AR083872A1 - Derivados de acido carbamoil-cicloalquil-acetico sustituidos como inhibidores de nep - Google Patents
Derivados de acido carbamoil-cicloalquil-acetico sustituidos como inhibidores de nepInfo
- Publication number
- AR083872A1 AR083872A1 ARP110104249A ARP110104249A AR083872A1 AR 083872 A1 AR083872 A1 AR 083872A1 AR P110104249 A ARP110104249 A AR P110104249A AR P110104249 A ARP110104249 A AR P110104249A AR 083872 A1 AR083872 A1 AR 083872A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heteroaryl
- alkoxy
- halogen
- independently selected
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 5
- 125000001424 substituent group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 cyano, hydroxyl Chemical group 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000006719 (C6-C10) aryl (C1-C6) alkyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910003827 NRaRb Inorganic materials 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/52—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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- Gynecology & Obstetrics (AREA)
Abstract
Se proporciona además una composición farmacéutica de los compuestos de la presente, y una combinación de agentes famacológicamente activos. Su uso como medicamento para el tratamiento de enfermedades mediadas por NEP.Reivindicación 1: Un compuesto de la fórmula (1) o una sal farmacéuticamente aceptable del mismo, en donde: R3 y R4 son H, o R3 y R4 junto con los átomos de carbono con los que están unidos, forman un anillo de fenilo; n es 0 ó 1; R1, por cada presentación, es independientemente halógeno, alquilo C1-6, alcoxilo C1-6, hidroxilo, heteroarilo o fenilo; en donde el heteroarilo y fenilo pueden estar opcionalmente sustituidos con uno o más sustituyentes seleccionados independientemente a partir de halógeno, alquilo C1-6, halo-alquilo C1-6, ciano, alcoxilo C1-6, hidroxilo y NRcRd; en donde Rc y Rd son independientemente H o alquilo C1-6; o dos grupos R1 adyacentes forman, junto con los átomos de carbono con los que están unidos, un anillo de heteroarilo de 5 ó 6 miembros opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados a partir de halógeno, alquilo C1-6, halo-alquilo C1-6, ciano, hidroxilo y alcoxilo C1-6; R2 es (CH2)pC(O)X1 o (CH2)s-heteroarilo; en donde el heteroarilo es un anillo de heteroarilo mono- o bi-cíclico que contiene de 5 a 10 miembros del anillo seleccionados a partir de átomos de carbono, y de 1 a 5 heteroátomos, y cada heteroátomo se selecciona independientemente a partir de O, N o S, en donde S y N se pueden oxidar hasta diferentes estados de oxidación, y el heteroarilo está opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente a partir de halógeno, alquilo C1-6, halo-alquilo C1-6, ciano, hidroxilo, alcoxilo C1-6, carboxilo y C(O)O-alquilo C1-6; R5 es H, alquilo C1-6, o arilo C6-10-alquilo C1-6; p es 0 ó 1; s es 0, 1, 2, 3 ó 4; m es 0, 1, 2, 3, 4 ó 5; X y X1 son independientemente OH, O-alquilo C1-6, O-bencilo o NRaRb, en donde Ra y Rb son independientemente H, alquilo C1-6 opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente a partir de halógeno, hidroxilo, alcoxilo C1-6, y carboxilo; o Ra y Rb, junto con el átomo de nitrógeno con el que están unidos, forman un heterociclilo de 5 ó 6 miembros opcionalmente sustituido con uno o más sustituyentes seleccionados independientemente a partir de alquilo C1-6, halógeno, hidroxilo, alcoxilo C1-6, carboxilo, C(O)O-alquilo C1-6, y C(O)O-bencilo; y B es C(O)NH o NHC(O), con la condición de que el compuesto no es el ácido 4-(bisfenil-4-il)-3-(1-carboxi-metil)-ciclopentan-carboxamido)-butanoico, el ácido 4-([1,1’-bifenil]-4-il)-3-(1-(2-(benciloxi)-2-oxo-etil)-ciclopentan-carboxamido)-butanoico, ni el 4-([1,1’-bifenil]-4-il)-3-(1-(2-(benciloxi)-2-oxo-etil)-ciclopentan-carboxamido)-butanoato de terbutilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41417110P | 2010-11-16 | 2010-11-16 |
Publications (1)
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|---|---|
| AR083872A1 true AR083872A1 (es) | 2013-03-27 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| ARP110104249A AR083872A1 (es) | 2010-11-16 | 2011-11-14 | Derivados de acido carbamoil-cicloalquil-acetico sustituidos como inhibidores de nep |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8877815B2 (es) |
| EP (1) | EP2640689A1 (es) |
| JP (1) | JP2014507372A (es) |
| CN (1) | CN103249715A (es) |
| AR (1) | AR083872A1 (es) |
| TW (1) | TW201300353A (es) |
| WO (1) | WO2012065953A1 (es) |
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| US11835503B2 (en) | 2009-05-28 | 2023-12-05 | The Cleveland Clinic Foundation | TMA-formation inhibitor treatment for elevated TMA-containing compound diseases |
| US10241093B2 (en) * | 2009-05-28 | 2019-03-26 | The Cleveland Clinic Foundation | Trimethylamine-containing compounds for diagnosis and prediction of disease |
| EA028583B1 (ru) | 2013-02-14 | 2017-12-29 | Новартис Аг | Замещенные бис-фенилбутановые производные фосфоновой кислоты в качестве ингибиторов nep (нейтральная эндопептидаза) |
| AU2014216417B2 (en) | 2013-02-14 | 2016-05-12 | Novartis Ag | Substituted bisphenyl butanoic acid derivatives as NEP inhibitors with improved in vivo efficacy |
| GB201704476D0 (en) | 2017-03-21 | 2017-05-03 | Antabio Sas | Chemical compounds |
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| WO2020064175A1 (en) * | 2018-09-25 | 2020-04-02 | Antabio Sas | Indane derivatives for use in the treatment of bacterial infection |
| SG11202102790PA (en) * | 2018-09-25 | 2021-04-29 | Antabio Sas | Indane derivatives for use in the treatment of bacterial infection |
| EP3628672A1 (en) * | 2018-09-25 | 2020-04-01 | Antabio SAS | Indane derivatives for use in the treatment of bacterial infection |
| EP3628666A1 (en) * | 2018-09-25 | 2020-04-01 | Antabio SAS | Indane derivatives for use in the treatment of bacterial infection |
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-
2011
- 2011-11-10 US US13/293,560 patent/US8877815B2/en not_active Expired - Fee Related
- 2011-11-14 JP JP2013539217A patent/JP2014507372A/ja active Pending
- 2011-11-14 AR ARP110104249A patent/AR083872A1/es not_active Application Discontinuation
- 2011-11-14 WO PCT/EP2011/070066 patent/WO2012065953A1/en not_active Ceased
- 2011-11-14 CN CN2011800551969A patent/CN103249715A/zh active Pending
- 2011-11-14 EP EP11785381.2A patent/EP2640689A1/en not_active Withdrawn
- 2011-11-15 TW TW100141689A patent/TW201300353A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN103249715A (zh) | 2013-08-14 |
| US20120122764A1 (en) | 2012-05-17 |
| US8877815B2 (en) | 2014-11-04 |
| JP2014507372A (ja) | 2014-03-27 |
| WO2012065953A1 (en) | 2012-05-24 |
| EP2640689A1 (en) | 2013-09-25 |
| TW201300353A (zh) | 2013-01-01 |
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