CO5320600A1 - Agentes antibacterianos de 3-aminoquinazolin-2,4-dionas - Google Patents

Agentes antibacterianos de 3-aminoquinazolin-2,4-dionas

Info

Publication number
CO5320600A1
CO5320600A1 CO01004183A CO01004183A CO5320600A1 CO 5320600 A1 CO5320600 A1 CO 5320600A1 CO 01004183 A CO01004183 A CO 01004183A CO 01004183 A CO01004183 A CO 01004183A CO 5320600 A1 CO5320600 A1 CO 5320600A1
Authority
CO
Colombia
Prior art keywords
substituted
alkyl
alkynyl
alkenyl
heterocyclic
Prior art date
Application number
CO01004183A
Other languages
English (en)
Inventor
Paul Bird
Edmund Lee Ellsworth
Dai Quoc Nguyen
Joseph Peter Sanchez
Howard Daniel Hollis Showalter
Rajesshwar Singh
Michael Andrew Stier
Tuan Phong Tran
Brian Morgan Watson
Judy Yip
Original Assignee
Warner Lambert Co
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 Warner Lambert Co filed Critical Warner Lambert Co
Publication of CO5320600A1 publication Critical patent/CO5320600A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C07D239/96Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Paper (AREA)

Abstract

Un compuespo de la fórmula I<EMI FILE="01004183_1" ID="1" IMF=JPEG >o una sal farmacéuticamente aceptable de ellos en donde:R1 y R3 independientemente son H,Alquilo y alquilo sustituido de C1-C12,AIquenilo y alquenilo sustituido de C2-C12,AlquiniIo y alquinilo sustituido de C2-C12,Cicloalquilo y cicloalquiIo sustituido de C3-C12,Arilo y arilo sustituido,Heterocíclico y heterocíclico sustituido,o heteroarilo y heteroarilo sustituido;R5, R6 y R8 independientemente son H,(O)nalquilo de C1-C12, y alquilo sustituido;(O)nalquenilo de C2-C12 y alquenilo sustituido;(O)nalquinilo de C2-C12 y alquinilo sustituido,en donde n es 0 o 1,halo,NO2,CN,NR´R´´;R´ y R´´ independientemente son H,alquilo y alquilo sustituido de C1-C12,alquenilo y alquenilo sustituido de C2-C12,alquinilo y alquinilo sustituido de C2-C12,CO-alquilo de C1-C12 y alquilo sustituido,o R´ y R´´ tomados junto con el nitrógeno al cual están unidos forman un anillo de 3 a 7 miembros que contiene de 1 a 3 heteroátomos seleccionados de N, O y S, dicho anillo es no sustituido o sustituido con hasta 4 grupos sustituyentes;R1 y R8 pueden ser tomados junto con los átomos a los cuales están unidos para formar un anillo cíclico que tiene de 1 a 3 heteroátomos seleccionados de N, O y S y optativamente sustituidos por R´ y R´´; - 2 -R7 es hidrógeno,alquilo y alquilo sustituido de C1-C12,alquenilo y alquenilo sustituido de C2-C12,alquinilo y alquinilo sustituido de C2-C12,halo,NO2,CN,NR´R´´,COOR´ ,arilo,arilo fusionado,heterocíclico,heterocíclico bicíclico, oespiro heterocíclicoen donde todos los grupos del anillo pueden ser sustituidos; yJ y K independientemente son C o N, siempre que cuando J o K es N, R6 o R8 esté ausente en esa posición.
CO01004183A 2000-01-24 2001-01-22 Agentes antibacterianos de 3-aminoquinazolin-2,4-dionas CO5320600A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US17825200P 2000-01-24 2000-01-24
US24126700P 2000-10-18 2000-10-18

Publications (1)

Publication Number Publication Date
CO5320600A1 true CO5320600A1 (es) 2003-09-30

Family

ID=26874138

Family Applications (1)

Application Number Title Priority Date Filing Date
CO01004183A CO5320600A1 (es) 2000-01-24 2001-01-22 Agentes antibacterianos de 3-aminoquinazolin-2,4-dionas

Country Status (38)

Country Link
US (2) US7094780B1 (es)
EP (1) EP1255739B1 (es)
JP (1) JP4811978B2 (es)
KR (1) KR20020067701A (es)
CN (1) CN1425008A (es)
AP (1) AP2002002603A0 (es)
AR (1) AR030186A1 (es)
AT (1) ATE398110T1 (es)
AU (1) AU783078B2 (es)
BG (1) BG107023A (es)
BR (1) BR0017010A (es)
CA (1) CA2393802C (es)
CO (1) CO5320600A1 (es)
CR (1) CR6709A (es)
DE (1) DE60039194D1 (es)
EA (1) EA005585B1 (es)
EE (1) EE200200412A (es)
ES (1) ES2304992T3 (es)
GE (1) GEP20053429B (es)
HK (1) HK1054237A1 (es)
HN (1) HN2001000009A (es)
HR (1) HRP20020696A2 (es)
HU (1) HUP0204101A3 (es)
IL (1) IL150393A0 (es)
IS (1) IS6448A (es)
MA (1) MA26866A1 (es)
MX (1) MXPA02005989A (es)
NO (1) NO20023516L (es)
OA (1) OA12316A (es)
PA (1) PA8510101A1 (es)
PE (1) PE20011060A1 (es)
PL (1) PL356837A1 (es)
SK (1) SK10572002A3 (es)
SV (1) SV2001000288A (es)
TN (1) TNSN01011A1 (es)
UY (1) UY26551A1 (es)
WO (1) WO2001053273A1 (es)
YU (1) YU55902A (es)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUP0100051A3 (en) 1997-09-15 2002-08-28 Procter & Gamble Antimicrobial quinolones, their compositions and uses
JP2004532876A (ja) 2001-05-30 2004-10-28 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 抗菌剤
BR0210028A (pt) * 2001-06-19 2004-06-22 Warner Lambert Co Agentes antibacterianos
US6900224B2 (en) * 2002-07-31 2005-05-31 The Procter & Gamble Company Antimicrobial quinolones, their compositions and uses
CA2538420A1 (en) * 2003-09-12 2005-03-24 Warner-Lambert Company Llc Quinolone antibacterial agents
WO2005026153A1 (en) * 2003-09-12 2005-03-24 Warner-Lambert Company Llc Quinazoline-2, 4-diones as antibacterial agents
MXPA06005550A (es) * 2003-11-18 2006-08-17 Warner Lambert Co Agentes antibacterianos.
WO2006019965A2 (en) * 2004-07-16 2006-02-23 Takeda San Diego, Inc. Dipeptidyl peptidase inhibitors
GB0416730D0 (en) 2004-07-27 2004-09-01 Novartis Ag Organic compounds
ES2332529T3 (es) * 2005-01-26 2010-02-08 F. Hoffmann-La Roche Ag Derivados de fenil-metanona y su empleo como inhibidores del transportador 1 de glicina.
GB0507298D0 (en) 2005-04-11 2005-05-18 Novartis Ag Organic compounds
US7977346B2 (en) 2006-01-17 2011-07-12 Guoqing Paul Chen Spiro compounds and methods of use
KR101084521B1 (ko) 2006-03-28 2011-11-18 워너 칠콧 컴퍼니 엘엘씨 퀴놀론 중간체를 제조하기 위한 커플링 방법
MX2008012328A (es) 2006-03-28 2008-10-09 Procter & Gamble Sales de malato, y polimorfos de acido (3s,5s)-7-[3-amino-5-metil- piperidinil]-1-ciclopropil-1,4-dihidro-8-metoxi-4-oxo-3-quinolinc arboxilico.
US20080139574A1 (en) 2006-11-30 2008-06-12 Cadila Healthcare Limited Novel quinoline derivatives
ES2387539T3 (es) * 2008-01-30 2012-09-25 Shin Poong Pharmaceutical Co. Ltd. Nuevo derivado de quinazolina-2,4-diona, y composiciones para la profilaxis y tratamiento de enfermedades nerviosas craneales conteniendo el mismo derivado
WO2011031745A1 (en) 2009-09-09 2011-03-17 Achaogen, Inc. Antibacterial fluoroquinolone analogs
WO2012088266A2 (en) 2010-12-22 2012-06-28 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3
US9732083B2 (en) 2011-03-15 2017-08-15 Merck Sharp & Dohme Corp. Tricyclic gyrase inhibitors
ES2682755T3 (es) * 2011-12-21 2018-09-21 Jiangsu Hengrui Medicine Co. Ltd. Derivado del anillo heteroarilo de seis miembros de pirrol, método de preparación del mismo y sus usos medicinales
CN107383009B (zh) 2012-06-13 2020-06-09 因塞特控股公司 作为fgfr抑制剂的取代的三环化合物
WO2014026125A1 (en) 2012-08-10 2014-02-13 Incyte Corporation Pyrazine derivatives as fgfr inhibitors
TWI639602B (zh) 2012-09-12 2018-11-01 默沙東藥廠 三環旋轉酶抑制劑
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
SG11201508328PA (en) 2013-04-19 2015-11-27 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
CN107438607B (zh) 2015-02-20 2021-02-05 因赛特公司 作为fgfr抑制剂的双环杂环
CN108530448A (zh) * 2017-03-02 2018-09-14 浙江司太立制药股份有限公司 含有碱性氮杂螺环片段的苯并噻嗪-4-酮类化合物及其制备方法
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
CA3099116A1 (en) 2018-05-04 2019-11-07 Incyte Corporation Salts of an fgfr inhibitor
AU2019262195B2 (en) 2018-05-04 2024-09-12 Incyte Corporation Solid forms of an FGFR inhibitor and processes for preparing the same
CN111620866A (zh) * 2019-02-27 2020-09-04 南京药石科技股份有限公司 一种顺式-7,7-二氟-六氢-1H 吡咯并[3,4-c]吡啶衍生物及其制备方法
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
JP2022552324A (ja) 2019-10-14 2022-12-15 インサイト・コーポレイション Fgfr阻害剤としての二環式複素環
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
CA3163875A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
KR20220131900A (ko) 2019-12-04 2022-09-29 인사이트 코포레이션 Fgfr 억제제의 유도체
WO2021146424A1 (en) 2020-01-15 2021-07-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
CN111499513B (zh) * 2020-04-24 2023-03-14 上海毕得医药科技股份有限公司 一种2,3,4,5-四溴苯甲酸酯的合成方法
US12065494B2 (en) 2021-04-12 2024-08-20 Incyte Corporation Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent
JP2024522189A (ja) 2021-06-09 2024-06-11 インサイト・コーポレイション Fgfr阻害剤としての三環式ヘテロ環

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1068263B (es) * 1959-11-05
FR1203542A (fr) * 1958-02-25 1960-01-19 Rhone Poulenc Sa Nouveaux dérivés de la phénothiazine comportant en position 10 une chaîne pipérazinique et leurs procédés de préparation
DE3068648D1 (de) * 1980-03-10 1984-08-30 Berri Balzac Derivatives of 3-amino-(1h,3h)-2,4-quinazolin-diones
GB2097784A (en) * 1981-04-28 1982-11-10 Davidson Dr John Stirton Dihydrobenzotriazepine diones; aminoquinazoline diones
WO1994014809A1 (de) 1992-12-23 1994-07-07 Byk Gulden Lomberg Chemische Fabrik Gmbh Anellierte uracilderivate
WO1998018781A2 (en) 1996-10-28 1998-05-07 Versicor, Inc. Fused 2,4-pyrimidinedione combinatorial libraries, their preparation and the use of fused 2,4-pyrimidinediones derivatives as antimicrobial agents
DK1028950T3 (da) * 1997-10-28 2003-09-01 Warner Lambert Co 7-substituerede quinazolin-2,4-dioner nyttige som antibakterielle midler
ES2310039T3 (es) 1998-05-26 2008-12-16 Warner-Lambert Company Llc Pirimidinas biciclicas y 3,4-dihidropirimidinas biciclicas como inhibidores de la proliferacion celular.
ATE305003T1 (de) * 1998-12-11 2005-10-15 Hoffmann La Roche Zyklische hydrazinderivate als tnf-alpha inhibitoren

Also Published As

Publication number Publication date
HUP0204101A3 (en) 2004-05-28
EA005585B1 (ru) 2005-04-28
US7582627B2 (en) 2009-09-01
US20060287308A1 (en) 2006-12-21
CR6709A (es) 2003-11-25
JP4811978B2 (ja) 2011-11-09
YU55902A (sh) 2006-01-16
BG107023A (en) 2003-04-30
PA8510101A1 (es) 2003-06-30
WO2001053273A1 (en) 2001-07-26
JP2003520277A (ja) 2003-07-02
IS6448A (is) 2002-06-27
TNSN01011A1 (en) 2005-11-10
PL356837A1 (en) 2004-07-12
KR20020067701A (ko) 2002-08-23
US7094780B1 (en) 2006-08-22
SV2001000288A (es) 2001-11-30
CA2393802C (en) 2011-04-19
CN1425008A (zh) 2003-06-18
NO20023516D0 (no) 2002-07-23
AU2089901A (en) 2001-07-31
HN2001000009A (es) 2001-06-13
GEP20053429B (en) 2005-01-25
IL150393A0 (en) 2002-12-01
ES2304992T3 (es) 2008-11-01
CA2393802A1 (en) 2001-07-26
EP1255739B1 (en) 2008-06-11
BR0017010A (pt) 2002-11-05
MA26866A1 (fr) 2004-12-20
US20060183762A1 (en) 2006-08-17
HUP0204101A2 (hu) 2003-04-28
OA12316A (en) 2006-05-15
AU783078B2 (en) 2005-09-22
MXPA02005989A (es) 2002-10-23
PE20011060A1 (es) 2001-10-12
ATE398110T1 (de) 2008-07-15
HRP20020696A2 (en) 2003-12-31
UY26551A1 (es) 2001-04-30
SK10572002A3 (sk) 2003-10-07
EA200200661A1 (ru) 2003-02-27
DE60039194D1 (de) 2008-07-24
AP2002002603A0 (en) 2002-09-30
NO20023516L (no) 2002-07-23
EP1255739A1 (en) 2002-11-13
AR030186A1 (es) 2003-08-13
HK1054237A1 (zh) 2003-11-21
EE200200412A (et) 2003-10-15

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