AR119698A2 - Compuesto amida n-urea sustituida derivado de aminoácido - Google Patents
Compuesto amida n-urea sustituida derivado de aminoácidoInfo
- Publication number
- AR119698A2 AR119698A2 ARP200100544A ARP200100544A AR119698A2 AR 119698 A2 AR119698 A2 AR 119698A2 AR P200100544 A ARP200100544 A AR P200100544A AR P200100544 A ARP200100544 A AR P200100544A AR 119698 A2 AR119698 A2 AR 119698A2
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- hydrogen
- aryl
- cycloalkyl
- Prior art date
Links
- -1 AMIDE COMPOUND Chemical class 0.000 title abstract 3
- 150000001413 amino acids Chemical class 0.000 title abstract 2
- 239000004202 carbamide Substances 0.000 title abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 16
- 229910052739 hydrogen Inorganic materials 0.000 abstract 14
- 239000001257 hydrogen Substances 0.000 abstract 14
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 11
- 150000002431 hydrogen Chemical group 0.000 abstract 10
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 150000003862 amino acid derivatives Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/417—Imidazole-alkylamines, e.g. histamine, phentolamine
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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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
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- 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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- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- 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
- A61K31/198—Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
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- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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- C07C323/39—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 at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
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- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
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- C07D233/64—Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- Indole Compounds (AREA)
Abstract
Compuestos amida N-urea sustituida derivados de aminoácidos representados por la fórmula (1). Reivindicación 1: Un compuesto amida N-urea sustituida derivado de aminoácido caracterizado porque está representado por la fórmula (1), sus enantiómeros, diastereoisómeros, tautómeros, hidratos, solvatos o sales farmacéuticamente aceptables del mismo, en donde: a es 1 y b es 0; a es 0 y b es 1; a es 1 y b es 1; R¹ es alquilo C₁₋₈ opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, heterociclo opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, arilo C₆₋₁₀ opcionalmente sustituido, cicloalquenilo C₃₋₈ opcionalmente sustituido, -NR¹¹R¹² o -OR¹³; R² es alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R³ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido, halógeno, -COOR¹⁵, -OR¹³, -NR¹¹R¹², NO₂, heterociclo opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, arilo C₆₋₁₀ opcionalmente sustituido o cicloalquenilo C₃₋₈ opcionalmente sustituido; R⁴ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido, halógeno, -COOR¹⁵, -OR¹³, -NR¹¹R¹², NO₂, heterociclo opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, arilo C₆₋₁₀ opcionalmente sustituido o cicloalquenilo C₃₋₈ opcionalmente sustituido; R⁵ es halógeno, -CF₃ o -S(O)ₙR¹⁴; n es 0, 1 ó 2; R⁶ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido, halógeno, -COOR¹⁵, -OR¹³, -NR¹¹R¹², NO₂, heterociclo opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, arilo C₆₋₁₀ opcionalmente sustituido o cicloalquenilo C₃₋₈ opcionalmente sustituido; R⁷ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido, halógeno, -COOR¹⁵, -OR¹³, -NR¹¹R¹², NO₂, heterociclo opcionalmente sustituido, cicloalquilo C₃₋₈ opcionalmente sustituido, arilo C₆₋₁₀ opcionalmente sustituido o cicloalquenilo C₃₋₈ opcionalmente sustituido; R⁸ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R⁹ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R¹⁰ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R⁹ᵃ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R¹⁰ᵃ es hidrógeno, alquilo C₁₋₈ opcionalmente sustituido o arilo C₆₋₁₀ opcionalmente sustituido; R¹¹ es hidrógeno o alquilo C₁₋₈ opcionalmente sustituido; R¹² es hidrógeno o alquilo C₁₋₈ opcionalmente sustituido; R¹³ es hidrógeno o alquilo C₁₋₈ opcionalmente sustituido; R¹⁴ es hidrógeno, CF₃ o alquilo C₁₋₈ opcionalmente sustituido; R¹⁵ es hidrógeno o alquilo C₁₋₈ opcionalmente sustituido; con la condición de que: a). cuando a = 1 y b = 0 entonces: R⁹ no es bencilo opcionalmente sustituido; y R¹¹ no es: un compuesto del grupo de fórmulas (2); y el compuesto de la fórmula (1) no es de las estructuras: del grupo de fórmulas (3); y b). cuando a = 0 y b = 1 entonces: R¹ es OR¹³; y el compuesto de la fórmula (1) no es de la estructura: de fórmula (4); y c). cuando a = 1 y b = 1 entonces: R¹¹ no es: un resto de fórmula (5).
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| US201161551772P | 2011-10-26 | 2011-10-26 |
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| ARP200100544A AR119698A2 (es) | 2011-10-26 | 2020-02-27 | Compuesto amida n-urea sustituida derivado de aminoácido |
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| ARP120104004A AR088535A1 (es) | 2011-10-26 | 2012-10-25 | Derivados de amidas de aminoacidos sustituidos con n-urea como moduladores de receptor formil peptido del receptor del tipo 1 (fprl-1) |
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2016
- 2016-04-26 US US15/138,823 patent/US9579307B2/en active Active
- 2016-07-29 JP JP2016150311A patent/JP6496689B2/ja active Active
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2017
- 2017-01-18 US US15/408,643 patent/US9974772B2/en active Active
- 2017-10-23 AU AU2017251683A patent/AU2017251683C1/en active Active
- 2017-12-25 IL IL256555A patent/IL256555B/en active IP Right Grant
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2018
- 2018-04-10 US US15/949,335 patent/US10172832B2/en active Active
- 2018-11-19 CY CY20181101220T patent/CY1121604T1/el unknown
- 2018-12-10 US US16/215,400 patent/US10993931B2/en active Active
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2019
- 2019-03-11 JP JP2019043998A patent/JP6804580B2/ja active Active
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- 2019-11-12 AU AU2019264555A patent/AU2019264555B2/en active Active
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2020
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2021
- 2021-04-13 US US17/229,347 patent/US20220202777A1/en not_active Abandoned
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2023
- 2023-09-29 US US18/478,718 patent/US20240285584A1/en active Pending
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