PE20090519A1 - Composicion farmaceutica que contiene n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)-etil]-amino]-metil]-fenil]-2e-2-propenamida - Google Patents
Composicion farmaceutica que contiene n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)-etil]-amino]-metil]-fenil]-2e-2-propenamidaInfo
- Publication number
- PE20090519A1 PE20090519A1 PE2008000314A PE2008000314A PE20090519A1 PE 20090519 A1 PE20090519 A1 PE 20090519A1 PE 2008000314 A PE2008000314 A PE 2008000314A PE 2008000314 A PE2008000314 A PE 2008000314A PE 20090519 A1 PE20090519 A1 PE 20090519A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- propenamide
- indol
- hydroxy
- phenyl
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 abstract 2
- ZDZOTLJHXYCWBA-VCVYQWHSSA-N N-debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol Chemical compound O([C@H]1[C@H]2[C@@](C([C@H](O)C3=C(C)[C@@H](OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)C=4C=CC=CC=4)C[C@]1(O)C3(C)C)=O)(C)[C@@H](O)C[C@H]1OC[C@]12OC(=O)C)C(=O)C1=CC=CC=C1 ZDZOTLJHXYCWBA-VCVYQWHSSA-N 0.000 abstract 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- 206010006187 Breast cancer Diseases 0.000 abstract 1
- 208000026310 Breast neoplasm Diseases 0.000 abstract 1
- 108010033040 Histones Proteins 0.000 abstract 1
- 239000005411 L01XE02 - Gefitinib Substances 0.000 abstract 1
- 239000002136 L01XE07 - Lapatinib Substances 0.000 abstract 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 abstract 1
- 206010035226 Plasma cell myeloma Diseases 0.000 abstract 1
- -1 TRASTUZUMAB Chemical compound 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- MMIMIFULGMZVPO-UHFFFAOYSA-N benzyl 3-bromo-2,6-dinitro-5-phenylmethoxybenzoate Chemical compound [O-][N+](=O)C1=C(C(=O)OCC=2C=CC=CC=2)C([N+](=O)[O-])=C(Br)C=C1OCC1=CC=CC=C1 MMIMIFULGMZVPO-UHFFFAOYSA-N 0.000 abstract 1
- 229960005395 cetuximab Drugs 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229960003668 docetaxel Drugs 0.000 abstract 1
- 229960004679 doxorubicin Drugs 0.000 abstract 1
- 229960002584 gefitinib Drugs 0.000 abstract 1
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical compound C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229960004891 lapatinib Drugs 0.000 abstract 1
- BCFGMOOMADDAQU-UHFFFAOYSA-N lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 abstract 1
- 208000032839 leukemia Diseases 0.000 abstract 1
- 201000005202 lung cancer Diseases 0.000 abstract 1
- 208000020816 lung neoplasm Diseases 0.000 abstract 1
- 201000001441 melanoma Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 201000000050 myeloid neoplasm Diseases 0.000 abstract 1
- FWZRWHZDXBDTFK-ZHACJKMWSA-N panobinostat Chemical compound CC1=NC2=CC=C[CH]C2=C1CCNCC1=CC=C(\C=C\C(=O)NO)C=C1 FWZRWHZDXBDTFK-ZHACJKMWSA-N 0.000 abstract 1
- 229960005184 panobinostat Drugs 0.000 abstract 1
- 229960001586 procarbazine hydrochloride Drugs 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 229940063683 taxotere Drugs 0.000 abstract 1
- 229960000575 trastuzumab Drugs 0.000 abstract 1
Classifications
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- 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
- A61K31/404—Indoles, e.g. pindolol
-
- 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
-
- 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
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- 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
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/529—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim forming part of bridged ring systems
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/548—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame having two or more sulfur atoms in the same ring
-
- 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
- A61K31/69—Boron compounds
-
- 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
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
REFERIDA A UNA COMPOSICION FARMACEUTICA QUE CONTIENE LA COMBINACION DE: A) UN INHIBIDOR DE LA DESACETILASA DE HISTONA (HDA) TAL COMO N-HIDROXI-3-[4-[[[2-(2-METIL-1H-INDOL-3-IL)-ETIL]-AMINO]-METIL]-FENIL]-2E-2-PROPENAMIDA (LBH589); Y B) UNO O MAS AGENTES FARMACEUTICAMENTE ACTIVOS TALES COMO TAXOTERE, CLORHIDRATO DE PROCARBAZINA, LAPATINIB, DOXORRUBICINA, TRASTUZUMAB, GEFITINIB, DOCETAXEL, GEMCITABINA, CETUXIMAB, RITUXIMAB, PEMETREXED, ETOPOSIDA, 5-FLUOROURACILO, MESILATO DE IMATINIB, PACLITAXEL, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCESO DE PREPARACION DE LA COMBINACION. DICHA COMPOSICION ES UTIL EN EL TRATAMIENTO DE ENFERMEDADES PROLIFERATIVAS TALES COMO CANCER DE MAMA, CANCER DE PULMON, MELANOMA, MIELOMA, LEUCEMIA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89000507P | 2007-02-15 | 2007-02-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090519A1 true PE20090519A1 (es) | 2009-05-29 |
Family
ID=39560929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008000314A PE20090519A1 (es) | 2007-02-15 | 2008-02-13 | Composicion farmaceutica que contiene n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)-etil]-amino]-metil]-fenil]-2e-2-propenamida |
Country Status (21)
| Country | Link |
|---|---|
| US (7) | US20100069458A1 (es) |
| EP (3) | EP2120900A2 (es) |
| JP (1) | JP2010519209A (es) |
| KR (1) | KR20090110913A (es) |
| CN (1) | CN101626758A (es) |
| AR (1) | AR065335A1 (es) |
| AU (1) | AU2008216327A1 (es) |
| BR (1) | BRPI0807812A2 (es) |
| CA (1) | CA2677651A1 (es) |
| CL (1) | CL2008000470A1 (es) |
| CO (1) | CO6220928A2 (es) |
| EC (1) | ECSP099576A (es) |
| IL (1) | IL200193A0 (es) |
| MA (1) | MA31205B1 (es) |
| MX (1) | MX2009008584A (es) |
| PE (1) | PE20090519A1 (es) |
| RU (1) | RU2009134223A (es) |
| TN (1) | TN2009000344A1 (es) |
| TW (1) | TW200848022A (es) |
| WO (1) | WO2008100985A2 (es) |
| ZA (1) | ZA200905159B (es) |
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| US20080051380A1 (en) | 2006-08-25 | 2008-02-28 | Auerbach Alan H | Methods and compositions for treating cancer |
| AU2008204928B2 (en) * | 2007-01-10 | 2011-03-31 | Novartis Ag | Formulations of deacetylase inhibitors |
| MX2009009233A (es) | 2007-03-01 | 2010-06-02 | Novartis Ag | Sales de adicion de acido, hidratos y polimorfos de la etil-amida del acido 5-(2,4-dihidroxi-5-isopropil-fenil)-4-(4-morfolin-4-il-m etil-fenil)-isoxazol-3-carboxilico, yformulaciones que comprenden estas formas. |
| CL2008002786A1 (es) * | 2007-09-20 | 2009-05-15 | Novartis Ag | Torta farmceuticamente aceptable, formada por liofilizacion, que comprende: n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il]-etil]-amino]-metil]-fenil]-2e-2-propenamida o una sal, un regulador de ph seleciondo de lactato o acidop lactico, fodfato o acido fosforico o una combinacion y un agente de volumen; proceso de elaboracion. |
| HRP20150947T1 (hr) | 2009-01-08 | 2015-10-09 | Curis, Inc. | Inhibitori fosfoinositid 3-kinaze sa skupinom koja veže cink |
| JO3002B1 (ar) | 2009-08-28 | 2016-09-05 | Irm Llc | مركبات و تركيبات كمثبطات كيناز بروتين |
| US8491927B2 (en) | 2009-12-02 | 2013-07-23 | Nimble Epitech, Llc | Pharmaceutical composition containing a hypomethylating agent and a histone deacetylase inhibitor |
| AU2011239537A1 (en) * | 2010-04-16 | 2012-11-15 | Curis, Inc. | Treatment of cancers having K-ras mutations |
| CN102241628B (zh) * | 2010-05-14 | 2015-11-25 | 中国人民解放军总医院 | (2e)-3-苯基-n-[2,2,2-三氯-1-[[(8-喹啉基氨基)硫代甲基]氨基]乙基]-2-丙烯酰胺及其医药用途 |
| US20120087915A1 (en) | 2010-06-03 | 2012-04-12 | Pharmacyclics, Inc. | Use of inhibitors of bruton's tyrosine kinase (btk) |
| RU2013114246A (ru) * | 2010-09-01 | 2014-10-20 | Новартис Аг | Комбинация hdac ингибиторов с лекарственными средствами против тромбоцитопении |
| LT3111938T (lt) | 2011-04-01 | 2019-06-25 | Curis, Inc. | Fosfoinozitido 3-kinazės inhibitorius su cinko rišamąja dalimi |
| EA201391587A1 (ru) * | 2011-04-28 | 2014-08-29 | Слоан-Кеттеринг Инститьют Фор Кэнсер Рисерч | Комбинированная терапия на основе hsp90 |
| US20140113919A1 (en) * | 2011-06-14 | 2014-04-24 | Novartis Ag | Combination of panobinostat and ruxolitinib in the treatment of cancer such as a myeloproliferative neoplasm |
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| EP3795145A3 (en) | 2011-08-17 | 2021-06-09 | Dennis M. Brown | Compositions and methods to improve the therapeutic benefit of suboptimally administered chemical compounds including substituted hexitols such as dibromodulcitol |
| CN102949722A (zh) * | 2011-08-26 | 2013-03-06 | 中国医学科学院放射医学研究所 | 基于p38抑制剂和细胞生长因子的新颖药物组合物 |
| US11007194B2 (en) | 2011-11-11 | 2021-05-18 | Array Biopharma Inc. | Method of treating a proliferative disease |
| US20150087687A1 (en) | 2012-03-23 | 2015-03-26 | Dennis Brown | Compositions and methods to improve the therapeutic benefit of indirubin and analogs thereof, including meisoindigo |
| US20150182490A1 (en) | 2012-06-26 | 2015-07-02 | Del Mar Pharmaceuticals | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| MX2015001081A (es) | 2012-07-24 | 2015-10-14 | Pharmacyclics Inc | Mutaciones asociadas a resistencia a inhibidores de la tirosina cinasa de bruton (btk). |
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| JP2016512549A (ja) * | 2013-03-14 | 2016-04-28 | ファーマサイクリックス エルエルシー | ブルトン型チロシンキナーゼ阻害剤及びcyp3a4阻害剤の組み合わせ |
| KR20160061911A (ko) | 2013-04-08 | 2016-06-01 | 데니스 엠. 브라운 | 최적하 투여된 화학 화합물의 치료 효과 |
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| US10398672B2 (en) | 2014-04-29 | 2019-09-03 | Whitehead Institute For Biomedical Research | Methods and compositions for targeting cancer stem cells |
| US9956228B2 (en) * | 2014-05-02 | 2018-05-01 | Oncoethix Gmbh | Method of treating acute myeloid leukemia and/or acute lymphoblastic leukemia using thienotriazolodiazepine compounds |
| CN106794184A (zh) * | 2014-06-02 | 2017-05-31 | 黄奇英 | 抗药性癌症的治疗方法 |
| AU2015296968A1 (en) * | 2014-06-10 | 2017-02-02 | University Of South Carolina | Methods and compositions for treatment of HER-positive cancers |
| MA41544A (fr) * | 2015-02-19 | 2017-12-26 | Novartis Ag | Dosages de panobinostat pour le traitement du myélome multiple |
| FI3490560T3 (fi) | 2016-07-29 | 2025-02-27 | Janssen Pharmaceutica Nv | Niraparibi käytettäväksi eturauhassyövän hoitomenetelmässä |
| KR101941045B1 (ko) * | 2017-08-09 | 2019-01-22 | 연세대학교 산학협력단 | 암의 예방 또는 치료용 약학적 조성물 |
| KR101988124B1 (ko) * | 2017-08-31 | 2019-06-11 | 사회복지법인 삼성생명공익재단 | 암 연관 섬유아세포 표적용 약학적 조성물 |
| PL3833670T3 (pl) * | 2018-08-10 | 2024-08-19 | Navire Pharma, Inc. | Pochodne 6-(4-amino-3-metylo-2-oksa-8-azaspiro[4.5]dekan-8-ylo)-3-(2,3-dichlorofenylo)-2-metylopirymidyn-4(3h)-onu oraz powiązane związki jako inhibitory ptpn11 (shp2) do leczenia raka |
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| CN115137716A (zh) * | 2021-04-19 | 2022-10-04 | 海军军医大学第一附属医院第二军医大学第一附属医院上海长海医院 | 紫草素及其药学上可接受的盐类在制备预防或治疗绝经后骨质疏松症药物中的应用 |
| CN118615291A (zh) * | 2024-04-19 | 2024-09-10 | 三峡大学 | 角鲨烯环氧酶新型抑制剂及其在制备治疗抗乳腺癌的药物上的应用 |
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| ATE28864T1 (de) | 1982-07-23 | 1987-08-15 | Ici Plc | Amide-derivate. |
| GB8327256D0 (en) | 1983-10-12 | 1983-11-16 | Ici Plc | Steroid derivatives |
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-
2008
- 2008-02-13 EP EP08729719A patent/EP2120900A2/en not_active Withdrawn
- 2008-02-13 AR ARP080100618A patent/AR065335A1/es unknown
- 2008-02-13 RU RU2009134223/15A patent/RU2009134223A/ru not_active Application Discontinuation
- 2008-02-13 AU AU2008216327A patent/AU2008216327A1/en not_active Abandoned
- 2008-02-13 CA CA002677651A patent/CA2677651A1/en not_active Abandoned
- 2008-02-13 KR KR1020097016980A patent/KR20090110913A/ko not_active Withdrawn
- 2008-02-13 BR BRPI0807812-2A patent/BRPI0807812A2/pt not_active Application Discontinuation
- 2008-02-13 PE PE2008000314A patent/PE20090519A1/es not_active Application Discontinuation
- 2008-02-13 EP EP12150317A patent/EP2491923A3/en not_active Withdrawn
- 2008-02-13 MX MX2009008584A patent/MX2009008584A/es not_active Application Discontinuation
- 2008-02-13 JP JP2009549693A patent/JP2010519209A/ja active Pending
- 2008-02-13 WO PCT/US2008/053798 patent/WO2008100985A2/en not_active Ceased
- 2008-02-13 CN CN200880005098A patent/CN101626758A/zh active Pending
- 2008-02-13 US US12/526,962 patent/US20100069458A1/en not_active Abandoned
- 2008-02-13 EP EP11157791A patent/EP2359818A1/en not_active Withdrawn
- 2008-02-14 TW TW097105218A patent/TW200848022A/zh unknown
- 2008-02-14 CL CL200800470A patent/CL2008000470A1/es unknown
-
2009
- 2009-07-23 ZA ZA200905159A patent/ZA200905159B/xx unknown
- 2009-07-30 IL IL200193A patent/IL200193A0/en unknown
- 2009-08-13 CO CO09085032A patent/CO6220928A2/es not_active Application Discontinuation
- 2009-08-13 EC EC2009009576A patent/ECSP099576A/es unknown
- 2009-08-14 TN TNP2009000344A patent/TN2009000344A1/fr unknown
- 2009-08-31 MA MA32192A patent/MA31205B1/fr unknown
-
2012
- 2012-07-25 US US13/557,731 patent/US20130029927A1/en not_active Abandoned
-
2014
- 2014-12-08 US US14/563,430 patent/US20150094274A1/en not_active Abandoned
-
2016
- 2016-07-28 US US15/222,370 patent/US20170027909A1/en not_active Abandoned
-
2017
- 2017-05-17 US US15/597,718 patent/US20170246147A1/en not_active Abandoned
- 2017-11-14 US US15/812,141 patent/US20180071251A1/en not_active Abandoned
-
2018
- 2018-06-12 US US16/006,137 patent/US20180289670A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20130029927A1 (en) | 2013-01-31 |
| ZA200905159B (en) | 2010-05-26 |
| CA2677651A1 (en) | 2008-08-21 |
| EP2491923A3 (en) | 2012-12-26 |
| US20150094274A1 (en) | 2015-04-02 |
| AU2008216327A1 (en) | 2008-08-21 |
| EP2359818A1 (en) | 2011-08-24 |
| MX2009008584A (es) | 2009-08-18 |
| BRPI0807812A2 (pt) | 2020-06-23 |
| WO2008100985A3 (en) | 2008-10-30 |
| AR065335A1 (es) | 2009-06-03 |
| KR20090110913A (ko) | 2009-10-23 |
| RU2009134223A (ru) | 2011-03-20 |
| CL2008000470A1 (es) | 2008-08-29 |
| TW200848022A (en) | 2008-12-16 |
| IL200193A0 (en) | 2010-04-15 |
| CN101626758A (zh) | 2010-01-13 |
| US20180071251A1 (en) | 2018-03-15 |
| ECSP099576A (es) | 2009-09-29 |
| US20170027909A1 (en) | 2017-02-02 |
| WO2008100985A2 (en) | 2008-08-21 |
| US20180289670A1 (en) | 2018-10-11 |
| EP2491923A2 (en) | 2012-08-29 |
| US20170246147A1 (en) | 2017-08-31 |
| EP2120900A2 (en) | 2009-11-25 |
| CO6220928A2 (es) | 2010-11-19 |
| US20100069458A1 (en) | 2010-03-18 |
| MA31205B1 (fr) | 2010-02-01 |
| TN2009000344A1 (en) | 2010-12-31 |
| JP2010519209A (ja) | 2010-06-03 |
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