AR060873A1 - Derivados biciclicos como inhibidores de cetp - Google Patents
Derivados biciclicos como inhibidores de cetpInfo
- Publication number
- AR060873A1 AR060873A1 ARP070101992A ARP070101992A AR060873A1 AR 060873 A1 AR060873 A1 AR 060873A1 AR P070101992 A ARP070101992 A AR P070101992A AR P070101992 A ARP070101992 A AR P070101992A AR 060873 A1 AR060873 A1 AR 060873A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- alkoxy
- cycloalkyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed 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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero rings
Abstract
La presente se refiere además, al uso de los compuestos de la presente para el tratamiento de, demora de progreso para superar, las enfermedades en donde esté involucrada la proteína de transferencia de colesteril-éster. Reivindicacion 1: Un compuesto de la formula (1), en donde el anillo A, que está templado al anillo B, representa un radical aromático carbocíclico insustituido o sustituido; o un radical aromático heterocíclico insustituido o sustituido; en donde Ar representa un radical aromático carbocíclico Insustituido o sustituido; R1 es el elemento -C(=O)-R3, -C(=O)-O-R3, -C(=O)-NR4R5, -S(O)m-R3, -S(O)mN(R4)(R5), siendo m en cada caso el entero 0, 1, o 2 o R1 es Z; Z se selecciona a partir del grupo que consiste en: cicloalquilo monocíclico insustituido o sustituido, o cicloalquenilo monocíclico Insustituido o sustituido, un radical aromático carbocíclico insustituido o sustituido, o un radical heterocíclico insustituido o sustituido; R3 representa Independientemente hidrogeno, alquilo, haloalquilo, cicloalquilo insustituido o sustituido, cicloalquenilo insustituido o sustituido; en la fraccion de cicloalquilo, cicloalquil-alquilo insustituido o sustituido; en la fraccion de cicloalquenilo, cicloalquenil-alquilo insustituido o sustituido; un radical aromático carbocíclico insustituido o sustituido, un radical heterocíclico insustituido o sustituido; o, en la fraccion de arilo, aralquilo insustituido o sustituido; R4 y R5, independientemente uno del otro, representan hidrogeno, alquilo, o cicloalquilo, y el alquilo está sustituido por uno o más sustituyentes seleccionados a partir del grupo que consiste en cicloalquilo insustituido o sustituido, cicloalquenilo insustituido o sustituido, y un radical heterocíclico insustituido o sustituido; R7 y R8, independientemente uno del otro, representan cicloalquilo insustituido o sustituido, cicloalquenilo insustituido o sustituido, o un radical aromático carbocíclico insustituido o sustituido, o un radical heterocíclico insustituido o sustituido; o R4 y R5 son juntos alquileno insustituido o sustituido, o alquileno insustituido o sustituido que está interrumpido por O, NR3, o S; R3' es R3 o -C(=O)- OR3 y m es el entero 0, 1, o 2; X es CR6 o N, e Y es N; o X es N, e Y es CR6; R6 es hidrogeno, halogeno, NO2, CN, OH, alquilo, alcoxi-alquilo, hidroxi-alquilo, halo-alquilo, alcoxilo, alcoxi-alcoxilo, halo-alcoxilo, -C(=O)-R3, -C(=O)-O-R3, - N(R4)(R5), -C(=O)-NR4R5, -S(O)m-R3, -S(O)m-N(R4)(R5), -NR3-S(O)m-N(R4)(R5), siendo m en cada caso el entero 0, 1, o 2; alcanoilo, cicloalquilo insustituido o sustituido, cicloalquenilo insustituido o sustituido; en la fraccion de arilo, aralquilo insustituido o sustituido; y en la fraccion de heterociclilo, heterociclil-alquilo insustituido o sustituido; y en donde el cicloalquilo sustituido, o el cicloalquenilo sustituido, o el alquileno sustituido, está cada uno de los cuales sustituido por uno o más sustituyentes seleccionados a partir del grupo que consiste en alquilo, alcoxilo, -C(=O)-O-R3, -C(=O)-N(alquil)(alquilo), -N(alquil)(alquilo), H2N-C(=O)-, H2N-C(=O)-alquilo--, formilo, formal-alquilo--, cicloalquil-alquilo, un radical aromático carbocíclico, un radical heterocíclico, aralquilo, y heterociclil-alquilo; y en donde un radical aromático carbocíclico, o un radical aromático heterocíclico, o un radical heterocíclico, en la fraccion de arilo es aralquilo insustituido o sustituido, en la fraccion de heterociclilo es heterociclil-alquilo insustituido o sustituido; o los anillos A o Ar, independientemente uno del otro, están insustituidos o sustituidos por uno o más sustituyentes seleccionados a partir del grupo que consiste en halogeno, NO2, CN, OH, alquilo, alcoxi-alquilo, hidroxi-alquilo, halo-alquilo, alcoxilo, alcoxi-alcoxilo, halo-alcoxilo, -C(=O)-R3, -C(=O)-O-R3, -N(R4)(R5), -C(=O)-NR4R5, -S(O)m-R3, -S(O)mN(R4)(R5), -NR3-S(O)m-N(R4)(R5), y alcanoilo, siendo m en cada caso el entero 0, 1, o 2; y cicloalquilo Insustituido o sustituido, cicloalquenilo insustituido o sustituido; en la fraccion de arilo, aralquilo insustituido o sustituido, y en la fraccion de heterociclilo, heterociclil-alquilo insustituido o sustituido; en forma libre o en forma de sal, o una sal del mismo.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0609268.8A GB0609268D0 (en) | 2006-05-10 | 2006-05-10 | Organic compounds |
US86648006P | 2006-11-20 | 2006-11-20 | |
US89614207P | 2007-03-21 | 2007-03-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR060873A1 true AR060873A1 (es) | 2008-07-16 |
Family
ID=38445602
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070101992A AR060873A1 (es) | 2006-05-10 | 2007-05-08 | Derivados biciclicos como inhibidores de cetp |
Country Status (17)
Country | Link |
---|---|
US (2) | US8232403B2 (es) |
EP (1) | EP2024356A1 (es) |
KR (1) | KR101172120B1 (es) |
AR (1) | AR060873A1 (es) |
AU (1) | AU2007247385B2 (es) |
CA (1) | CA2650954C (es) |
CL (1) | CL2007001325A1 (es) |
CR (1) | CR10420A (es) |
EC (1) | ECSP088891A (es) |
GT (1) | GT200800242A (es) |
IL (1) | IL195010A0 (es) |
MA (1) | MA30427B1 (es) |
MX (1) | MX2008014284A (es) |
NO (1) | NO20084912L (es) |
TN (1) | TNSN08444A1 (es) |
TW (1) | TW200813009A (es) |
WO (1) | WO2007128568A1 (es) |
Families Citing this family (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8604055B2 (en) | 2004-12-31 | 2013-12-10 | Dr. Reddy's Laboratories Ltd. | Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors |
EP1848430B1 (en) * | 2004-12-31 | 2017-08-02 | Dr. Reddy's Laboratories Ltd. | Novel benzylamine derivatives as cetp inhibitors |
KR20080086917A (ko) * | 2005-12-29 | 2008-09-26 | 노파르티스 아게 | 콜레스테릴 에스테르 전달 단백질 (cetp) 억제제로서의피리디닐 아민 유도체 |
AU2007247385B2 (en) * | 2006-05-10 | 2011-07-14 | Novartis Ag | Bicyclic derivatives as CETP inhibitors |
CA2650515A1 (en) * | 2006-05-11 | 2007-11-22 | Novartis Ag | Benzylamine derivatives as cetp inhibitors |
US7750019B2 (en) | 2006-08-11 | 2010-07-06 | Kowa Company, Ltd. | Pyrimidine compound having benzyl(pyridylmethyl)amine structure and medicament comprising the same |
US7790737B2 (en) | 2007-03-13 | 2010-09-07 | Kowa Company, Ltd. | Substituted pyrimidine compounds and their utility as CETP inhibitors |
EP2149563B9 (en) | 2007-04-13 | 2015-04-22 | Kowa Company, Ltd. | Novel pyrimidine compound having dibenzylamine structure, and medicine comprising the compound |
EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
WO2010061621A1 (ja) | 2008-11-28 | 2010-06-03 | 興和株式会社 | trans-{4-[(アルキルアミノ)メチル]シクロヘキシル}酢酸エステルの製造方法 |
AU2010289397B2 (en) * | 2009-09-03 | 2016-05-26 | Bioenergenix | Heterocyclic compounds for the inhibition of PASK |
EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120054A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
US8901114B2 (en) | 2011-03-08 | 2014-12-02 | Sanofi | Oxathiazine derivatives substituted with carbocycles or heterocycles, method for producing same, drugs containing said compounds, and use thereof |
RU2609200C2 (ru) | 2011-07-08 | 2017-01-30 | Новартис Аг | Способ лечения атеросклероза у субъектов с высоким уровнем триглицеридов |
MX2014001849A (es) | 2011-08-18 | 2014-10-24 | Reddys Lab Ltd Dr | Compuestos de amina heterociclicos sustituidos como inhibidores de proteina de transferencia de ester colesterilo (cetp). |
CN103958511A (zh) | 2011-09-27 | 2014-07-30 | 雷迪博士实验室有限公司 | 作为胆固醇酯转移蛋白(CETP)抑制剂用于治疗动脉粥样硬化的5-苄基氨基甲基-6-氨基吡唑并[3,4-b]吡啶衍生物 |
AU2013346501B2 (en) * | 2012-11-19 | 2017-07-13 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions of CETP inhibitors |
UY35144A (es) | 2012-11-20 | 2014-06-30 | Novartis Ag | Miméticos lineales sintéticos de apelina para el tratamiento de insuficiencia cardiaca |
WO2014128564A2 (en) * | 2013-02-21 | 2014-08-28 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions of cetp inhibitors |
UY35670A (es) | 2013-07-25 | 2015-02-27 | Novartis Ag | Polipéptidos cíclicos para el tratamiento de insuficiencia cardíaca |
BR112016001376A2 (pt) | 2013-07-25 | 2017-10-24 | Novartis Ag | bioconjugados de polipeptídeos de apelin sintéticos |
MX2017009534A (es) | 2015-01-23 | 2018-04-10 | Novartis Ag | Conjugados de acidos grasos y apelina sintetica con mayor vida media. |
US20230076506A1 (en) * | 2019-12-11 | 2023-03-09 | Ryvu Therapeutics S.A. | Heterocyclic compounds as modulators of stimulator of interferon genes (sting) |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6458852B1 (en) * | 1999-09-23 | 2002-10-01 | G.D. Searle & Co. | Use of substituted N, N-bis-phenyl aminoalcohol compounds for inhibiting cholesteryl ester transfer protein activity |
EP1325006A2 (en) * | 2000-08-07 | 2003-07-09 | Neurogen Corporation | Heterocyclic compounds as ligands of the gaba a? receptor |
DK1533292T3 (da) * | 2002-08-30 | 2007-06-04 | Japan Tobacco Inc | Dibenzylaminforbindelse og medicinsk anvendelse deraf |
CA2504941C (en) | 2002-11-08 | 2012-06-26 | Neurogen Corporation | 3-substituted-6-aryl pyridines |
EA200501376A1 (ru) | 2003-03-28 | 2006-04-28 | Пфайзер Продактс Инк. | Производные 1,2,4-замещённых 1,2,3,4-тетрагидро- и 1,2-дигидрохинолинов и 1,2,3,4-тетрагидрохиноксалина в качестве ингибиторов сетр для лечения атеросклероза и тучности |
US7371759B2 (en) * | 2003-09-25 | 2008-05-13 | Bristol-Myers Squibb Company | HMG-CoA reductase inhibitors and method |
WO2005100298A1 (en) | 2004-04-13 | 2005-10-27 | Merck & Co., Inc. | Cetp inhibitors |
JP2008520645A (ja) | 2004-11-23 | 2008-06-19 | ファイザー・プロダクツ・インク | ジベンジルアミン化合物および誘導体 |
US7668830B2 (en) | 2004-11-29 | 2010-02-23 | Nokia Corporation | Access rights |
EP1848430B1 (en) * | 2004-12-31 | 2017-08-02 | Dr. Reddy's Laboratories Ltd. | Novel benzylamine derivatives as cetp inhibitors |
KR101184807B1 (ko) | 2005-01-06 | 2012-09-20 | 톰슨 라이센싱 | 디지털 광 프로젝션 시스템에서 레인보우 아티팩트를줄이는 방법 및 장치 |
US20100203504A1 (en) | 2005-07-07 | 2010-08-12 | Yoichi Katsumoto | Substance-Information Acquisition Method Using Evanescent Light Beam, Substance-Information Measurement Apparatus, Base-Sequence Determination Method and Base-Sequence Determination Apparatus |
WO2007008899A2 (en) | 2005-07-11 | 2007-01-18 | University Of Florida Research Foundation, Inc. | Variable feathering field splitting for intensity modulated fields of large size |
AU2006330072B2 (en) * | 2005-12-28 | 2012-08-02 | Dr. Reddy's Laboratories Ltd. | Selective benzylamine derivatives and their utility as cholesterol ester-transfer protein inhibitors |
KR20080086917A (ko) * | 2005-12-29 | 2008-09-26 | 노파르티스 아게 | 콜레스테릴 에스테르 전달 단백질 (cetp) 억제제로서의피리디닐 아민 유도체 |
PE20071025A1 (es) * | 2006-01-31 | 2007-10-17 | Mitsubishi Tanabe Pharma Corp | Compuesto amina trisustituido |
AU2007247385B2 (en) * | 2006-05-10 | 2011-07-14 | Novartis Ag | Bicyclic derivatives as CETP inhibitors |
CA2650515A1 (en) * | 2006-05-11 | 2007-11-22 | Novartis Ag | Benzylamine derivatives as cetp inhibitors |
BRPI0718809A2 (pt) * | 2006-11-15 | 2013-12-03 | Novartis Ag | Compostos orgânicos |
EP2086961A1 (en) * | 2006-11-15 | 2009-08-12 | Novartis AG | Heterocyclic derivatives as cetp inhibitors |
-
2007
- 2007-05-08 AU AU2007247385A patent/AU2007247385B2/en not_active Ceased
- 2007-05-08 MX MX2008014284A patent/MX2008014284A/es active IP Right Grant
- 2007-05-08 WO PCT/EP2007/004058 patent/WO2007128568A1/en active Application Filing
- 2007-05-08 CA CA2650954A patent/CA2650954C/en not_active Expired - Fee Related
- 2007-05-08 US US12/300,208 patent/US8232403B2/en not_active Expired - Fee Related
- 2007-05-08 AR ARP070101992A patent/AR060873A1/es unknown
- 2007-05-08 KR KR1020087030049A patent/KR101172120B1/ko not_active IP Right Cessation
- 2007-05-08 EP EP07724982A patent/EP2024356A1/en not_active Withdrawn
- 2007-05-09 CL CL200701325A patent/CL2007001325A1/es unknown
- 2007-05-09 TW TW096116482A patent/TW200813009A/zh unknown
-
2008
- 2008-10-30 IL IL195010A patent/IL195010A0/en unknown
- 2008-10-30 CR CR10420A patent/CR10420A/es not_active Application Discontinuation
- 2008-11-06 TN TNP2008000444A patent/TNSN08444A1/en unknown
- 2008-11-07 GT GT200800242A patent/GT200800242A/es unknown
- 2008-11-10 EC EC2008008891A patent/ECSP088891A/es unknown
- 2008-11-21 NO NO20084912A patent/NO20084912L/no not_active Application Discontinuation
- 2008-11-24 MA MA31408A patent/MA30427B1/fr unknown
-
2012
- 2012-05-17 US US13/473,649 patent/US8410275B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
TW200813009A (en) | 2008-03-16 |
EP2024356A1 (en) | 2009-02-18 |
US8410275B2 (en) | 2013-04-02 |
IL195010A0 (en) | 2009-08-03 |
CL2007001325A1 (es) | 2008-07-18 |
AU2007247385B2 (en) | 2011-07-14 |
GT200800242A (es) | 2009-04-29 |
NO20084912L (no) | 2009-02-03 |
AU2007247385A1 (en) | 2007-11-15 |
MX2008014284A (es) | 2008-11-18 |
KR20090017580A (ko) | 2009-02-18 |
KR101172120B1 (ko) | 2012-08-10 |
CA2650954C (en) | 2014-02-11 |
WO2007128568A1 (en) | 2007-11-15 |
US20090227580A1 (en) | 2009-09-10 |
US20120225874A1 (en) | 2012-09-06 |
MA30427B1 (fr) | 2009-05-04 |
TNSN08444A1 (en) | 2010-04-14 |
CR10420A (es) | 2009-02-02 |
ECSP088891A (es) | 2008-12-30 |
US8232403B2 (en) | 2012-07-31 |
CA2650954A1 (en) | 2007-11-15 |
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