AR080357A1 - Derivados de fumaratos de acidos grasos, composiciones farmaceuticas y sus usos - Google Patents
Derivados de fumaratos de acidos grasos, composiciones farmaceuticas y sus usosInfo
- Publication number
- AR080357A1 AR080357A1 ARP110100061A ARP110100061A AR080357A1 AR 080357 A1 AR080357 A1 AR 080357A1 AR P110100061 A ARP110100061 A AR P110100061A AR P110100061 A ARP110100061 A AR P110100061A AR 080357 A1 AR080357 A1 AR 080357A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- independently
- null
- optionally substituted
- compound
- Prior art date
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/70—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/72—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atoms of the carboxamide groups bound to acyclic carbon atoms
- C07C235/76—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups and doubly-bound oxygen atoms bound to the same carbon skeleton with the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
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- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/221—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin with compounds having an amino group, e.g. acetylcholine, acetylcarnitine
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Abstract
Derivados de fumaratos de ácidos grasos; composiciones que comprenden cantidades eficaces de un derivado de fumarato de ácido graso; y métodos para tratar o prevenir el cáncer, un trastorno metabolico o un trastorno neurodegenerativo, que comprende administrar una cantidad eficaz de un derivado de fumarato de ácido graso. Reivindicacion 2: Un compuesto caracterizado porque es de formula (1) o una sal aceptable farmacéuticamente, hidrato, solvato, prodroga, enantiomero, o estereoisomero del mismo; donde cada W1 y W2 es en forma independiente nulo, O, S, NH, o NR, o W1 y W2 pueden tomarse juntos para formar un grupo imidazolidina o piperazina opcionalmente sustituido; cada a, b, c, y d, es en forma independiente -H, -D, -CH3, -OCH3, -OCH2CH3, -C(O)O, -O-Z, o bencilo, o dos de a, b, c, y d pueden tomarse juntos, junto con el unico carbono al que están unidos, para formar un cicloalquilo o heterociclo; cada n, o, p, q, es en forma independiente 0, 1 o 2; cada L es en forma independiente nulo, -O-, -C(O)-,-S-, -S(O)-, -S(O)2-, -S-S-, -alquil C1-6-, -cicloalquil C3-6-, un heterociclo, un heteroarilo, una de los compuestos del grupo de formulas (2) donde la representacion de L no constituye una limitacion direccional de izquierda a derecha como se ilustra, sino que el lado derecho o el lado izquierdo de L puede estar unido al lado W1 del compuesto de formula (1); cada R6 es en forma independiente -H, -D, alquilo C1-4, -halogeno, ciano, oxo, tiooxo, -OH, -C(O)alquilo C1-4, -O-arilo, -O-bencilo, -OC(O)alquilo C1-4, alqueno C1-3, alquino C1-3, -C(O)alquilo C1-4, -NH2, -NH(alquilo C1-3), -N(alquil C1-3)2, -NH(C(O)alquilo C1-3), -N(C(O)alquil C1-3)2, -SH, -S(alquilo C1-3), -S(O)alquilo C1-3, -S(O)2alquilo C1-3; cada g es en forma independiente 2, 3 o 4; cada h es en forma independiente 1, 2, o 4; cada m y m' es en forma independiente 0, 1, 2, o 3; si m es mayor a 1, luego L o L' pueden ser iguales o diferentes; cada m1 es en forma independiente 0, 1, 2 o 3; k es 0, 1, 2, o 3; z es 1, 2, o 3; cada R4 es en forma independiente H o alquilo C1-6 opcionalmente sustituido, donde una unidad metileno del alquilo C1-6 puede reemplazarse opcionalmente por O o NR, y en NR4R4, ambos R4 cuando se toman junto con el nitrogeno al cual están unidos pueden formar un anillo heterocíclico como por ejemplo una pirrolidina, piperidina, morfolina, piperazina o pirrol; cada Z es en forma independiente H, o un resto de las formulas (3), (4) o (5) con las siguientes condiciones se encuentra presente al menos un resto (3) o (4) o en el compuesto; cada t es en forma independiente 0 o 1; cada r es en forma independiente 2, 3, o 7; cada s es en forma independiente 3, 5, o 6; cada v es en forma independiente 1, 2, o 6; cada R1 y R2 es en forma independiente -H, -O, alquilo C1-4, -halogeno, -OH, -C(O)alquilo C1-4, -O-arilo, -O-bencilo, -OC(O)alquilo C1-4, -alqueno C1-3, alquino C1-3, -C(O)alquilo C1-4, -NH2, -NH(alquilo C1-3), -N(alquil C1-3)2, -NH(C(O)alquilo C1-3), -N(C(O)alquil C1-3)2, -SH, -S(alquilo C1-3), -S(O)alquilo C1-3, -S(O)2alquilo C1-3; cada R3 es en forma independiente H, -alquilo C1-6 o -C(CH2OH)2; cada R5 es en forma independiente e, H o alquilo C1-10 de cadena lineal o ramificada que puede estar opcionalmente sustituido con OH, NH2, CO2R, CONH2, fenilo, C6H4OH, imidazol o arginina; cada e es en forma independiente H o cualquiera de las cadenas laterales de los aminoácidos naturales; cada R es en forma independiente -H, -alquilo C1-3, o alquilo C1-4 de cadena lineal o ramificada opcionalmente sustituido con OH, o halogeno; con las siguientes condiciones cuando cada uno de m, n, o, p, y q es 0, W1 y W2 son cada uno nulo, y Z es un resto (3) o (5) luego t debe ser 0; cuando cada uno de m, n, o, p, y q es 0, y W1 y W2 son cada uno nulo, luego Z no debe ser un resto (4). Reivindicacion 13: Una composicion farmacéutica caracterizada porque comprende un compuesto de formula 1, 1A, 1B, 1C o 2 y un vehículo farmacéuticamente aceptable. Reivindicacion 16: El método de la reivindicacion 15, caracterizado porque el trastorno metabolico es la diabetes tipo II, la enfermedad cardiovascular con resistencia a la insulina, la arritmia, la aterosclerosis, la enfermedad de la arteria coronaria, la hipertrigliceridemia, la dislipidemia, la retinopatía, la neuropatía, el edema macular, la nefropatía diabética, la nefropatía asociada a la lgA, la enfermedad renal cronica (CKD) y las enfermedades inflamatorias del rinon, que incluyen las complicaciones urémicas, la glomerulonefritis y la nefrosis.
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| US29339610P | 2010-01-08 | 2010-01-08 | |
| US29457810P | 2010-01-13 | 2010-01-13 |
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| ARP110100061A AR080357A1 (es) | 2010-01-08 | 2011-01-07 | Derivados de fumaratos de acidos grasos, composiciones farmaceuticas y sus usos |
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| CA3160676A1 (en) | 2019-11-12 | 2021-05-20 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of cardiovascular events in a subject with atrial fibrillation and/or atrial flutter |
| US11986452B2 (en) | 2021-04-21 | 2024-05-21 | Amarin Pharmaceuticals Ireland Limited | Methods of reducing the risk of heart failure |
| CA3249056A1 (en) * | 2022-01-19 | 2023-07-27 | Ian Hodgdon | SHORT CHAIN FATTY ACIDS FOR CANCER TREATMENT |
| CN114853628B (zh) * | 2022-05-07 | 2023-10-13 | 自然资源部第三海洋研究所 | 一种二十二碳六烯酰酯衍生物及其制备方法和应用 |
| CN114886892B (zh) * | 2022-05-07 | 2023-09-12 | 四川大学 | 氧化吲哚螺双环[2,2,1]庚烷类化合物在制备治疗胃癌药物中的应用 |
| WO2025242146A1 (zh) * | 2024-05-21 | 2025-11-27 | 中国科学院生物物理研究所 | 活性化合物在预防、延缓或治疗认知和/或运动功能障碍中的用途 |
Family Cites Families (10)
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|---|---|---|---|---|
| IL83775A (en) | 1987-09-04 | 1991-12-15 | Dexter Chemical Corp | Amino acid esters and amides of fumaric acid and pharmaceutical compositions containing them for use in the treatment of psoriasis |
| US5242905A (en) | 1987-09-04 | 1993-09-07 | Dexter Chemical Corporation | Pharmaceutical compositions for the treatment of psoriasis |
| JPH0987176A (ja) * | 1995-09-26 | 1997-03-31 | Shiseido Co Ltd | 糸球体腎炎抑制剤 |
| US5795909A (en) * | 1996-05-22 | 1998-08-18 | Neuromedica, Inc. | DHA-pharmaceutical agent conjugates of taxanes |
| US6090842A (en) * | 1998-03-10 | 2000-07-18 | The Regents Of The University Of California | Lipoic acid analogs |
| SE514226C2 (sv) | 1999-04-30 | 2001-01-22 | Uddeholm Tooling Ab | Kallarbetsverktyg av stål, dess användning och tillverkning |
| US6387945B2 (en) * | 2000-04-11 | 2002-05-14 | The Regents Of The University Of California | Lipoic acid analogs |
| GB0112324D0 (en) | 2001-05-21 | 2001-07-11 | Croda Int Plc | Compounds |
| EP2653873B8 (en) * | 2007-02-08 | 2022-08-24 | Biogen MA Inc. | Compositions and uses for treating Multiple Sclerosis |
| AU2011204277B2 (en) | 2010-01-08 | 2015-12-24 | Catabasis Pharmaceuticals, Inc. | Fatty Acid Fumarate Derivatives and their uses |
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2011
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- 2011-01-07 CA CA2786605A patent/CA2786605A1/en not_active Abandoned
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- 2011-01-07 WO PCT/US2011/020534 patent/WO2011085211A1/en not_active Ceased
- 2011-01-07 EP EP11732212.3A patent/EP2521447B1/en not_active Not-in-force
- 2011-01-07 BR BRBR112012016879-7A patent/BR112012016879A2/pt not_active IP Right Cessation
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- 2011-01-07 ES ES11732212.3T patent/ES2637266T3/es active Active
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