PL3468966T3 - Inhibitory interakcji menina-mll - Google Patents

Inhibitory interakcji menina-mll

Info

Publication number
PL3468966T3
PL3468966T3 PL17739383T PL17739383T PL3468966T3 PL 3468966 T3 PL3468966 T3 PL 3468966T3 PL 17739383 T PL17739383 T PL 17739383T PL 17739383 T PL17739383 T PL 17739383T PL 3468966 T3 PL3468966 T3 PL 3468966T3
Authority
PL
Poland
Prior art keywords
menin
inhibitors
mll interaction
mll
interaction
Prior art date
Application number
PL17739383T
Other languages
English (en)
Inventor
Salvacion Cacatian
David A. Claremon
Lawrence Wayne Dillard
Chengguo DONG
Yi Fan
Lanqi Jia
Stephen D. Lotesta
Andrew Marcus
Angel Morales-Ramos
Suresh B. Singh
Shankar Venkatraman
Jing Yuan
Yajun Zheng
Linghang Zhuang
Stephan D. Parent
Travis L. Houston
Original Assignee
Vitae Pharmaceuticals, Llc
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 Vitae Pharmaceuticals, Llc filed Critical Vitae Pharmaceuticals, Llc
Publication of PL3468966T3 publication Critical patent/PL3468966T3/pl

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • 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
    • C07D403/14Heterocyclic 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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
    • C07D491/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic 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
    • C07D491/02Heterocyclic 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
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic System
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
PL17739383T 2016-06-10 2017-06-08 Inhibitory interakcji menina-mll PL3468966T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662348496P 2016-06-10 2016-06-10
EP17739383.2A EP3468966B1 (en) 2016-06-10 2017-06-08 Inhibitors of the menin-mll interaction
PCT/US2017/036506 WO2017214367A1 (en) 2016-06-10 2017-06-08 Inhibitors of the menin-mll interaction

Publications (1)

Publication Number Publication Date
PL3468966T3 true PL3468966T3 (pl) 2021-04-06

Family

ID=59325631

Family Applications (1)

Application Number Title Priority Date Filing Date
PL17739383T PL3468966T3 (pl) 2016-06-10 2017-06-08 Inhibitory interakcji menina-mll

Country Status (21)

Country Link
US (3) US10683302B2 (pl)
EP (2) EP3805215A1 (pl)
JP (3) JP7007302B2 (pl)
KR (2) KR20220123727A (pl)
CN (1) CN109743875B (pl)
AU (2) AU2017278950B2 (pl)
BR (2) BR112018075260A2 (pl)
CA (1) CA3024180A1 (pl)
CY (1) CY1124834T1 (pl)
DK (1) DK3468966T3 (pl)
ES (1) ES2831084T3 (pl)
HR (1) HRP20201771T1 (pl)
HU (1) HUE051451T2 (pl)
IL (3) IL298381A (pl)
LT (1) LT3468966T (pl)
MX (3) MX2018015252A (pl)
PL (1) PL3468966T3 (pl)
PT (1) PT3468966T (pl)
SI (1) SI3468966T1 (pl)
WO (1) WO2017214367A1 (pl)
ZA (1) ZA201900150B (pl)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE49687E1 (en) 2014-09-09 2023-10-10 The Regents Of The University Of Michigan Thienopyrimidine and thienopyridine compounds and methods of use thereof
TWI703150B (zh) 2015-06-04 2020-09-01 美商庫拉腫瘤技術股份有限公司 用於抑制menin及mll蛋白之交互作用的方法及組合物
EP3302057A4 (en) 2015-06-04 2018-11-21 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with mll proteins
JP7000333B2 (ja) 2016-03-16 2022-02-10 クラ オンコロジー,インク. メニン-mllの架橋された二環式阻害剤及びその使用方法
EP4219449A3 (en) 2016-03-16 2023-10-11 Kura Oncology, Inc. Substituted indole derivatives and methods of preparation thereof
KR20190015275A (ko) 2016-05-02 2019-02-13 더 리젠츠 오브 더 유니버시티 오브 미시간 메닌 억제제로서의 피페리딘
LT3468966T (lt) 2016-06-10 2021-02-25 Vitae Pharmaceuticals, Llc Menino-mll sąveikos inhibitoriai
WO2018050684A1 (en) 2016-09-14 2018-03-22 Janssen Pharmaceutica Nv Fused bicyclic inhibitors of menin-mll interaction
EP3512857B1 (en) 2016-09-14 2021-02-24 Janssen Pharmaceutica NV Spiro bicyclic inhibitors of menin-mll interaction
US10745409B2 (en) 2016-12-15 2020-08-18 Janssen Pharmaceutica Nv Azepane inhibitors of menin-MLL interaction
US11944627B2 (en) 2017-03-24 2024-04-02 Kura Oncology, Inc. Methods for treating hematological malignancies and Ewing's sarcoma
SG11201909083UA (en) 2017-03-31 2019-10-30 Univ Michigan Regents Piperidines as covalent menin inhibitors
CA3059675A1 (en) 2017-04-10 2018-10-18 Mitsui Chemicals Agro, Inc. Pyridone compounds and agricultural and horticultural fungicides comprising the same as active ingredients
US11542248B2 (en) 2017-06-08 2023-01-03 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with MLL proteins
US11649251B2 (en) 2017-09-20 2023-05-16 Kura Oncology, Inc. Substituted inhibitors of menin-MLL and methods of use
US11396517B1 (en) 2017-12-20 2022-07-26 Janssen Pharmaceutica Nv Exo-aza spiro inhibitors of menin-MLL interaction
AU2018389145B2 (en) * 2017-12-20 2023-02-02 Janssen Pharmaceutica Nv Exo-aza spiro inhibitors of menin-MLL interaction
US11325921B2 (en) 2018-03-30 2022-05-10 Sumitomo Dainippon Pharma Co., Ltd. Optically active crosslinked cyclic secondary amine derivative
CN112585140B (zh) 2018-08-27 2023-07-04 住友制药株式会社 光学活性氮杂双环衍生物
US10815241B2 (en) 2018-08-27 2020-10-27 Sumitomo Dainippon Pharma Co., Ltd. Optically active azabicyclo ring derivative
CN111285875B (zh) * 2018-12-06 2023-02-03 苏州信诺维医药科技股份有限公司 一种杂环化合物、其应用及含其的药物组合物
US20230030720A1 (en) 2018-12-06 2023-02-02 Daiichi Sankyo Company, Limited Cycloalkane-1,3-diamine derivative
CA3125353A1 (en) 2018-12-31 2020-07-09 Biomea Fusion, Llc Inhibitors of menin-mll interaction
MX2022004213A (es) 2019-10-09 2022-05-03 Novartis Ag Derivados de 2-azaspiro[3.4]octano como agonistas de m4.
CN114555606A (zh) * 2019-10-09 2022-05-27 诺华股份有限公司 作为m4激动剂的5-氧杂-2-氮杂螺[3.4]辛烷衍生物
CN114867721A (zh) * 2019-12-19 2022-08-05 詹森药业有限公司 取代的直链螺环衍生物
JP7454520B2 (ja) 2020-02-26 2024-03-22 住友ファーマ株式会社 光学活性なアザビシクロ環誘導体からなる医薬
CN111297863B (zh) * 2020-03-30 2021-06-25 四川大学华西医院 menin-MLL抑制剂在制备治疗子宫内膜癌的药物中的应用
CN115698013A (zh) * 2020-04-07 2023-02-03 赛达克斯制药股份有限公司 Menin抑制剂和cyp3a4抑制剂的组合及其使用方法
CN114516873A (zh) * 2020-11-18 2022-05-20 苏州优理生物医药科技有限公司 一种螺环类化合物、包含其药物组合物及其应用
RU2752079C1 (ru) * 2020-12-01 2021-07-22 Федеральное государственное автономное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" (Е)-(6-(2-гидроксифенил)-2-иминио-4,7,8-триоксо-1,3-дифенил-1,3,6-триазаспиро[4.4]нонан-9-илиден)(4-метоксифенил)метаноат, обладающий противомикробной активностью, и способ его получения
AU2022272692A1 (en) 2021-05-08 2024-01-04 Janssen Pharmaceutica Nv Substituted spiro derivatives
CN117730081A (zh) 2021-05-08 2024-03-19 詹森药业有限公司 取代的螺环衍生物
PE20240593A1 (es) * 2021-05-11 2024-03-21 Janssen Pharmaceutica Nv Terapias de combinacion
EP4337215A1 (en) * 2021-05-11 2024-03-20 JANSSEN Pharmaceutica NV Combination therapies
IL308476A (en) 2021-05-14 2024-01-01 Syndax Pharmaceuticals Inc Inhibitors of the menin-mil interaction
US20230250096A1 (en) 2021-06-01 2023-08-10 Janssen Pharmaceutica Nv SUBSTITUTED PHENYL-1H-PYRROLO[2,3-c] PYRIDINE DERIVATIVES
CN117412964A (zh) * 2021-06-03 2024-01-16 首药控股(北京)股份有限公司 取代的杂环化合物及其应用
CN117425659A (zh) 2021-06-03 2024-01-19 詹森药业有限公司 哒嗪或被螺环胺取代的1,2,4-三嗪
WO2022257047A1 (en) * 2021-06-09 2022-12-15 Acerand Therapeutics (Hong Kong) Limited Diazaspirobicylic compounds as protein-protein interaction inhibitors and applications thereof
KR20240021808A (ko) 2021-06-17 2024-02-19 얀센 파마슈티카 엔브이 암과 같은 질환의 치료를 위한 (r)-n-에틸-5-플루오로-n-아이소프로필-2-((5-(2-(6-((2-메톡시에틸)(메틸)아미노)-2-메틸헥산-3-일)-2,6-다이아자스피로[3.4]옥탄-6-일)-1,2,4-트라이아진-6-일)옥시)벤즈아미드 베실레이트 염
WO2023011446A1 (zh) * 2021-08-04 2023-02-09 成都苑东生物制药股份有限公司 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途
CN115515958B (zh) * 2021-08-04 2023-09-29 成都苑东生物制药股份有限公司 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途
CN113769098B (zh) * 2021-09-22 2022-09-30 中国医学科学院肿瘤医院深圳医院 MLL-menin抑制剂组合物在制备抗肝癌药物中的应用
TW202333690A (zh) * 2021-12-03 2023-09-01 大陸商燁輝醫藥科技(上海)有限公司 羰基取代的二氮雜螺化合物及其用途
CN116375707A (zh) * 2021-12-31 2023-07-04 成都先导药物开发股份有限公司 Menin抑制剂及其用途
WO2024046457A1 (en) * 2022-09-02 2024-03-07 Hutchmed Limited Triazine compounds and uses thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090281114A1 (en) 2008-05-08 2009-11-12 Fabre-Kramer Pharmaceuticals, Inc. Indolylalkyl derivatives of pyrimidinylpiperazine and metabolites thereof for treatment of anxiety, depression, and sexual dysfunction
AR071717A1 (es) 2008-05-13 2010-07-07 Array Biopharma Inc Pirrolo[2,3-b]piridinas inhibidoras de quinasas chk1 y chk2,composiciones farmaceuticas que las contienen,proceso para prepararlas y uso de las mismas en el tratamiento y prevencion del cancer.
KR20190011343A (ko) 2011-06-10 2019-02-01 메르크 파텐트 게엠베하 Btk 억제 활성을 갖는 피리미딘 및 피리딘 화합물의 조성물 및 제조방법
EP2968342B1 (en) 2013-03-13 2018-10-03 The Regents of the University of Michigan Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof
WO2015191701A1 (en) * 2014-06-10 2015-12-17 The Trustees Of The University Of Pennsylvania Scaffolds for inhibitors of menin-mll interactions
CN105732636B (zh) 2014-12-30 2020-04-21 广东东阳光药业有限公司 杂芳化合物及其在药物中的应用
AU2016378579A1 (en) 2015-12-22 2018-06-14 Vitae Pharmaceuticals, Inc. Inhibitors of the menin-MLL interaction
LT3468966T (lt) 2016-06-10 2021-02-25 Vitae Pharmaceuticals, Llc Menino-mll sąveikos inhibitoriai

Also Published As

Publication number Publication date
IL298381A (en) 2023-01-01
US20230174541A1 (en) 2023-06-08
IL283267B2 (en) 2023-04-01
CA3024180A1 (en) 2017-12-14
SI3468966T1 (sl) 2021-03-31
ES2831084T3 (es) 2021-06-07
JP2022058514A (ja) 2022-04-12
AU2021258089A1 (en) 2021-11-25
HRP20201771T1 (hr) 2021-02-19
RU2019100040A3 (pl) 2020-07-15
CN109743875B (zh) 2022-04-29
EP3468966A1 (en) 2019-04-17
JP2019517548A (ja) 2019-06-24
PT3468966T (pt) 2020-11-10
EP3805215A1 (en) 2021-04-14
US10683302B2 (en) 2020-06-16
DK3468966T3 (da) 2020-11-09
AU2021258089B2 (en) 2024-01-25
MX2023002982A (es) 2023-04-10
CN109743875A (zh) 2019-05-10
CY1124834T1 (el) 2022-07-22
JP7007302B2 (ja) 2022-01-24
MX2021003939A (es) 2021-05-27
BR112018075260A2 (pt) 2019-03-12
KR20190017012A (ko) 2019-02-19
US11479557B2 (en) 2022-10-25
ZA201900150B (en) 2023-04-26
KR20220123727A (ko) 2022-09-08
MX2018015252A (es) 2019-04-25
JP7461390B2 (ja) 2024-04-03
EP3468966B1 (en) 2020-08-05
LT3468966T (lt) 2021-02-25
AU2017278950B2 (en) 2021-07-29
IL263586B (en) 2021-06-30
US20210053974A1 (en) 2021-02-25
AU2017278950A1 (en) 2019-01-03
US20190144459A1 (en) 2019-05-16
HUE051451T2 (hu) 2021-03-01
RU2019100040A (ru) 2020-07-13
KR102436430B1 (ko) 2022-08-24
BR122024002146A2 (pt) 2024-03-05
IL283267A (en) 2021-07-29
IL283267B (en) 2022-12-01
IL263586A (en) 2019-01-31
JP2024045176A (ja) 2024-04-02
WO2017214367A1 (en) 2017-12-14

Similar Documents

Publication Publication Date Title
IL283267A (en) Inhibitors of menin–mll interaction
IL259560A (en) Inhibitors of the menin-mll interaction
PL3512850T3 (pl) Inhibitory interakcji menina-mll
IL251584B (en) Dihydropyrrolopyridines ror–gamma inhibitors
IL246902B (en) Dihydropyrrolopyridine ror–gamma inhibitors
AU364417S (en) Back of the case
GB201403536D0 (en) Inhibitor compounds
IL265139B (en) Dopamine-b-hydroxylase inhibitors
GB201521059D0 (en) Inhibitors of metallo-beta-lactamases
ZA201907136B (en) Ip6k inhibitors
GB201505658D0 (en) Inhibitor compounds
GB201612860D0 (en) Inhibitors
GB201501004D0 (en) Inhibitors
IL274550A (en) Dopamine-B-hydroxylase inhibitors
IL262111B1 (en) Monovalent inhibitors of hutnfr1 interaction
GB201401005D0 (en) Inhibitor
GB201520949D0 (en) Inhibitors
AU2024202700A1 (en) Inhibitors of the menin-MLL Interaction
GB201721465D0 (en) Inhibitors
GB201720189D0 (en) Dopamine-B-hydroxylase inhibitors
GB201621619D0 (en) Inhibitor compounds
GB201500644D0 (en) Inhibitor compounds
GB201402924D0 (en) The theory of instantransmission