SG11201804360XA - Mat2a inhibitors for treating mtap null cancer - Google Patents

Mat2a inhibitors for treating mtap null cancer

Info

Publication number
SG11201804360XA
SG11201804360XA SG11201804360XA SG11201804360XA SG11201804360XA SG 11201804360X A SG11201804360X A SG 11201804360XA SG 11201804360X A SG11201804360X A SG 11201804360XA SG 11201804360X A SG11201804360X A SG 11201804360XA SG 11201804360X A SG11201804360X A SG 11201804360XA
Authority
SG
Singapore
Prior art keywords
international
mat2a
mtap
massachusetts
publication
Prior art date
Application number
SG11201804360XA
Inventor
Katya Marjon
Sung Eun Choe
Original Assignee
Agios Pharmaceuticals 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 Agios Pharmaceuticals Inc filed Critical Agios Pharmaceuticals Inc
Publication of SG11201804360XA publication Critical patent/SG11201804360XA/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/01Hydrocarbons
    • A61K31/015Hydrocarbons carbocyclic
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • C12Q1/6886Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/02Halogenated hydrocarbons
    • A61K31/025Halogenated hydrocarbons carbocyclic
    • A61K31/03Halogenated hydrocarbons carbocyclic aromatic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/136Amines having aromatic rings, e.g. ketamine, nortriptyline having the amino group directly attached to the aromatic ring, e.g. benzeneamine
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

Abstract

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property -' Organization International Bureau ... .... 0Y)1 (43) International Publication Date .... ......) 8 June 2017 (08.06.2017) WI P0 I P CT ID Hit (10) WO 111111111111111111IIIIIIII International II 2017/096165 Publication IIIIIIIIIIIIIIIIIIIIIIIIIIIIII Al Number RIO IIII IIIIIIII (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61K 31/015 (2006.01) A61K 31/505 (2006.01) kind of national protection available): AE, AG, AL, AM, A61K 45/00 (2006.01) A61P 35/00 (2006.01) 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, (21) International Application Number: DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, PCT/US2016/064619 HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, (22) International Filing Date: KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, 2 December 2016 (02.12.2016) 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, (25) Filing Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, (26) Publication Language: English TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 62/262,750 3 December 2015 (03.12.2015) US (84) Designated States (unless otherwise indicated, for every 62/297,572 19 February 2016 (19.02.2016) US kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, (71) Applicant: AGIOS PHARMACEUTICALS, INC. TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, [US/US]; 88 Sidney Street, Cambridge, Massachusetts TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, 02139 (US). DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (72) Inventors: MARJON, Katya; 117 Maskwonicut Street, 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, Sharon, Massachusetts 02067 (US). CHOE, Sung Eun; 12 Kimball Road, Lexington, Massachusetts 02421 (US). GW, KM, ML, MR, NE, SN, TD, TG). Published: (74) Agents: PERDOK, Monique M., Reg. No. 42,989 et al.; 21(3)) P.O. Box 2938, Minneapolis, Minnesota 55402 (US). — with international search report (Art (54) Title: MAT2A INHIBITORS FOR TREATING MTAP NULL CANCER (57) : The present invention provides diagnostic and prognostic methods for predicting the effectiveness of MAT2A inhibitor. AG1-512 treatment of a cancer patient with a Methods are for predicting the sensitivity of tu- .40>o , ... 150 provided 1 ;. mor cell growth to inhibition by a MAT2A inhibitor, 1 comprising assessing whether the tumor cell is absent an MTAP MTAP whereby cells that are MTAP null are sensit- wt gene : ive to inhibition by MAT2A inhibitors. ,....- I tX9 ,,,, ,,,,„...„ \; —.1.—.4.\...$ . ‘ ;., I . 1 1: MIA? nu 1 eo i 0 io 1.0 10 4 10 104 1O .4t \"4 1-1 C\ C It - -- 1-1 C ei io 1-1 ilA FIGUREA . 2). M S O
SG11201804360XA 2015-12-03 2016-12-02 Mat2a inhibitors for treating mtap null cancer SG11201804360XA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562262750P 2015-12-03 2015-12-03
US201662297572P 2016-02-19 2016-02-19
PCT/US2016/064619 WO2017096165A1 (en) 2015-12-03 2016-12-02 Mat2a inhibitors for treating mtap null cancer

Publications (1)

Publication Number Publication Date
SG11201804360XA true SG11201804360XA (en) 2018-06-28

Family

ID=57614465

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201804360XA SG11201804360XA (en) 2015-12-03 2016-12-02 Mat2a inhibitors for treating mtap null cancer

Country Status (12)

Country Link
US (1) US20180371551A1 (en)
EP (1) EP3383375A1 (en)
JP (2) JP6877429B2 (en)
KR (1) KR20180100125A (en)
CN (1) CN108601752A (en)
AU (1) AU2016364855B2 (en)
CA (1) CA3006743A1 (en)
EA (1) EA201891304A1 (en)
IL (1) IL259773A (en)
MX (1) MX2018006781A (en)
SG (1) SG11201804360XA (en)
WO (1) WO2017096165A1 (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3795215A1 (en) 2012-05-30 2021-03-24 Chugai Seiyaku Kabushiki Kaisha Target tissue-specific antigen-binding molecule
MX2016007312A (en) 2013-12-04 2017-01-13 Chugai Pharmaceutical Co Ltd Antigen-binding molecules, the antigen-binding activity of which varies according to the concentration of compounds, and libraries of said molecules.
US11376256B2 (en) 2018-07-19 2022-07-05 Agency For Science, Technology And Research Method of treating a methionine-dependent cancer
MX2021006841A (en) 2018-12-10 2021-07-02 Ideaya Biosciences Inc 2-oxoquinazoline derivatives as methionine adenosyltransferase 2a inhibitors.
WO2020189748A1 (en) * 2019-03-19 2020-09-24 中外製薬株式会社 Antigen-binding molecule containing antigen-binding domain of which binding activity to antigen is changed depending on mta, and library for obtaining said antigen-binding domain
WO2021023609A1 (en) * 2019-08-02 2021-02-11 Glaxosmithkline Intellectual Property Development Limited Combination of a type i protein arginine methyltransferase (type i prmt) inhibitor and a methionine adenosyltransferase ii alpha (mat2a) inhibitor
WO2021158792A1 (en) * 2020-02-04 2021-08-12 Agios Pharmaceuticals, Inc. Methods of treating autoimmune or inflammatory diseases or disorders
TW202227082A (en) * 2020-08-12 2022-07-16 美商施維雅製藥有限公司 Combination therapies for use in treating cancer
BR112023025360A2 (en) * 2021-06-02 2024-02-20 Ideaya Biosciences Inc USE OF A METHIONINE ADENOSYLTRANSFERASE II ALPHA (MAT2A) INHIBITOR AND A PROTEIN ARGININE METHYLTRANSFERASE TYPE II (PRMT TYPE II) INHIBITOR, USE OF A COMPOUND A, COMBINATION PRODUCTS AND MAT2A INHIBITORS
CN113476450B (en) * 2021-08-10 2023-04-28 江南大学 Application of EPZ015666 in preparation of medicine for preventing and treating vascular intimal hyperplasia diseases
CN114028572B (en) * 2021-11-30 2022-11-25 清华大学 Novel use of MAT2A inhibitor for treating asthma

Family Cites Families (84)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4503035B1 (en) 1978-11-24 1996-03-19 Hoffmann La Roche Protein purification process and product
US4530901A (en) 1980-01-08 1985-07-23 Biogen N.V. Recombinant DNA molecules and their use in producing human interferon-like polypeptides
US5231176A (en) 1984-08-27 1993-07-27 Genentech, Inc. Distinct family DNA encoding of human leukocyte interferons
US4683202A (en) 1985-03-28 1987-07-28 Cetus Corporation Process for amplifying nucleic acid sequences
US4868103A (en) 1986-02-19 1989-09-19 Enzo Biochem, Inc. Analyte detection by means of energy transfer
US4843155A (en) 1987-11-19 1989-06-27 Piotr Chomczynski Product and process for isolating RNA
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
US5587458A (en) 1991-10-07 1996-12-24 Aronex Pharmaceuticals, Inc. Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof
EP0552108B1 (en) 1992-01-17 1999-11-10 Lakowicz, Joseph R. Energy transfer phase-modulation fluoro-immunoassay
ATE419355T1 (en) 1992-02-06 2009-01-15 Novartis Vaccines & Diagnostic MARKER FOR CANCER AND BIOSYNTHETIC BINDING PROTEIN FOR IT
US6177401B1 (en) 1992-11-13 2001-01-23 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
US5942393A (en) 1993-12-29 1999-08-24 The Regents Of The University Of California Method for the detection of the presence or absence of methylthioadenosine phosphorylase (MTASE) in a cell sample by detection of the presence or absence of MTASE encoding nucleic acid in the cell sample
IL112248A0 (en) 1994-01-25 1995-03-30 Warner Lambert Co Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
PT821671E (en) 1995-04-20 2001-04-30 Pfizer ARYLSULFONYL HYDROXAMIC ACID DERIVATIVES AS MMP AND TNF INHIBITORS
US5880141A (en) 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
GB9520822D0 (en) 1995-10-11 1995-12-13 Wellcome Found Therapeutically active compounds
ES2206602T3 (en) 1995-10-23 2004-05-16 The Children's Medical Center Corporation INHIBITING THERAPEUTIC COMPOUNDS AND METHODS OF ANGIOGENESIS.
US5854033A (en) 1995-11-21 1998-12-29 Yale University Rolling circle replication reporter systems
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
DE69624081T2 (en) 1995-12-20 2003-06-12 Hoffmann La Roche Matrix metalloprotease inhibitors
US6291455B1 (en) 1996-03-05 2001-09-18 Zeneca Limited 4-anilinoquinazoline derivatives
JPH11512750A (en) 1996-06-27 1999-11-02 ファイザー インク. Derivatives of 2- (2-oxo-ethylidene) -imidazolidin-4-one and their use as farnesyl protein transferase inhibitors
EP0818442A3 (en) 1996-07-12 1998-12-30 Pfizer Inc. Cyclic sulphone derivatives as inhibitors of metalloproteinases and of the production of tumour necrosis factor
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
AU3693697A (en) 1996-07-13 1998-02-09 Glaxo Group Limited Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
ATE227283T1 (en) 1996-07-13 2002-11-15 Glaxo Group Ltd CONDENSED HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS
KR20000067904A (en) 1996-07-18 2000-11-25 디. 제이. 우드, 스피겔 알렌 제이 Phosphinate Based Inhibitors of Matrix Metalloproteases
PL331895A1 (en) 1996-08-23 1999-08-16 Pfizer Arylosulphonylamino derivatives of hydroxamic acid
CA2277100C (en) 1997-01-06 2005-11-22 Pfizer Inc. Cyclic sulfone derivatives
CN1113862C (en) 1997-02-03 2003-07-09 辉瑞产品公司 Arylsulfonylamino hydroxamic acid derivs
JP2000507975A (en) 1997-02-07 2000-06-27 ファイザー・インク N-hydroxy-β-sulfonylpropionamide derivatives and their use as matrix metalloproteinase inhibitors
NZ336836A (en) 1997-02-11 2001-02-23 Pfizer Arylsulfonyl hydroxamic acid derivatives suitable for a broad range of medicinal treatments
JP2002511852A (en) 1997-05-07 2002-04-16 スージェン・インコーポレーテッド 2-indolinone derivatives as modulators of protein kinase activity
AU734009B2 (en) 1997-05-30 2001-05-31 Merck & Co., Inc. Novel angiogenesis inhibitors
ATE263147T1 (en) 1997-08-08 2004-04-15 Pfizer Prod Inc DERIVATIVES OF ARYLOXYARYLSULFONYLAMINO HYDROXYAMINE ACIDS
JP4959049B2 (en) 1997-08-22 2012-06-20 アストラゼネカ・ユーケイ・リミテッド Oxyindolylquinazoline derivatives as angiogenesis inhibitors
EP1017682A4 (en) 1997-09-26 2000-11-08 Merck & Co Inc Novel angiogenesis inhibitors
EA005889B1 (en) 1997-11-11 2005-06-30 Пфайзер Продактс Инк. Thienopyrimidine and thienopyridine derivatives useful as anticancer agents
GB9725782D0 (en) 1997-12-05 1998-02-04 Pfizer Ltd Therapeutic agents
US6506559B1 (en) 1997-12-23 2003-01-14 Carnegie Institute Of Washington Genetic inhibition by double-stranded RNA
JPH11236333A (en) 1997-12-30 1999-08-31 Pfizer Prod Inc Imidazolin-4-one derivative as anticancer agent
GB9800569D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9801690D0 (en) 1998-01-27 1998-03-25 Pfizer Ltd Therapeutic agents
AUPP249298A0 (en) 1998-03-20 1998-04-23 Ag-Gene Australia Limited Synthetic genes and genetic constructs comprising same I
PA8469501A1 (en) 1998-04-10 2000-09-29 Pfizer Prod Inc HYDROXAMIDES OF THE ACID (4-ARILSULFONILAMINO) -TETRAHIDROPIRAN-4-CARBOXILICO
PA8469401A1 (en) 1998-04-10 2000-05-24 Pfizer Prod Inc BICYCLE DERIVATIVES OF HYDROXAMIC ACID
SK17282000A3 (en) 1998-05-15 2002-04-04 Imclone Systems Incorporated Non-radiolabeled protein receptor tyrosine kinase inhibitor
TR200003514T2 (en) 1998-05-29 2002-05-21 Sugen Inc. Pyrrole substituted 2-indolinone protein kinase inhibitors
UA60365C2 (en) 1998-06-04 2003-10-15 Пфайзер Продактс Інк. Isothiazole derivatives, a method for preparing thereof, a pharmaceutical composition and a method for treatment of hyperproliferative disease of mammal
US6576420B1 (en) 1998-06-23 2003-06-10 Regents Of The University Of California Method for early diagnosis of, and determination of prognosis in, cancer
US6566131B1 (en) 2000-10-04 2003-05-20 Isis Pharmaceuticals, Inc. Antisense modulation of Smad6 expression
AU4925199A (en) 1998-08-27 2000-03-21 Pfizer Products Inc. Quinolin-2-one derivatives useful as anticancer agents
CN1314904A (en) 1998-08-27 2001-09-26 辉瑞产品公司 Alkynyl-substituted quinoline-2-one derivatives useful as anticancer agents
US6410323B1 (en) 1999-08-31 2002-06-25 Isis Pharmaceuticals, Inc. Antisense modulation of human Rho family gene expression
DK1004578T3 (en) 1998-11-05 2004-06-28 Pfizer Prod Inc 5-oxo-pyrrolidine-2-carboxylic acid hydroxamide derivatives
EP1006113A1 (en) 1998-12-02 2000-06-07 Pfizer Products Inc. Derivatives of 2-(2-oxo-ethylidene)-imidazolidin-4-one and their use to inhibit abnormal cell growth
US6107091A (en) 1998-12-03 2000-08-22 Isis Pharmaceuticals Inc. Antisense inhibition of G-alpha-16 expression
US5981732A (en) 1998-12-04 1999-11-09 Isis Pharmaceuticals Inc. Antisense modulation of G-alpha-13 expression
US6682736B1 (en) 1998-12-23 2004-01-27 Abgenix, Inc. Human monoclonal antibodies to CTLA-4
UA71945C2 (en) 1999-01-27 2005-01-17 Pfizer Prod Inc Substituted bicyclic derivatives being used as anticancer agents
JP3270834B2 (en) 1999-01-27 2002-04-02 ファイザー・プロダクツ・インク Heteroaromatic bicyclic derivatives useful as anticancer agents
SK11002001A3 (en) 1999-02-11 2002-05-09 Pfizer Products Inc. Heteroaryl-substituted quinolin-2-one derivatives useful as anticancer agents
US6586447B1 (en) 1999-04-01 2003-07-01 Pfizer Inc 3,3-disubstituted-oxindole derivatives useful as anticancer agents
US6046321A (en) 1999-04-09 2000-04-04 Isis Pharmaceuticals Inc. Antisense modulation of G-alpha-i1 expression
GB9927444D0 (en) 1999-11-19 2000-01-19 Cancer Res Campaign Tech Inhibiting gene expression
UA75055C2 (en) 1999-11-30 2006-03-15 Пфайзер Продактс Інк. Benzoimidazole derivatives being used as antiproliferative agent, pharmaceutical composition based thereon
EP1106612B1 (en) 1999-11-30 2004-02-11 Pfizer Products Inc. Quinoline derivatives useful for inhibiting farnesyl protein transferase
HN2000000266A (en) 2000-01-21 2001-05-21 Pfizer Prod Inc ANTI-TARGET COMPOUND AND METHOD OF SEPARATION OF ENANTIOMERS USEFUL TO SYNTHEIZE SUCH COMPOUND.
EP1272630A2 (en) 2000-03-16 2003-01-08 Genetica, Inc. Methods and compositions for rna interference
US6365354B1 (en) 2000-07-31 2002-04-02 Isis Pharmaceuticals, Inc. Antisense modulation of lysophospholipase I expression
US6566135B1 (en) 2000-10-04 2003-05-20 Isis Pharmaceuticals, Inc. Antisense modulation of caspase 6 expression
AU2003303094A1 (en) 2002-12-30 2004-08-13 Exelixis, Inc. MAT2As AS MODIFIERS OF THE p53 PATHWAY AND METHODS OF USE
US9044432B2 (en) 2009-12-22 2015-06-02 Ohio State Innovation Foundation Compositions and methods for cancer detection and treatment
WO2012103457A2 (en) 2011-01-28 2012-08-02 University Of Kentucky Stilbene analogs and methods of treating cancer
WO2014100716A1 (en) 2012-12-21 2014-06-26 Epizyme, Inc. Prmt5 inhibitors and uses thereof
JP2016505000A (en) 2012-12-21 2016-02-18 エピザイム,インコーポレイティド PRMT5 inhibitors and uses thereof
US9221794B2 (en) 2012-12-21 2015-12-29 Epizyme, Inc. PRMT5 inhibitors and uses thereof
WO2014100730A1 (en) 2012-12-21 2014-06-26 Epizyme, Inc. Prmt5 inhibitors containing a dihydro- or tetrahydroisoquinoline and uses thereof
EP2975938A4 (en) 2013-03-15 2017-02-15 Ohio State Innovation Foundation Inhibitors of prmt5 and methods of their use
TWI533873B (en) 2014-02-12 2016-05-21 中央研究院 Pharmaceutical composition for treating liver diseases
CN105039342B (en) 2015-08-06 2017-12-01 李家平 SiRNA and its application of MAT2A gene expressions can be suppressed

Also Published As

Publication number Publication date
IL259773A (en) 2018-07-31
EA201891304A1 (en) 2019-01-31
CA3006743A1 (en) 2017-06-08
JP6877429B2 (en) 2021-05-26
WO2017096165A1 (en) 2017-06-08
KR20180100125A (en) 2018-09-07
CN108601752A (en) 2018-09-28
US20180371551A1 (en) 2018-12-27
AU2016364855A1 (en) 2018-07-05
EP3383375A1 (en) 2018-10-10
MX2018006781A (en) 2018-11-09
JP2018537473A (en) 2018-12-20
AU2016364855B2 (en) 2019-08-29
JP2021098736A (en) 2021-07-01

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