AR053451A1 - Antagonistas del receptor de proquineticina 1 - Google Patents

Antagonistas del receptor de proquineticina 1

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Publication number
AR053451A1
AR053451A1 ARP060101155A ARP060101155A AR053451A1 AR 053451 A1 AR053451 A1 AR 053451A1 AR P060101155 A ARP060101155 A AR P060101155A AR P060101155 A ARP060101155 A AR P060101155A AR 053451 A1 AR053451 A1 AR 053451A1
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Argentina
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alkyl
phenyl
proviso
alkoxy
optionally substituted
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ARP060101155A
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English (en)
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Janssen Pharmaceutica Nv
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Publication of AR053451A1 publication Critical patent/AR053451A1/es

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12—Antidiarrhoeals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/20—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with no nitrogen atoms directly attached to a ring carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/30—Only oxygen atoms
    • C07D251/34—Cyanuric or isocyanuric esters
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/38—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40—Nitrogen atoms
    • C07D251/42—One nitrogen atom
    • C07D251/46—One nitrogen atom with oxygen or sulfur atoms attached to the two other ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Reivindicacion 1: Un compuesto de formula (1) donde A1 es H, arilo, heteroarilo, cicloalquilo C5-8, o heterociclilo, con la condicion de que A1 sea diferente de piridin-4-ilo, N-t-butoxicarbonil-piperidin-4-ilo, o N-metil-piperidin-3-ilo; y donde los sustituyentes de A1 diferentes de H están opcionalmente sustituidos con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6, halogeno, nitro, alquilo C1-6 halogenado, alcoxi C1-6 halogenado, alquiltio C1-6, alcoxi C1-6carbonilo, amino, alquilamino C1-6, di(alquil C1-6)amino, ciano, hidroxi, aminocarbonilo, alquilamino, C1-6 carbonilo, di(alquil C1-6)aminocarbonilo, alcoxi C1-6carbonilamino, alquil C1-6carbonilo, alquiltio C1-6carbonilo, formilo, alquilsulfonilo C1-6, alquilsulfonilamino C1-6, aminosulfonilo, alquilaminosulfonilo C1-6, y di(alquil C1-6)aminosulfonilo; L1 es -(CH2)r- o -CH2CH2X(CH2)s-, opcionalmente sustituido con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-6, alquenilo C2-6, alquinilo C2-6, y halogeno; con la condicion de que cuando A1 es H, r es mayor o igual a 4; r es un numero entero de 1 a 5; s es un numero entero de 1 a 3; X es O o S; D es -P-A2, donde cuando A2 es H, P es -(CH2)4-6-, y cuando A2 es diferente de H, P es -(CH2)1-2- o -CH2CH=CH-; A2 es H, benzodioxalilo, heteroarilo diferente de piridin-2-ilo no sustituido, cicloalquilo C3-8, o fenilo opcionalmente sustituido en las posiciones meta y para con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-6, alcoxi C1-6, halogeno, alquiloC1-6 halogenado, alcoxi C1-6 halogenado, arilalcoxi C1-6, fenilo, alquiltio C1-6, alcoxi C1-6carbonilo, amino, alquilamino C1-6, di(alquil C1-6)amino, ciano, hidroxi, nitro, alquil C1-6carbonilo, alquiltio C1-6carbonilo, aminocarbonilo, alquilamino C1-6carbonilo, di(alquil C1-6)aminocarbonilo, alquil C1-6carbonilamino, y un cicloalquiloxi C3-6 no fusionado, donde benzodioxalilo, heteroarilo, y cicloalquilo C3-8 están opcionalmente sustituidos con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-6, alcoxi C1-6, halogeno, alquilo C1-6 halogenado, alcoxi C1-6 halogenado, arilalcoxi C1-6, fenilo, alquiltio C1-6, alcoxi C1-6carbonilo, amino, alquilamino C1-6, di(alquil C1-6)amino, ciano, hidroxi, nitro, alquil C1-6carbonilo, alquiltio C1-6carbonilo, aminocarbonilo, alquilaminoC1-6carbonilo, di(alquil C1-6)aminocarbonilo, alquil C1-6carbonilamino y un cicloalquiloxi C3-6 no fusionado; con la condicion de que no más de dos sustituyentes de A2 sean arilalcoxi C1-6, fenilo o un cicloalquiloxi C3-6 no fusionado; con la condicion de que cuando A1 es fenilo no sustituido y L2 es -X1- CH(Rx)-(CRyRz)-, donde X1 es NH, y Rx, Ry y Rz son H, A2 sea diferente de fenilo no sustituido; fenilo sustituido con arilalcoxi C1-6 o fenilo; o fenilo sustituido en la posicion meta con ciano; y, además con al condicion de que cuando A1 es fenilo no sustituido y L2 es - X1-CH(Rx)-(CRyRz)2-, donde X1 es NH y Rx, Ry y Rz son cada uno H, A2 sea diferente de fenilo sustituido con metoxi; y con la condicion de que cuando A1 es 3,4-dicloro-fenilo y P es -CH2-, A2 sea diferente de fenilo sustituido en la posicion meta con trifluorometilo o trifluorometoxi; y además con la condicion de que cuando A1 es 3,4-dicloro-fenilo y P es -(CH2)2-, A2 sea diferente de 4-metoxi-fenilo; W es N o C(Rw); donde Rw es H o alquilo C1-2; L2 es un radical bivalente seleccionado del grupo que consiste en: pirrolidinilo o piperidinilo unido al anillo de triazina de formula (1) por medio de su átomo de N, donde dicho pirrolidinilo o piperidinilo está sustituido con un átomo de C con -(CH2)0-2-; NH-cicloalquilo C5-7-(CH2)0-2-, con la condicion de que cuando cicloalquilo C5-7 es ciclohexilo, Q está unido a la posicion 2- cis-4- en relacion con la posicion de -NH-; X1-alquilo C2- 6; X1-(CH2)u-X2-(CH2)v-; donde u es un numero entero de 1 a 3; y donde v es un numero entero de 1 a 4; con la condicion de que cuando X1 es un enlace directo y W es C(Rw), entonces u es 1 y v es 2 a 4; X2-(CH2)0-4; X1-(CH2)2-3-X3-(CH2)2-3-;NH(CH2)1- 4C(=O)-, con la condicion de que al menos uno de Rb, Rc, o Rd es diferente de H y m es 0; NHC(=O)-(CH2)1-4-; C(=O)NH(CRyRz)2-5; y X1-CH(Rx)-(CRyRz)1-5-; de manera tal que cuando X1 es un enlace directo y W es C(Rw), entonces Rx es H; donde X1 es -NH- , O, S, o un enlace directo, de manera tal que X1 es diferente de O cuando W es N; X2 es -CH=CH-; X3 es O, S, NH, o C=O; Rx, Ry y Rz son independientemente H o alquilo C1-4; y con la condicion de que L2 en ningun caso exceda de 7 átomos de longitud; y además con la condicion de que cando L2 es -X2-(CH2) 0-4- o -C(=O)NH(CRyRz)2-5-, entonces Rw es H; es -(O)mN(Ra)-G; y m es 0 o1; G es-C(=NRb)NRcRd; Ra y Rd son independientemente H, alquilo C1-6, alquenilo C1-6 o alquinilo C3-6, donde los sustituyentes de Ra y Rd diferentes de H están opcionalmente sustituidos con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en hidroxi, alcoxi C1-4, fluoro, amino, alquilamino C1-4, dialquilamino C1-4 y alquil C1- 4carbonilo; Ra y Rc se toman junto con los átomos a los cuales están unidos para formar un anillo monocíclico de 5-8 miembros opcionalmente sustituido con oxo; Rb es H, alquilo C1-6, alquenilo C2-6, alquinilo C3-6, alcoxi C3-6carbonilo, o ciano; o Rb y Rc se toman junto con los átomos a los cuales están unidos para formar un anillo monocíclico de 5-8 miembros, opcionalmente sustituido con oxo; Rc es H, alquilo C1-10, alquenilo C2-10, alquinilo C3-10, cicloalquilo C3-7, adamantilo, amino, alquilamino C1-6, di(alquil C1-6)amino, alquil C1-6carbonilo, alcoxi C1-6carbonilo, arilcarbonilo, heteroarilcarbonilo, heterociclilcarbonilo, arilo, heteroarilo o heterociclilo; donde alquilo C1-10, alquenilo C2-10, y alquinilo C2-10 están opcionalmente sustituidos con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en hidroxi, alcoxi C1-6, trifluorometilo, arilo, heteroarilo y heterociclilo; y donde cualquier sustituyente de Rc que contiene arilo o heteroarilo está opcionalmente sustituido con uno a tres sustituyentes seleccionados independientemente del grupo que consiste en alquilo C1-6, alcoxi C1-6, halogeno, alquilo C1-6 fluorado, alcoxi C1-6 fluorado, alquil 1-6carbonilo, alcoxi C1- 6carbonilo, aminocarbonilo, alquilamino C1-6carbonilo, di(alquil C1-6)aminocarbonilo, alcoxi C1-6carbonilamino, formilo, alquilsulfonilo C1-6, alquilsulfonilamino C1-6, aminosulfonilo, alquilaminosulfonilo C1-6, y di(alquil C1-6)aminosulfonilo, nitro, metiltio, hidroxi y ciano; o Rc y Rd se toman con los átomos a los cuales están unidos para formar un anillo monocíclico de 5-8 miembros que opcionalmente incluye 1 a 2 heteroátomos O o S en el anillo y dicho anillo está opcionalmente sustituido con oxo; con la condicion de que en cualquier caso, solo exista un anillo opcionalmente entre Ra y Rb, Rb y Rc, o Rc y Rd; y enantiomeros, diastereomeros, tautomeros, solvatos, y sus sales aceptables para uso farmacéutico.
ARP060101155A 2005-03-24 2006-03-23 Antagonistas del receptor de proquineticina 1 AR053451A1 (es)

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US (2) US7968710B2 (es)
EP (1) EP1866290B1 (es)
JP (1) JP2008534500A (es)
KR (1) KR20080006564A (es)
CN (2) CN101326168A (es)
AR (1) AR053451A1 (es)
AU (1) AU2006229793A1 (es)
BR (1) BRPI0609315A2 (es)
CA (1) CA2602576A1 (es)
MX (1) MX2007011848A (es)
MY (1) MY153719A (es)
TW (1) TW200720260A (es)
WO (1) WO2006104715A1 (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101326168A (zh) * 2005-03-24 2008-12-17 詹森药业有限公司 激肽原1受体拮抗剂
EP1959959B1 (en) * 2005-12-06 2013-04-10 Merck Sharp & Dohme Corp. Morpholine carboxamide prokineticin receptor antagonists
US7902358B2 (en) * 2005-12-29 2011-03-08 Janssen Pharmaceutica Nv Prokineticin 1 receptor antagonists
CA2635845A1 (en) * 2005-12-29 2007-07-12 Janssen Pharmaceutica N.V. Prokineticin 2 receptor antagonists
CA2704185C (en) * 2007-10-30 2016-02-16 Janssen Pharmaceutica N.V. Amino-heteroaryl-containing prokineticin 1 receptor antagonists
WO2010077976A2 (en) * 2008-12-17 2010-07-08 The Regents Of The University Of California Prokineticin receptor antagonists and uses thereof
PL2399910T3 (pl) * 2009-02-13 2014-09-30 Shionogi & Co Pochodne triazyny jako antagoniści receptora p2x3 i/albo p2x2/3 i kompozycja farmaceutyczna zawierająca je
WO2012006003A1 (en) * 2010-06-28 2012-01-12 Janssen Pharmaceutica Nv Prokineticin 1 receptor antagonists for the treatment of pain
WO2012006004A1 (en) * 2010-06-28 2012-01-12 Janssen Pharmaceutica Nv Prokineticin 1 receptor antagonists for the treatment of pain
US9212130B2 (en) 2010-08-10 2015-12-15 Shionogi & Co., Ltd. Heterocyclic derivative and pharmaceutical composition comprising the same
RU2565073C2 (ru) 2010-08-10 2015-10-20 Сионоги Энд Ко., Лтд. Триазиновое производное и включающая его фармацевтическая композиция, обладающая анальгетической активностью
JP6124351B2 (ja) 2012-02-09 2017-05-10 塩野義製薬株式会社 複素環および炭素環誘導体
NZ626112A (en) * 2012-03-30 2016-04-29 Nissan Chemical Ind Ltd Triazinone compound and t-type calcium channel inhibitor
WO2014078306A1 (en) 2012-11-13 2014-05-22 Regeneron Pharmaceuticals, Inc. Anti-prokineticin receptor (prokr) antibodies and uses thereof
TWI637949B (zh) 2013-06-14 2018-10-11 塩野義製藥股份有限公司 胺基三衍生物及含有其等之醫藥組合物
US9988373B2 (en) 2013-12-26 2018-06-05 Shionogi & Co., Ltd. Nitrogen-containing six-membered cyclic derivatives and pharmaceutical composition comprising the same
BR112017022654A2 (pt) 2015-04-24 2018-07-10 Shionogi & Co., Ltd. derivado heterocíclico de 6 membros e composição farmacêutica compreendendo o mesmo
KR102528627B1 (ko) 2016-10-17 2023-05-03 시오노기 앤드 컴파니, 리미티드 2환성 함질소 헤테로환 유도체 및 그를 함유하는 의약 조성물
KR102494188B1 (ko) * 2021-04-14 2023-01-31 시오노기 앤드 컴파니, 리미티드 바이러스 증식 저해 작용을 갖는 트라이아진 유도체 및 그들을 함유하는 의약 조성물

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1504304A (en) * 1974-02-15 1978-03-15 Ici Ltd Process of combating fungal and bacterial infections of plants with triazine dione derivatives
US6485938B1 (en) 1999-11-16 2002-11-26 Zymogenetics, Inc. Nucleic acid molecules that encodes human Zven1
JP2004532609A (ja) 2000-11-03 2004-10-28 ザ リージェント オブ ザ ユニバーシティ オブ カリフォルニア プロキネチシンポリペプチド、関連組成物および方法
AU2003216591A1 (en) 2002-04-10 2003-10-20 Orichid Chemicals And Pharmaceuticals Limited Amino substituted pyrimidinone derivatives useful in the treatment of inflammation and immunological
EP1558287A4 (en) 2002-10-07 2009-07-08 Zymogenetics Inc USES OF HUMAN ZVEN ANTAGONISTS
US7115560B2 (en) 2003-03-25 2006-10-03 The Regents Of The University Of California Methods for modulating gastric secretion using prokineticin receptor antagonists
US20050170455A1 (en) 2003-06-20 2005-08-04 Qun-Yong Zhou Novel prokineticin receptor isoforms and methods of use
CN100376246C (zh) 2003-07-07 2008-03-26 纽罗克里生物科学有限公司 作为促性激素释放激素受体拮抗剂的嘧啶-2,4-二酮衍生物
US20060019338A1 (en) 2004-03-05 2006-01-26 Qun-Yong Zhou Primate prokineticin and prokineticin receptor polypeptides, related compositions and methods
KR20070116915A (ko) 2005-03-24 2007-12-11 얀센 파마슈티카 엔.브이. 프로키네티신 2 수용체 길항제로서의 피리미딘디온 유도체
JP2008537548A (ja) * 2005-03-24 2008-09-18 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ プロキネチシン１受容体
CN101326168A (zh) * 2005-03-24 2008-12-17 詹森药业有限公司 激肽原1受体拮抗剂
US7902358B2 (en) * 2005-12-29 2011-03-08 Janssen Pharmaceutica Nv Prokineticin 1 receptor antagonists

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CA2602576A1 (en) 2006-10-05
BRPI0609315A2 (pt) 2010-03-09
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TW200720260A (en) 2007-06-01
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