AU2017383102B2 - Inhibitors of SOX18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases - Google Patents
Inhibitors of SOX18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases Download PDFInfo
- Publication number
- AU2017383102B2 AU2017383102B2 AU2017383102A AU2017383102A AU2017383102B2 AU 2017383102 B2 AU2017383102 B2 AU 2017383102B2 AU 2017383102 A AU2017383102 A AU 2017383102A AU 2017383102 A AU2017383102 A AU 2017383102A AU 2017383102 B2 AU2017383102 B2 AU 2017383102B2
- Authority
- AU
- Australia
- Prior art keywords
- sox18
- cancer
- alkyl
- protein
- group
- Prior art date
- Legal status (The legal status 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 status listed.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/66—Polycyclic acids with unsaturation outside the aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
- C07C65/105—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups polycyclic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/075—Ethers or acetals
- A61K31/085—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon
- A61K31/09—Ethers or acetals having an ether linkage to aromatic ring nuclear carbon having two or more such linkages
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/65—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/44—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C235/46—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/15—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with all hydroxy groups on non-condensed rings, e.g. phenylphenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/215—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring having unsaturation outside the six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/33—Polycyclic acids
- C07C63/331—Polycyclic acids with all carboxyl groups bound to non-condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
- C07C65/24—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups polycyclic
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Ophthalmology & Optometry (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyrane Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2016905362A AU2016905362A0 (en) | 2016-12-23 | Compounds and use thereof in methods of treatment | |
| AU2016905362 | 2016-12-23 | ||
| PCT/AU2017/051439 WO2018112545A1 (en) | 2016-12-23 | 2017-12-21 | Inhibitors of sox18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2017383102A1 AU2017383102A1 (en) | 2019-08-01 |
| AU2017383102B2 true AU2017383102B2 (en) | 2023-05-11 |
Family
ID=62624141
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2017383102A Active AU2017383102B2 (en) | 2016-12-23 | 2017-12-21 | Inhibitors of SOX18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US11434190B2 (enExample) |
| EP (1) | EP3558293A4 (enExample) |
| JP (2) | JP7579057B2 (enExample) |
| KR (1) | KR102572077B1 (enExample) |
| CN (1) | CN110536685A (enExample) |
| AU (1) | AU2017383102B2 (enExample) |
| CA (1) | CA3048040A1 (enExample) |
| WO (1) | WO2018112545A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018112545A1 (en) | 2016-12-23 | 2018-06-28 | The University Of Queensland | Inhibitors of sox18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases |
| CN110143941B (zh) * | 2019-06-04 | 2021-05-25 | 北京四环制药有限公司 | 一种巴罗萨韦玛波酯中间体的合成方法 |
| AU2020464868A1 (en) * | 2020-08-26 | 2023-04-13 | Gertrude Biomedical Pty Ltd | Antiviral SOX inhibitors |
| CN118834915A (zh) * | 2024-08-15 | 2024-10-25 | 扬州大学 | 一种在羊毛乳头细胞中稳定过表达的sox18慢病毒重组标签载体的构建及应用 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001074753A1 (de) * | 2000-03-30 | 2001-10-11 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Synthetische derivate von lunularsäure, arzneimittel enthaltend diese verbindungen, verfahren zur herstellung der lunularsäurederivate sowie deren verwendung |
| US20080234369A1 (en) * | 2007-02-01 | 2008-09-25 | The Jiang Cell Biomedical Research Co., Ltd. | 3,4,5,4' - tetramethoxyl- alpha,beta-diphenylethane -3' -0- sodiumsulphate and its use |
| CN102050759A (zh) * | 2010-12-09 | 2011-05-11 | 江苏天晟药业有限公司 | 白藜芦醇酰胺类衍生物及其制备方法 |
| WO2011119866A1 (en) * | 2010-03-24 | 2011-09-29 | Ohio University | Compositions and methods for glucose transport inhibition |
| WO2014134202A1 (en) * | 2013-02-26 | 2014-09-04 | Triact Therapeutics, Inc. | Cancer therapy |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0314725A1 (en) | 1987-05-19 | 1989-05-10 | FISONS plc | 2-(3,4-dihydroxyphenyl)ethylamines, their preparation and use as pharmaceutical |
| US6326507B1 (en) | 1998-06-19 | 2001-12-04 | Trustees Of Dartmouth College | Therapeutic compounds and methods of use |
| KR20060031809A (ko) * | 2003-06-09 | 2006-04-13 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | 암 치료 및 진단용 조성물 및 방법 |
| ITRM20030355A1 (it) * | 2003-07-18 | 2005-01-19 | Sigma Tau Ind Farmaceuti | Composti ad attivita' citotossica derivati della combretastatina. |
| UA94724C2 (en) * | 2005-12-08 | 2011-06-10 | Новартис Аг | Thiadiazolidinone derivatives as antidiabetic agents |
| CN101062043B (zh) * | 2006-04-30 | 2011-06-08 | 浙江天皇药业有限公司 | 3,4,5,4'-四甲氧基二苯乙烷-3’-o-磷酸二钠在抗肿瘤及其转移药物的应用 |
| EA201100615A1 (ru) * | 2008-10-13 | 2011-12-30 | Новартис Аг | Производные салициловой кислоты в качестве ингибиторов активности фарнезилпирофосфатсинтазы |
| EP3060237B1 (en) * | 2013-10-25 | 2021-08-18 | Wayne State University | Modified reprogramming protein for use in treating a cancer |
| WO2018112545A1 (en) * | 2016-12-23 | 2018-06-28 | The University Of Queensland | Inhibitors of sox18 protein activity for treating angiogenesis- and/or lymphangiogenesis-related diseases |
| AU2020464868A1 (en) * | 2020-08-26 | 2023-04-13 | Gertrude Biomedical Pty Ltd | Antiviral SOX inhibitors |
-
2017
- 2017-12-21 WO PCT/AU2017/051439 patent/WO2018112545A1/en not_active Ceased
- 2017-12-21 US US16/472,882 patent/US11434190B2/en active Active
- 2017-12-21 CA CA3048040A patent/CA3048040A1/en active Pending
- 2017-12-21 CN CN201780086511.1A patent/CN110536685A/zh active Pending
- 2017-12-21 EP EP17884538.4A patent/EP3558293A4/en active Pending
- 2017-12-21 KR KR1020197021576A patent/KR102572077B1/ko active Active
- 2017-12-21 AU AU2017383102A patent/AU2017383102B2/en active Active
- 2017-12-21 JP JP2019534124A patent/JP7579057B2/ja active Active
-
2022
- 2022-05-10 US US17/741,065 patent/US20230100768A1/en active Pending
- 2022-10-07 JP JP2022162614A patent/JP2023011613A/ja active Pending
-
2023
- 2023-06-27 US US18/342,312 patent/US12410116B2/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001074753A1 (de) * | 2000-03-30 | 2001-10-11 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Synthetische derivate von lunularsäure, arzneimittel enthaltend diese verbindungen, verfahren zur herstellung der lunularsäurederivate sowie deren verwendung |
| US20080234369A1 (en) * | 2007-02-01 | 2008-09-25 | The Jiang Cell Biomedical Research Co., Ltd. | 3,4,5,4' - tetramethoxyl- alpha,beta-diphenylethane -3' -0- sodiumsulphate and its use |
| WO2011119866A1 (en) * | 2010-03-24 | 2011-09-29 | Ohio University | Compositions and methods for glucose transport inhibition |
| CN102050759A (zh) * | 2010-12-09 | 2011-05-11 | 江苏天晟药业有限公司 | 白藜芦醇酰胺类衍生物及其制备方法 |
| WO2014134202A1 (en) * | 2013-02-26 | 2014-09-04 | Triact Therapeutics, Inc. | Cancer therapy |
Non-Patent Citations (7)
| Title |
|---|
| CHARLOTTE GéNY, ET AL.: "Anacardic Acids from Knema hookeriana as Modulators of Bcl-xL/Bak and Mcl-1/Bid Interactions", JOURNAL OF NATURAL PRODUCTS, AMERICAN CHEMICAL SOCIETY, US, vol. 79, no. 4, 22 April 2016 (2016-04-22), US , pages 838 - 844, XP055496052, ISSN: 0163-3864, DOI: 10.1021/acs.jnatprod.5b00915 * |
| ELISABETH BERTL, KARIN KLIMO, ELKE HEISS, FRANK KLENKE, PETER PESCHKE, HANS BECKER, THEOPHIL EICHER, CHRISTIAN HERHAUS, GOVIND KAP: "Identification of novel inhibitors of angiogenesis using a human in vitro anti-angiogenic assay", INTERNATIONAL JOURNAL OF CANCER RESEARCH AND PREVENTION, NOVA SCIENCE PUBLISHERS INC., US, vol. 1, no. 1, 1 January 2004 (2004-01-01), US , pages 47 - 61, XP009515336, ISSN: 1554-1134 * |
| FRANKIE LAM; TRACEY D. BRADSHAW; HUI MAO; SCOTT ROBERTS; YUANJIANG PAN; SHUDONG WANG: "ZJU-6, a novel derivative of Erianin, shows potent anti-tubulin polymerisation and anti-angiogenic activities", INVESTIGATIONAL NEW DRUGS, KLUWER ACADEMIC PUBLISHERS, BO, vol. 30, no. 5, 14 October 2011 (2011-10-14), Bo , pages 1899 - 1907, XP035107062, ISSN: 1573-0646, DOI: 10.1007/s10637-011-9755-9 * |
| GONG Y-Q ET AL: "In vivo and in vitro evaluation of erianin, a novel anti-angiogenic agent", EUROPEAN JOURNAL OF CANCER, ELSEVIER, AMSTERDAM, NL, vol. 40, no. 10, 1 July 2004 (2004-07-01), pages 1554 - 1565, * |
| QIAN LIU, ET AL.: "Synthesis of 3′-methoxy-E-diethylstilbestrol and its analogs as tumor angiogenesis inhibitors", STEROIDS, ELSEVIER SCIENCE PUBLISHERS, NEW YORK, NY., US, vol. 77, no. 5, 1 April 2012 (2012-04-01), US , pages 419 - 423, XP055496045, ISSN: 0039-128X, DOI: 10.1016/j.steroids.2011.12.024 * |
| SAYAKA NOMURA, KAORI ENDO-UMEDA, MAKOTO MAKISHIMA, YUICHI HASHIMOTO, MINORU ISHIKAWA: "Development of Tetrachlorophthalimides as Liver X Receptor β (LXRβ)-Selective Agonists", CHEMMEDCHEM COMMUNICATIONS, WILEY-VCH, DE, vol. 11, no. 20, 19 October 2016 (2016-10-19), DE , pages 2347 - 2360, XP055679637, ISSN: 1860-7179, DOI: 10.1002/cmdc.201600305 * |
| YU-CHEN CAI ET AL: INVESTIGATIONAL NEW DRUGS; THE JOURNAL OF NEW ANTICANCER AGENTS, KLUWER ACADEMIC PUBLISHERS, BO, vol. 29, no. 2, 11 December 2009 (2009-12-11), pages 300 -311 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP3558293A1 (en) | 2019-10-30 |
| CN110536685A (zh) | 2019-12-03 |
| JP7579057B2 (ja) | 2024-11-07 |
| KR20190105018A (ko) | 2019-09-11 |
| JP2023011613A (ja) | 2023-01-24 |
| JP2020506884A (ja) | 2020-03-05 |
| EP3558293A4 (en) | 2020-10-28 |
| AU2017383102A1 (en) | 2019-08-01 |
| US12410116B2 (en) | 2025-09-09 |
| KR102572077B1 (ko) | 2023-08-29 |
| US11434190B2 (en) | 2022-09-06 |
| WO2018112545A1 (en) | 2018-06-28 |
| US20230100768A1 (en) | 2023-03-30 |
| US20190337880A1 (en) | 2019-11-07 |
| US20240002326A1 (en) | 2024-01-04 |
| CA3048040A1 (en) | 2018-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12410116B2 (en) | Compounds and use thereof in methods of treatment | |
| Holden et al. | Small molecule dysregulation of TEAD lipidation induces a dominant-negative inhibition of hippo pathway signaling | |
| JP6592071B2 (ja) | ヒトezh2の阻害剤およびその使用方法 | |
| Bouché et al. | Benzoisoquinolinediones as potent and selective inhibitors of BRPF2 and TAF1/TAF1L bromodomains | |
| Wang et al. | Development of potent type I protein arginine methyltransferase (PRMT) inhibitors of leukemia cell proliferation | |
| JP6027110B2 (ja) | ノッチ経路シグナリングインヒビター化合物 | |
| Freeman-Cook et al. | Design of selective, ATP-competitive inhibitors of Akt | |
| JP2019508496A (ja) | 癌の治療法のためのtaf1阻害剤 | |
| Chang et al. | Discovery of novel PROTAC degraders of p300/CBP as potential therapeutics for hepatocellular carcinoma | |
| Gradl et al. | Discovery of the SMYD3 inhibitor BAY-6035 using thermal shift assay (TSA)-based high-throughput screening | |
| CA2925127A1 (en) | Pyrido[2,3-d]pyrimidin-4-one compounds as tankyrase inhibitors | |
| Shukla et al. | Mutations of RNA splicing factors in hematological malignancies | |
| Miller et al. | Diarylthiophenes as inhibitors of the pore-forming protein perforin | |
| Sun et al. | Structure-guided discovery of potent and selective CLK2 inhibitors for the treatment of knee osteoarthritis | |
| Lim et al. | Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists | |
| Liao et al. | Discovery of Thiadiazoleamide Derivatives as Potent, Selective, and Orally Available Antagonists Disrupting Androgen Receptor Homodimer | |
| Liu et al. | ZJK-807: A Selective PROTAC Degrader of KRASG12D Overcoming Resistance in Pancreatic Cancer | |
| Manka et al. | Inhibitors of the menin-mixed lineage leukemia (MLL) interaction | |
| Poluri et al. | Small-Molecule Inhibitors of Protein–Protein Interactions as Therapeutics | |
| TWI361068B (en) | Compounds for the inhibition of histone deacetylase | |
| WO2021039824A1 (ja) | Rnaメチルトランスフェラーゼ阻害剤、そのスクリーニング方法、抗がん剤有効性判定マーカー、及びftsj1阻害剤の有効性予測のためのキット |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) |