AR032434A1 - Norbornilamino-derivados substituidos, procedimientos para su preparacion, su empleo para la preparcion de medicamentos, asi como el medicamento que los contiene - Google Patents
Norbornilamino-derivados substituidos, procedimientos para su preparacion, su empleo para la preparcion de medicamentos, asi como el medicamento que los contieneInfo
- Publication number
- AR032434A1 AR032434A1 ARP000106577A ARP000106577A AR032434A1 AR 032434 A1 AR032434 A1 AR 032434A1 AR P000106577 A ARP000106577 A AR P000106577A AR P000106577 A ARP000106577 A AR P000106577A AR 032434 A1 AR032434 A1 AR 032434A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- substituted
- preparation
- independently
- Prior art date
Links
- 239000003814 drug Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 2
- 229940126601 medicinal product Drugs 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 12
- 229910052731 fluorine Inorganic materials 0.000 abstract 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 239000011737 fluorine Substances 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 229940079593 drug Drugs 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 238000011282 treatment Methods 0.000 abstract 2
- 206010048962 Brain oedema Diseases 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 208000002249 Diabetes Complications Diseases 0.000 abstract 1
- 206010012655 Diabetic complications Diseases 0.000 abstract 1
- 206010048554 Endothelial dysfunction Diseases 0.000 abstract 1
- 206010020880 Hypertrophy Diseases 0.000 abstract 1
- 102000004895 Lipoproteins Human genes 0.000 abstract 1
- 108090001030 Lipoproteins Proteins 0.000 abstract 1
- 206010041235 Snoring Diseases 0.000 abstract 1
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 abstract 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical class OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 230000000879 anti-atherosclerotic effect Effects 0.000 abstract 1
- 229940030600 antihypertensive agent Drugs 0.000 abstract 1
- 239000002220 antihypertensive agent Substances 0.000 abstract 1
- 230000003143 atherosclerotic effect Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 208000006752 brain edema Diseases 0.000 abstract 1
- 230000001413 cellular effect Effects 0.000 abstract 1
- 201000001883 cholelithiasis Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 244000078703 ectoparasite Species 0.000 abstract 1
- 230000008694 endothelial dysfunction Effects 0.000 abstract 1
- 230000003176 fibrotic effect Effects 0.000 abstract 1
- 239000003574 free electron Substances 0.000 abstract 1
- 208000001130 gallstones Diseases 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 206010020718 hyperplasia Diseases 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 239000008141 laxative Substances 0.000 abstract 1
- 230000002475 laxative effect Effects 0.000 abstract 1
- 238000002483 medication Methods 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 210000000653 nervous system Anatomy 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- -1 phenyloxy Chemical group 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 239000003169 respiratory stimulant agent Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 210000002966 serum Anatomy 0.000 abstract 1
- 230000035939 shock Effects 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000011477 surgical intervention Methods 0.000 abstract 1
Classifications
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- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C—CHEMISTRY; METALLURGY
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- C07C211/33—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
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- C07C211/38—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of a saturated carbon skeleton containing condensed ring systems
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
- C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
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- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
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- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/60—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/38—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to acyclic carbon atoms and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
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- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton
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- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
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- C07C2603/66—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing five-membered rings
- C07C2603/68—Dicyclopentadienes; Hydrogenated dicyclopentadienes
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Abstract
Norbornilamino-derivados substituidos con nitrogeno exo-configurado y sistemas de 5, 6 o 7 anillos endo-condensados de la Formula (1) y con nitrogeno exo-configurado y sistemas de 5, 6 o 7 anillos exo-condensados de la Formula (1a), en las cuales significan: A alquileno C1-4; S1 un par de electrones libres o alquilo C1-4; S2 alquilo C1-4 o H; correspondiendo, cuando S1 y S2 representan alquilo, X- en el agrupamiento resultante [-N+(S1S2)-X-] a un anion farmacologicamente aceptable o trifluoroacetato; B un sistema anular de carbono de 5, 6 o 7 anillos saturado o no saturado, que puede estar substituido sencillamente o repetidas veces independientemente entre sí con oxo, hidroxilo, alcoxilo C1-4 y alquilo C1-4; y R1, R2, R3, R4 y R5, independientemente entre sí, H, OH, F, Cl, Br, I, CN, NO2, amidino, -CO2R11, -CONR11R12, SOrR11, -SOsNR11R12, alquilo C1-4, alcoxilo C1-4, alcoxi C1-4-alquilo C1-4, alcoxi C1-4-alquiloxilo C1-4, hidroxi-alquilo C1-4, cicloalcoxilo C3-7 o feniloxilo, pudiendo estar el fenilo sin substituir o substituido con hasta tres substituyentes, que son independientes entre sí, seleccionados del grupo formado por F, Cl, Br y metoxilo; amino, alquilamino C1-4, dialquilamino C1-4, aminoalquilo C1-4, dialquilamino C1-4-alquilo C1-4, alquilamino C1-4-alquilo C1-4, pudiendo estar los átomos de hidrogeno de los radicales alquilo total o parcialmente substituidos por fluor; R11 y R12 independientemente entre sí, son H o alquilo C1-4, pudiendo estar los átomos de hidrogeno en los radicales alquilo total o parcialmente substituidos por fluor; r es 0, 1 o 2; s es 1 o 2; o R1 y R2, R2 y R3, R3 y R4 y R4 y R5 conjuntamente en cada caso un grupo -O-(CH2)n-O-; n es 1 o 2; y los restantes radicales R1, R2, R3, R4 o R5 en cada caso, independientemente entre sí, H, OH, F, Cl, Br, I, CN, NO2, amidino, -CO2R11, -CONR(R11)R12, SOrR11, -SOsNR11R12, alquilo C1-4, alcoxilo C1-4, alcoxi C1-4-alquilo C1-4, cicloalcoxilo C3-7, hidroxi-alquilo C1-4, amino, alquilamino C1-4, dialquilamino C1-4, aminoalquilo C1-4, dialquilamino C1-4-alquilo C1-4, alquilamino C1-4-alquilo C1-4, pudiendo estar los átomos de hidrogeno de los radicales alquilo total o parcialmente substituidos por fluor; R11 y R12 independientemente entre sí, son H o alquilo C1-4, pudiendo estar los átomos de hidrogeno en los radicales alquilo total o parcialmente substituidos por fluor; r es 0, 1 o 2; s es 1 o 2; con la excepcion de la bencil-(octahidro-4,7-metano-inden-5-il)-amina, así como sus sales tolerables farmacéuticamente o trifluoroacetatos; que son agentes notablemente adecuados como agentes antihipertensores, para la reduccion o impedimento de danos inducidos isquémicamente, como medicamentos para intervenciones quirurgicas, para el tratamiento de isquemias del sistema nervioso, de la apoplejía y del edema cerebral, del shock, del estímulo respiratorio perturbado, para el tratamiento del ronquido, como laxante, como agente contra ectoparásitos, como prevencion contra la formacion de cálculos biliares, como agentes antiateroscleroticos, agentes contra complicaciones diabéticas tardías, enfermedades cancerosas, enfermedades fibroticas, disfuncion endotelial, hipertrofias e hiperplasias de organos. Estos compuestos son inhibidores del antiporter de sodio-protones celular. Influencian las lipoproteínas en suero y pueden por lo tanto emplearse para la profilaxis y la regresion de alteraciones ateroscleroticas; procedimientos para su preparacion, su empleo para la preparacion de medicamentos, así como el medicamento que los contiene.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19960204A DE19960204A1 (de) | 1999-12-14 | 1999-12-14 | Substituierte Norlbornylamino-Derivate, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR032434A1 true AR032434A1 (es) | 2003-11-12 |
Family
ID=7932583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000106577A AR032434A1 (es) | 1999-12-14 | 2000-12-12 | Norbornilamino-derivados substituidos, procedimientos para su preparacion, su empleo para la preparcion de medicamentos, asi como el medicamento que los contiene |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6825231B2 (es) |
| EP (1) | EP1255724B1 (es) |
| JP (1) | JP2003517033A (es) |
| KR (1) | KR20030004308A (es) |
| CN (1) | CN1210251C (es) |
| AR (1) | AR032434A1 (es) |
| AT (1) | ATE338022T1 (es) |
| AU (1) | AU778888B2 (es) |
| BR (1) | BR0016360A (es) |
| CA (1) | CA2394130A1 (es) |
| CZ (1) | CZ20022006A3 (es) |
| DE (2) | DE19960204A1 (es) |
| EE (1) | EE200200292A (es) |
| HK (1) | HK1049655B (es) |
| HR (1) | HRP20020517A2 (es) |
| HU (1) | HUP0204360A3 (es) |
| IL (1) | IL150228A0 (es) |
| MX (1) | MXPA02003763A (es) |
| NO (1) | NO20022801L (es) |
| NZ (1) | NZ519511A (es) |
| PL (1) | PL356235A1 (es) |
| RU (1) | RU2260584C2 (es) |
| SK (1) | SK8202002A3 (es) |
| WO (1) | WO2001044164A1 (es) |
| YU (1) | YU30302A (es) |
| ZA (1) | ZA200204663B (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10063294A1 (de) | 2000-12-19 | 2002-07-04 | Aventis Pharma Gmbh | Substituierte Heterocyclo-Norbornylamino-Derivate, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| DE10156617A1 (de) | 2001-11-17 | 2003-05-28 | Biosphings Ag | Herstellung reiner Stereoisomere von Tricyclo[5.2.1.0··2··.··6··]-dec-9-yl-xanthogenat und Arzneimittel daraus |
| US20030187045A1 (en) * | 2001-12-21 | 2003-10-02 | Uwe Heinelt | Substituted imidazolidines, process for their preparation, and their use as a medicament or diagnostic |
| DE10163239A1 (de) * | 2001-12-21 | 2003-07-10 | Aventis Pharma Gmbh | Substituierte Imidazolidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie enthaltendes Medikament |
| US7049333B2 (en) | 2002-06-04 | 2006-05-23 | Sanofi-Aventis Deutschland Gmbh | Substituted thiophenes: compositions, processes of making, and uses in disease treatment and diagnosis |
| DE10224892A1 (de) * | 2002-06-04 | 2003-12-18 | Aventis Pharma Gmbh | Substituierte Thiophene, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| DE10304374A1 (de) * | 2003-02-04 | 2004-08-05 | Aventis Pharma Deutschland Gmbh | Neue substituierte 2-Aminoimidazole, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| US20050054705A1 (en) * | 2003-02-04 | 2005-03-10 | Aventis Pharma Deutschland Gmbh | N-substituted (benzoimidazol-2-yl) phenylamines, process for their preparation, their use as medicament or diagnostic aid, and medicament comprising them |
| DE102005001411A1 (de) | 2005-01-12 | 2006-07-27 | Sanofi-Aventis Deutschland Gmbh | Substituierte 4-Phenyltetrahydroisochinoline, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament, sowie sie enthaltendes Medikament |
| ATE479679T1 (de) | 2007-06-28 | 2010-09-15 | Sanofi Aventis Us Llc | Verfahren zur herstellung von n-(2-chlor-4-methyl-3-thienyl)-1h-benzimidazol- 2-amin hydrochlorid und zwischenprodukte dafür |
| BRPI0918502A2 (pt) | 2008-09-02 | 2015-12-01 | Sanofi Aventis | aminoindanos substituídos e análogos dos mesmos, e o uso farmacêutico dos mesmos |
| DE102009030291A1 (de) * | 2009-06-24 | 2011-01-05 | Cu Chemie Uetikon Gmbh | Enantiomerenreine tricyclische Verbindung und Verfahren zur diastereomerenreinen und enantiomerenreinen Herstellung bicyclischer und tricyclischer Verbindungen |
| CN105408428B (zh) | 2013-08-13 | 2017-07-07 | 色彩矩阵控股股份有限公司 | 流体状颜料分散体 |
| EP4541784A1 (en) * | 2022-06-20 | 2025-04-23 | Mitsubishi Chemical Corporation | Quaternary ammonium salt, organic structure-directing agent, method for producing quaternary ammonium salt, con-type zeolite, method for producing con-type zeolite, catalyst, and method for producing lower olefin |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2403138A1 (de) * | 1974-01-23 | 1975-07-31 | Hoechst Ag | Benzylaminderivate und verfahren zu ihrer herstellung |
| US5157034A (en) * | 1991-02-27 | 1992-10-20 | Pfizer Inc. | Neuroleptic perhydro-1H-pyrido[1,2-a]pyrazines |
| EP0556674B1 (de) * | 1992-02-15 | 1996-06-19 | Hoechst Aktiengesellschaft | 3,5-Substituierte Benzoylguanidine, mit antiarrythmischer Wirkung und inhibierender Wirkung auf die Proliferationen von Zellen |
| DE19518073A1 (de) * | 1995-05-17 | 1996-11-21 | Hoechst Ag | Substituierte Benzyloxycarbonylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
| US5792635A (en) * | 1995-06-07 | 1998-08-11 | Magainin Pharmaceuticals, Inc. | Method of inhibiting the sodium/proton exchanger NHE3 and method of inhibiting growth by administering squalamine |
| DE19633966A1 (de) * | 1996-08-22 | 1998-02-26 | Hoechst Ag | Phenylsubstituierte Alkenylcarbonsäure-guanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament |
-
1999
- 1999-12-14 DE DE19960204A patent/DE19960204A1/de not_active Withdrawn
-
2000
- 2000-12-01 YU YU30302A patent/YU30302A/sh unknown
- 2000-12-01 PL PL00356235A patent/PL356235A1/xx not_active Application Discontinuation
- 2000-12-01 EE EEP200200292A patent/EE200200292A/xx unknown
- 2000-12-01 SK SK820-2002A patent/SK8202002A3/sk unknown
- 2000-12-01 RU RU2002118700/04A patent/RU2260584C2/ru not_active IP Right Cessation
- 2000-12-01 HU HU0204360A patent/HUP0204360A3/hu unknown
- 2000-12-01 AT AT00977604T patent/ATE338022T1/de not_active IP Right Cessation
- 2000-12-01 HK HK03101859.5A patent/HK1049655B/zh not_active IP Right Cessation
- 2000-12-01 HR HR20020517A patent/HRP20020517A2/hr not_active Application Discontinuation
- 2000-12-01 BR BR0016360-0A patent/BR0016360A/pt not_active IP Right Cessation
- 2000-12-01 NZ NZ519511A patent/NZ519511A/en unknown
- 2000-12-01 IL IL15022800A patent/IL150228A0/xx unknown
- 2000-12-01 CA CA002394130A patent/CA2394130A1/en not_active Abandoned
- 2000-12-01 CZ CZ20022006A patent/CZ20022006A3/cs unknown
- 2000-12-01 WO PCT/EP2000/012107 patent/WO2001044164A1/de not_active Ceased
- 2000-12-01 DE DE50013410T patent/DE50013410D1/de not_active Expired - Lifetime
- 2000-12-01 MX MXPA02003763A patent/MXPA02003763A/es active IP Right Grant
- 2000-12-01 AU AU15254/01A patent/AU778888B2/en not_active Ceased
- 2000-12-01 KR KR1020027007555A patent/KR20030004308A/ko not_active Ceased
- 2000-12-01 CN CNB008144648A patent/CN1210251C/zh not_active Expired - Fee Related
- 2000-12-01 JP JP2001545253A patent/JP2003517033A/ja active Pending
- 2000-12-01 EP EP00977604A patent/EP1255724B1/de not_active Expired - Lifetime
- 2000-12-12 US US09/734,008 patent/US6825231B2/en not_active Expired - Fee Related
- 2000-12-12 AR ARP000106577A patent/AR032434A1/es unknown
-
2002
- 2002-06-11 ZA ZA200204663A patent/ZA200204663B/en unknown
- 2002-06-12 NO NO20022801A patent/NO20022801L/no not_active Application Discontinuation
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