AR099029A1 - MODULADORES DE PIRROLIDINILSULFONA RORg - Google Patents
MODULADORES DE PIRROLIDINILSULFONA RORgInfo
- Publication number
- AR099029A1 AR099029A1 ARP150100016A ARP150100016A AR099029A1 AR 099029 A1 AR099029 A1 AR 099029A1 AR P150100016 A ARP150100016 A AR P150100016A AR P150100016 A ARP150100016 A AR P150100016A AR 099029 A1 AR099029 A1 AR 099029A1
- Authority
- AR
- Argentina
- Prior art keywords
- cr2er2f
- substituted
- alkyl
- nr11r11
- occurrence
- Prior art date
Links
- 101100091494 Mus musculus Rorc gene Proteins 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 22
- 125000005842 heteroatom Chemical group 0.000 abstract 16
- 229910052739 hydrogen Inorganic materials 0.000 abstract 16
- 239000001257 hydrogen Substances 0.000 abstract 16
- 229910052760 oxygen Inorganic materials 0.000 abstract 16
- 229910052717 sulfur Inorganic materials 0.000 abstract 16
- 125000000623 heterocyclic group Chemical group 0.000 abstract 15
- 125000004432 carbon atom Chemical group C* 0.000 abstract 14
- 125000005843 halogen group Chemical group 0.000 abstract 9
- 150000002431 hydrogen Chemical class 0.000 abstract 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 abstract 2
- 108010081348 HRT1 protein Hairy Proteins 0.000 abstract 2
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 abstract 2
- -1 OCF2 Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/12—Oxygen or sulfur atoms
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- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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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- Pyridine Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1), o uno de sus estereoisómeros sales farmacéuticamente aceptables, en donde: R¹ se selecciona de H, halo, alquilo C₁₋₆ sustituido con 0 - 3 R¹ᵃ y -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 R¹ᵃ; R¹ᵃ es, de modo independiente en cada aparición, hidrógeno, =O, halo, CF₃, OCF₃, CN, NO₂, -(CR²ᵉR²ᶠ)ʳ-ORᵇ, -(CR²ᵉR²ᶠ)ʳ-S(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)ʳ-OC(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)Rᶜ, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, alquenilo C₂₋₆ sustituido con 0 - 3 Rᵃ, alquinilo C₂₋₆ sustituido con 0 - 3 Rᵃ, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; R² se selecciona de hidrógeno, -(CR²ᵉR²ᶠ)ʳ-C(O)R²ᵈ, -(CR²ᵉR²ᶠ)ʳ-C(O)OR²ᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-S(O)₂R²ᶜ, alquilo C₁₋₆ sustituido con 0 - 3 R²ᵃ, alquenilo C₂₋₆ sustituido con 0 - 3 R²ᵃ, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 10 miembros sustituido con 0 - 3 Rᵃ y -(CR²ᵉR²ᶠ)ʳ-heterociclo de 4 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; R²ᵃ es, de modo independiente en cada aparición, hidrógeno, =O, halo, OCF₃, CN, NO₂, -(CR²ᵉR²ᶠ)ʳ-ORᵇ, -(CR²ᵉR²ᶠ)ʳ-S(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)ʳ-OC(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)Rᶜ, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, alquenilo C₂₋₆ sustituido con 0 - 3 Rᵃ, alquinilo C₂₋₆ sustituido con 0 - 3 Rᵃ, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 4 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; R²ᵇ es, de modo independiente en cada aparición, hidrógeno, CF₃, -(CR²ᵉR²ᶠ)qORᵇ, -(CR²ᵉR²ᶠ)qS(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)R¹ᵈ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)qOC(O)Rᵇ, -(CR²ᵉR²ᶠ)qNR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)qNRᵇC(O)R¹ᶜ, -(CR²ᵉR²ᶠ)qNRᵇC(O)ORᶜ, -(CR²ᵉR²ᶠ)qNRᵇC(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)qS(O)₂NR¹¹R¹¹, -(CR²ᵉR²ᶠ)qNRᵇS(O)₂Rᶜ, alquilo C₁₋₆ sustituido con 0 - 2 Rᵃ, haloalquilo C₁₋₆, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 2 Rᵃ; R²ᶜ es, de modo independiente en cada aparición, hidrógeno, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, alquenilo C₂₋₆ sustituido con 0 - 3 Rᵃ, cicloalquilo C₃₋₁₀ sustituido con 0 - 3 Rᵃ, arilo C₆₋₁₀ sustituido con 0 - 3 Rᵃ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 10 miembros que contiene 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ, sustituido con 0 - 3 Rᵃ; R²ᵈ es, de modo independiente en cada aparición, hidrógeno, alquilo C₁₋₆ sustituido con 0 - 2 Rᵈ, haloalquilo C₁₋₆, C₍O₎NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-cicloalquilo C₃₋₁₀ sustituido con 0 - 3 Rᵈ, -(CR²ᵉR²ᶠ)ʳ-fenilo sustituido con 0 - 2 Rᵃ o un -(CR²ᵉR²ᶠ)ʳ-heterociclo de 4 - 10 miembros donde el heterociclo puede ser fusionado, en puente o espirocíclico, que contiene 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ, sustituido con 0 - 3 Rᵃ; R²ᵉ y R²ᶠ son, de modo independiente en cada aparición, hidrógeno, halógeno o alquilo C₁₋₆; R³ se selecciona de hidrógeno, halo, N₃, CN, -(CR²ᵉR²ᶠ)ʳ-OR³ᵇ, -(CR²ᵉR²ᶠ)ʳ-NR¹¹R¹¹, alquilo C₁₋₆ sustituido con 0 - 3 R³ᵃ, cicloalquilo C₃₋₁₀ sustituido con 0 - 3 R³ᵃ; y fenilo sustituido con 0 - 3 R³ᵃ o heterociclo de 4 - 10 miembros que contiene 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ, sustituido con 0 - 3 R³ᵃ o dos R³ ubicados en átomos de carbono adyacentes ligados para formar un carbociclo de 5 - 7 miembros o un heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ, ambos opcionalmente sustituidos con 0 - 3 R³ᵃ; R³ᵃ es, de modo independiente en cada aparición, hidrógeno, =O, halo, OCF₃, OCF₂, CF₃, CHF₂, CN, NO₂, -(CR²ᵉR²ᶠ)ʳ-ORᵇ, -(CR²ᵉR²ᶠ)ʳ-S(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)ʳ-OC(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)Rᶜ, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᵃ, alquenilo C₂₋₆, sustituido con 0 - 3 Rᵃ, alquinilo C₂₋₆ sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 10 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; R³ᵇ es, de modo independiente en cada aparición, hidrógeno, CF₃, -(CR²ᵉR²ᶠ)qORᵇ, -(CR²ᵉR²ᶠ)qS(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)R¹ᵈ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)qOC(O)Rᵇ, -(CR²ᵉR²ᶠ)qNR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)qNRᵇC(O)R¹ᶜ, -(CR²ᵉR²ᶠ)qNRᵇC(O)ORᶜ, -(CR²ᵉR²ᶠ)qNRᵇC(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)qS(O)₂NR¹¹R¹¹, (CR²ᵉR²ᶠ)qNRᵇS(O)₂Rᶜ, alquilo C₁₋₆, sustituido con 0 - 3 Rᵃ, haloalquilo C₁₋₆, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros sustituido con 0 - 3 Rᵃ o-(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵃ; R¹¹ es, de modo independiente en cada aparición, hidrógeno, alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, CF₃, cicloalquilo C₃₋₁₀ sustituido con 0 - 3 Rᶠ, -(CR²ᵉR²ᶠ)ʳ-fenilo sustituido con 0 - 3 Rᵈ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵈ; o un R¹¹ y un segundo R¹¹, ambos unidos al mismo átomo de nitrógeno, se combinan para formar un heterociclo que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᵈ; Rᵃ es, de modo independiente en cada aparición, hidrógeno, =O, halo, OCF₃, CF₃, CHF₂, CN, NO₂, -(CR²ᵉR²ᶠ)ʳ-ORᵇ, -(CR²ᵉR²ᶠ)ʳ-S(O)ₚRᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-C(O)ORᵇ, -(CR²ᵉR²ᶠ)ʳ-OC(O)Rᵇ, -(CR²ᵉR²ᶠ)ʳ-NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-C(O)NR¹¹R¹¹, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)Rᶜ, -(CR²ᵉR²ᶠ)ʳ-NRᵇC(O)ORᶜ, -NRᵇC(O)NR¹¹R¹¹, -S(O)ₚNR¹¹R¹¹, -NRᵇS(O)ₚRᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, haloalquilo C₁₋₆, alquenilo C₂₋₆, sustituido con 0 - 3 Rᵃ, alquinilo C₂₋₆ sustituido con 0 - 3 Rᵃ, -(CR²ᵉR²ᶠ)ʳ-carbociclo de 3 - 14 miembros o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᶠ; Rᵇ es, de modo independiente en cada aparición, hidrógeno, alquilo C₁₋₆ sustituido con 0 - 3 Rᵈ, haloalquilo C₁₋₆, cicloalquilo C₃₋₆,sustituido con 0 - 3 Rᵈ, -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᶠ o -(CR²ᵉR²ᶠ)ʳ-carbociclo de 6 - 10 miembros sustituido con 0 - 3 Rᵈ; Rᶜ es, de modo independiente en cada aparición, alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, -(CR²ᵉR²ᶠ)ʳ-cicloalquilo C₃₋₆ sustituido con 0 - 3 Rᶠ o -(CR²ᵉR²ᶠ)ʳ-fenilo sustituido con 0 - 3 Rᶠ; Rᵈ es, de modo independiente en cada aparición, hidrógeno, =O, halo, OCF₃ CF₃, CN, NO₂, -ORᵉ, -(CR²ᵉR²ᶠ)ʳ-C(O)Rᶜ, -NRᵉRᵉ, -NRᵉC(O)ORᶜ, C(O)NRᵉRᵉ, -NRᵉC(O)Rᶜ, CO₂Rᶜ, -NRᵉSO₂Rᶜ, SO₂Rᶜ, alquilo C₁₋₆ sustituido con 0 - 3 Rᶠ, cicloalquilo C₃₋₆ sustituido con 0 - 3 Rᶠ, -(CR²ᵉR²ᶠ)ʳ-fenilo sustituido con 0 - 3 Rᶠ o -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 7 miembros que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ sustituido con 0 - 3 Rᶠ; Rᵉ está seleccionado, de modo independiente en cada aparición, de hidrógeno, C(O)NRᶠRᶠ, alquilo C₁₋₆, cicloalquilo C₃₋₆ o -(CR²ᵉR²ᶠ)ʳ-fenilo sustituido con 0 - 3 Rᶠ; Rᶠ es, de modo independiente en cada aparición, hidrógeno, =O, halo, CN, NH₂, NH(alquilo C₁₋₆), N(alquilo C₁₋₆)₂, SO₂(alquilo C₁₋₆), CO₂H, CO₂(alquilo C₁₋₆), OH, cicloalquilo C₃₋₆, CF₃ u O(alquilo C₁₋₆); o Rᶠ es, de modo independiente en cada aparición, un -(CR²ᵉR²ᶠ)ʳ-heterociclo de 5 - 10 miembros opcionalmente sustituido que comprende átomos de carbono y 1 - 4 heteroátomos seleccionados de N, O y S(O)ₚ, fenilo o cicloalquilo C₃₋₆, cada grupo opcionalmente sustituido con halo, CN, CF₃, alquilo C₁₋₆ u O(alquilo C₁₋₆); m y n se seleccionan, de modo independiente, de 0, 1, 2 y 3; p y q, independientemente de cada aparición, son 0, 1 ó 2; y r es 0, 1, 2, 3 ó 4.
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| CN105705501B (zh) | 2013-09-09 | 2019-04-19 | 百时美施贵宝公司 | RORγ调节剂 |
| JP6397488B2 (ja) | 2013-09-20 | 2018-09-26 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | RORγ調節因子 |
| JP6476205B2 (ja) | 2014-01-06 | 2019-02-27 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | RORγ修飾因子としてのヘテロ環式スルホン |
| CN106132931B (zh) | 2014-01-06 | 2019-08-02 | 百时美施贵宝公司 | 碳环砜RORγ调节剂 |
| CN106061947B (zh) | 2014-01-06 | 2019-12-03 | 百时美施贵宝公司 | 环己基砜RORγ调节剂 |
| SI3212641T1 (sl) | 2014-10-30 | 2019-02-28 | Janssen Pharmaceutica Nv | Tiazoli kot modulatorji RORyt |
| JOP20200117A1 (ar) | 2014-10-30 | 2017-06-16 | Janssen Pharmaceutica Nv | كحولات ثلاثي فلوروميثيل كمُعدلات للمستقبل النووي جاما تي المرتبط بحمض الريتيونَويك ROR?t |
| US9845319B2 (en) | 2014-10-30 | 2017-12-19 | Janssen Pharmaceutiuca NV | Amide substituted thiazoles as modulators of RORyt |
| PE20180119A1 (es) | 2015-05-07 | 2018-01-18 | Bristol Myers Squibb Co | Sulfonas triciclicas como moduladores del receptor huerfano relacionado con retinoide gamma (rorgamma) |
| US10610520B2 (en) | 2016-03-31 | 2020-04-07 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| TW201803869A (zh) | 2016-04-27 | 2018-02-01 | 健生藥品公司 | 作為RORγT調節劑之6-胺基吡啶-3-基噻唑 |
| EP3523279A1 (en) * | 2016-10-10 | 2019-08-14 | Bristol-Myers Squibb Company | Tricyclic sulfones as ror gamma modulators |
| WO2018071620A1 (en) * | 2016-10-13 | 2018-04-19 | Bristol-Myers Squibb Company | Heterocyclic sulfones as ror gamma modulators |
| AU2017356911A1 (en) * | 2016-11-09 | 2019-06-20 | Bristol-Myers Squibb Company | Tricyclic sulfones as ROR gamma modulators |
| EP3538522A1 (en) * | 2016-11-10 | 2019-09-18 | Bristol-Myers Squibb Company | Ror gamma modulators |
| CA3103770A1 (en) | 2018-06-18 | 2019-12-26 | Janssen Pharmaceutica Nv | Phenyl and pyridinyl substituted imidazoles as modulators of roryt |
| JP2021528405A (ja) | 2018-06-18 | 2021-10-21 | ヤンセン ファーマシューティカ エヌ.ベー. | RORγtのモジュレータとしてのアミド置換チアゾール |
| US11034658B2 (en) | 2018-06-18 | 2021-06-15 | Janssen Pharmaceutica Nv | Pyridinyl pyrazoles as modulators of RORγT |
| US10975057B2 (en) | 2018-06-18 | 2021-04-13 | Janssen Pharmaceutica Nv | 6-aminopyridin-3-yl pyrazoles as modulators of RORgT |
| US11034669B2 (en) | 2018-11-30 | 2021-06-15 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| US12012374B2 (en) | 2019-05-13 | 2024-06-18 | Bristol-Myers Squibb Company | Agonists of ROR GAMMAt |
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| GB0108591D0 (en) * | 2001-04-05 | 2001-05-23 | Merck Sharp & Dohme | Therapeutic agents |
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| US20130190356A1 (en) * | 2011-12-22 | 2013-07-25 | Genentech, Inc. | Benzyl sulfonamide derivatives as rorc modulators |
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| CN106132931B (zh) | 2014-01-06 | 2019-08-02 | 百时美施贵宝公司 | 碳环砜RORγ调节剂 |
| JP6476205B2 (ja) | 2014-01-06 | 2019-02-27 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | RORγ修飾因子としてのヘテロ環式スルホン |
| CN106061947B (zh) | 2014-01-06 | 2019-12-03 | 百时美施贵宝公司 | 环己基砜RORγ调节剂 |
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2015
- 2015-01-05 ES ES15700613.1T patent/ES2669208T3/es active Active
- 2015-01-05 EP EP15700613.1A patent/EP3092229B1/en not_active Not-in-force
- 2015-01-05 TW TW104100097A patent/TW201609634A/zh unknown
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- 2015-01-05 JP JP2016562465A patent/JP6530764B2/ja not_active Expired - Fee Related
- 2015-01-05 MX MX2016008845A patent/MX369347B/es active IP Right Grant
- 2015-01-05 US US15/109,719 patent/US20160326108A1/en not_active Abandoned
- 2015-01-05 CA CA2936116A patent/CA2936116A1/en not_active Abandoned
- 2015-01-05 WO PCT/US2015/010089 patent/WO2015103509A1/en not_active Ceased
- 2015-01-05 CN CN201580011338.XA patent/CN106061971B/zh not_active Expired - Fee Related
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| US9458171B2 (en) | 2016-10-04 |
| ES2669208T3 (es) | 2018-05-24 |
| CA2936116A1 (en) | 2015-07-09 |
| US20160326108A1 (en) | 2016-11-10 |
| MX369347B (es) | 2019-11-06 |
| EP3092229A1 (en) | 2016-11-16 |
| CN106061971A (zh) | 2016-10-26 |
| US20150191483A1 (en) | 2015-07-09 |
| EP3092229B1 (en) | 2018-03-28 |
| MX2016008845A (es) | 2016-09-07 |
| EA030849B1 (ru) | 2018-10-31 |
| WO2015103509A1 (en) | 2015-07-09 |
| CN106061971B (zh) | 2019-03-12 |
| JP6530764B2 (ja) | 2019-06-12 |
| EA201691368A1 (ru) | 2016-10-31 |
| JP2017501236A (ja) | 2017-01-12 |
| TW201609634A (zh) | 2016-03-16 |
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