UA118233C2 - Сполуки, які інгібують білок mcl-1 - Google Patents

Сполуки, які інгібують білок mcl-1

Info

Publication number
UA118233C2
UA118233C2 UAA201702910A UAA201702910A UA118233C2 UA 118233 C2 UA118233 C2 UA 118233C2 UA A201702910 A UAA201702910 A UA A201702910A UA A201702910 A UAA201702910 A UA A201702910A UA 118233 C2 UA118233 C2 UA 118233C2
Authority
UA
Ukraine
Prior art keywords
protein
compounds
tetrahydronaphthalene derivatives
mcl
inhibit mcl
Prior art date
Application number
UAA201702910A
Other languages
English (en)
Ukrainian (uk)
Inventor
Шон П. Браун
Юньсяо Лі
Майк Еліас Лісарсабуру
Браян С. Лукас
Нік А. Парас
Джошуа Тейджерлі
Марк Вімолратана
Сянхун Ван
Мін Юй
Мануель Санканела
Люшен Чжу
Буенростро Ана Ґонсалес
Чжихун Лі
Original Assignee
Емджен Інк.
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 Емджен Інк. filed Critical Емджен Інк.
Publication of UA118233C2 publication Critical patent/UA118233C2/uk

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
    • C07D513/10Spiro-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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (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)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
UAA201702910A 2014-08-29 2015-08-28 Сполуки, які інгібують білок mcl-1 UA118233C2 (uk)

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
UA118233C2 true UA118233C2 (uk) 2018-12-10

Family

ID=54238507

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA201702910A UA118233C2 (uk) 2014-08-29 2015-08-28 Сполуки, які інгібують білок 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) PH12017500367A1 (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
WO2017147410A1 (en) * 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein
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
WO2017197036A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
WO2017197046A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. C3-carbon linked glutarimide degronimers for target protein degradation
EP3454856B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
AU2017300738A1 (en) 2016-07-22 2019-02-07 Les Laboratoires Servier Combination of a BCL-2 inhibitor and a MCL-1 inhibitor, uses and pharmaceutical compositions thereof
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
SG10202106345VA (en) * 2017-08-15 2021-07-29 Abbvie Inc Macrocyclic mcl-1 inhibitors and methods of use
US20200239494A1 (en) * 2017-08-15 2020-07-30 Abbvie Inc. Macrocyclic mcl-1 inhibitors and methods of use
EP3668878B1 (en) 2017-08-18 2025-05-21 Amgen Inc. Compounds that inhibit mcl-1 protein
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
EP4029868A1 (en) 2018-05-14 2022-07-20 Gilead Sciences, Inc. Mcl-1 inhibitors
BR112021008796A2 (pt) * 2018-11-09 2021-08-03 Prelude Therapeutics, Incorporated derivados de espiro-sulfonamida como inibidores de proteína de leucemia-1 de células mieloides (mcl-1)
EP3897631A4 (en) 2018-12-20 2022-11-23 C4 Therapeutics, Inc. TARGETED PROTEIN BREAKDOWN
TWI745836B (zh) * 2019-01-18 2021-11-11 大陸商蘇州亞盛藥業有限公司 作為mcl-1抑製劑的大螺環醚
GEAP202515825A (en) 2019-05-20 2025-07-25 Servier Lab 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
MA56505A (fr) * 2019-06-21 2022-04-27 Janssen Pharmaceutica Nv Inhibiteurs macrocycliques de mcl-1
KR102776925B1 (ko) 2019-06-25 2025-03-11 길리애드 사이언시즈, 인코포레이티드 Flt3l-fc 융합 단백질 및 사용 방법
JP7573591B2 (ja) 2019-07-09 2024-10-25 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1阻害剤としての大環状スピロ環誘導体
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
EP4045083B1 (en) 2019-10-18 2024-01-10 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
CA3153636A1 (en) 2019-10-31 2021-05-06 Forty Seven, Inc. Anti-cd47 and anti-cd20 based treatment of blood cancer
CN114901366A (zh) * 2019-11-04 2022-08-12 锐新医药公司 Ras抑制剂
WO2021091982A1 (en) 2019-11-04 2021-05-14 Revolution Medicines, Inc. Ras inhibitors
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
CN120098025A (zh) 2019-11-26 2025-06-06 吉利德科学公司 用于制备mcl1抑制剂的方法和中间体
PH12022551441A1 (en) 2019-12-24 2023-11-20 Carna Biosciences Inc Diacylglycerol kinase modulating compounds
MX2022009947A (es) 2020-02-14 2022-11-07 Jounce Therapeutics Inc Anticuerpos y proteinas de fusion que se unen a ccr8 y usos de estos.
EP4107161A1 (en) * 2020-02-21 2022-12-28 Janssen Pharmaceutica NV Macrocyclic indole derivatives as inhibitors of mcl-1
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
US20230212191A1 (en) * 2020-04-16 2023-07-06 Prelude Therapeutics, Incorporated Spiro-sulfonimidamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
EP4143194A1 (en) 2020-05-01 2023-03-08 Gilead Sciences, Inc. Cd73 inhibiting 2,4-dioxopyrimidine compounds
IL297522A (en) * 2020-05-06 2022-12-01 Amgen Inc Synthesis of vinylic intermediates
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
WO2021225823A1 (en) * 2020-05-06 2021-11-11 Amgen Inc. Synthesis of vinylic protected alcohol intermediates
KR20230006544A (ko) 2020-05-06 2023-01-10 암젠 인크 설폰아미드 중간체의 합성
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
EP4165050A1 (en) 2020-06-10 2023-04-19 JANSSEN Pharmaceutica NV Macrocyclic 2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1
AU2021337589A1 (en) * 2020-09-03 2023-03-30 Amgen Inc. Diol desymmetrization by nucleophilic aromatic substitution
JP2023541916A (ja) 2020-09-15 2023-10-04 レボリューション メディシンズ インコーポレイテッド がんの治療における、ras阻害剤としてのインドール誘導体
CN116457334A (zh) * 2020-11-19 2023-07-18 吉利德科学公司 用于制备大环mcl1抑制剂的方法和中间体
IL303079A (en) 2020-11-24 2023-07-01 Novartis Ag Mcl-1 inhibitor antibody-drug conjugates and methods of use
MX2023006144A (es) * 2020-11-25 2023-06-06 Amgen Inc Alquenilacion enantioselectiva de aldehidos.
EP4255409A1 (en) 2020-12-07 2023-10-11 Cellestia Biotech AG Pharmaceutical combinations for treating cancer
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
ES3026771T3 (en) 2020-12-17 2025-06-12 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
CN118852330A (zh) 2021-05-05 2024-10-29 锐新医药公司 用于治疗癌症的ras抑制剂
TW202313094A (zh) 2021-05-18 2023-04-01 美商基利科學股份有限公司 使用FLT3L—Fc融合蛋白之方法
CA3222269A1 (en) 2021-06-11 2022-12-15 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
KR20240005901A (ko) 2021-06-23 2024-01-12 길리애드 사이언시즈, 인코포레이티드 디아실글리세롤 키나제 조절 화합물
CN117355531A (zh) 2021-06-23 2024-01-05 吉利德科学公司 二酰基甘油激酶调节化合物
US11999733B2 (en) 2021-06-23 2024-06-04 Gilead Sciences, Inc. Diacylglycerol kinase modulating compounds
CN117480155A (zh) 2021-06-23 2024-01-30 吉利德科学公司 二酰基甘油激酶调节化合物
AR127308A1 (es) 2021-10-08 2024-01-10 Revolution Medicines Inc Inhibidores ras
US20230183216A1 (en) 2021-10-28 2023-06-15 Gilead Sciences, Inc. Pyridizin-3(2h)-one derivatives
CA3235986A1 (en) 2021-10-29 2023-05-04 Gilead Science, Inc. Cd73 compounds
EP4433484A1 (en) 2021-11-16 2024-09-25 JANSSEN Pharmaceutica NV Macrocyclic 2-amino-but-3-enamides as inhibitors of mcl-1
US20230203202A1 (en) 2021-12-08 2023-06-29 Dragonfly Therapeutics, Inc. Proteins binding nkg2d, cd16 and 5t4
US20230220106A1 (en) 2021-12-08 2023-07-13 Dragonfly Therapeutics, Inc. Antibodies targeting 5t4 and uses thereof
AU2022417491A1 (en) 2021-12-22 2024-05-23 Gilead Sciences, Inc. Ikaros zinc finger family degraders and uses thereof
JP2024546851A (ja) 2021-12-22 2024-12-26 ギリアード サイエンシーズ, インコーポレイテッド Ikarosジンクフィンガーファミリー分解剤及びその使用
TW202340168A (zh) 2022-01-28 2023-10-16 美商基利科學股份有限公司 Parp7抑制劑
CR20240386A (es) 2022-03-17 2024-10-24 Gilead Sciences Inc Degradadores de dedos de zinc de la familia ikaros y usos de estos
AU2023240346A1 (en) 2022-03-24 2024-09-19 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
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
CA3254998A1 (en) * 2022-04-05 2023-10-12 Amgen Inc. MCI-1 ANTAGONIST SALT AND SOLVATES FORMS
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
AU2023256670A1 (en) 2022-04-21 2024-10-17 Gilead Sciences, Inc. Kras g12d modulating compounds
CR20240553A (es) 2022-05-20 2025-05-02 Servier Lab Conjugados de anticuerpo-fármaco de compuestos antineoplásicos y métodos de uso de los mismos
CA3260083A1 (en) 2022-07-01 2024-01-04 Gilead Sciences, Inc. CD73 COMPOUNDS
US20240091351A1 (en) 2022-09-21 2024-03-21 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPa DISRUPTION ANTICANCER COMBINATION THERAPY
AU2023409398A1 (en) 2022-12-22 2025-06-05 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
AU2024252725A1 (en) 2023-04-11 2025-11-06 Gilead Sciences, Inc. Kras modulating compounds
AU2024259556A1 (en) 2023-04-21 2025-10-23 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
WO2025006720A1 (en) 2023-06-30 2025-01-02 Gilead Sciences, Inc. Kras modulating compounds
TW202519517A (zh) 2023-07-26 2025-05-16 美商基利科學股份有限公司 Parp7抑制劑
WO2025024663A1 (en) 2023-07-26 2025-01-30 Gilead Sciences, Inc. Parp7 inhibitors
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
WO2025054530A1 (en) 2023-09-08 2025-03-13 Gilead Sciences, Inc. Pyrimidine-containing polycyclic derivatives as kras g12d modulating compounds
US20250101042A1 (en) 2023-09-08 2025-03-27 Gilead Sciences, Inc. Kras g12d modulating compounds
US20250154172A1 (en) 2023-11-03 2025-05-15 Gilead Sciences, Inc. Prmt5 inhibitors and uses thereof
TW202540185A (zh) 2023-11-22 2025-10-16 法商施維雅藥廠 抗cd74抗體藥物結合物及其使用方法
TW202540186A (zh) 2023-11-22 2025-10-16 瑞士商諾華公司 抗cd7抗體藥物結合物及其使用方法
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
WO2025245003A1 (en) 2024-05-21 2025-11-27 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
ES2400371T3 (es) * 2005-07-07 2013-04-09 Abbott Laboratories Promotores de la apoptosis
NZ579833A (en) 2007-04-16 2012-11-30 Abbott Lab 7-substituted indole mcl-1 inhibitors
ES2562218T3 (es) * 2007-07-27 2016-03-03 Janssen Pharmaceutica, N.V. Pirrolopirimidinas útiles para el tratamiento de enfermedades proliferativas
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
EP2528893B1 (en) * 2010-01-29 2018-10-10 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
EP2831067B1 (en) * 2012-03-29 2017-11-01 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
WO2017147410A1 (en) 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein

Also Published As

Publication number Publication date
MX379155B (es) 2025-03-11
JP6502479B2 (ja) 2019-04-17
MA40111B1 (fr) 2018-12-31
PE20170892A1 (es) 2017-07-12
CR20170116A (es) 2017-04-28
EP3424931A3 (en) 2019-02-20
JO3474B1 (ar) 2020-07-05
US20230271981A1 (en) 2023-08-31
KR102466351B1 (ko) 2022-11-10
US9562061B2 (en) 2017-02-07
US12024529B2 (en) 2024-07-02
BR112017004209B1 (pt) 2022-08-09
US20170088560A1 (en) 2017-03-30
SG11201701525WA (en) 2017-03-30
ES2706309T3 (es) 2019-03-28
LT3186259T (lt) 2019-02-25
TWI676628B (zh) 2019-11-11
EP3424931A2 (en) 2019-01-09
PH12017500367B1 (en) 2017-07-10
US10836779B2 (en) 2020-11-17
EA031223B1 (ru) 2018-12-28
US20210040120A1 (en) 2021-02-11
IL257942A (en) 2018-05-31
BR112017004209A2 (pt) 2018-07-31
ES2777478T3 (es) 2020-08-05
ZA201701763B (en) 2018-08-29
NZ729768A (en) 2021-06-25
MY176235A (en) 2020-07-24
AR101729A1 (es) 2017-01-11
US11001598B2 (en) 2021-05-11
CY1121195T1 (el) 2020-05-29
US11685747B2 (en) 2023-06-27
CL2017000469A1 (es) 2017-11-03
MA40111A1 (fr) 2018-06-29
HUE041806T2 (hu) 2019-05-28
IL250843A0 (en) 2017-04-30
EP3424931B1 (en) 2020-02-12
HRP20190053T1 (hr) 2019-02-22
IL257942B (en) 2020-05-31
WO2016033486A1 (en) 2016-03-03
ME03313B (me) 2019-10-20
US20160068545A1 (en) 2016-03-10
CN107001387A (zh) 2017-08-01
DK3186259T3 (en) 2019-02-25
SI3186259T1 (sl) 2019-03-29
PH12017500367A1 (en) 2017-07-10
US20200062780A1 (en) 2020-02-27
EP3186259A1 (en) 2017-07-05
CO2017002998A2 (es) 2017-07-19
SMT201900048T1 (it) 2019-02-28
KR20170043661A (ko) 2017-04-21
US10494381B2 (en) 2019-12-03
TR201901312T4 (tr) 2019-02-21
AU2015308735A1 (en) 2017-03-23
EA201790492A1 (ru) 2017-07-31
PL3186259T3 (pl) 2019-04-30
IL250843B (en) 2018-03-29
CA2959615A1 (en) 2016-03-03
AU2015308735B2 (en) 2019-03-14
EP3186259B1 (en) 2018-12-19
US20190016736A1 (en) 2019-01-17
AP2017009827A0 (en) 2017-03-31
UY36285A (es) 2016-04-01
RS58276B1 (sr) 2019-03-29
CN107001387B (zh) 2019-03-05
ZA201802865B (en) 2022-05-25
TW201625645A (zh) 2016-07-16
PT3186259T (pt) 2019-02-06
CA2959615C (en) 2023-01-17
MX2017002656A (es) 2017-10-12
US20190023720A1 (en) 2019-01-24
US10100063B2 (en) 2018-10-16
TN2017000067A1 (en) 2018-07-04
JP2017525730A (ja) 2017-09-07

Similar Documents

Publication Publication Date Title
PH12017500367B1 (en) Compounds that inhibit mcl-1 protein
PH12019502245A1 (en) Compounds that inhibit mcl-1 protein
MX389597B (es) Inhibidores de cdk2/4/6 de piridopirimidinona.
TN2016000529A1 (en) Substituted dihydroisoquinolinone compounds
MD20170016A2 (ro) Compuşi aminopirimidinici ca inhibitori JAK
MX376639B (es) Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer.
MX375323B (es) Inhibidores de cinasa de interacción con proteína cinasa activada por mitógeno (mnk) y métodos relacionados con los mismos.
PH12015502159A1 (en) Chemical entities
PH12018501285A1 (en) Alkyl dihydroquinoline sulfonamide compounds
PH12016501997A1 (en) Cycloalkyl-linked diheterocycle derivatives
MX2017002544A (es) Derivados de isoquinolinona utiles en el tratamiento contra el cancer.
MX2017002627A (es) Derivados de polieteres macrociclicos de n-aril-2-amino-4-aril-pir imidina como inhibidores de ftl3 y jak.
MX2015015290A (es) Compuestos furanona como inhibidores de quinasa.
EA201992303A1 (ru) СОЕДИНЕНИЯ, КОТОРЫЕ ИНГИБИРУЮТ БЕЛОК Mcl-1
MX2017002747A (es) Derivados de polieteres macrociclicos de n-aril-triciclopirimidin- 2-amino como inhibidores de ftl3 y jak.