SG11201908553SA - Combination of isoindolinone derivatives with sgi-110 - Google Patents
Combination of isoindolinone derivatives with sgi-110Info
- Publication number
- SG11201908553SA SG11201908553SA SG11201908553SA SG11201908553SA SG 11201908553S A SG11201908553S A SG 11201908553SA SG 11201908553S A SG11201908553S A SG 11201908553SA SG 11201908553S A SG11201908553S A SG 11201908553SA
- Authority
- SG
- Singapore
- Prior art keywords
- international
- sgi
- cambridge
- rule
- oqa
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
- A61K31/708—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid having oxo groups directly attached to the purine ring system, e.g. guanosine, guanylic acid
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic 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
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/14—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
- C07H19/207—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids the phosphoric or polyphosphoric acids being esterified by a further hydroxylic compound, e.g. flavine adenine dinucleotide or nicotinamide-adenine dinucleotide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/04—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
International Publication Date (19) World Intellectual Property Organization International Bureau (10) International Publication Number WO 2018/178679 Al °mono n o VII IE (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) 04 October 2018 (04.10.2018) WIPO I PCT (51) International Patent Classification: (72) Inventors: CHESSARI, Gianni; c/o Astex Therapeutics C07D 401/06 (2006.01) C07D 405/12 (2006.01) Limited, 436 Cambridge Science Park, Milton Road, Cam- A61K 31/4035 (2006.01) CO7H 19/207 (2006.01) bridge Cambridgeshire CB4 OQA (GB). LYONS, John A61K 31/708 (2006.01) C07C 403/12 (2006.01) Francis; c/o Astex Therapeutics Limited, 436 Cambridge C07D 403/06 (2006.01) C07D 209/46 (2006.01) Science Park, Milton Road, Cambridge Cambridgeshire C07D 405/06 (2006.01) A61P 35/00 (2006.01) CB4 OQA (GB). C07D 405/10 (2006.01) (74) Agent: ELKINGTON AND FIFE LLP; Thavies Inn (21) International Application Number: PCT/GB2018/050832 (22) International Filing Date: 28 March 2018 (28.03.2018) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 1704966.9 28 March 2017 (28.03.2017) GB (71) Applicants: ASTEX THERAPEUTICS LIMITED [GB/GB]; 436 Cambridge Science Park, Milton Road, Cambridge Cambridgeshire CB4 OQA (GB). CANCER RESEARCH TECHNOLOGY LIMITED [GB/GB]; An- gel Building, 407 St John Street, London Greater London EC1V 4AD (GB). House, 3-4 Holborn Circus, London Greater London EC1N 2HA (GB). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, W O 20 18/ 17 867 9 Al (54) Title: COMBINATION OF ISOINDOLINONE DERIVATIVES WITH SGI-110 (10) (57) : The invention provides a combination comprising: (i) a com- pound of formula (Io) : (Io) or a tautomer or a solvate or a pharmaceutically acceptable salt thereof, wherein the various substituents are as defined in the claims; and (ii) a compound which is SGI-110 (SGI-110) or a tautomer or a solvate or a pharmaceutically acceptable salt thereof. Also provided are phar- maceutical compositions containing the combinations and medical uses of the combinations. (SGI-110) [Continued on next page] WO 2018/178679 Al MIDEDIMOIMEMIEHNOMOIMIIMICHMEMOIMIE TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Declarations under Rule 4.17: as to applicant's entitlement to apply for and be granted a patent (Rule 4.17(H)) as to the applicant's entitlement to claim the priority of the earlier application (Rule 4.17(iii)) of inventorship (Rule 4.17(iv)) Published: — with international search report (Art. 21(3))
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1704966.9A GB201704966D0 (en) | 2017-03-28 | 2017-03-28 | Pharmaceutical compounds |
PCT/GB2018/050832 WO2018178679A1 (en) | 2017-03-28 | 2018-03-28 | Combination of isoindolinone derivatives with sgi-110 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201908553SA true SG11201908553SA (en) | 2019-10-30 |
Family
ID=58687832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201908553S SG11201908553SA (en) | 2017-03-28 | 2018-03-28 | Combination of isoindolinone derivatives with sgi-110 |
Country Status (15)
Country | Link |
---|---|
US (1) | US11236047B2 (en) |
EP (1) | EP3601251A1 (en) |
JP (1) | JP2020518554A (en) |
KR (1) | KR20190133702A (en) |
CN (1) | CN110603251A (en) |
AU (1) | AU2018244798A1 (en) |
BR (1) | BR112019019276A2 (en) |
CA (1) | CA3056308A1 (en) |
GB (1) | GB201704966D0 (en) |
IL (1) | IL269034A (en) |
MX (1) | MX2019011182A (en) |
RU (1) | RU2019131584A (en) |
SG (1) | SG11201908553SA (en) |
TW (1) | TW201838628A (en) |
WO (1) | WO2018178679A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
WO2021248231A1 (en) * | 2020-06-09 | 2021-12-16 | Relive Therapeutics Inc. | Compounds comprising a three ring core as pd-1/pd-l1 blockers |
Family Cites Families (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH374071A (en) | 1959-04-30 | 1963-12-31 | Geigy Ag J R | Process for the preparation of new isoindoline derivatives |
US3466298A (en) | 1967-03-14 | 1969-09-09 | American Home Prod | Process for the preparation of 2-(2-aminoethyl)isoindolines |
US3763178A (en) | 1968-09-05 | 1973-10-02 | American Home Prod | Imidazolinyl phenyl carbonyl acid addition salts and related compounds |
GB1325065A (en) | 1970-02-12 | 1973-08-01 | American Home Prod | Imidazoline derivatives |
AR203991A1 (en) | 1972-03-16 | 1975-11-12 | Rhone Poulenc Sa | PROCEDURE FOR PREPARING DERIVATIVES OF (HYDROXY-2-AMINO-3-PROPOXI) -3-ISOINDOLINONE-1 |
FR2217000B1 (en) | 1973-02-08 | 1976-04-09 | Rhone Poulenc Ind | |
GB1601701A (en) | 1977-07-22 | 1981-11-04 | Delmar Chem | Production of heterocyclic benzamide compounds |
US4200759A (en) | 1978-07-20 | 1980-04-29 | Delmar Chemicals, Limited | Preparation of imidazo[2,1-a]isoindole compounds |
US4244966A (en) | 1979-09-24 | 1981-01-13 | American Home Products Corporation | 1,3-Dihydro-3-(2-hydroxy-, 2-bromo- or 2-chloroethyl)-2H-isoindol-1-one derivatives |
US4312809A (en) | 1980-10-31 | 1982-01-26 | E. R. Squibb & Sons, Inc. | Lactam derivatives of mercaptoacylamino acids |
US4331600A (en) | 1980-10-31 | 1982-05-25 | Usv Pharmaceutical Corporation | Intermediates for the synthesis of phthalimidines |
FR2533563A1 (en) | 1982-09-23 | 1984-03-30 | Adir | NOVEL SULFONYLUREE DERIVATIVES, PROCESSES FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME |
HU212435B (en) | 1990-06-07 | 1996-06-28 | Sandoz Ag | Herbicidal compositions containing substituted phthalides and heterocyclic phthalides as active ingredient and process for preparation of their active ingredients. |
TW448172B (en) | 1996-03-08 | 2001-08-01 | Pharmacia & Upjohn Co Llc | Novel hydroxamic acid derivatives useful for the treatment of diseases related to connective tissue degradation |
DE19807423A1 (en) | 1998-02-21 | 1999-08-26 | Hoechst Marion Roussel De Gmbh | New isoindolone derivatives useful as soluble guanylate cyclase activators for treating cardiovascular disorders, asthma, renal insufficiency, diabetes, cirrhosis or cognitive dysfunction |
ES2251395T3 (en) | 1999-07-26 | 2006-05-01 | Banyu Pharmaceutical Co., Ltd. | BIARILURE DERIVATIVES. |
AU1466001A (en) | 1999-11-05 | 2001-05-14 | Phase-1 Molecular Toxicology | Methods of determining individual hypersensitivity to an agent |
DE10134482A1 (en) | 2001-07-16 | 2003-01-30 | Bayer Ag | Substituted isoindoles and their use |
DE60225719T2 (en) | 2001-12-18 | 2009-04-23 | F. Hoffmann-La Roche Ag | CIS-2,4,5-TRIPHENYL-IMIDAZOLINE AND ITS USE IN THE TREATMENT OF TUMORS |
FR2840302B1 (en) | 2002-06-03 | 2004-07-16 | Aventis Pharma Sa | ISOINDOLONE DERIVATIVES, PREPARATION METHOD AND INTERMEDIARY THEREOF AS MEDICAMENTS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME |
DK1566378T3 (en) | 2002-11-26 | 2012-11-12 | Maruishi Pharma | isoindoline |
JP2004217591A (en) | 2003-01-16 | 2004-08-05 | Dai Ichi Seiyaku Co Ltd | Method for producing cis-selective fluorocyclopropane derivative |
US7320992B2 (en) | 2003-08-25 | 2008-01-22 | Amgen Inc. | Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use |
JP2005255660A (en) | 2004-03-10 | 2005-09-22 | Katsuhiko Tomooka | Polyfunctional group-containing lactams and method for producing the same |
WO2005095341A1 (en) | 2004-03-30 | 2005-10-13 | Kyowa Hakko Kogyo Co., Ltd. | Nitrogen-containing heterocyclic compound |
TW200613272A (en) | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
GB0419481D0 (en) | 2004-09-02 | 2004-10-06 | Cancer Rec Tech Ltd | Isoindolin-1-one derivatives |
CN101160314B (en) | 2005-02-22 | 2012-05-23 | 密执安州立大学董事会 | Small molecule inhibitors of mdm2 and the uses thereof |
US7705021B2 (en) | 2005-05-02 | 2010-04-27 | Fox Chase Cancer Center | Isoindolone compounds, compositions containing the same, and methods of use thereof for the treatment of viral infections related to the etiology of cancer |
WO2007021308A1 (en) | 2005-08-12 | 2007-02-22 | Astrazeneca Ab | Metabotropic glutamate-receptor-potentiating isoindolones |
US7727978B2 (en) | 2006-08-24 | 2010-06-01 | Bristol-Myers Squibb Company | Cyclic 11-beta hydroxysteroid dehydrogenase type I inhibitors |
EP2108642A1 (en) | 2006-10-17 | 2009-10-14 | Kyowa Hakko Kirin Co., Ltd. | Jak inhibitor |
GB0706072D0 (en) | 2007-03-28 | 2007-05-09 | Sterix Ltd | Compound |
NZ581817A (en) | 2007-06-03 | 2012-05-25 | Univ Vanderbilt | Benzamide mglur5 positive allosteric modulators and methods of making and using same |
GB0811643D0 (en) * | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
PL2340021T3 (en) | 2008-09-18 | 2013-04-30 | Hoffmann La Roche | Substituted pyrrolidine-2-carboxamides |
US8354444B2 (en) | 2008-09-18 | 2013-01-15 | Hoffmann-La Roche Inc. | Substituted pyrrolidine-2-carboxamides |
JP2013510860A (en) | 2009-11-12 | 2013-03-28 | ザ、リージェンツ、オブ、ザ、ユニバーシティ、オブ、ミシガン | Spiro-oxindole MDM2 antagonist |
US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
JO2998B1 (en) | 2010-06-04 | 2016-09-05 | Amgen Inc | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
DK2684880T3 (en) | 2011-03-10 | 2018-05-22 | Daiichi Sankyo Co Ltd | DISPIROPYRROLIDINE DERIVATIVES |
US8859586B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Cyclohexyl isoquinolinone compounds |
US8859535B2 (en) | 2011-06-20 | 2014-10-14 | Novartis Ag | Hydroxy substituted isoquinolinone derivatives |
PT2750768T (en) | 2011-08-30 | 2018-12-19 | Astex Pharmaceuticals Inc | Decitabine derivative formulations |
JO3357B1 (en) | 2012-01-26 | 2019-03-13 | Novartis Ag | Imidazopyrrolidinone compounds |
KR101401705B1 (en) | 2012-01-31 | 2014-06-27 | 울산대학교 산학협력단 | Synthetic Method for Isoindoline Derivatives Using Rhodium Catalyst |
US9365512B2 (en) | 2012-02-13 | 2016-06-14 | AbbVie Deutschland GmbH & Co. KG | Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy |
SI2914254T1 (en) | 2012-10-30 | 2020-07-31 | Mei Pharma, Inc. | Combination therapies to treat chemoresistant cancers |
SG10201707135RA (en) * | 2013-03-01 | 2017-10-30 | Astex Pharmaceuticals Inc | Drug combinations |
CA2912547A1 (en) | 2013-07-03 | 2015-01-08 | F. Hoffmann-La Roche Ag | Mrna-based gene expression for personalizing patient cancer therapy with an mdm2 antagonist |
WO2015108175A1 (en) | 2014-01-14 | 2015-07-23 | Daiichi Sankyo Company, Limited | Gene signatures associated with sensitivity to mdm2 inhibitors |
WO2015161032A1 (en) | 2014-04-17 | 2015-10-22 | The Regents Of The University Of Michigan | Mdm2 inhibitors and therapeutic methods using the same |
WO2016056673A1 (en) | 2014-10-09 | 2016-04-14 | Daiichi Sankyo Company, Limited | Algorithms for gene signature-based predictor of sensitivity to mdm2 inhibitors |
BR112018000054A2 (en) | 2015-07-02 | 2018-09-04 | Otsuka Pharmaceutical Co., Ltd. | lyophilized pharmaceutical compositions |
GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
CN114948963A (en) | 2015-10-21 | 2022-08-30 | 大冢制药株式会社 | Protein kinase inhibitor benzolactam compounds |
TWI734715B (en) | 2015-11-19 | 2021-08-01 | 美商卡默森屈有限公司 | Modulators of chemokine receptors |
GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
CA3050645A1 (en) | 2018-07-27 | 2020-01-27 | Ottawa Hospital Research Institute | Treatment of acute myeloid leukemia |
TWI772753B (en) | 2019-02-24 | 2022-08-01 | 大陸商蘇州亞盛藥業有限公司 | Treatment methods and biomarkers for mdm2 inhibitors |
-
2017
- 2017-03-28 GB GBGB1704966.9A patent/GB201704966D0/en not_active Ceased
-
2018
- 2018-03-28 AU AU2018244798A patent/AU2018244798A1/en not_active Abandoned
- 2018-03-28 CN CN201880023272.XA patent/CN110603251A/en active Pending
- 2018-03-28 WO PCT/GB2018/050832 patent/WO2018178679A1/en unknown
- 2018-03-28 TW TW107110712A patent/TW201838628A/en unknown
- 2018-03-28 SG SG11201908553S patent/SG11201908553SA/en unknown
- 2018-03-28 EP EP18715917.3A patent/EP3601251A1/en not_active Withdrawn
- 2018-03-28 KR KR1020197030380A patent/KR20190133702A/en not_active Application Discontinuation
- 2018-03-28 US US16/497,135 patent/US11236047B2/en active Active
- 2018-03-28 CA CA3056308A patent/CA3056308A1/en active Pending
- 2018-03-28 MX MX2019011182A patent/MX2019011182A/en unknown
- 2018-03-28 JP JP2019552469A patent/JP2020518554A/en active Pending
- 2018-03-28 RU RU2019131584A patent/RU2019131584A/en unknown
- 2018-03-28 BR BR112019019276-0A patent/BR112019019276A2/en not_active Application Discontinuation
-
2019
- 2019-09-01 IL IL26903419A patent/IL269034A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CN110603251A (en) | 2019-12-20 |
GB201704966D0 (en) | 2017-05-10 |
RU2019131584A3 (en) | 2021-07-23 |
EP3601251A1 (en) | 2020-02-05 |
CA3056308A1 (en) | 2018-10-04 |
AU2018244798A1 (en) | 2019-09-26 |
JP2020518554A (en) | 2020-06-25 |
TW201838628A (en) | 2018-11-01 |
IL269034A (en) | 2019-10-31 |
US20200207711A1 (en) | 2020-07-02 |
RU2019131584A (en) | 2021-04-29 |
BR112019019276A2 (en) | 2020-05-26 |
US11236047B2 (en) | 2022-02-01 |
KR20190133702A (en) | 2019-12-03 |
MX2019011182A (en) | 2020-01-20 |
WO2018178679A1 (en) | 2018-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SG11201805300QA (en) | Heterocyclic compounds as immunomodulators | |
SG11201809559UA (en) | Substituted pyridines as inhibitors of dnmt1 | |
SG11201906891RA (en) | Methods for the administration of certain vmat2 inhibitors | |
SG11201810600WA (en) | Fxr (nr1h4) modulating compounds | |
SG11201809857TA (en) | Anti-CTLA-4 Antibodies | |
SG11201903487SA (en) | PROCESS FOR THE PREPARATION OF PYRAZOLO[1,5-a]PYRIMIDINES AND SALTS THEREOF | |
SG11201908553SA (en) | Combination of isoindolinone derivatives with sgi-110 | |
SG11201907544VA (en) | Jak inhibitors containing a 4-membered heterocyclic amide | |
SG11201809499UA (en) | Processes for preparing phosphorodiamidate morpholino oligomers | |
SG11201803627XA (en) | N-substituted indole derivatives as pge2 receptor modulators | |
SG11201900633XA (en) | Piperidine cxcr7 receptor modulators | |
SG11201901558VA (en) | Pth compounds with low peak-to-trough ratios | |
SG11201808686VA (en) | Synthesis of indazoles | |
SG11201810965YA (en) | 1h-pyrazolo[4,3-b]pyridines as pde1 inhibitors | |
SG11201408750VA (en) | NOVEL FUSED PYRIDINE DERIVATIVES USEFUL AS c-MET TYROSINE KINASE INHIBITORS | |
SG11201805149XA (en) | Compositions comprising 15-hepe and methods of using the same | |
SG11201909807TA (en) | Methods of manufacturing of niraparib | |
SG11201806480UA (en) | Derivatives of pyrroloimidazole or analogues thereof which are useful for the treatment of inter alia cancer | |
SG11201407345QA (en) | Pyrazole compounds as sglt1 inhibitors | |
SG11201811686UA (en) | 18f-labeled triazole containing psma inhibitors | |
SG11201901048VA (en) | Pharmaceutical compositions and uses directed to lysosomal storage disorders | |
SG11201806424TA (en) | Therapeutic compounds | |
SG11201903795WA (en) | Salts of indazole derivative and crystals thereof | |
SG11201903091VA (en) | Quinoxaline compounds as type iii receptor tyrosine kinase inhibitors | |
SG11202000331YA (en) | Therapeutic modulators of the reverse mode of atp synthase |