PE20191153A1 - Moduladores de calpainas y usos terapeuticos de los mismos - Google Patents

Moduladores de calpainas y usos terapeuticos de los mismos

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Publication number
PE20191153A1
PE20191153A1 PE2019000732A PE2019000732A PE20191153A1 PE 20191153 A1 PE20191153 A1 PE 20191153A1 PE 2019000732 A PE2019000732 A PE 2019000732A PE 2019000732 A PE2019000732 A PE 2019000732A PE 20191153 A1 PE20191153 A1 PE 20191153A1
Authority
PE
Peru
Prior art keywords
optionally substituted
aryl
membered heteroaryl
membered
modulators
Prior art date
Application number
PE2019000732A
Other languages
English (en)
Inventor
Brad Owen Buckman
John Beamond Nicholas
Shendong Yuan
Marc Adler
Kumaraswamy Emayan
Jingyuang Ma
Original Assignee
Blade Therapeutics Inc
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 Blade Therapeutics Inc filed Critical Blade Therapeutics Inc
Publication of PE20191153A1 publication Critical patent/PE20191153A1/es

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    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • A61K31/41641,3-Diazoles
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Abstract

Referido a un compuesto que tiene la estructura seleccionada de las formulas (I-a, I-b, I-c, I-d, I-e, I-f, I-g, I-h, I-m, I-n) o una de sus sales farmaceuticamente aceptables, en donde: A2 es heterociclilo opcionalmente sustituido de 3-10 miembros, arilo C6-10 opcionalmente sustituido, entre otros; A4 es arilo C6-10 opcionalmente sustituido, heteroarilo opcionalmente sustituido con 5-10 miembros, entre otros; A3 es arilo C6-10 opcionalmente sustituido, heteroarilo opcionalmente sustituido de 5-10 miembros, entre otros; A5 es heterociclilo opcionalmente sustituido de 3-10 miembros, arilo C6-10 opcionalmente sustituido, entre otros; A6 es arilo C6-10 opcionalmente sustituido, heteroarilo opcionalmente sustituido de 5-10 miembros, entre otros; A7 es arilo C6-10 opcionalmente sustituido, heteroarilo opcionalmente sustituido de 5-10 miembros. R1 es H, -COOH, -CH2NO2, entre otros; R6 es -H o alquilo C1-4opcionalmente sustituido; A, B, D, X y Z se seleccionan de modo independiente entre C(R4) y N; R4 es -H, alquilo C1-4, entre otros; Y es NR5, O, S o SO2. Estos compuestos de alfa-cetoamida no macrolidos son moduladores de calpaina de pequena molecula, utiles en el tratamiento de la enfermedad fibrotica o un estado secundario de la misma, artritis reumatoide, entre otros. Tambien se refiere a metodos de preparacion y una composicion farmaceutica que comprende dichos compuestos.
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