AR049583A2 - Compuesto derivado de pirazolo-pirimidina, composicion farmaceutica y el uso de dicho compuesto en la fabricacion de medicamentos - Google Patents
Compuesto derivado de pirazolo-pirimidina, composicion farmaceutica y el uso de dicho compuesto en la fabricacion de medicamentosInfo
- Publication number
- AR049583A2 AR049583A2 ARP050102868A ARP050102868A AR049583A2 AR 049583 A2 AR049583 A2 AR 049583A2 AR P050102868 A ARP050102868 A AR P050102868A AR P050102868 A ARP050102868 A AR P050102868A AR 049583 A2 AR049583 A2 AR 049583A2
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- haloalkyl
- optionally substituted
- case
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 8
- 239000003814 drug Substances 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 14
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 14
- 125000001475 halogen functional group Chemical group 0.000 abstract 11
- -1 2,3-dihydrobenzofuranyl Chemical group 0.000 abstract 10
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 10
- 125000001072 heteroaryl group Chemical group 0.000 abstract 10
- 125000003118 aryl group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 5
- 125000001624 naphthyl group Chemical group 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 4
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 4
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 abstract 4
- 125000002541 furyl group Chemical group 0.000 abstract 4
- 125000001544 thienyl group Chemical group 0.000 abstract 4
- 125000004306 triazinyl group Chemical group 0.000 abstract 4
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 abstract 3
- 125000004076 pyridyl group Chemical group 0.000 abstract 3
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 3
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 abstract 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 208000035475 disorder Diseases 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 abstract 1
- 208000017194 Affective disease Diseases 0.000 abstract 1
- 206010053164 Alcohol withdrawal syndrome Diseases 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 208000000103 Anorexia Nervosa Diseases 0.000 abstract 1
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- 206010013754 Drug withdrawal syndrome Diseases 0.000 abstract 1
- 208000030814 Eating disease Diseases 0.000 abstract 1
- 208000019454 Feeding and Eating disease Diseases 0.000 abstract 1
- 208000018522 Gastrointestinal disease Diseases 0.000 abstract 1
- 206010019233 Headaches Diseases 0.000 abstract 1
- 241000725303 Human immunodeficiency virus Species 0.000 abstract 1
- 208000013016 Hypoglycemia Diseases 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 208000019022 Mood disease Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 206010033799 Paralysis Diseases 0.000 abstract 1
- 208000006011 Stroke Diseases 0.000 abstract 1
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 abstract 1
- 208000025865 Ulcer Diseases 0.000 abstract 1
- 208000029650 alcohol withdrawal Diseases 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- 230000036506 anxiety Effects 0.000 abstract 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 210000004556 brain Anatomy 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- OGEBRHQLRGFBNV-RZDIXWSQSA-N chembl2036808 Chemical compound C12=NC(NCCCC)=NC=C2C(C=2C=CC(F)=CC=2)=NN1C[C@H]1CC[C@H](N)CC1 OGEBRHQLRGFBNV-RZDIXWSQSA-N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 235000014632 disordered eating Nutrition 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 206010013663 drug dependence Diseases 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 230000035558 fertility Effects 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 231100000869 headache Toxicity 0.000 abstract 1
- 230000002008 hemorrhagic effect Effects 0.000 abstract 1
- 230000002218 hypoglycaemic effect Effects 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 230000008629 immune suppression Effects 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 230000036512 infertility Effects 0.000 abstract 1
- 208000000509 infertility Diseases 0.000 abstract 1
- 231100000535 infertility Toxicity 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 208000014674 injury Diseases 0.000 abstract 1
- 208000002551 irritable bowel syndrome Diseases 0.000 abstract 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 208000028173 post-traumatic stress disease Diseases 0.000 abstract 1
- 230000000750 progressive effect Effects 0.000 abstract 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 208000011117 substance-related disease Diseases 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 abstract 1
- 230000008733 trauma Effects 0.000 abstract 1
- 231100000397 ulcer Toxicity 0.000 abstract 1
- 230000009385 viral infection Effects 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Coloring (AREA)
Abstract
Un compuesto derivado de pirazolo-pirimidina, que responde a las formulas (1) o (2), e isomeros del mismo, forma estereoisoméricas del mismo, o mezclas de formas estereoisoméricas del mismo, y sus sales aceptables para uso farmacéutico o sus formas de prodroga en donde: A es CR; Z es N o CR2; Ar se selecciona entre fenilo, naftilo, piridilo, pirimidinilo, triazinilo, furanilo, tienilo, benzotienilo, benzofuranilo, 2,3-dihidrobenzofuranilo, 2,3-dihidrobenzotienilo, indanilo, 1,2-benzopiranilo, 3,4-dihidro-1,2-benzopiranilo, tetralinilo, cada Ar está opcionalmente sustituido con entre 1 y 5 grupos R4 y cada Ar está unido a un átomo de C insaturado; R se selecciona en forma independiente en cada caso entre H, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, cicloalquilo C3-6, cicloalquilalquilo C4-7, halo, CN, haloalquilo C1-4; R1 se selecciona en forma independiente en cada caso entre H, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, halo, CN, haloalquilo C1-4, hidroxialquilo C1-12, alcoxialquilo C2-12, cianoalquilo C2-10, cicloalquilo C3-6, cicloalquilalquilo C4-10, NR9R10, alquil C1-4-NR9R10, NR9COR10, OR11, SH o S(O)nR12; R2 se selecciona entre H, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, cicloalquilo C3-6, cicloalquilalquilo C4-10, hidroxialquilo C1-4, halo, CN, -NR6R7, NR9COR10, haloalquilo C1-4, -OR7, SH o -S(O)nR12; R3 se selecciona entre -H, OR7, SH, S(O)nR13, COR7, CO2R7, OC(O)R13, NR8COR7, N(COR7)2, NR8CONR6R7, NR8CO2R13, NR6R7, NR6aR7a, N(OR7)R6, CONR6R7, arilo, heteroarilo y heterociclilo, o alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C5-8, cicloalquilalquilo C4-12 o cicloalquenilalquilo C6-10, cada uno opcionalmente sustituido con entre 1 y 3 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR13, COR15, CO2R15, OC(O)R13, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R13, NR16R15, CONR16R15, arilo, heteroarilo y heterociclilo; R4 se selecciona en forma independiente en cada caso entre: alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-6, cicloalquilalquilo C4-12, NO2, halo, CN, haloalquilo C1-4, NR6R7, NR8COR7, NR8CO2R7, COR7, OR7, CONR6R7, CO(NOR9)R7, CO2R7, o S(O)nR7, donde cada uno de tales alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-6 y cicloalquilalquilo C4-12 son opcionalmente sustituidos con entre 1 y 3 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-4, NO2, halo, CN, NR6R7, NR8COR7, NR8CO2R7, COR7, OR7, CONR6R7, CO2R7, CO(NOR9)R7, o S(O)nR7; R6 y R7, R6a y R7a se seleccionan en forma independiente en cada caso entre -H, alquilo C1-10, alquenilo C3-10, alquinilo C3-10, haloalquilo C1-10 con 1-10 halogenos, alcoxialquilo C2-8, cicloalquilo C3-6, cicloalquilalquilo C4-12, cicloalquenilo C5-10, o cicloalquenilalquilo C6-14, cada uno opcionalmente sustituido con entre 1 y 3 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR13, COR15, CO2R15, OC(O)R13, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R13, NR16R15, CONR16R15, arilo, heteroarilo o heterociclilo, -arilo, aril(alquilo C1-4), heteroarilo, heteroaril(alquilo C1-4), heterociclilo o heterociclil(alquilo C1-4), como alternativa, NR6R7 y NR6aR7a en forma independiente piperidina, pirrolidina, piperazina, N-metilpiperazina, morfolina o tiomorfolina, cada uno opcionalmente sustituido con 1-3 grupos alquilo C1-4; R8 se selecciona en forma independiente en cada caso entre H o alquilo C1-4; R9 y R10 se seleccionan en forma independiente en cada caso entre H, alquilo C1-4, o cicloalquilo C3-6; R11 se selecciona entre alquilo C1-4, haloalquilo C1-4, o cicloalquilo C3-6; R12 es alquilo C1-4 o haloalquilo C1-4; R13 se selecciona entre alquilo C1-4, haloalquilo C1-4, alcoxialquilo C2-8, cicloalquilo C3-6, cicloalquilalquilo C4-12, arilo, aril(alquil C1-4)-, heteroarilo o heteroaril(alquil C1-4)-; R14 se selecciona entre alquilo C1-10, alquenilo C3-10, alquinilo C3-10, cicloalquilo C3-8 o cicloalquilalquilo C4-12, cada uno opcionalmente sustituido con entre 1 y 3 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR15, COR15, CO2R15, OC(O)R15, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R15, NR16R15, CONR16R15, y alquiltio C1-6, alquilsulfinilo C1-6 y alquilsulfonilo C1-6; R15 y R16 se seleccionan en forma independiente en cada caso entre H, alquilo C1-6, cicloalquilo C3-10, cicloalquilalquilo C4-16, excepto que para S(O)nR15, R15 no puede ser H; arilo es fenilo o naftilo, cada uno opcionalmente sustituido con entre 1 y 5 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR15, COR15, CO2R15, OC(O)R15, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R15, NR16R15, y CONR16R15; heteroarilo es piridilo, pirimidinilo, triazinilo, furanilo, piranilo, quinolinilo, isoquinolinilo, tienilo, imidazolilo, tiazolilo, indolilo, pirrolilo, oxazolilo, benzofuranilo, benzotienilo, benzotiazolilo, isoxazolilo, pirazolilo, 2,3-dihidrobenzotienilo o 2,3-dihidrobenzofuranilo, cada uno opcionalmente sustituido con entre 1 y 5 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR15, -COR15, CO2R15, OC(O)R15, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R15, NR16R15, y CONR16R15; heterociclilo es heteroarilo saturado o parcialmente saturado, opcionalmente sustituido con entre 1 y 5 sustituyentes seleccionados en forma independiente en cada caso entre alquilo C1-6, cicloalquilo C3-6, halo, haloalquilo C1-4, ciano, OR15, SH, S(O)nR15, COR15, CO2R15, OC(O)R15, NR8COR15, N(COR15)2, NR8CONR16R15, NR8CO2R15, NR15R16, y CONR16R15; n es en forma independiente en cada caso 0, 1 o 2, a condicion de que: (A) cuando R es H, y Z es CR2, Ar no sea fenilo o fenilo sustituido; (B) cuando Z es CR2, entonces R2 no sea -NR6SO2R7 o -SO2NR6R7; (C) cuando R es H, Z es CR2, R1 es OR11, R2 es H, R3 es OR7, y R7 y R11 son ambos H, entonces Ar no sea piridilo o naftilo; (D) cuando R1 es -(alquilen C1-2)-O-(alquil C1-2) o -(alquilen C1-2)-OH, entonces que se cumpla al menos una de las siguientes condiciones (i), (ii) y (iii): (i) que el compuesto sea un compuesto de formula (2); (ii) que Ar se selecciona entre naftilo, triazinilo, furanilo, tienilo, benzotienilo, benzofuranilo, 2,3-dihidrobenzofuranilo, 2,3-dihidrobenzotienilo, indanilo, 1,2- benzopiranilo, 3,4-dihidro-1,2-benzopiranilo, y tetralinilo opcionalmente sustituido; (iii) que R3 se seleccione entre H, SH, S(O)nR13 en donde n = 1, CO2R7, OC(O)R13, NR8COR7, N(COR7)2, NR8CONR6R7, NR8CO2R13, N(OR7)R6, CONR6R7, arilo distinto de fenilo opcionalmente sustituido, heteroarilo distinto de (a) pirazinilo opcionalmente sustituido, (b) pirimidilo opcionalmente sustituido o (c) piradizinilo o heterociclilo opcionalmente sustituido; y (E) cuando R3 es cicloalquenilo C5-8 o cicloalquenilalquilo C6-10, entonces que se cumpla al menos una de las siguientes condiciones (i), (ii) y (iii): (i) que el compuesto sea un compuesto de formula (2); (ii) que Ar se seleccione entre naftilo, triazinilo, furanilo, tienilo, benzotienilo, benzofuranilo, 2,3-dihidrobenzofuranilo, 2,3-dihidrobenzotienilo, indanilo, 1,2-benzopiranilo, 3,4-dihidro-1,2-benzopiranilo, y tetralinilo opcionalmente sustituido; (iii) que R1 se selecciona entre alquenilo C2-4, alquinilo C2-4, CN, haloalquilo C1-4, hidroxialquilo C3-12, alcoxialquilo C4-12 distinto de -(alquilen C1-2)-O-(alquilo C1-2), cianoalquilo C2-10, cicloalquilo C3-6, cicloalquilalquilo C4-10, NR9R16, alquil C1-4-NR9R10, NR9COR16, OR11, SH o S(O)nR12. También se describen las composiciones farmacéuticas que comprenden dichos compuestos y el uso de los mismos en la fabricacion de medicamentos para el tratamiento de un trastorno afectivo, ansiedad, depresion, dolor de cabeza, síndrome de intestino irritable, trastorno de estrés post-traumático, parálisis supranuclear progresiva, supresion inmune, enfermedad de Alzheimer, enfermedades gastrointestinales, anorexia nervosa u otros trastornos de la alimentacion, drogadiccion, síndrome de abstinencia a las drogas o al alcohol, enfermedades inflamatorias, problemas de fertilidad, infecciones por el virus de inmunodeficiencia humana, estrés hemorrágico, obesidad, infertilidad, traumatismos cerebrales y de la espina dorsal, epilepsia, accidente cerebrovascular, ulceras, esclerosis lateral amiotrofica, hipoglucemia o un trastorno cuyo tratamiento pueda ser efectuado o facilitado antagonizando el CRF, incluyendo sin carácter limitativo los trastornos inducidos o facilitados por el CRF, en mamíferos.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2329096P | 1996-07-24 | 1996-07-24 | |
| US68604796A | 1996-07-24 | 1996-07-24 | |
| US08/899,242 US6124289A (en) | 1996-07-24 | 1997-07-23 | Azolo triazines and pyrimidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR049583A2 true AR049583A2 (es) | 2006-08-16 |
Family
ID=27362048
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050102868A AR049583A2 (es) | 1996-07-24 | 2005-07-11 | Compuesto derivado de pirazolo-pirimidina, composicion farmaceutica y el uso de dicho compuesto en la fabricacion de medicamentos |
Country Status (15)
| Country | Link |
|---|---|
| JP (2) | JP4704521B2 (es) |
| CN (3) | CN1104432C (es) |
| AR (1) | AR049583A2 (es) |
| BR (1) | BR9710544A (es) |
| CA (1) | CA2259583C (es) |
| CZ (1) | CZ299451B6 (es) |
| EA (1) | EA004403B1 (es) |
| EE (1) | EE04316B1 (es) |
| HR (1) | HRP970413A2 (es) |
| IL (4) | IL127871A0 (es) |
| NO (1) | NO315610B1 (es) |
| NZ (1) | NZ333777A (es) |
| PL (1) | PL195762B1 (es) |
| SI (1) | SI9720045B (es) |
| SK (1) | SK286461B6 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2282401T3 (es) * | 2001-03-13 | 2007-10-16 | Bristol-Myers Squibb Pharma Company | 4-(2-butilamino)-2,7-dimetil-8-(2-metil-6-metoxipirid-3-il) pirazolo - 1,5-a-1,3,5-triazina, sus enantiomeros y sales farmaceuticamente aceptables como ligandos del receptor del factor liberador de croticotropina. |
| WO2004110454A1 (ja) * | 2003-06-13 | 2004-12-23 | Ishihara Sangyo Kaisha, Ltd. | アデノシンA2a受容体アゴニストの投与が必要な疾患を治療又は予防するための組成物 |
| US7329662B2 (en) * | 2003-10-03 | 2008-02-12 | Hoffmann-La Roche Inc. | Pyrazolo-pyridine |
| GB0519957D0 (en) * | 2005-09-30 | 2005-11-09 | Sb Pharmco Inc | Chemical compound |
| EP2094709B1 (en) * | 2006-09-20 | 2010-09-15 | Eli Lilly And Company | Thiazole pyrazolopyrimidines as crf1 receptor antagonists |
| CN103694242B (zh) * | 2013-12-10 | 2016-01-06 | 昆明翔昊科技有限公司 | 吡唑并嘧啶类化合物及其药物组合物和其在制药中的应用 |
| US20210361664A1 (en) | 2017-08-14 | 2021-11-25 | Spruce Biosciences, Inc. | Corticotropin releasing factor receptor antagonists |
| CN112608316B (zh) * | 2019-07-30 | 2022-10-21 | 厦门宝太生物科技股份有限公司 | 一种吡唑并三嗪类腺苷受体拮抗剂 |
| MX2023001688A (es) | 2020-08-12 | 2023-02-22 | Spruce Biosciences Inc | Metodos y composiciones para tratar el sindrome de ovario poliquistico. |
| US11708372B2 (en) | 2021-11-19 | 2023-07-25 | Spruce Biosciences, Inc. | Crystalline composition of tildacerfont and methods of use and preparation thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3995039A (en) * | 1975-05-27 | 1976-11-30 | Merck & Co., Inc. | Pyrazolo [1,5-a] [1,3,5] triazines |
| JPS6157587A (ja) * | 1984-08-29 | 1986-03-24 | Shionogi & Co Ltd | 縮合複素環誘導体および抗潰瘍剤 |
| US4824834A (en) * | 1986-10-31 | 1989-04-25 | Otsuka Pharmaceutical Company, Limited | Pyrazolotriazine compounds |
| JP2691317B2 (ja) * | 1989-08-25 | 1997-12-17 | 株式会社大塚製薬工場 | 4―ヒドロキシ―8―(3―低級アルコキシ―4―フェニルスルフィニルフェニル)ピラゾロ〔1,5―a〕―1,3,5―トリアジン光学活性体の塩類及びその製造方法 |
| AU639615B2 (en) * | 1990-10-09 | 1993-07-29 | Otsuka Pharmaceutical Co., Ltd. | Pyrimidine derivative, production thereof, and androgen inhibitor |
| ES2126573T3 (es) * | 1991-04-22 | 1999-04-01 | Otsuka Pharma Co Ltd | Derivado de pirazol (1,5-a)pirimidina y agente antiinflamatorio que contiene este derivado. |
| US5356897A (en) * | 1991-09-09 | 1994-10-18 | Fujisawa Pharmaceutical Co., Ltd. | 3-(heteroaryl)-pyrazololi[1,5-a]pyrimidines |
-
1997
- 1997-07-23 EE EEP199900019A patent/EE04316B1/xx unknown
- 1997-07-23 PL PL97331523A patent/PL195762B1/pl unknown
- 1997-07-23 EA EA199900158A patent/EA004403B1/ru not_active IP Right Cessation
- 1997-07-23 CA CA002259583A patent/CA2259583C/en not_active Expired - Lifetime
- 1997-07-23 BR BR9710544A patent/BR9710544A/pt not_active IP Right Cessation
- 1997-07-23 JP JP50723398A patent/JP4704521B2/ja not_active Expired - Fee Related
- 1997-07-23 SK SK97-99A patent/SK286461B6/sk not_active IP Right Cessation
- 1997-07-23 IL IL12787197A patent/IL127871A0/xx unknown
- 1997-07-23 CN CN97196525A patent/CN1104432C/zh not_active Expired - Lifetime
- 1997-07-23 SI SI9720045A patent/SI9720045B/sl active Search and Examination
- 1997-07-23 CZ CZ0018499A patent/CZ299451B6/cs not_active IP Right Cessation
- 1997-07-23 NZ NZ333777A patent/NZ333777A/en not_active IP Right Cessation
- 1997-07-24 HR HRP970413 patent/HRP970413A2/hr not_active Application Discontinuation
-
1998
- 1998-12-30 IL IL127871A patent/IL127871A/en not_active IP Right Cessation
-
1999
- 1999-01-21 NO NO19990264A patent/NO315610B1/no not_active IP Right Cessation
-
2001
- 2001-05-30 CN CN 01120849 patent/CN1250223C/zh not_active Expired - Lifetime
-
2002
- 2002-04-25 CN CN 02118589 patent/CN1388126A/zh active Pending
- 2002-06-11 IL IL150163A patent/IL150163A/en not_active IP Right Cessation
-
2004
- 2004-07-23 JP JP2004216483A patent/JP4194539B2/ja not_active Expired - Fee Related
- 2004-10-12 IL IL164513A patent/IL164513A/en not_active IP Right Cessation
-
2005
- 2005-07-11 AR ARP050102868A patent/AR049583A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002513382A (ja) | 2002-05-08 |
| IL164513A (en) | 2010-04-29 |
| IL127871A (en) | 2010-04-29 |
| CN1327793A (zh) | 2001-12-26 |
| IL127871A0 (en) | 1999-10-28 |
| PL195762B1 (pl) | 2007-10-31 |
| NZ333777A (en) | 2000-07-28 |
| JP4194539B2 (ja) | 2008-12-10 |
| EE04316B1 (et) | 2004-06-15 |
| SK9799A3 (sk) | 2005-04-01 |
| IL164513A0 (en) | 2005-12-18 |
| CZ18499A3 (cs) | 1999-11-17 |
| SI9720045A (sl) | 1999-10-31 |
| NO315610B3 (no) | 2003-09-29 |
| PL331523A1 (en) | 1999-07-19 |
| EA004403B1 (ru) | 2004-04-29 |
| SK286461B6 (sk) | 2008-10-07 |
| CN1225637A (zh) | 1999-08-11 |
| NO315610B1 (no) | 2003-09-29 |
| CA2259583C (en) | 2009-11-17 |
| IL150163A (en) | 2010-12-30 |
| CZ299451B6 (cs) | 2008-07-30 |
| CN1104432C (zh) | 2003-04-02 |
| CA2259583A1 (en) | 1998-01-29 |
| NO990264D0 (no) | 1999-01-21 |
| HRP970413A2 (en) | 1998-10-31 |
| BR9710544A (pt) | 1999-08-17 |
| JP4704521B2 (ja) | 2011-06-15 |
| NO990264L (no) | 1999-03-10 |
| CN1388126A (zh) | 2003-01-01 |
| EE9900019A (et) | 1999-08-16 |
| SI9720045B (sl) | 2008-02-29 |
| CN1250223C (zh) | 2006-04-12 |
| EA199900158A1 (ru) | 1999-10-28 |
| JP2005097257A (ja) | 2005-04-14 |
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| FA | Abandonment or withdrawal |