutical Co., Ltd. Pyrazole derivatives, processes for preparation thereof and pharmaceutical composition comprising the same
CN1312807A (en) * 1998-06-19 2001-09-12 希龙公司 Inhibitors of glycogen synthase kinase 3
EP1397142A4 (en) * 2001-06-19 2004-11-03 Bristol Myers Squibb Co Pyrimidine inhibitors of phosphodiesterase (pde) 7
MXPA05005477A (en) * 2002-11-21 2005-07-25 Chiron Corp 2,4,6-trisubstituted pyrimidines as phosphotidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer.
US7183287B2 (en) 2003-04-03 2007-02-27 Pharmacia Corporation Substituted pyrimidinones
TW200526641A (en) * 2003-12-26 2005-08-16 Daiichi Seiyaku Co Amidopyrazole derivatives
WO2008070908A1 (en) * 2006-12-11 2008-06-19 Bionomics Limited Chemical compounds and processes
AU2009275957A1 (en) * 2008-07-29 2010-02-04 Boehringer Ingelheim International Gmbh 5-alkynyl-pyrimidines
TWI435874B (en) * 2008-10-31 2014-05-01 Toray Industries A cyclohexane derivative and the medical and pharmaceutical use
US9365539B2 (en) * 2010-05-11 2016-06-14 Merck Sharp & Dohme Corp. Prolylcarboxypeptidase inhibitors
WO2012034116A2 (en) 2010-09-10 2012-03-15 The Johns Hopkins University Small molecules as epigenetic modulators of lysine-specific demethylase 1 and methods of treating disorders
PH12013501871A1 (en) 2011-03-25 2019-06-03 Glaxosmithkline Ip No 2 Ltd Cyclopropylamines as lsd1 inhibitors
WO2013175789A1 (en) 2012-05-24 2013-11-28 出光興産株式会社 Material for organic electroluminescent elements, and organic electroluminescent element using same
EP2970285B1 (en) 2013-03-11 2019-04-17 AbbVie Inc. Fused tetracyclic bromodomain inhibitors
WO2015018522A1 (en) 2013-08-06 2015-02-12 Oncoethix Sa Bet-bromodomain inhibitor shows synergism with several anti-cancer agents in pre-clinical models of diffuse large b-cell lymphoma (dlbcl)
RS63733B1 (en) 2013-10-18 2022-12-30 Celgene Quanticel Research Inc BROMODOMAIN INHIBITORS
JP6430512B2 (en) * 2013-12-11 2018-11-28 セルジーン クオンティセル リサーチ,インク. Inhibitors of lysine-specific demethylase-1
SI3137169T1 (en) 2014-05-01 2022-04-29 Celgene Quanticel Research, Inc. Inhibitors of lysine specific demethylase-1
US20160022684A1 (en) 2014-07-25 2016-01-28 Pharmacyclics Llc Bet inhibitor and bruton's tyrosine kinase inhibitor combinations
US20190055235A1 (en) 2014-12-17 2019-02-21 Zenith Epigenetics Ltd. Substituted bicyclic compounds as bromodomain inhibitors
PT3371152T (en) * 2015-11-05 2021-02-01 Celgene Quanticel Res Inc Compositions comprising an inhibitor of lysine specific demethylase-1

Also Published As

Publication number Publication date
EP3137169A1 (en) 2017-03-08
EA201692079A1 (en) 2017-04-28
CA2947283C (en) 2023-01-24
CN106659914A (en) 2017-05-10
KR20160144506A (en) 2016-12-16
SA519410025B1 (en) 2022-06-01
AU2015253040A1 (en) 2016-11-24
HRP20220096T1 (en) 2022-04-15
CY1124959T1 (en) 2023-01-05
SMT202200066T1 (en) 2022-03-21
US20170114024A1 (en) 2017-04-27
TW201623254A (en) 2016-07-01
ES2903423T3 (en) 2022-04-01
IL248505A0 (en) 2016-12-29
US20160152595A1 (en) 2016-06-02
CN106659914B (en) 2020-06-19
US20220153706A1 (en) 2022-05-19
NI201600165A (en) 2017-03-13
US10654810B2 (en) 2020-05-19
MX2016014253A (en) 2017-02-08
ZA201607613B (en) 2017-11-29
EA036672B1 (en) 2020-12-07
SA516380201B1 (en) 2019-11-20
US11084793B2 (en) 2021-08-10
US20160130247A1 (en) 2016-05-12
US20170349555A1 (en) 2017-12-07
US20150315187A1 (en) 2015-11-05
JP2017514830A (en) 2017-06-08
EP3137169A4 (en) 2018-01-10
US10207999B2 (en) 2019-02-19
US9771329B2 (en) 2017-09-26
US9573930B2 (en) 2017-02-21
CL2016002736A1 (en) 2017-06-23
IL248505B (en) 2021-01-31
JP6493890B2 (en) 2019-04-03
LT3137169T (en) 2022-04-11
PT3137169T (en) 2022-01-25
CA2947283A1 (en) 2015-11-05
DK3137169T3 (en) 2022-02-14
PL3137169T3 (en) 2022-02-28
WO2015168466A1 (en) 2015-11-05
AR100251A1 (en) 2016-09-21
BR112016025248B1 (en) 2022-12-13
AU2015253040B2 (en) 2020-04-09
SI3137169T1 (en) 2022-04-29
US9776974B2 (en) 2017-10-03
AU2015253040A8 (en) 2017-06-15
PH12016502179A1 (en) 2017-02-13
HUE057895T2 (en) 2022-06-28
US11987560B2 (en) 2024-05-21
BR112016025248A2 (en) 2018-06-19
TWI676620B (en) 2019-11-11
MX373373B (en) 2020-05-12
PE20161438A1 (en) 2017-01-18
US20170349556A1 (en) 2017-12-07
US20200231549A1 (en) 2020-07-23
WO2015168466A8 (en) 2016-11-24
NZ725914A (en) 2023-09-29
US9255097B2 (en) 2016-02-09
RS62874B1 (en) 2022-02-28
US10023543B2 (en) 2018-07-17
EP3137169B1 (en) 2021-11-10
KR102400920B1 (en) 2022-05-20
US20180325900A1 (en) 2018-11-15
EA036672B8 (en) 2021-01-13

Similar Documents

Publication Publication Date Title
IL272130B (en) Inhibitors of lysine specific demethylase-1
IL250876B (en) Inhibitors of lysine specific demethylase-1
ZA201607613B (en) Inhibitors of lysine specific demethylase-1
ZA201700069B (en) Inhibitors of lysine specific demethylase-1
ZA201700072B (en) Inhibitors of lysine specific demethylase-1
PL3204352T3 (en) Inhibitors of lysine gingipain
HK1234047A1 (en) Inhibitors of lysine specific demethylase-1
HK1231134A1 (en) Inhibitors of lysine specific demethylase-1
HK1231843A1 (en) Inhibitors of lysine specific demethylase-1