AR065854A1 - Derivados de 1-oxa-3,9-diaza-espiro[5.5]undecan-2-ona,medicamentos que los contienen y usos como agentes anti vih,entre otros. - Google Patents
Derivados de 1-oxa-3,9-diaza-espiro[5.5]undecan-2-ona,medicamentos que los contienen y usos como agentes anti vih,entre otros.Info
- Publication number
- AR065854A1 AR065854A1 ARP080101248A ARP080101248A AR065854A1 AR 065854 A1 AR065854 A1 AR 065854A1 AR P080101248 A ARP080101248 A AR P080101248A AR P080101248 A ARP080101248 A AR P080101248A AR 065854 A1 AR065854 A1 AR 065854A1
- Authority
- AR
- Argentina
- Prior art keywords
- dimethyl
- compound
- formula
- alkoxy
- alkyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-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
- A61K31/535—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
- A61K31/537—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 spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pain & Pain Management (AREA)
- AIDS & HIV (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Un compuesto de la formula I, en la que R es (a) cicloalquilo C3-6 dicho cicloalquilo está opcionalmente sustituido de una a tres veces por restos elegidos con independencia entre el grupo formado por hidroxi, alquilo C1-3, oxo, halogeno, alcoxi C1-6-oximino y alcoxi C1-6-alcoxi C1-6; (b) (cicloalquilo C3-6)-alquilo C1-3, dicho cicloalquilo está opcionalmente sustituido de una a tres veces por restos elegidos con independencia entre el grupo formado por hidroxi, alquilo C1-3, oxo, halogeno,alcoxi C1-6-oximino y alcoxi C1-6-alcoxi C1-6, con la condicion de que dicho (cicloalquilo C3-6)-alquilo C1-3 no sea 4,4-difluorociclohexil-metilo ni 1-hidroxil-ciclohexil-metilo, (c) el compuesto de la formula (2) en el que R6 es hidrogeno ohalogeno; (d) el compuesto de la formula (3); (e) el compuesto de la formula (4), (f) el compuesto de la formula (5) en el que m es 0 o 2; (g) heteroarilo, heteroaril-alquilo C1-3, fenilalquilo C1-3 en el que dicho heteroarilo es piridina,pirimidina, pirazina o piridazina y dicho heteroarilo o dicho fenilo está sustituido con independencia por 1-3 sustituyentes elegidos con independencia entre alquilo C1-3, halogeno, alcoxi C1-6, ciano y nitro (h) haloalquilo C1-3 (i) el compuesto dela formula (6), (j) el compuesto de la formula (7), (k) el compuesto de la formula (8), (m) el compuesto de la formula (9); R2 es alquilo C1-6; R3 es hidrogeno o alquilo C1-3; R4 es elegido entre el grupo formado por (a) - (i) y (j): (a) 4,6-dimetil-pirimidin-5-ilo; (b) 4,6-dimetil-2-trifluormetil-pirimidin-5-ilo; (c) 2,4-dimetil-piridin-3-ilo; (d) 2,4-dimetil-1-oxi-piridin-3-il Ç 6-ciano-2,4-dimetil-piridin-3-ilo; (f) 2,4-dimetil-6-oxo-6H-piran-3-il (g) 2,4-dimetil-6-oxo-1,6-dihidro-piridin-3-ilo; (h) 1,2,4-trimetil-6-oxo-1,6-dihidro-piridin-3-ilo; (i) 3,5-dimetil-1-oxi-1H-pirazol-4-ilo; y (j) 5-ciano-2,4-dimetil-1H-pirrol-3-ilo; o (k) 3-metil-5-trifluormetil-isoxasol-4-il (l) 3,5-dimetil-1-hidroxi-pirazol-4-ilo; R6 es acilo C1-6,(alcoxi C1-6)-carbonilo, (alquilo C1-6)-SO, haloalquilo C1-6, cicloalquilo C3-6, oxetanilo, tetrahidrofuranilo o tetrahidropiranilo y n es 0-3; p es el numero 1 o 3; o una sal de adicion de ácido farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92069407P | 2007-03-29 | 2007-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR065854A1 true AR065854A1 (es) | 2009-07-08 |
Family
ID=39535486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080101248A AR065854A1 (es) | 2007-03-29 | 2008-03-27 | Derivados de 1-oxa-3,9-diaza-espiro[5.5]undecan-2-ona,medicamentos que los contienen y usos como agentes anti vih,entre otros. |
Country Status (15)
Country | Link |
---|---|
US (1) | US7625891B2 (es) |
EP (1) | EP2142555A1 (es) |
JP (1) | JP2010522707A (es) |
KR (1) | KR20090127298A (es) |
CN (1) | CN101646679A (es) |
AR (1) | AR065854A1 (es) |
AU (1) | AU2008233930A1 (es) |
BR (1) | BRPI0809646A2 (es) |
CA (1) | CA2682639A1 (es) |
CL (1) | CL2008000863A1 (es) |
IL (1) | IL200661A0 (es) |
MX (1) | MX2009010503A (es) |
PE (1) | PE20090183A1 (es) |
TW (1) | TW200902020A (es) |
WO (1) | WO2008119663A1 (es) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5451611B2 (ja) * | 2007-07-26 | 2014-03-26 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1のサイクリックインヒビター |
WO2009037168A1 (en) * | 2007-09-19 | 2009-03-26 | F. Hoffmann-La Roche Ag | Heterocyclic antiviral compounds |
AR069207A1 (es) * | 2007-11-07 | 2010-01-06 | Vitae Pharmaceuticals Inc | Ureas ciclicas como inhibidores de la 11 beta - hidroxi-esteroide deshidrogenasa 1 |
WO2009075835A1 (en) | 2007-12-11 | 2009-06-18 | Vitae Pharmaceutical, Inc | CYCLIC UREA INHIBITORS OF 11β-HYDROXYSTEROID DEHYDROGENASE 1 |
TW200934490A (en) * | 2008-01-07 | 2009-08-16 | Vitae Pharmaceuticals Inc | Lactam inhibitors of 11 &abgr;-hydroxysteroid dehydrogenase 1 |
JP5490020B2 (ja) | 2008-01-24 | 2014-05-14 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1の環状カルバゼート及びセミカルバジドインヒビター |
JP5734666B2 (ja) * | 2008-02-11 | 2015-06-17 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1の1,3−オキサアゼパン−2−オン及び1,3−ジアゼパン−2−オン阻害剤 |
US8598160B2 (en) * | 2008-02-15 | 2013-12-03 | Vitae Pharmaceuticals, Inc. | Cycloalkyl lactame derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
US20110105504A1 (en) * | 2008-03-18 | 2011-05-05 | Vitae Pharmaceuticals ,Inc. | Inhibitors Of 11beta-Hydroxysteroid Dehydrogenase Type 1 |
JP5538365B2 (ja) | 2008-05-01 | 2014-07-02 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1の環状阻害剤 |
US8242111B2 (en) * | 2008-05-01 | 2012-08-14 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
CL2009001058A1 (es) | 2008-05-01 | 2010-09-10 | Vitae Pharmaceuticals Inc | Compuestos derivados de oxazinas sustituidas, inhibidores de la 11b-hidroxiesteroide deshidrogenasa de tipo-1; composicion farmaceutica; y uso del compuesto para inhibir la actividad de 11b-hsd1, como en el tratamiento de la diabetes, dislipidemia, hipertension, obesidad, cancer, glaucoma, entre otras. |
PL2300461T3 (pl) * | 2008-05-01 | 2013-09-30 | Vitae Pharmaceuticals Inc | Cykliczne inhibitory dehydrogenazy 11beta-hydroksysteroidów 1 |
CA2729998A1 (en) | 2008-07-25 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
EP2687525B1 (en) | 2008-07-25 | 2015-09-23 | Boehringer Ingelheim International GmbH | Cyclic inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
KR20110063438A (ko) | 2008-09-25 | 2011-06-10 | 베링거 인겔하임 인터내셔날 게엠베하 | Cb2 수용체를 선택적으로 조절하는 설포닐 화합물 |
WO2010089303A1 (en) | 2009-02-04 | 2010-08-12 | Boehringer Ingelheim International Gmbh | CYCLIC INHIBITORS OF 11 β-HYDROXYSTEROID DEHYDROGENASE 1 |
UA109255C2 (ru) | 2009-04-30 | 2015-08-10 | Берінгер Інгельхайм Інтернешнл Гмбх | Циклические ингибиторы 11бета-гидроксистероиддегидрогеназы 1 |
US8927539B2 (en) | 2009-06-11 | 2015-01-06 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1 based on the 1,3-oxazinan-2-one structure |
EP2448928B1 (en) | 2009-07-01 | 2014-08-13 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
WO2011109324A1 (en) | 2010-03-05 | 2011-09-09 | Boehringer Ingelheim International Gmbh | Tetrazole compounds which selectively modulate the cb2 receptor |
JP5860042B2 (ja) | 2010-06-16 | 2016-02-16 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 置換5、6及び7員複素環、そのような化合物を含有する医薬及びそれらの使用 |
WO2011161128A1 (en) | 2010-06-25 | 2011-12-29 | Boehringer Ingelheim International Gmbh | Azaspirohexanones as inhibitors of 11-beta-hsd1 for the treatment of metabolic disorders |
WO2012059416A1 (en) | 2010-11-02 | 2012-05-10 | Boehringer Ingelheim International Gmbh | Pharmaceutical combinations for the treatment of metabolic disorders |
KR20200003933A (ko) | 2011-03-04 | 2020-01-10 | 뉴젠 세러퓨틱스 인코포레이티드 | 알킨 치환된 퀴나졸린 화합물 및 그것의 사용 방법 |
WO2012155339A1 (zh) | 2011-05-17 | 2012-11-22 | 江苏康缘药业股份有限公司 | 4-苯胺-6-丁烯酰胺-7-烷醚喹唑啉衍生物及其制备方法和用途 |
WO2018048261A1 (ko) * | 2016-09-08 | 2018-03-15 | 가천대학교 산학협력단 | 신규 스피로퀴논 유도체 화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 신경계 질환의 예방 또는 치료용 약학적 조성물 |
CN109012748B (zh) * | 2018-07-27 | 2021-03-16 | 安徽师范大学 | 吡啶取代吡咯基稀土金属催化剂及其制备方法和应用 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL127065C (es) * | 1964-04-22 | |||
HU204529B (en) | 1989-08-10 | 1992-01-28 | Richter Gedeon Vegyeszet | Process for producing new 1-oxa-2-oxo-8-aza-spiro(4,5)decane derivatives and pharmaceutical compositions containing them |
US6291469B1 (en) | 1995-09-29 | 2001-09-18 | Eli Lilly And Company | Spiro compounds as inhibitors of fibrinogen-dependent platelet aggregation |
ATE299866T1 (de) | 1999-05-04 | 2005-08-15 | Schering Corp | Piperidinderivate verwendbar als ccr5 antagonisten |
US6689765B2 (en) * | 1999-05-04 | 2004-02-10 | Schering Corporation | Piperazine derivatives useful as CCR5 antagonists |
CZ20013940A3 (cs) | 1999-05-04 | 2002-04-17 | Schering Corporation | Piperazinové deriváty uľitečné jako CCR5 antagonisté |
US6391865B1 (en) * | 1999-05-04 | 2002-05-21 | Schering Corporation | Piperazine derivatives useful as CCR5 antagonists |
ATE283854T1 (de) | 1999-12-03 | 2004-12-15 | Ono Pharmaceutical Co | Triazaspiro(5.5)undecan-derivate und drogen, die dasselbe als aktiven inhaltsstoff enthalten |
AU2001230537A1 (en) | 2000-02-01 | 2001-08-14 | Daiichi Pharmaceutical Co., Ltd. | Pyridoxazine derivatives |
CN1264847C (zh) | 2001-05-14 | 2006-07-19 | 弗·哈夫曼-拉罗切有限公司 | 1-氧杂-3,9-二氮杂-螺[5.5]十一-2-酮衍生物及其作为神经激肽受体拮抗剂的用途 |
MXPA04006280A (es) | 2001-12-28 | 2004-09-27 | Acadia Pharm Inc | Compuestos espiroazaciclicos como moduladores de receptor de monoamina. |
KR100863854B1 (ko) * | 2004-02-10 | 2008-10-15 | 에프. 호프만-라 로슈 아게 | 케모카인 ccr5 수용체 조절제 |
CN101410414A (zh) * | 2006-01-30 | 2009-04-15 | 弗·哈夫曼-拉罗切有限公司 | 用于治疗hiv的具有协同作用的组合物 |
-
2008
- 2008-03-18 CA CA002682639A patent/CA2682639A1/en not_active Abandoned
- 2008-03-18 KR KR1020097020226A patent/KR20090127298A/ko not_active Application Discontinuation
- 2008-03-18 JP JP2010500218A patent/JP2010522707A/ja active Pending
- 2008-03-18 MX MX2009010503A patent/MX2009010503A/es unknown
- 2008-03-18 BR BRPI0809646-5A patent/BRPI0809646A2/pt not_active Application Discontinuation
- 2008-03-18 EP EP08717970A patent/EP2142555A1/en not_active Withdrawn
- 2008-03-18 AU AU2008233930A patent/AU2008233930A1/en not_active Abandoned
- 2008-03-18 WO PCT/EP2008/053238 patent/WO2008119663A1/en active Application Filing
- 2008-03-18 CN CN200880010622A patent/CN101646679A/zh active Pending
- 2008-03-26 PE PE2008000546A patent/PE20090183A1/es not_active Application Discontinuation
- 2008-03-26 TW TW097110847A patent/TW200902020A/zh unknown
- 2008-03-26 CL CL2008000863A patent/CL2008000863A1/es unknown
- 2008-03-27 AR ARP080101248A patent/AR065854A1/es unknown
- 2008-03-28 US US12/079,746 patent/US7625891B2/en not_active Expired - Fee Related
-
2009
- 2009-09-01 IL IL200661A patent/IL200661A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL200661A0 (en) | 2010-05-17 |
WO2008119663A1 (en) | 2008-10-09 |
TW200902020A (en) | 2009-01-16 |
JP2010522707A (ja) | 2010-07-08 |
US7625891B2 (en) | 2009-12-01 |
CA2682639A1 (en) | 2008-10-09 |
CN101646679A (zh) | 2010-02-10 |
AU2008233930A1 (en) | 2008-10-09 |
BRPI0809646A2 (pt) | 2014-09-23 |
KR20090127298A (ko) | 2009-12-10 |
EP2142555A1 (en) | 2010-01-13 |
PE20090183A1 (es) | 2009-03-12 |
MX2009010503A (es) | 2009-10-19 |
CL2008000863A1 (es) | 2008-11-07 |
US20080249087A1 (en) | 2008-10-09 |
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