CR20170116A - Compuestos que inhiben la proteina mcl-1 - Google Patents

Compuestos que inhiben la proteina mcl-1

Info

Publication number
CR20170116A
CR20170116A CR20170116A CR20170116A CR20170116A CR 20170116 A CR20170116 A CR 20170116A CR 20170116 A CR20170116 A CR 20170116A CR 20170116 A CR20170116 A CR 20170116A CR 20170116 A CR20170116 A CR 20170116A
Authority
CR
Costa Rica
Prior art keywords
compounds
inhibit
protein mcl
mcl
methods
Prior art date
Application number
CR20170116A
Other languages
English (en)
Spanish (es)
Inventor
Sean P Brown
Mike Elias Lizarzaburu
Nick A Paras
Xianghong Wang
Yunxiao Li
Manuel Zancanella
Liusheng Zhu
Marc Vimolratana
Brian S Lucas
Joshua Taygerly
Ming Yu
Buenrostro Ana Gonzalez
Zhihong Li
Original Assignee
Amgen 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 Amgen Inc filed Critical Amgen Inc
Publication of CR20170116A publication Critical patent/CR20170116A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/10Spiro-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
    • 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
    • A61K31/554Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/11Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/42Unsaturated compounds containing hydroxy or O-metal groups
    • C07C59/56Unsaturated compounds containing hydroxy or O-metal groups containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
    • C07C59/66Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
    • C07C59/68Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/16Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • C07D249/18Benzotriazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • Mycology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
CR20170116A 2014-08-29 2015-08-28 Compuestos que inhiben la proteina mcl-1 CR20170116A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462043929P 2014-08-29 2014-08-29
PCT/US2015/047472 WO2016033486A1 (en) 2014-08-29 2015-08-28 Tetrahydronaphthalene derivatives that inhibit mcl-1 protein

Publications (1)

Publication Number Publication Date
CR20170116A true CR20170116A (es) 2017-04-28

Family

ID=54238507

Family Applications (1)

Application Number Title Priority Date Filing Date
CR20170116A CR20170116A (es) 2014-08-29 2015-08-28 Compuestos que inhiben la proteina mcl-1

Country Status (41)

Country Link
US (7) US9562061B2 (enExample)
EP (2) EP3424931B1 (enExample)
JP (1) JP6502479B2 (enExample)
KR (1) KR102466351B1 (enExample)
CN (1) CN107001387B (enExample)
AP (1) AP2017009827A0 (enExample)
AR (1) AR101729A1 (enExample)
AU (1) AU2015308735B2 (enExample)
BR (1) BR112017004209B1 (enExample)
CA (1) CA2959615C (enExample)
CL (1) CL2017000469A1 (enExample)
CO (1) CO2017002998A2 (enExample)
CR (1) CR20170116A (enExample)
CY (1) CY1121195T1 (enExample)
DK (1) DK3186259T3 (enExample)
EA (1) EA031223B1 (enExample)
ES (2) ES2777478T3 (enExample)
HR (1) HRP20190053T1 (enExample)
HU (1) HUE041806T2 (enExample)
IL (2) IL250843B (enExample)
JO (1) JO3474B1 (enExample)
LT (1) LT3186259T (enExample)
MA (1) MA40111B1 (enExample)
ME (1) ME03313B (enExample)
MX (1) MX379155B (enExample)
MY (1) MY176235A (enExample)
PE (1) PE20170892A1 (enExample)
PH (1) PH12017500367B1 (enExample)
PL (1) PL3186259T3 (enExample)
PT (1) PT3186259T (enExample)
RS (1) RS58276B1 (enExample)
SG (1) SG11201701525WA (enExample)
SI (1) SI3186259T1 (enExample)
SM (1) SMT201900048T1 (enExample)
TN (1) TN2017000067A1 (enExample)
TR (1) TR201901312T4 (enExample)
TW (1) TWI676628B (enExample)
UA (1) UA118233C2 (enExample)
UY (1) UY36285A (enExample)
WO (1) WO2016033486A1 (enExample)
ZA (2) ZA201701763B (enExample)

Families Citing this family (94)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3474B1 (ar) 2014-08-29 2020-07-05 Amgen Inc مشتقات تيتراهيدرونافثالين التي تثبط بروتين mcl-1
US11306107B2 (en) 2016-02-25 2022-04-19 Amgen Inc. Compounds that inhibit MCL-1 protein
CN109562107A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的杂环降解决定子体
WO2017197046A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. C3-carbon linked glutarimide degronimers for target protein degradation
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
EP3454862B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
TWI759316B (zh) 2016-07-22 2022-04-01 法商施維雅藥廠 Bcl-2抑制劑及mcl1抑制劑之組合、其用途及醫藥組合物
JP6453507B2 (ja) * 2017-03-30 2019-01-16 アムジエン・インコーポレーテツド Mcl−1タンパク質を阻害する化合物
EP3641762A4 (en) 2017-06-20 2021-03-10 C4 Therapeutics, Inc. N / O-LINKED DEGRONES AND DEGRONIMERS FOR PROTEIN DEGRADATION
JP2020531433A (ja) * 2017-08-15 2020-11-05 アッヴィ・インコーポレイテッド 大環状mcl−1阻害剤及び使用の方法
MX2020001719A (es) * 2017-08-15 2020-11-06 Abbvie Inc Inhibidores macrocíclicos de mcl-1 y metodos de uso.
MA49908A (fr) 2017-08-18 2021-04-28 Amgen Inc Composés inhibant la protéine mcl-1
US11279712B2 (en) 2017-08-29 2022-03-22 Amgen Inc. Macrocyclic compounds that inhibit MCL-1 protein
WO2019173181A1 (en) 2018-03-05 2019-09-12 Amgen Inc. Alpha-hydroxy phenylacetic acid pharmacophore or bioisostere mcl-1 protein antagonists
MY198871A (en) * 2018-05-14 2023-10-02 Gilead Sciences Inc Mcl-1 inhibitors
MA54157A (fr) * 2018-11-09 2021-09-15 Prelude Therapeutics Inc Dérivés de spiro-sulfonamide en tant qu'inhibiteurs de la protéine de la leucémie myéloïde -1 (mcl-1)
CN120698985A (zh) 2018-12-20 2025-09-26 C4医药公司 靶向蛋白降解
WO2020147802A1 (en) * 2019-01-18 2020-07-23 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic spiroethers as mcl-1 inhibitors
AU2020279230A1 (en) 2019-05-20 2021-12-02 Les Laboratoires Servier Mcl-1 inhibitor antibody-drug conjugates and methods of use
US11453681B2 (en) 2019-05-23 2022-09-27 Gilead Sciences, Inc. Substituted eneoxindoles and uses thereof
KR20220024694A (ko) * 2019-06-21 2022-03-03 얀센 파마슈티카 엔.브이. Mcl-1의 거대환식 억제제
WO2020263830A1 (en) 2019-06-25 2020-12-30 Gilead Sciences, Inc. Flt3l-fc fusion proteins and methods of use
ES2987630T3 (es) 2019-07-09 2024-11-15 Janssen Pharmaceutica Nv Derivados de espirociclos macrocíclicos como inhibidores de MCL-1
EP3771469A1 (en) 2019-07-30 2021-02-03 Amgen, Inc Formulations and dosages for administering a compound that inhibits mcl1 protein
WO2021047616A1 (zh) * 2019-09-12 2021-03-18 苏州亚盛药业有限公司 氧氮杂环庚烷类螺环化合物、中间体及其制备方法
US11795223B2 (en) 2019-10-18 2023-10-24 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
MX2022005123A (es) 2019-10-31 2022-05-30 Forty Seven Inc Tratamiento basado en anti-cd47 y anti-cd20 para cancer hematologico.
CN114786777A (zh) 2019-11-04 2022-07-22 锐新医药公司 Ras抑制剂
CR20220240A (es) * 2019-11-04 2022-08-03 Revolution Medicines Inc Inhibidores de ras
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
PL4065567T3 (pl) * 2019-11-26 2025-01-20 Gilead Sciences, Inc. Procesy i związki pośrednie do wytwarzania inhibitorów mcl1
KR20220131918A (ko) 2019-12-24 2022-09-29 카나 바이오사이언스, 인코포레이션 다이아실글리세롤 키나제 조절 화합물
BR112022014623A2 (pt) 2020-02-14 2022-09-13 Jounce Therapeutics Inc Anticorpos e proteínas de fusão que se ligam a ccr8 e usos dos mesmos
JP2023514364A (ja) * 2020-02-21 2023-04-05 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1の阻害剤としての大環状インドール誘導体
JP2021161114A (ja) * 2020-03-31 2021-10-11 アムジエン・インコーポレーテツド Mcl−1化合物のメチル化
WO2021211922A1 (en) * 2020-04-16 2021-10-21 Prelude Therapeutics, Incorporated Spiro-sulfonimidamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
AU2021264550A1 (en) 2020-05-01 2022-11-17 Gilead Sciences, Inc. CD73 inhibiting 2,4-dioxopyrimidine compounds
MX2022013872A (es) * 2020-05-06 2022-11-30 Amgen Inc Sintesis de productos intermedios de alcohol vinilico.
TWI867217B (zh) * 2020-05-06 2024-12-21 美商安進公司 乙烯基環丁基中間體之合成
TWI827924B (zh) * 2020-05-06 2024-01-01 美商安進公司 大環Mcl-1抑制劑中間體的閉環合成
CN115485268B (zh) 2020-05-06 2024-06-18 安进公司 乙烯基保护的醇中间体的合成
US12441681B2 (en) 2020-05-06 2025-10-14 Amgen Inc. Synthesis of sulfonamide intermediates
AU2021288987A1 (en) * 2020-06-10 2023-02-09 Janssen Pharmaceutica Nv Macrocyclic 2-amino-3-fluoro-but-3-enamides as inhibitors of MCL-1
IL300977A (en) 2020-09-03 2023-04-01 Amgen Inc Removal of diol symmetry via nucleophilic aromatic substitution
EP4214209A1 (en) 2020-09-15 2023-07-26 Revolution Medicines, Inc. Indole derivatives as ras inhibitors in the treatment of cancer
KR20230107848A (ko) * 2020-11-19 2023-07-18 길리애드 사이언시즈, 인코포레이티드 거대고리형 mcl1 저해제를 제조하기 위한 방법 및 중간체
EP4251208A1 (en) 2020-11-24 2023-10-04 Novartis AG Mcl-1 inhibitor antibody-drug conjugates and methods of use
EP4251604A1 (en) * 2020-11-25 2023-10-04 Amgen Inc. Enantioselective alkenylation of aldehydes
EP4008324A1 (en) 2020-12-07 2022-06-08 Cellestia Biotech AG Combinations comprising an inhibitor of an anti-apoptotic protein, such as bcl-2, bcl-xl, bclw or mcl-1, and a notch signaling pathway inhibitor for treating cancer
WO2022122667A1 (en) 2020-12-07 2022-06-16 Cellestia Biotech Ag Pharmaceutical combinations for treating cancer
AU2021404501A1 (en) 2020-12-17 2023-08-03 Janssen Pharmaceutica Nv Macrocyclic branched 3-fluoro-but-3-enamides as inhibitors of mcl-1
TW202302145A (zh) 2021-04-14 2023-01-16 美商基利科學股份有限公司 CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症
BR112023020877A2 (pt) 2021-04-26 2023-12-12 Janssen Pharmaceutica Nv 2-aliltetra-hidrofuranos macrocíclicos como inibidores de mcl-1
EP4334325A1 (en) 2021-05-05 2024-03-13 Revolution Medicines, Inc. Ras inhibitors for the treatment of cancer
US20220389394A1 (en) 2021-05-18 2022-12-08 Gilead Sciences, Inc. METHODS OF USING FLT3L-Fc FUSION PROTEINS
US11957693B2 (en) 2021-06-11 2024-04-16 Gilead Sciences, Inc. Combination MCL-1 inhibitors with anti-cancer agents
KR20240019330A (ko) 2021-06-11 2024-02-14 길리애드 사이언시즈, 인코포레이티드 Mcl-1 저해제와 항체 약물 접합체의 조합
US11976072B2 (en) 2021-06-23 2024-05-07 Gilead Sciences, Inc. Diacylglycerol kinase modulating compounds
PE20242071A1 (es) 2021-06-23 2024-10-18 Gilead Sciences Inc Compuestos moduladores de diacilglicerol quinasa
CA3222439A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
AU2022297367B2 (en) 2021-06-23 2025-04-10 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
AR127308A1 (es) 2021-10-08 2024-01-10 Revolution Medicines Inc Inhibidores ras
JP2024539252A (ja) 2021-10-28 2024-10-28 ギリアード サイエンシーズ, インコーポレイテッド ピリジジン-3(2h)-オン誘導体
PE20241186A1 (es) 2021-10-29 2024-06-03 Gilead Sciences Inc Compuestos de cd73
EP4433484A1 (en) 2021-11-16 2024-09-25 JANSSEN Pharmaceutica NV Macrocyclic 2-amino-but-3-enamides as inhibitors of mcl-1
US20230220106A1 (en) 2021-12-08 2023-07-13 Dragonfly Therapeutics, Inc. Antibodies targeting 5t4 and uses thereof
WO2023107956A1 (en) 2021-12-08 2023-06-15 Dragonfly Therapeutics, Inc. Proteins binding nkg2d, cd16 and 5t4
US12122764B2 (en) 2021-12-22 2024-10-22 Gilead Sciences, Inc. IKAROS zinc finger family degraders and uses thereof
EP4452414A2 (en) 2021-12-22 2024-10-30 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
TW202340168A (zh) 2022-01-28 2023-10-16 美商基利科學股份有限公司 Parp7抑制劑
CA3253296A1 (en) 2022-03-17 2023-09-21 Gilead Sciences Inc Zinc Finger Degradation Agents of the Ikaros Family and Their Uses
CN119031937A (zh) 2022-03-24 2024-11-26 吉利德科学公司 用于治疗表达Trop-2的癌症的联合疗法
EP4504737A1 (en) 2022-04-05 2025-02-12 Amgen Inc. Salt forms and solvates of mci-1 antagonists
TWI876305B (zh) 2022-04-05 2025-03-11 美商基利科學股份有限公司 用於治療結腸直腸癌之組合療法
JP2025511331A (ja) 2022-04-05 2025-04-15 アムジエン・インコーポレーテツド Mci-1アンタゴニストの非晶質及び結晶性形態
CR20240451A (es) 2022-04-21 2024-12-04 Gilead Sciences Inc Compuestos de modulación de kras g12d
KR20250027285A (ko) 2022-05-20 2025-02-25 노파르티스 아게 항신생물 화합물의 항체-약물 접합체 및 그의 사용 방법
JP2025522762A (ja) 2022-07-01 2025-07-17 ギリアード サイエンシーズ, インコーポレイテッド Cd73化合物
US20240091351A1 (en) 2022-09-21 2024-03-21 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY
EP4638436A1 (en) 2022-12-22 2025-10-29 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
WO2024215754A1 (en) 2023-04-11 2024-10-17 Gilead Sciences, Inc. Kras modulating compounds
AU2024259556A1 (en) 2023-04-21 2025-10-23 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
US20250042922A1 (en) 2023-06-30 2025-02-06 Gilead Sciences, Inc. Kras modulating compounds
US20250066328A1 (en) 2023-07-26 2025-02-27 Gilead Sciences, Inc. Parp7 inhibitors
TW202519517A (zh) 2023-07-26 2025-05-16 美商基利科學股份有限公司 Parp7抑制劑
EP4516807A1 (en) 2023-08-28 2025-03-05 Consorcio Centro de Investigación Biomédica en Red Compositions for use in a method of providing improved hematopoietic stem cell engraftment
WO2025054347A1 (en) 2023-09-08 2025-03-13 Gilead Sciences, Inc. Kras g12d modulating compounds
WO2025054530A1 (en) 2023-09-08 2025-03-13 Gilead Sciences, Inc. Pyrimidine-containing polycyclic derivatives as kras g12d modulating compounds
US20250154172A1 (en) 2023-11-03 2025-05-15 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
WO2025111450A1 (en) 2023-11-22 2025-05-30 Les Laboratoires Servier Anti-cd74 antibody-drug conjugates and methods of use thereof
WO2025111431A1 (en) 2023-11-22 2025-05-30 Les Laboratoires Servier Anti-cd7 antibody-drug conjugates and methods of use thereof
WO2025126157A1 (en) 2023-12-15 2025-06-19 Advesya Anti-il-1rap binding domains and antibody-drug conjugates thereof
WO2025137640A1 (en) 2023-12-22 2025-06-26 Gilead Sciences, Inc. Azaspiro wrn inhibitors
US20250376484A1 (en) 2024-05-21 2025-12-11 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
US5858784A (en) 1991-12-17 1999-01-12 The Regents Of The University Of California Expression of cloned genes in the lung by aerosol- and liposome-based delivery
US6042820A (en) 1996-12-20 2000-03-28 Connaught Laboratories Limited Biodegradable copolymer containing α-hydroxy acid and α-amino acid units
US6472375B1 (en) 1998-04-16 2002-10-29 John Wayne Cancer Institute DNA vaccine and methods for its use
MX2007016070A (es) * 2005-07-07 2008-03-10 Abbott Lab Promotores de apoptosis.
NZ579833A (en) 2007-04-16 2012-11-30 Abbott Lab 7-substituted indole mcl-1 inhibitors
CA2693715C (en) * 2007-07-27 2015-10-27 Janssen Pharmaceutica Nv Pyrrolopyrimidines
EP2470527A4 (en) * 2009-08-20 2013-02-27 Merck Sharp & Dohme ETHER-benzotriazole
BR112012009388A2 (pt) * 2009-10-08 2016-06-14 Sanford Burnham Med Res Inst derivados de apogossipolone como agentes anticâncer
EP3138838A1 (en) 2010-01-29 2017-03-08 Dana-Farber Cancer Institute, Inc. Small molecules for the modulation of mcl-1 and methods of modulating cell death, cell division, cell differentiation and methods of treating disorders
WO2013052943A2 (en) 2011-10-06 2013-04-11 The Regents Of The University Of Michgian Small molecule inhibitors of mcl-1 and uses thereof
WO2013149124A1 (en) * 2012-03-29 2013-10-03 The Regents Of The University Of Michigan Small molecule inhibitors of mcl-1 and uses thereof
JO3474B1 (ar) 2014-08-29 2020-07-05 Amgen Inc مشتقات تيتراهيدرونافثالين التي تثبط بروتين mcl-1
US11306107B2 (en) 2016-02-25 2022-04-19 Amgen Inc. Compounds that inhibit MCL-1 protein

Also Published As

Publication number Publication date
US11001598B2 (en) 2021-05-11
ZA201802865B (en) 2022-05-25
JO3474B1 (ar) 2020-07-05
KR102466351B1 (ko) 2022-11-10
EP3424931B1 (en) 2020-02-12
DK3186259T3 (en) 2019-02-25
KR20170043661A (ko) 2017-04-21
ZA201701763B (en) 2018-08-29
UY36285A (es) 2016-04-01
EP3186259B1 (en) 2018-12-19
IL257942B (en) 2020-05-31
IL250843A0 (en) 2017-04-30
WO2016033486A1 (en) 2016-03-03
CO2017002998A2 (es) 2017-07-19
AR101729A1 (es) 2017-01-11
US20210040120A1 (en) 2021-02-11
CY1121195T1 (el) 2020-05-29
PH12017500367A1 (en) 2017-07-10
US20200062780A1 (en) 2020-02-27
ES2706309T3 (es) 2019-03-28
ME03313B (me) 2019-10-20
MA40111A1 (fr) 2018-06-29
US10494381B2 (en) 2019-12-03
EP3424931A2 (en) 2019-01-09
US10836779B2 (en) 2020-11-17
SMT201900048T1 (it) 2019-02-28
US11685747B2 (en) 2023-06-27
US20190016736A1 (en) 2019-01-17
CL2017000469A1 (es) 2017-11-03
NZ729768A (en) 2021-06-25
CA2959615C (en) 2023-01-17
CN107001387A (zh) 2017-08-01
SG11201701525WA (en) 2017-03-30
IL257942A (en) 2018-05-31
PE20170892A1 (es) 2017-07-12
US9562061B2 (en) 2017-02-07
US20170088560A1 (en) 2017-03-30
AP2017009827A0 (en) 2017-03-31
AU2015308735B2 (en) 2019-03-14
IL250843B (en) 2018-03-29
TW201625645A (zh) 2016-07-16
EA201790492A1 (ru) 2017-07-31
EA031223B1 (ru) 2018-12-28
TN2017000067A1 (en) 2018-07-04
BR112017004209A2 (pt) 2018-07-31
SI3186259T1 (sl) 2019-03-29
US12024529B2 (en) 2024-07-02
HRP20190053T1 (hr) 2019-02-22
US20160068545A1 (en) 2016-03-10
BR112017004209B1 (pt) 2022-08-09
RS58276B1 (sr) 2019-03-29
US20190023720A1 (en) 2019-01-24
US10100063B2 (en) 2018-10-16
EP3186259A1 (en) 2017-07-05
PT3186259T (pt) 2019-02-06
EP3424931A3 (en) 2019-02-20
HUE041806T2 (hu) 2019-05-28
PH12017500367B1 (en) 2017-07-10
MX379155B (es) 2025-03-11
US20230271981A1 (en) 2023-08-31
TR201901312T4 (tr) 2019-02-21
AU2015308735A1 (en) 2017-03-23
ES2777478T3 (es) 2020-08-05
LT3186259T (lt) 2019-02-25
TWI676628B (zh) 2019-11-11
MY176235A (en) 2020-07-24
JP2017525730A (ja) 2017-09-07
MA40111B1 (fr) 2018-12-31
CA2959615A1 (en) 2016-03-03
JP6502479B2 (ja) 2019-04-17
MX2017002656A (es) 2017-10-12
CN107001387B (zh) 2019-03-05
PL3186259T3 (pl) 2019-04-30
UA118233C2 (uk) 2018-12-10

Similar Documents

Publication Publication Date Title
CR20170116A (es) Compuestos que inhiben la proteina mcl-1
MX2019011693A (es) Compuestos que inhiben la proteina mcl-1.
CO2017004525A2 (es) Dihidropirrolopiridinas inhibidoras de ror-gamma
CO2018004857A2 (es) Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer
CL2013003160A1 (es) Compuestos derivados de 4h-cromen-4-ona moduladores de la proteina cinasa pi3k; compuestos intermediarios; composicion farmaceutica que los comprende; y utiles en el tratamiento del cancer, agentes antinflamatorios, inmunosupresores, esteroides, analgesicos, leucemia, entre otros.
CU20160109A7 (es) Compuestos de indazol como inhibidores de irak4
CR20150633A (es) Derivados del bipirazol como inhibidores jak
MX2019012847A (es) Compuestos de c5-anilinoquinazolina y su uso en el tratamiento del cancer.
UY35590A (es) Nuevos compuestos para el tratamiento del cáncer
NI201500096A (es) Compuesto químicos
UY35455A (es) Inhibidores tripeptidicos de la epoxicetona proteasa
NI201600176A (es) Compuestos de 1, 3, 4 - tiadiazol y uso de los mismos para el tratamiento del cáncer.
UY36875A (es) Composiciones inhibidoras de bromodominios para el tratamiento de diversas enfermedades
AR101414A1 (es) Derivados de pirrolidinona como inhibidores de metap-2
UY38228A (es) Compuestos de triazolopirimidina y su uso en el tratamiento del cáncer
SV2016005310A (es) Derivados de diheterociclo enlazado a cicloalquilo
CL2017002229A1 (es) Inhibidores de bace1.
DOP2016000325A (es) Compuestos, composición farmacéutica y su uso en el tratamiento de enfermedades neurodegenerativas
ECSP18056196A (es) Derivados de indano
EA201992303A1 (ru) СОЕДИНЕНИЯ, КОТОРЫЕ ИНГИБИРУЮТ БЕЛОК Mcl-1