MX2019004845A - Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico. - Google Patents
Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico.Info
- Publication number
- MX2019004845A MX2019004845A MX2019004845A MX2019004845A MX2019004845A MX 2019004845 A MX2019004845 A MX 2019004845A MX 2019004845 A MX2019004845 A MX 2019004845A MX 2019004845 A MX2019004845 A MX 2019004845A MX 2019004845 A MX2019004845 A MX 2019004845A
- Authority
- MX
- Mexico
- Prior art keywords
- proteasome inhibitors
- methods
- cylodextrin
- peptide proteasome
- complexation
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- 229940079156 Proteasome inhibitor Drugs 0.000 title abstract 4
- 239000003207 proteasome inhibitor Substances 0.000 title abstract 4
- 238000010668 complexation reaction Methods 0.000 title abstract 3
- 108090000765 processed proteins & peptides Proteins 0.000 title abstract 3
- 229920000858 Cyclodextrin Polymers 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229940097362 cyclodextrins Drugs 0.000 abstract 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 abstract 3
- 229960002438 carfilzomib Drugs 0.000 abstract 1
- 108010021331 carfilzomib Proteins 0.000 abstract 1
- BLMPQMFVWMYDKT-NZTKNTHTSA-N carfilzomib Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC(C)C)C(=O)[C@]1(C)OC1)NC(=O)CN1CCOCC1)CC1=CC=CC=C1 BLMPQMFVWMYDKT-NZTKNTHTSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- 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
- A61K38/07—Tetrapeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/55—Protease inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61K47/40—Cyclodextrins; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
- A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
- Y10S530/827—Proteins from mammals or birds
- Y10S530/829—Blood
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Nanotechnology (AREA)
- Immunology (AREA)
- Gastroenterology & Hepatology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Crystallography & Structural Chemistry (AREA)
- Molecular Biology (AREA)
- Medical Informatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Dermatology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
La presente divulgación proporciona procedimientos para formular composiciones que comprenden uno o más inhibidores del proteasoma peptídico y una ciclodextrina, en particular una ciclodextrina sustituida. Dichos procedimientos incrementan considerablemente la solubilidad y la estabilidad de estos inhibidores del proteasoma y facilitan tanto su fabricación como su administración.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261644122P | 2012-05-08 | 2012-05-08 | |
| US201361777475P | 2013-03-12 | 2013-03-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2019004845A true MX2019004845A (es) | 2021-03-31 |
Family
ID=48326170
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2014013552A MX364393B (es) | 2012-05-08 | 2013-05-08 | Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico. |
| MX2019004845A MX2019004845A (es) | 2012-05-08 | 2014-11-07 | Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico. |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2014013552A MX364393B (es) | 2012-05-08 | 2013-05-08 | Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US10159746B2 (es) |
| EP (2) | EP2662094B1 (es) |
| JP (1) | JP6410264B2 (es) |
| KR (5) | KR20220088949A (es) |
| CN (2) | CN107693772A (es) |
| AU (2) | AU2013259573B2 (es) |
| CA (1) | CA2873044C (es) |
| CL (1) | CL2014003055A1 (es) |
| DK (1) | DK2662094T3 (es) |
| EA (1) | EA033614B1 (es) |
| ES (1) | ES2981576T3 (es) |
| FI (1) | FI2662094T3 (es) |
| HK (2) | HK1207827A1 (es) |
| HR (1) | HRP20240724T1 (es) |
| HU (1) | HUE066956T2 (es) |
| IL (1) | IL235553B (es) |
| LT (1) | LT2662094T (es) |
| MX (2) | MX364393B (es) |
| PL (1) | PL2662094T3 (es) |
| PT (1) | PT2662094T (es) |
| RS (1) | RS65647B1 (es) |
| SG (2) | SG10201609318UA (es) |
| SI (1) | SI2662094T1 (es) |
| SM (1) | SMT202400264T1 (es) |
| WO (1) | WO2013169897A1 (es) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUE066956T2 (hu) | 2012-05-08 | 2024-09-28 | Onyx Therapeutics Inc | Peptid proteaszóma inhibitorok formulázására alkalmas ciklodextrin komplexálási eljárások |
| EP3021862B1 (en) | 2013-07-19 | 2017-08-30 | Onyx Therapeutics, Inc. | Peptide epoxyketone proteasome inhibitors in combination with pim kinase inhibitors for treatment of cancers |
| CN104945470B (zh) * | 2014-03-30 | 2020-08-11 | 浙江大学 | 杂环构建的三肽环氧酮类化合物及制备和应用 |
| DK3478670T3 (da) | 2016-06-29 | 2023-05-15 | Kezar Life Sciences | Krystallinske salte af peptidepoxyketon-immunproteasomhæmmer |
| JP7065044B2 (ja) | 2016-06-29 | 2022-05-11 | ケザール ライフ サイエンシズ | ペプチドエポキシケトン免疫プロテアソーム阻害剤、およびその前駆体の調製プロセス |
| WO2018038687A1 (en) | 2016-08-22 | 2018-03-01 | Mustafa Nevzat Ilaç Sanayii A.Ş. | Pharmaceutical formulations comprising a bortezomib-cyclodextrin complex |
| IL266964B2 (en) * | 2016-11-29 | 2024-06-01 | Oculis SA | Preparation of solid cyclodextrin complexes for ophthalmic active pharmaceutical ingredient delivery |
| JP7204670B2 (ja) * | 2017-05-03 | 2023-01-16 | サイデックス・ファーマシューティカルズ・インコーポレイテッド | シクロデキストリン及びブスルファンを含有する組成物 |
| TW202114697A (zh) | 2019-07-01 | 2021-04-16 | 瑞士商歐庫利斯公司 | 用於穩定包括藥物的水性組成物之pH值的方法 |
| CN110882221B (zh) * | 2019-11-29 | 2021-06-29 | 健进制药有限公司 | 一种注射用卡非佐米冻干制剂的生产工艺 |
| EP4134068A4 (en) * | 2020-04-09 | 2024-02-07 | Bika Biotechnology (Guangzhou) Co., Ltd. | Bendamustine composition and use thereof |
| WO2022159319A2 (en) * | 2021-01-19 | 2022-07-28 | Mountain Valley Md Inc | A porous aluminum nanoparticulate structure |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| US4870060A (en) | 1985-03-15 | 1989-09-26 | Janssen Pharmaceutica | Derivatives of γ-cylodextrin |
| US5340736A (en) | 1991-05-13 | 1994-08-23 | The President & Fellows Of Harvard College | ATP-dependent protease and use of inhibitors for same in the treatment of cachexia and muscle wasting |
| US5858784A (en) | 1991-12-17 | 1999-01-12 | The Regents Of The University Of California | Expression of cloned genes in the lung by aerosol- and liposome-based delivery |
| DE19505263A1 (de) * | 1995-02-16 | 1996-08-22 | Consortium Elektrochem Ind | Verfahren zur Reinigung von wasserlöslichen Cyclodextrinderivaten |
| AU4499697A (en) | 1996-09-13 | 1998-04-02 | New York University | Method for treating parasitic diseases with proteasome inhibitors |
| US6042820A (en) | 1996-12-20 | 2000-03-28 | Connaught Laboratories Limited | Biodegradable copolymer containing α-hydroxy acid and α-amino acid units |
| GB9713149D0 (en) | 1997-06-21 | 1997-08-27 | Pfizer Ltd | Pharmaceutical formulations |
| ATE323110T1 (de) | 1997-07-01 | 2006-04-15 | Pfizer Prod Inc | Verfahren zur herstellung von einem cyclodextrin |
| US6472375B1 (en) | 1998-04-16 | 2002-10-29 | John Wayne Cancer Institute | DNA vaccine and methods for its use |
| US6831099B1 (en) | 1999-05-12 | 2004-12-14 | Yale University | Enzyme inhibition |
| JP2004510826A (ja) | 2000-10-12 | 2004-04-08 | ヴィローミクス ゲゼルシャフト ミット ベシュレンクテル ハフツング | ウイルス感染の治療剤 |
| JP2003063965A (ja) | 2001-06-13 | 2003-03-05 | Otsuka Pharmaceut Factory Inc | 注射用シロスタゾール水性製剤 |
| JP2007517069A (ja) * | 2003-12-31 | 2007-06-28 | サイデックス・インコーポレイテッド | スルホアルキルエーテルγ−シクロデキストリンおよびコルチコステロイドを含む吸入製剤 |
| CA2562411A1 (en) * | 2004-04-15 | 2005-11-10 | Proteolix, Inc. | Compounds for enzyme inhibition |
| US7232818B2 (en) | 2004-04-15 | 2007-06-19 | Proteolix, Inc. | Compounds for enzyme inhibition |
| ES2408216T3 (es) * | 2004-12-07 | 2013-06-19 | Onyx Therapeutics, Inc. | Composición para la inhibición del proteasoma |
| CA2626122A1 (en) * | 2005-11-15 | 2007-05-24 | Baxter International, Inc. | Compositions comprising lipoxygenase inhibitors and cyclodextrin |
| MX2010003732A (es) * | 2007-10-04 | 2010-08-09 | Onyx Therapeutics Inc | Inhibidores de peptido cetona epoxi de proteasa cristalina y la sintesis de ceto-epoxidos de aminoacido. |
| US7635773B2 (en) | 2008-04-28 | 2009-12-22 | Cydex Pharmaceuticals, Inc. | Sulfoalkyl ether cyclodextrin compositions |
| PE20120059A1 (es) * | 2008-10-21 | 2012-02-27 | Onyx Therapeutics Inc | Combinaciones farmaceuticas con epoxicetonas peptidicas |
| CN102946879B (zh) | 2010-04-19 | 2015-04-22 | 尼基制药公司 | 一种蛋白酶体抑制剂和镓络合物在制备治疗增殖性疾病的药物中的应用 |
| KR20160033795A (ko) | 2012-02-28 | 2016-03-28 | 사이덱스 파마슈티칼스, 인크. | 알킬화된 시클로덱스트린 조성물 및 이의 제조 및 사용 방법 |
| BR112012028726B1 (pt) | 2012-05-08 | 2021-07-13 | Onyx Therapeutics, Inc. | Método para preparar uma composição farmacêutica com baixo teor de cloreto |
| HUE066956T2 (hu) | 2012-05-08 | 2024-09-28 | Onyx Therapeutics Inc | Peptid proteaszóma inhibitorok formulázására alkalmas ciklodextrin komplexálási eljárások |
| KR102112119B1 (ko) | 2012-10-22 | 2020-05-19 | 사이덱스 파마슈티칼스, 인크. | 알킬화된 시클로덱스트린 조성물 및 이의 제조 및 사용 방법 |
-
2013
- 2013-05-08 HU HUE13167148A patent/HUE066956T2/hu unknown
- 2013-05-08 KR KR1020227020311A patent/KR20220088949A/ko not_active Ceased
- 2013-05-08 EP EP13167148.9A patent/EP2662094B1/en active Active
- 2013-05-08 EA EA201491994A patent/EA033614B1/ru not_active IP Right Cessation
- 2013-05-08 RS RS20240704A patent/RS65647B1/sr unknown
- 2013-05-08 SG SG10201609318UA patent/SG10201609318UA/en unknown
- 2013-05-08 CN CN201710866757.2A patent/CN107693772A/zh active Pending
- 2013-05-08 CN CN201380036466.0A patent/CN104411334A/zh active Pending
- 2013-05-08 PT PT131671489T patent/PT2662094T/pt unknown
- 2013-05-08 HR HRP20240724TT patent/HRP20240724T1/hr unknown
- 2013-05-08 KR KR1020197035904A patent/KR20190137963A/ko not_active Ceased
- 2013-05-08 KR KR1020147034238A patent/KR102054329B1/ko active Active
- 2013-05-08 ES ES13167148T patent/ES2981576T3/es active Active
- 2013-05-08 JP JP2015511660A patent/JP6410264B2/ja active Active
- 2013-05-08 WO PCT/US2013/040127 patent/WO2013169897A1/en not_active Ceased
- 2013-05-08 SG SG11201407337QA patent/SG11201407337QA/en unknown
- 2013-05-08 FI FIEP13167148.9T patent/FI2662094T3/fi active
- 2013-05-08 CA CA2873044A patent/CA2873044C/en active Active
- 2013-05-08 KR KR1020207032107A patent/KR20200130748A/ko not_active Ceased
- 2013-05-08 PL PL13167148.9T patent/PL2662094T3/pl unknown
- 2013-05-08 HK HK15108517.0A patent/HK1207827A1/xx unknown
- 2013-05-08 AU AU2013259573A patent/AU2013259573B2/en active Active
- 2013-05-08 EP EP24170493.1A patent/EP4410374A3/en active Pending
- 2013-05-08 MX MX2014013552A patent/MX364393B/es active IP Right Grant
- 2013-05-08 DK DK13167148.9T patent/DK2662094T3/da active
- 2013-05-08 SM SM20240264T patent/SMT202400264T1/it unknown
- 2013-05-08 LT LTEP13167148.9T patent/LT2662094T/lt unknown
- 2013-05-08 SI SI201332084T patent/SI2662094T1/sl unknown
- 2013-05-08 KR KR1020247025639A patent/KR20240119191A/ko active Pending
- 2013-05-08 US US14/399,582 patent/US10159746B2/en active Active
-
2014
- 2014-11-06 IL IL235553A patent/IL235553B/en active IP Right Grant
- 2014-11-07 MX MX2019004845A patent/MX2019004845A/es unknown
- 2014-11-10 CL CL2014003055A patent/CL2014003055A1/es unknown
-
2018
- 2018-01-19 AU AU2018200444A patent/AU2018200444B2/en active Active
- 2018-08-14 HK HK18110388.9A patent/HK1250927A1/zh unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2019004845A (es) | Procedimientos para la formacion de complejos de ciclodextrina para formular inhibidores del proteasoma peptidico. | |
| MY196510A (en) | Cylodextrin Complexation Methods for Formulating Peptide Proteasome Inhibitors | |
| CY1124690T1 (el) | Σκευασματα ενδοφλεβιου διαλυματος ποσακοναζολης σταθεροποιημενα με υποκατεστημενη βητα-κυκλοδεξτρινη | |
| UA105229C2 (uk) | Фармацевтичний склад | |
| AU2012214029A8 (en) | Rorgammat inhibitors | |
| UA109868C2 (ru) | Соединения n-алкилтриазола как антагонисты лизофосфатидной кислоты (lpar) | |
| EA201390908A1 (ru) | Производные бицикло[3.2.1]октиламида и их применение | |
| EA201490724A1 (ru) | Замещенные соединения тетрагидроизохинолина в качестве ингибиторов фактора xia | |
| MX2013007336A (es) | Compuestos de bi-heteroarilo como inhibidores de vps34. | |
| TN2015000324A1 (en) | Substituted bisphenyl butanoic phosphonic acid derivatives as nep (neutral endopeptidase) inhibitors | |
| WO2013009527A3 (en) | Factor ixa inhibitors | |
| EP4582424A3 (en) | 1,2-naphthoquinone derivative and method for preparing same | |
| UA109281C2 (uk) | Фармацевтична композиція, яка містить похідне аміду або його фармацевтично прийнятну сіль | |
| MY165902A (en) | Substituted pyridine derivatives as fabi inhibitors | |
| NZ708821A (en) | Lfa-1 inhibitor formulations | |
| MX343540B (es) | Compuesto de tiazol y metodo de preparacion y uso del mismo. | |
| EA201291014A1 (ru) | Трициклическое индазольное соединение, способ его получения и содержащая его фармацевтическая композиция | |
| MX2015007309A (es) | Derivado de hidantoina. | |
| TN2014000060A1 (en) | Benzothiazolone compound | |
| MX2010003112A (es) | Formas de dosificacion solubles que contienen derivados de cephem adecuados para administracion parenteral. | |
| MX2010009513A (es) | Composicion farmaceutica. | |
| SMT201300112B (it) | Sale citrato di 9E-15-(2-pirrolidin-1-il-etossi)-7,12,25-triossa-19,21,24-triaza-tetracicloÄ18.3.1.1(2,5).1(14,18)Üesacos a-1(24),2,4,9,14,16,18(26),20,22-nonaene | |
| MX2015010434A (es) | Derivados de acido bisfenil-butanoico sustituido como inhibidores de la endopeptidasa neutra (nep), con una mayor eficacia in vivo. | |
| MX2015017864A (es) | Metodo de preparacion de derivados de acido pirrolidina-2-carboxil ico. | |
| SA114350532B1 (ar) | عملية لتخليق 3، 4-داي ميثوكسي باي سيكلو [4، 2، 0] أوكتا-1، 3، 5- ترايين-7-كربو نيتريل، والاستخدام في تخليق إيفابرادين وأملاح إضافة منه باستخدام حمض مقبول صيدلانياً |