EA202092317A1 - Ингибитор белок-белковых взаимодействий фенилтриазольных соединений mll1-wdr5 - Google Patents

Ингибитор белок-белковых взаимодействий фенилтриазольных соединений mll1-wdr5

Info

Publication number
EA202092317A1
EA202092317A1 EA202092317A EA202092317A EA202092317A1 EA 202092317 A1 EA202092317 A1 EA 202092317A1 EA 202092317 A EA202092317 A EA 202092317A EA 202092317 A EA202092317 A EA 202092317A EA 202092317 A1 EA202092317 A1 EA 202092317A1
Authority
EA
Eurasian Patent Office
Prior art keywords
protein
wdr5
mll1
phenyltriazole
inhibitor
Prior art date
Application number
EA202092317A
Other languages
English (en)
Inventor
Цидун Ю
Сяокэ Го
Дундун Ли
Вэйлинь ЧЭНЬ
Чжихуэй Ван
Original Assignee
Чайна Фармасьютикал Юниверсити
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 Чайна Фармасьютикал Юниверсити filed Critical Чайна Фармасьютикал Юниверсити
Publication of EA202092317A1 publication Critical patent/EA202092317A1/ru

Links

Classifications

    • 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
    • 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
    • C07D405/02Heterocyclic 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
    • C07D405/12Heterocyclic 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
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/041,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
    • C07D249/061,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
    • 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
    • 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
    • C07D403/10Heterocyclic 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 carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Настоящее изобретение относится к области медицинской химии, в частности к классу ингибиторов белок-белкового взаимодействия фенилтриазол MLL1-WDR5 (I) и способу его получения, и фармакодинамические исследования доказывают, что соединение по настоящему изобретению характеризуется относительно сильной ингибиторной активностью белок-белкового взаимодействия MLL1-WDR5.
EA202092317A 2018-04-23 2018-12-25 Ингибитор белок-белковых взаимодействий фенилтриазольных соединений mll1-wdr5 EA202092317A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201810365880.0A CN108715585A (zh) 2018-04-23 2018-04-23 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂
PCT/CN2018/123500 WO2019205687A1 (zh) 2018-04-23 2018-12-25 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂

Publications (1)

Publication Number Publication Date
EA202092317A1 true EA202092317A1 (ru) 2021-07-23

Family

ID=63899366

Family Applications (1)

Application Number Title Priority Date Filing Date
EA202092317A EA202092317A1 (ru) 2018-04-23 2018-12-25 Ингибитор белок-белковых взаимодействий фенилтриазольных соединений mll1-wdr5

Country Status (17)

Country Link
US (2) US11479545B2 (ru)
EP (1) EP3786157B1 (ru)
JP (1) JP7274765B2 (ru)
KR (1) KR20210019414A (ru)
CN (2) CN108715585A (ru)
AU (1) AU2018420231B2 (ru)
BR (1) BR112020021569A2 (ru)
CA (1) CA3097925A1 (ru)
CL (1) CL2020002736A1 (ru)
CO (1) CO2020014430A2 (ru)
EA (1) EA202092317A1 (ru)
IL (1) IL278255B2 (ru)
MX (1) MX2020011205A (ru)
PH (1) PH12020551756A1 (ru)
SG (1) SG11202010492SA (ru)
WO (1) WO2019205687A1 (ru)
ZA (1) ZA202006581B (ru)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2019261273B2 (en) 2018-04-23 2023-03-09 Celgene Corporation Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma
CN108715585A (zh) 2018-04-23 2018-10-30 中国药科大学 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂
CN109734674B (zh) * 2019-02-26 2022-08-26 中国药科大学 苯胺类wdr5蛋白-蛋白相互作用抑制剂及其制法和用途
US20230286948A1 (en) * 2022-03-14 2023-09-14 Huyabio International, Llc Haloalkylpyridyl triazole mll1-wdr5 protein-protein interaction inhibitor
WO2023177593A1 (en) * 2022-03-14 2023-09-21 Huyabio International, Llc Phenyl triazole mll1-wdr5 protein-protein interaction inhibitor
WO2024002379A1 (zh) * 2022-07-01 2024-01-04 甘李药业股份有限公司 一种用作wdr5抑制剂的化合物或其可药用盐及其应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1692116B1 (en) * 2003-12-03 2011-03-09 Boehringer Ingelheim Pharmaceuticals Inc. 1,2,3-triazole amide derivatives as inhibitors of cytokine production
WO2011149827A1 (en) 2010-05-24 2011-12-01 Glaxosmithkline Llc Compounds and methods
CN104844573A (zh) 2015-04-17 2015-08-19 中国药科大学 嘧啶类btk抑制剂、其制备方法及医药用途
CN105175284B (zh) * 2015-07-21 2017-06-16 中国药科大学 酰胺类化合物、制备方法及其医药用途
RU2018128334A (ru) 2016-02-09 2020-03-10 Инвентисбио Инк. Ингибиторы индоламин-2,3-диоксигеназы (ido)
AU2017226005A1 (en) * 2016-03-01 2018-09-06 Propellon Therapeutics Inc. Inhibitors of WDR5 protein-protein binding
US11319299B2 (en) 2016-03-01 2022-05-03 Propellon Therapeutics Inc. Substituted carboxamides as inhibitors of WDR5 protein-protein binding
CN107382840B (zh) 2016-05-16 2020-09-01 四川大学 吡啶类化合物及其作为idh功能变异突变体抑制剂类药物的用途
WO2019127385A1 (en) 2017-12-29 2019-07-04 Shenzhen United Imaging Healthcare Co., Ltd. Systems and methods for patient positioning
CN108715585A (zh) 2018-04-23 2018-10-30 中国药科大学 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂

Also Published As

Publication number Publication date
CN112368268A (zh) 2021-02-12
IL278255B1 (en) 2023-05-01
CN108715585A (zh) 2018-10-30
US20230098016A1 (en) 2023-03-30
EP3786157B1 (en) 2024-08-07
AU2018420231A1 (en) 2020-12-10
AU2018420231B2 (en) 2024-08-22
JP7274765B2 (ja) 2023-05-17
US11479545B2 (en) 2022-10-25
MX2020011205A (es) 2021-02-09
SG11202010492SA (en) 2020-11-27
US20210139466A1 (en) 2021-05-13
CA3097925A1 (en) 2019-10-31
EP3786157A4 (en) 2022-01-05
BR112020021569A2 (pt) 2021-04-13
WO2019205687A1 (zh) 2019-10-31
PH12020551756A1 (en) 2021-08-16
JP2021525226A (ja) 2021-09-24
ZA202006581B (en) 2023-05-31
EP3786157A1 (en) 2021-03-03
IL278255B2 (en) 2023-09-01
CL2020002736A1 (es) 2021-05-28
US12054478B2 (en) 2024-08-06
CO2020014430A2 (es) 2021-05-20
IL278255A (ru) 2020-12-31
KR20210019414A (ko) 2021-02-22

Similar Documents

Publication Publication Date Title
EA202092317A1 (ru) Ингибитор белок-белковых взаимодействий фенилтриазольных соединений mll1-wdr5
EA201990851A1 (ru) Новые аналоги карбануклеозида, замещенные моноциклической и бициклической кольцевой системой, для применения в качестве ингибиторов prmt5
CL2018000374A1 (es) Sales de un inhibidor de lsd1
EA202191890A1 (ru) Ингибиторы pcsk9 и способы их применения
AR110381A2 (es) Inhibidores biarilo de tirosina cinasa de bruton
EA201890573A1 (ru) Новые замещенные 6-6-бициклическим ароматическим кольцом аналоги нуклеозидов для применения в качестве ингибиторов prmt5
EA201890338A1 (ru) Оксадиазольные производные, пригодные в качестве ингибиторов hdac
EA201891974A1 (ru) Ингибиторы связывания белка wdr5 с белками
EA201692249A1 (ru) Ингибиторы фосфатидилинозитол-3-киназы
EA201591382A1 (ru) Ингибиторы гистондеметилаз
EA201792535A1 (ru) Гетероциклические амиды в качестве ингибиторов киназ
EA201691401A1 (ru) Индазольные соединения в качестве ингибиторов irak4
EA202092263A1 (ru) Аминопиридиновые производные в качестве ингибиторов ctps1
EA201792259A1 (ru) Бензимидазольные и имидазопиридиновые карбоксимидамидные соединения
EA201400735A1 (ru) Производные альфа-амино бороновой кислоты, селективные ингибиторы иммунопротеасомы
EA202191892A1 (ru) Ингибиторы pcsk9 и способы их применения
EA201690598A1 (ru) Аминогетероарил бензамиды в качестве ингибиторов киназы
EA201792548A1 (ru) 4-гидрокси-3-(гетероарил)пиридин-2-оновые агонисты apj для применения в лечении сердечно-сосудистых заболеваний
EA201991884A3 (ru) Ингибиторы g12c kras
EA201791955A1 (ru) ИНГИБИТОРЫ TGF-β
EA201692265A1 (ru) Ингибиторы фосфатидилинозитол-3-киназы
EA201592182A1 (ru) Ингибиторы фосфатидилинозитол-3-киназы
EA201692266A1 (ru) Ингибиторы фосфатидилинозитол-3-киназы
EA201790599A1 (ru) Соединения и композиции в качестве ингибиторов киназ
EA201992137A1 (ru) ПИРИМИДОПИРИМИДИНОНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ КИНАЗЫ Wee-1