KR100558506B1 - 과도한 물질 p에 의해 야기된 문제점을 치료하기 위한약물 제조에 사용되는 아릴(또는헤테로아릴)아졸일카르비놀 유도체의 용도 - Google Patents
과도한 물질 p에 의해 야기된 문제점을 치료하기 위한약물 제조에 사용되는 아릴(또는헤테로아릴)아졸일카르비놀 유도체의 용도 Download PDFInfo
- Publication number
- KR100558506B1 KR100558506B1 KR1020017001560A KR20017001560A KR100558506B1 KR 100558506 B1 KR100558506 B1 KR 100558506B1 KR 1020017001560 A KR1020017001560 A KR 1020017001560A KR 20017001560 A KR20017001560 A KR 20017001560A KR 100558506 B1 KR100558506 B1 KR 100558506B1
- Authority
- KR
- South Korea
- Prior art keywords
- methyl
- imidazole
- dimethylamino
- benzyl
- pyrazole
- Prior art date
Links
Classifications
-
- 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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
-
- 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
-
- 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
- A61K31/41—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
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
Landscapes
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Addiction (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
Claims (4)
- 화학식(I)의 아릴(또는 헤테로아릴)아졸일카르비놀 유도체 및 이들의 생리학적으로 수용가능한 염을 활성성분으로 하고, 불안, 우울증, 정신분열증, 조울증, 성기능장애, 약물중독, 인지장애, 운동성질환의 치료용 조성물,[화학식1]여기서, Ar은 페닐 또는 티에닐 라디컬로, 치환되지 않거나 또는 동일한 혹은 상이한 1개, 2개 또는 3개의 치환체로 치환되고, 상기 치환체는 플루오린, 클로린, 브로민, 메틸, 트리플루오르메틸, 메톡시에서 선택되고;R1은 수소 원자, 사이클로헥실기, N-메틸피페리딜기, 페닐기, 비닐기 또는 C1-C4알킬기이고;R2는 수소원자, 디(C1-C4알킬)아미노(C2-C3알킬), (C1-C2알킬)아자헤테르시클릴(C2-C3알킬), 또는 아자헤테로시클릴(C2-C3알킬)이고;Het는 질소(N)이 1 내지 3개인 아졸로써, 치환되지 않거나 또는 동일한 혹은 상이한 1개 또는 2개의 치환체로 치환되고, 상기 치환체는 플루오린, 클로린, 브로민, C1-C12알킬기, 벤질라디컬, 시아노(C2-C3알킬)라디컬, 카르복시알킬(C2-C3알킬)라디컬, 메톡시카르보닐(C2-C3알킬)라디컬, 하이드록시(C2-C3알킬)라디컬, 아미노(C2-C3알킬)라디컬, 디(C1-C4알킬)아미노(C2-C3알킬)라디컬, 아자헤테로시클릴(C2-C3알킬)라디컬에서 선택된다.
- 제 1항에 있어서, 화학식(I)의 화합물은 다음에서 선택되는 것을 특징으로 하는 조성물:[1] 2-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-이미다졸[2] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-이미다졸[3] 2-4-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-이미다졸[4] 2-3-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-이미다졸[5] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-이미다졸[6] 2-4-플루오르-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-이미다졸[7] 2-α-[2-(디메틸아미노)에톡시]-α-메틸-3-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[8] 2-3-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-이미다졸[9] 2-3-클로로-α-[2-(디메틸아미노)에톡시]-α-프로필벤질-1-메틸-1H-이미다졸[10] 1-부틸-2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1H-이미다졸[11] 2-α-[2-(디메틸아미노)에톡시]-α-메틸-4-메톡시벤질-1-메틸-1H-이미다졸[12] 2-3-클로로-α-메틸-α-[2-(N-피롤리딜)에톡시]벤질-1-메틸-1H-이미다졸[13] 2-α-[2-(디메틸아미노)에톡시]-α-프로필-3,4,5-트리메톡시벤질-1-도데실-1H-이미다졸[14] 1-부틸-2-α-[2-(디메틸아미노)에톡시]-4-(트리플루오르메틸)벤질-1H-이미다졸[15] 1-메틸-2-α-메틸-α-[2-(N-피페리딜)에톡시]-3-(트리플루오르메틸)벤질-1H-이미다졸[16] 2-α-사이클로헥실-3,4-디클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-이미다졸[17] 2-3,4-디클로로-α-[2-(디메틸아미노)에톡시]-α-프로필벤질-1-메틸-1H-이미다졸[18] 2-3,4-디클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-이미다졸[19] 2-3,4-디클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-이미다졸[20] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-[2-(N-피페리딜)에틸]-1H-이미다졸[21] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-[2-(N-피페리딜)프로필]-1H-이미다졸[22] 1-(3-시아노프로필)-2-4-클로로-α-[2-(디메틸아미노)에톡시]벤질]-1H-이미다졸[23] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-(N-메틸-4-피페리딜)벤질-1-메틸-1H-이미다졸[24] 1-벤질-2-α-[2-(N-벤질-N-메틸아미노)에톡시]-4-클로로벤질-1H-이미다졸[25] 2-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메톡시벤질-7-메틸-6,7,8,9-테트라하이드로-1H-이미다졸[1,5-a][1,4]디아제피나[26] 2-4-클로로-α-[2-(디메틸아미노)에톡시]벤질-7-메틸-6,7,8,9-테트라하이드로-1H-이미다졸[1,5-a][1,4]디아제피나[27] 1-부틸-5-α-[2-(디메틸아미노)에톡시]벤질]-1H-피라졸[28] 5-α-(4-클로로페닐)-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[29] 1-부틸-5-α-[2-(디메틸아미노)에톡시]-3,4,5-트리메톡시벤질]-1H-피라졸[30] 1-부틸-5-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질]-1H-피라졸[31] 5-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[32] 5-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-피라졸[33] 5-α-[2-(디메틸아미노)에톡시]-3,4,5-트리메톡시벤질-1-메틸-1H-피라졸[34] 1-메틸-5-α-[2-(N-피롤리딜)에톡시]벤질-1H-피라졸[35] 1-메틸-5-α-[2-(N-모르폴리닐)에톡시]벤질-1H-피라졸[36] 5-α-[2-(디메틸아미노)에톡시]-α-메틸-3,4,5-트리메톡시벤질-1-메틸-1H-피라졸[37] 4-브로모-5-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[38] 1,3-디메틸-5-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1H-피라졸[39] 1,3-디메틸-5-α-[2-(디메틸아미노)에톡시]벤질-1H-피라졸[40] 5-α-[2-(디메틸아미노)에톡시]-2-메틸벤질-1-메틸-1H-피라졸[41] 4-클로로-5-4-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[42] 5-4-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[43] 5-3-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[44] 5-α-[2-(디메틸아미노)에톡시]-4-메틸벤질-1-메틸-1H-피라졸[45] 5-2-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[46] 1-메틸-5-α-[2-(N-피페리딜)에톡시]벤질-1H-피라졸[47] 1-메틸-5-α-[2-(N-프로필-2-피페리딜)에톡시]벤질-1H-피라졸[48] 5-α-[2-(N-에틸-2-피페리딜)에톡시]벤질-1-메틸-1H-피라졸[49] 1-메틸-5-α-[2-(N-메틸-2-피롤리딜)에톡시]벤질-1H-피라졸[50] 5-α-[2-(디이소프로필아미노)에톡시]벤질-1-메틸-1H-피라졸[51] 1-메틸-5-α-[2-(N-메틸-2-피페리딜)에톡시]벤질-1H-피라졸[52] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-메틸-1H-이미다졸[53] 2-3-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[54] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-에틸벤질-1-메틸-1H-이미다졸[55] 2-α-부틸-3-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[56] 2-α-사이클로헥실-4-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[57] 2-α-[3-(디메틸아미노)프로폭시]-4-플루오르-α-메틸벤질-1-메틸-1H-이미다졸[58] 2-α-[3-(디메틸아미노)프로폭시]-α-메틸-3-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[59] 2-2-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-메틸-1H-이미다졸[60] 2-3-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-메틸-1H-이미다졸[61] 2-α-[3-(디메틸아미노)프로폭시]-α-메틸-3,4,5-트리메톡시벤질-1-메틸-1H-이미다졸[62] 2-α-[3-(디메틸아미노)프로폭시]-α-메틸-4-메톡시벤질-1-메틸-1H-이미다졸[63] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[64] 2-α-[3-(디메틸아미노)프로폭시]-3,4,5-트리메톡시벤질-1-메틸-1H-이미다졸[65] 2-α-[3-(디메틸아미노)프로폭시]-α-메틸-4-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[66] 2-α-[3-(디메틸아미노)프로폭시]-3-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[67] 2-α-[3-(디메틸아미노)프로폭시]-4-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[68] 2-α-[3-(디메틸아미노)프로폭시]-4-메톡시벤질-1-메틸-1H-이미다졸[69] 2-α-부틸-α-[3-(디메틸아미노)프로폭시]-3-(트리플루오르메틸)벤질-1-메틸-1H-이미다졸[70] 1-부틸-2-4-클로로-α-[3-(디메틸아미노)프록시]-α-메틸벤질-1H-이미다졸[71] 1-부틸-2-α-부틸-α-[3-(디메틸아미노)프로폭시]-3,4,5-트리메톡시벤질-1H-이미다졸[72] 1-부틸-2-α-부틸-2-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1H-이미다졸[73] 1-부틸-2-α-부틸-2,4-디클로로-α-[3-(디메틸아미노)프로폭시]벤질-1H-이미다졸[74] 1-부틸-2-α-[3-(디메틸아미노)프로폭시]-4-(트리플루오르메틸)벤질-1H-이미다졸[75] 2-4-클로로-α-[3-(N-피페리딜)프로폭시]벤질-1-메틸-1H-이미다졸[76] 1-메틸-2-α-메틸-α-[3-(N-피페리딜)프로폭시]-4-(트리플루오르메틸)벤질-1H-이미다졸[77] 2-α-부틸-2-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[78] 2-α-부틸-3,4-디클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[79] 2-3,4-디클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-메틸-1H-이미다졸[80] 2-3,4-디클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[81] 2-α-사이클로헥실-3,4-디클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-이미다졸[82] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-α-[2-(N-피페리딜)에틸]-1H-이미다졸[83] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-[2-(N-피페리딜)프로필]-1H-이미다졸[84] 2-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-(N-메틸-4-피페리딜)벤질-1-메틸-1H-이미다졸[85] 1-부틸-5-α-[3-(디메틸아미노)프로폭시]벤질-1H-피라졸[86] 1-부틸-5-4-클로로-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1H-피라졸[87] 5-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-피라졸[88] 5-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1-메틸-1H-피라졸[89] 1,3-디메틸-5-α-[3-(디메틸아미노)프로폭시]-α-메틸벤질-1H-피라졸[90] 1,3-디메틸-5-α-[3-(디메틸아미노)프로폭시]벤질-1H-피라졸[91] 5-α-[3-(디메틸아미노)프로폭시]-2-메틸벤질-1-메틸-1H-피라졸[92] 5-클로로-5-4-클로로-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-피라졸[93] 1-메틸-5-α-[3-(N-피페리딜)프로폭시]벤질-1H-피라졸[94] 1-메틸-5-α-[3-(N-피롤리딜)프로폭시]벤질-1H-피라졸[95] 4-4-클로로-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸[96] 4-4-클로로-α-[2-(디메틸아미노)에톡시]-α-메틸벤질-1-메틸-1H-피라졸[97] 4-4-클로로-α-[2-(N-프로필-2-피페리딜)에톡시]벤질-1-메틸-1H-피라졸[98] 4-4-클로로-α-[2-(N-메틸-2-피페리딜)에톡시]벤질-1-메틸-1H-피라졸[99] 4-4-클로로-α-[2-(N-에틸-2-피페리딜)에톡시]벤질-1-메틸-1H-피라졸[100] 4-4-클로로-α-[2-(디이소프로필아미노)에톡시]벤질-1-메틸-1H-피라졸[101] 4-4-클로로-α-[2-(N-메틸-2-피롤리딜)에톡시]벤질-1-메틸-1H-피라[102] 4-α-[3-(디메틸아미노)프로폭시]벤질-1-메틸-1H-피라졸[103] 4-4-클로로-α-[3-(N-모르폴리닐)프로폭시]벤질-1-메틸-1H-피라졸[104] 4-4-클로로-α-[3-(N-피롤리딜)프로폭시]벤질-1-메틸-1H-피라졸[105] 2-(α-하이드록시벤질)-1H-이미다졸[106] 2-(4-클로로-α-하이드록시벤질)-1H-이미다졸[107] 2-(4-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[108] 2-(3-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[109] 2-(4-플루오르-α-하이드록시벤질)-1-메틸-1H-이미다졸[110] 2-[α-하이드록시-3-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[111] 2-[α-하이드록시-4-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[112] 2-(α-하이드록시-3,4,5-트리메톡시벤질)-1-메틸-1H-이미다졸[113] 2-(3,4-디클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[114] 1-부틸-2-[α-하이드록시-4-(트리플루오르메틸)벤질]-1H-이미다졸[115] 1-부틸-2-(3,4-디클로로-α-하이드록시벤질)-1H-이미다졸[116] 1-부틸-2-(4-클로로-α-하이드록시벤질)-1H-이미다졸[117] 1-부틸-2-(α-하이드록시-3,4,5-트리메톡시벤질)-1H-이미다졸[118] 1-도데실-2-(α-하이드록시-3,4,5-트리메톡시벤질)-1H-이미다졸[119] 2-(α-부틸-3-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[120] 2-(3-클로로-α-하이드록시-α-메틸벤질)-1-메틸-1H-이미다졸[121] 2-(4-클로로-α-하이드록시-α-메틸벤질)-1-메틸-1H-이미다졸[122] 2-[4-클로로-α-하이드록시-α-(N-메틸-4-피페리딜)벤질]-1-메틸-1H-이미다졸[123] 2-(4-클로로-α-에틸-α-하이드록시벤질)-1-메틸-1H-이미다졸[124] 2-(α-부틸-4-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[125] 2-(α-사이클로헥실-4-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[126] 2-(2-클로로-α-하이드록시-α-메틸벤질)-1-메틸-1H-이미다졸[127] 2-(α-부틸-2-클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[128] 2-[α-하이드록시-α-메틸-3-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[129] 2-[α-부틸-α-하이드록시-3-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[130] 2-[α-사이클로헥실-α-하이드록시-3-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[131] 2-[α-하이드록시-α-메틸-4-(트리플루오르메틸)벤질]-1-메틸-1H-이미다졸[132] 2-(4-플루오르-α-하이드록시-α-메틸벤질)-1-메틸-1H-이미다졸[133] 2-(α-하이드록시-α-메틸-4-메틸벤질)-1-메틸-1H-이미다졸[134] 2-(3,4-디클로로-α-하이드록시-α-메틸벤질)-1-메틸-1H-이미다졸[135] 2-(α-부틸-3,4-디클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[136] 2-(α-사이클로헥실-3,4-디클로로-α-하이드록시벤질)-1-메틸-1H-이미다졸[137] 2-(α-하이드록시-α-메틸-3,4,5-트리메톡시벤질)-1-메틸-1H-이미다졸[138] 1-부틸-2-(4-클로로-α-하이드록시--α메틸벤질)-1H-이미다졸[139] 1-부틸-2-(α-부틸-4-클로로-α-하이드록시벤질)-1H-이미다졸[140] 1-부틸-2-[4-클로로-α-하이드록시-α-(N-메틸-4-피페리딜)벤질]-1H-이미다졸[141] 1-부틸-2-(α-부틸-α-하이드록시-3,4,5-트리메톡시벤질)-1H-이미다졸[142] 1-부틸-2-(α-부틸-2-클로로-α-하이드록시벤질)-1H-이미다졸[143] 1-부틸-2-[α-에틸-α-하이드록시-3-(트리플루오르메틸)벤질]-1H-이미다졸[144] 1-부틸-2-(α-부틸-2,4-디클로로-α-하이드록시벤질)-1H-이미다졸[145] 2-(4-클로로-α-하이드록시-α-메틸벤질)-1-[2-(N-피페리딜)에틸]-1H-이미다졸[146] 2-(4-클로로-α-하이드록시-α-메틸벤질)-1-(3-디메틸아미노프로필)-1H-이미다졸[147] 2-(α-부틸-α-하이드록시-3,4,5-트리메톡시벤질)-1-도데실-1H-이미다졸[148] 1-벤질-2-[α-부틸-α-하이드록시-3-(트리플루오르메틸)벤질]-1H-이미다졸[149] 1-벤질-2-(4-클로로-α-하이드록시-α-메틸벤질)-1H-이미다졸[150] 1-(2-시아노에틸)-2-(4-클로로-α-하이드록시벤질)-1H-이미다졸[151] 1-(3-아미노프로필)-2-(4-클로로-α-하이드록시벤질)-1H-이미다졸[152] 3-[2-(3-클로로-α-하이드록시벤질)-1H-이미다졸-1-일]프로파논산[153] 2-(4-클로로-α-하이드록시벤질)-1-(3-하이드록시프로필)-1H-이미다졸[154] 3-[2-(3-클로로-α-하이드록시벤질)-1H-이미다졸-1-일]메틸 프로파노산염[155] 2-(α-하이드록시벤질)-1-(3-하이드록시프로필)-1H-이미다졸[156] 2-(α-하이드록시-4-메틸벤질)-1-(3-하이드록시프로필)-1H-이미다졸[157] 2-(α-하이드록시-4-메톡시벤질)-1-(3-하이드록시프로필)-1H-이미다졸[158] 2-(3,4-디클로로-α-하이드록시벤질)-1-(3-하이드록시프로필)-1H-이미다졸[159] 3-[2-(α-하이드록시벤질)-1H-이미다졸-1-일]메틸 프로파논산염[160] 2-(4-클로로-α-하이드록시벤질)-1-(4-하이드록시부틸)-1H-이미다졸[161] 1-(3-시아노프로필)-2-(4-클로로-α-하이드록시벤질)-1H-이미다졸[162] 4-[2-(4-클로로-α-하이드록시벤질)-1H-이미다졸-1-일]부타논산[163] 4-[2-(4-클로로-α-하이드록시벤질)-1H-이미다졸-1-일]메틸 부타논산염[164] 1-부틸-5-(α-하이드록시벤질)-1H-피라졸[165] 5-(4-클로로-α-하이드록시벤질)-1-메틸-1H-피라졸[166] 5-(α-하이드록시-3,4,5-트리메톡시벤질)-1-메틸-1H-피라졸[167] 1-부틸-5-(α-하이드록시-3,4,5-트리메톡시벤질)-1H-피라졸[168] 4-브로모-5-(α-하이드록시벤질)-1-메틸-1H-피라졸[169] 5-[α-(4-클로로페닐)-α-하이드록시벤질]-1-메틸-1H-피라졸[170] 1-부틸-5-(4-클로로-α-하이드록시-α-메틸벤질)-1H-피라졸[171] 5-(α-하이드록시-α-메틸벤질)-1-메틸-1H-피라졸[172] 5-(α-하이드록시-α-메틸-3,4,5-트리메톡시벤질)-1-메틸-1H-피라졸[173] 1,3-디메틸-5-(α-하이드록시-α-메틸벤질)-1H-피라졸[174] 1-부틸-5-(α-하이드록시-α-비닐벤질)-1H-피라졸[175] 1-부틸-5-(4-클로로-α-하이드록시-α-비닐벤질)-1H-피라졸[176] 4-클로로-5-(α-하이드록시벤질)-1-메틸-1H-피라졸[177] 5-(α-하이드록시-2-메틸벤질)-1-메틸-1H-피라졸[178] 5-(3-클로로-α-하이드록시벤질)-1-메틸-1H-피라졸[179] 5-(α-하이드록시-4-메틸벤질)-1-메틸-1H-피라졸[180] 5-(2-클로로-α-하이드록시벤질)-1-메틸-1H-피라졸[181] 5-(α-하이드록시-4-메톡시벤질)-1-메틸-1H-피라졸[182] 5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸[183] 5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸시트레이트[184] 5-α-[2-(디메틸아미노)에톡시]-3-티에닐메틸-1-메틸-1H-피라졸[185] 2-α-[2-(디메틸아미노)에톡시]-3-티에닐메틸-1-메틸-1H-이미다졸[186] 5-α-[2-(디메틸아미노)에톡시]-3-메틸-2-티에닐메틸-1-메틸-1H-피라졸[187] 5-α-[2-(디메틸아미노)에톡시]-5-메틸-2-티에닐메틸-1-메틸-1H-피라졸[188] 5-5-브로모-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸[189] 5-4-브로모-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸[190] 5-α-[2-(디메틸아미노)에톡시]-α-메틸-2-티에닐메틸-1-메틸-1H-피라졸[191] 5-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸시트레이트[192](+)-5-α-[2-(디메틸아미노)-1-(메틸)에톡시]벤질-1-메틸-1H-피라졸[193](-)-5-α-[2-(디메틸아미노)-1-(메틸)에톡시]벤질-1-메틸-1H-피라졸[194](+)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸[195](-)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸[196](+)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸스트레이트[197](-)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸스트레이트[198](+)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸 D-디톨루오일타르트레이트[199](-)-5-α-[2-(디메틸아미노)에톡시]-2-티에닐메틸-1-메틸-1H-피라졸 L-디톨루오일타르트레이트[200](+)-5-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸 시트레이트[201](-)-5-α-[2-(디메틸아미노)에톡시]벤질-1-메틸-1H-피라졸 시트레이트[202] 5-(α-하이드록시-2-티에닐메틸)-1-메틸-1H-피라졸[203] 5-(α-하이드록시-3-메틸-2-티에닐메틸)-1-메틸-1H-피라졸[204] 5-(α-하이드록시-5-메틸-2-티에닐메틸)-1-메틸-1H-피라졸[205] 5-(5-브로모-α-하이드록시-2-티에닐메틸)-1-메틸-1H-피라졸[206] 5-(4-브로모-α-하이드록시-2-티에닐메틸)-1-메틸-1H-피라졸[207] 5-(α-하이드록시-α-메틸-2-티에닐메틸)-1-메틸-1H-피라졸.
- 삭제
- 삭제
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES009801708A ES2150378B1 (es) | 1998-08-07 | 1998-08-07 | Empleo de derivados de aril(o heteroaril)azolilcarbinoles en la elaboracion de un medicamento para el tratamiento de los trastornos mediados por un exceso de substancia p. |
ESP9801708 | 1998-08-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20010079616A KR20010079616A (ko) | 2001-08-22 |
KR100558506B1 true KR100558506B1 (ko) | 2006-03-07 |
Family
ID=8304839
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020017001560A KR100558506B1 (ko) | 1998-08-07 | 1999-08-05 | 과도한 물질 p에 의해 야기된 문제점을 치료하기 위한약물 제조에 사용되는 아릴(또는헤테로아릴)아졸일카르비놀 유도체의 용도 |
Country Status (26)
Country | Link |
---|---|
US (1) | US6518295B1 (ko) |
EP (1) | EP1103243B1 (ko) |
JP (1) | JP2002522359A (ko) |
KR (1) | KR100558506B1 (ko) |
CN (1) | CN1151789C (ko) |
AR (1) | AR019999A1 (ko) |
AT (1) | ATE257379T1 (ko) |
AU (1) | AU754124B2 (ko) |
BR (1) | BR9912807A (ko) |
CA (1) | CA2339661C (ko) |
CO (1) | CO5080747A1 (ko) |
CZ (1) | CZ292065B6 (ko) |
DE (1) | DE69914085T8 (ko) |
DK (1) | DK1103243T3 (ko) |
ES (2) | ES2150378B1 (ko) |
HU (1) | HUP0105428A3 (ko) |
IL (1) | IL141295A0 (ko) |
NO (1) | NO20010634L (ko) |
NZ (1) | NZ509645A (ko) |
PL (1) | PL193802B1 (ko) |
PT (1) | PT1103243E (ko) |
RU (1) | RU2223116C2 (ko) |
TR (1) | TR200100378T2 (ko) |
TW (1) | TW445259B (ko) |
WO (1) | WO2000007542A2 (ko) |
ZA (1) | ZA200100867B (ko) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2174756B2 (es) * | 2001-04-06 | 2003-11-16 | Esteve Labor Dr | Derivados de aril (o heteroaril) azolilcarbinoles para el tratamiento de enfermedades respiratorias. |
US20040142929A1 (en) * | 2001-07-06 | 2004-07-22 | Ramon Merce-Vidal | Derivatives of aryl (or heteroaryl) azolylcarbinoles for the treatment of urinary incontinence |
ES2180449B1 (es) * | 2001-07-06 | 2004-01-16 | Esteve Labor Dr | Derivados de aril (o heteroaril) azolilcarbinoles para el tratamiento de la incontinencia urinaria. |
DE10335566A1 (de) * | 2003-07-31 | 2005-02-24 | Grünenthal GmbH | Arzneimittel enthaltend Derivate von Aryl( oder Heteroaryl)azolylcarbinolen |
ES2244326B1 (es) * | 2004-04-05 | 2007-02-16 | Laboratorios Del Dr. Esteve, S.A. | Combinacion de substancias activas. |
EP1584335A3 (en) * | 2004-04-05 | 2006-02-22 | Laboratorios Del Dr. Esteve, S.A. | Active substance combination comprising a carbinol composition and an opioid |
WO2006010627A1 (en) * | 2004-07-30 | 2006-02-02 | Laboratorios Del Dr. Esteve, S.A. | Aryl (or heteroaryl) azolylcarbinols |
US20080045610A1 (en) * | 2004-09-23 | 2008-02-21 | Alexander Michalow | Methods for regulating neurotransmitter systems by inducing counteradaptations |
JP2008514612A (ja) * | 2004-09-23 | 2008-05-08 | ミシャロウ、アレクサンダー | 対抗適応を誘発することにより神経伝達物質系を調節する方法 |
WO2006087147A2 (en) * | 2005-02-15 | 2006-08-24 | Laboratorios Del Dr. Esteve, S.A. | Derivatives of aryl (or heteroaryl) azolylcarbinols for the treatment of fibromyalgia |
EP1695704A1 (en) * | 2005-02-28 | 2006-08-30 | Laboratorios Del Dr. Esteve, S.A. | Derivatives of aryl (or heteroaryl) azolylcarbinols for the treatment of fibromyalgia |
EP1690537A1 (en) * | 2005-02-15 | 2006-08-16 | Laboratorios Del Dr. Esteve, S.A. | Derivatives of aryl(or heteroaryl) azolycarbinols for the treatment of fibromyalgia |
ES2286920B1 (es) * | 2005-02-15 | 2008-08-16 | Laboratorios Del Dr. Esteve, S.A. | Derivados de aril (o heteroaril)azolilcarbinoles para el tratamiento de la fibromialgia. |
CN101374516A (zh) * | 2006-01-27 | 2009-02-25 | 弗·哈夫曼-拉罗切有限公司 | 取代的咪唑啉的2-咪唑衍生物的用途 |
EP1820502A1 (en) * | 2006-02-10 | 2007-08-22 | Laboratorios Del Dr. Esteve, S.A. | Active substance combination comprising azolylcarbinol compounds |
EP2076497B1 (en) | 2006-10-19 | 2012-02-22 | F. Hoffmann-La Roche AG | Aminomethyl-4-imidazoles |
ES2375578T3 (es) | 2006-11-02 | 2012-03-02 | F. Hoffmann-La Roche Ag | 2-imidazoles sustituidos como moduladores de receptores asociados a aminas trazas. |
WO2008058867A2 (en) | 2006-11-16 | 2008-05-22 | F. Hoffmann-La Roche Ag | Substituted 4-imidazoles |
CN101190330A (zh) | 2006-11-30 | 2008-06-04 | 深圳市鼎兴生物医药技术开发有限公司 | 胆碱酯酶在拮抗速激肽药物中的应用 |
CA2672617A1 (en) | 2006-12-13 | 2008-06-19 | F. Hoffmann-La Roche Ag | Novel 2-imidazoles as ligands for trace amine associated receptors (taar) |
WO2008092785A1 (en) | 2007-02-02 | 2008-08-07 | F. Hoffmann-La Roche Ag | Novel 2-aminooxazolines as taar1 ligands for cns disorders |
RU2460725C2 (ru) | 2007-02-15 | 2012-09-10 | Ф. Хоффманн-Ля Рош Аг | Новые 2-аминооксазолины в качестве лигандов taar1 |
EP2173720A2 (en) | 2007-07-02 | 2010-04-14 | F. Hoffmann-Roche AG | 2-imidazolines having a good affinity to the trace amine associated receptors (taars) |
EP2173719A1 (en) | 2007-07-03 | 2010-04-14 | F. Hoffmann-Roche AG | 4-imidazolines and their use as antidepressants |
KR101133862B1 (ko) | 2007-07-27 | 2012-04-06 | 에프. 호프만-라 로슈 아게 | Taar 리간드로서의 2-아제티딘메테인아민 및 2-피롤리딘메테인아민 |
EP2185502A1 (en) | 2007-08-03 | 2010-05-19 | F. Hoffmann-Roche AG | Pyridinecarboxamide and benzamide derivatives as taar1 ligands |
US8242153B2 (en) | 2008-07-24 | 2012-08-14 | Hoffmann-La Roche Inc. | 4,5-dihydro-oxazol-2YL derivatives |
US20100291151A1 (en) * | 2009-04-21 | 2010-11-18 | Auspex Pharmaceuticals, Inc. | 1-methylpyrazole modulators of substance p, calcitonin gene-related peptide, adrenergic receptor, and/or 5-ht receptor |
US8354441B2 (en) | 2009-11-11 | 2013-01-15 | Hoffmann-La Roche Inc. | Oxazoline derivatives |
US9452980B2 (en) | 2009-12-22 | 2016-09-27 | Hoffmann-La Roche Inc. | Substituted benzamides |
MX377836B (es) | 2016-03-17 | 2025-03-11 | F Hoffmann La Roche Ag | Derivado de 5-etil-4-metil-pirazol-3-carboxamida teniendo actividad como agonista de receptor asociado con aminas trazas (taar). |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2613720B1 (fr) * | 1987-04-10 | 1990-01-19 | Esteve Labor Dr | Derives d'aryl-heteroaryl carbinols avec activite analgesique |
FR2681322B1 (fr) * | 1991-09-12 | 1993-12-17 | Laboratorios Dr Esteve Sa | Derives d'aryl-heteroaryl-{n-[2-(3,4-dimethoxyphenyl)-ethyl]-n-methyl-3-aminopropoxy}-methane leur preparation et leur application en tant que medicaments . |
CA2154116A1 (en) * | 1994-07-22 | 1996-01-23 | Philip Arthur Hipskind | 1-aryl-2-acetamidopentanone derivatives for use as tachykinin receptor antagonists |
AU732633B2 (en) * | 1996-12-02 | 2001-04-26 | Merck Sharp & Dohme Limited | Use of NK-1 receptor antagonists for treating schizophrenic disorders |
JP2001504848A (ja) * | 1996-12-02 | 2001-04-10 | メルク シヤープ エンド ドーム リミテツド | 重症不安障害の治療のためのnk−1受容体拮抗薬の使用 |
JP2001504847A (ja) * | 1996-12-02 | 2001-04-10 | メルク シヤープ エンド ドーム リミテツド | 重抑鬱障害の治療のためのnk−1受容体拮抗薬の使用 |
ATE293975T1 (de) * | 1996-12-02 | 2005-05-15 | Merck Sharp & Dohme | Die verwendung von nk-1 rezeptor antagonisten für die behandlung von kognitiven störungen |
ES2150353B1 (es) * | 1998-04-15 | 2001-07-01 | Esteve Labor Dr | Tienilazolilalcoxietanaminas, su preparacion y su aplicacion como medicamentos. |
-
1998
- 1998-08-07 ES ES009801708A patent/ES2150378B1/es not_active Expired - Fee Related
-
1999
- 1999-08-04 CO CO99049291A patent/CO5080747A1/es unknown
- 1999-08-04 AR ARP990103870A patent/AR019999A1/es unknown
- 1999-08-05 EP EP99940199A patent/EP1103243B1/en not_active Expired - Lifetime
- 1999-08-05 DE DE69914085T patent/DE69914085T8/de not_active Expired - Fee Related
- 1999-08-05 PT PT99940199T patent/PT1103243E/pt unknown
- 1999-08-05 KR KR1020017001560A patent/KR100558506B1/ko not_active IP Right Cessation
- 1999-08-05 JP JP2000563228A patent/JP2002522359A/ja active Pending
- 1999-08-05 NZ NZ509645A patent/NZ509645A/xx unknown
- 1999-08-05 DK DK99940199T patent/DK1103243T3/da active
- 1999-08-05 CZ CZ2001412A patent/CZ292065B6/cs not_active IP Right Cessation
- 1999-08-05 TW TW088113353A patent/TW445259B/zh not_active IP Right Cessation
- 1999-08-05 RU RU2001106644/15A patent/RU2223116C2/ru not_active IP Right Cessation
- 1999-08-05 TR TR2001/00378T patent/TR200100378T2/xx unknown
- 1999-08-05 CA CA002339661A patent/CA2339661C/en not_active Expired - Fee Related
- 1999-08-05 HU HU0105428A patent/HUP0105428A3/hu unknown
- 1999-08-05 AU AU54229/99A patent/AU754124B2/en not_active Ceased
- 1999-08-05 BR BR9912807-1A patent/BR9912807A/pt not_active Application Discontinuation
- 1999-08-05 CN CNB998109150A patent/CN1151789C/zh not_active Expired - Fee Related
- 1999-08-05 US US09/762,079 patent/US6518295B1/en not_active Expired - Fee Related
- 1999-08-05 WO PCT/ES1999/000255 patent/WO2000007542A2/es active IP Right Grant
- 1999-08-05 AT AT99940199T patent/ATE257379T1/de not_active IP Right Cessation
- 1999-08-05 PL PL99346221A patent/PL193802B1/pl not_active IP Right Cessation
- 1999-08-05 ES ES99940199T patent/ES2213380T3/es not_active Expired - Lifetime
-
2001
- 2001-01-31 ZA ZA200100867A patent/ZA200100867B/en unknown
- 2001-02-06 NO NO20010634A patent/NO20010634L/no not_active Application Discontinuation
- 2001-02-07 IL IL14129501A patent/IL141295A0/xx unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100558506B1 (ko) | 과도한 물질 p에 의해 야기된 문제점을 치료하기 위한약물 제조에 사용되는 아릴(또는헤테로아릴)아졸일카르비놀 유도체의 용도 | |
JP2003509371A (ja) | 5−ヒドロキシトリプタミン・レセプタ/α2アドレナリン作用性レセプタ拮抗薬組成物の投与による運動障害の処置 | |
JP2002522359A5 (ko) | ||
RU2001106644A (ru) | Применение производных арил (или гетероарил) азолилкарбинолов в приготовлении лекарственного средства для лечения нарушений, опосредованных избытком вещества p | |
AU2007265088B2 (en) | Method of modulating neurite outgrowth by the use of a galanin-3 receptor antagonist | |
US20050107356A1 (en) | Combination of a CB1 receptor antagonist and of a product which activates dopaminergic neurotransmission in the brain, the pharmaceutical compositions comprising them and their use in the treatment of parkinson's disease | |
JP6247004B2 (ja) | 帯状疱疹関連通の急性期疼痛の予防又は治療剤 | |
EP1040829A2 (en) | Prokinetic agents for treating gastric hypomotility and related disorders | |
WO1997021439A1 (fr) | Medicament destine au traitement des troubles obsessifs compulsifs, de l'apnee du sommeil, des dysfonctions sexuelles, de l'emese et du mal des transports | |
KR102023748B1 (ko) | 순수한 5-ht6 수용체 길항제 및 nmda 수용체 길항제의 조합물 | |
WO1999059524A2 (es) | Empleo de derivados de aril(o heteroaril)azolilcarbinoles en la elaboracion de un medicamento para el tratamiento de la inflamacion neurogenica | |
CZ355998A3 (cs) | Pyridil a pyrimidylpiperaziny pro léčení poruch způsobených odejmutím drogy | |
AU2005222399A1 (en) | Ion channel modulators | |
MXPA01001438A (en) | Utilization of aryl(or heteroaryl)azolylcarbinol derivatives in the preparation of a medicament for the treatment of troubles mediated by an excess of substance p | |
ES2286920B1 (es) | Derivados de aril (o heteroaril)azolilcarbinoles para el tratamiento de la fibromialgia. | |
AU2018229062A1 (en) | Therapeutic agent for alcohol use disorders | |
CN101466685A (zh) | 酶抑制剂 | |
CN103998446A (zh) | 新的三氟甲基-*二唑衍生物及它们在治疗疾病中的应用 | |
WO2006060202A2 (en) | Imidazole derivatives for the treatment of psychiatric disorders |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0105 | International application |
Patent event date: 20010206 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20031014 Comment text: Request for Examination of Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20050720 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20060109 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20060228 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20060227 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |