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    • 1. 发明授权
    • 세포 손상 및 염증 질환의 치료 또는 예방용 약학 조성물
    • 细胞的药物损害和炎症性疾病的组合物治疗或预防
    • KR101335029B1
    • 2013-11-28
    • KR1020117013031
    • 2007-04-13
    • 주식회사 지엔티파마
    • 곽병주조성익조제영이영애변한열임두순함기백권영배이진환윤복선안춘산유근실
    • A61K31/136A61P29/00
    • A61K31/606A61K31/136A61K31/196
    • 본 발명은 세포 손상과 염증 질환의 치료 또는 예방에 유용한 약학 조성물 및 이를 이용하는 세포 손상과 염증 질환의 치료 또는 예방 방법에 관한 것으로서, 특정 화학식으로 표시되는 2-하이드록시 벤조산 유도체 또는 이의 약학적으로 허용가능한 염을 유효성분으로 이용하는 것을 특징으로 한다. 본 발명의 2-하이드록시 벤조산 유도체 및 이의 약학적으로 허용가능한 염은 매우 안전하고 세포보호효과와 염증억제 작용이 우수하여 위염, 위궤양, 췌장염, 대장염, 관절염, 당뇨병, 동맥경화, 신장염, 간염, 알츠하이머성 치매, 파킨슨병, 루게릭병 등을 포함하는 세포 손상과 염증 질환의 치료 또는 예방에 효과적이다.
    • 本发明涉及细胞用于治疗或使用在治疗或预防炎性疾病的有用的预防损伤和炎性疾病,和药物组合物它们损伤和细胞的方法,其2-羟基苯甲酸衍生物或其药学上可接受的,由特定式表示的 可溶性盐作为有效成分。 2-羟基酸衍生物及其药学上可接受的盐是高度安全和细胞保护作用和炎症抑制作用优于胃炎,胃溃疡,胰腺炎,大肠炎,关节炎,糖尿病,动脉硬化,肾炎,肝炎,根据本发明, 是有效的阿耳茨海默氏老年痴呆症,帕金森氏病,葛雷克氏病,包括治疗或预防细胞损伤和炎性疾病,包括的。
    • 3. 发明公开
    • 통증의 치료 또는 예방용 약학 조성물
    • 用于预防和治疗疼痛的药物组合物
    • KR1020100053027A
    • 2010-05-20
    • KR1020080111976
    • 2008-11-12
    • 주식회사 지엔티파마
    • 김기원권영배정낙신곽병주이영애
    • A61K31/075A61P23/00
    • PURPOSE: A composition containing an effective compound for pain for preventing neuropathic and inflammatory pain based on sigma 1 receptor suppression is provided. CONSTITUTION: A pharmaceutical composition contains a compound of chemical formula 1 or pharmaceutically acceptable salt thereof. In chemical formula 1, R1 is hydrogen or straight chain or side chain alkyl of C1-C6, and side chain alkyl, or cycloalkyl; R2 and R3 is straight chain or side chain alkyl of C1-C3; and R4 is straight chain or side chain linker containing C1-C4 alkyl or OH. The treatment or prevention for neuropathic or inflammatory pain is performed by administering a compound of chemical formula 1 or 2 or pharmaceutically acceptable salt.
    • 目的:提供一种含有基于西格玛1受体抑制的用于预防神经性和炎性疼痛的疼痛的有效化合物的组合物。 构成:药物组合物含有化学式1的化合物或其药学上可接受的盐。 在化学式1中,R 1是氢或C1-C6的直链或侧链烷基,和侧链烷基或环烷基; R2和R3是C1-C3的直链或侧链烷基; 并且R 4是含有C 1 -C 4烷基或OH的直链或侧链接头。 神经性或炎性疼痛的治疗或预防是通过施用化学式1或化合物2或其药学上可接受的盐来进行的。
    • 6. 发明公开
    • 재관류 손상의 치료 또는 예방용 약학 조성물
    • 用于预防和治疗再灌注损伤的药物组合物
    • KR1020090113424A
    • 2009-11-02
    • KR1020080039141
    • 2008-04-28
    • 주식회사 지엔티파마주식회사 아라온테크
    • 곽병주조제영조성익이영애나흥식
    • A61K31/136A61K31/137A61P9/10
    • PURPOSE: A pharmaceutical composition for preventing or treating reperfusion injury is provided to treat or prevent various damages such as myocardial stunning or necrosis. CONSTITUTION: A pharmaceutical composition for preventing or treating reperfusion injury comprises tetrafluorobenzyl derivative of the chemical formula 1 or its pharmaceutically acceptable salt as an active ingredient. The tetrafluorobenzyl derivative is 2-hydroxy is 2-hydroxy-5-(2,3,5,6-tetrafluoro-4- trifluoromethyl-benzylamino)benzoic acid, 2-nitro-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl- benzylamino)-benzoic acid, 2-methyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)- benzoic acid, and 2-methoxy-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl-benzylamino)-benzoic acid.
    • 目的:提供预防或治疗再灌注损伤的药物组合物,用于治疗或预防各种损伤,如心肌梗塞或坏死。 构成:用于预防或治疗再灌注损伤的药物组合物包括化学式1的四氟苄基衍生物或其药学上可接受的盐作为活性成分。 四氟苄基衍生物是2-羟基是2-羟基-5-(2,3,5,6-四氟-4-三氟甲基 - 苄基氨基)苯甲酸,2-硝基-5-(2,3,5,6-四氟 -4-三氟甲基 - 苄基氨基) - 苯甲酸,2-甲基-5-(2,3,5,6-四氟-4-三氟甲基 - 苄基氨基) - 苯甲酸和2-甲氧基-5- 5,6-四氟-4-三氟甲基 - 苄基氨基) - 苯甲酸。
    • 8. 发明授权
    • 2-하이드록시-5-페닐알킬아미노벤조산 유도체 및 이의 염의제조방법
    • 2-羟基-5-苯甲酰氨基苯甲酸衍生物及其盐的制备方法
    • KR100852962B1
    • 2008-08-20
    • KR1020070114660
    • 2007-11-12
    • 주식회사 지엔티파마
    • 곽병주조제영이영애쳉퀼링우유리앙리징
    • C07C229/64C07C229/38
    • C07C227/18C07C229/64
    • A method for preparing 2-hydroxy-5-phenylalkylaminobenzoic acid derivatives useful for treating diseases in the central nervous system is provided to enable mass product of the target compound through a simple process including a simple purification step. A method for preparing a 2-hydroxy-5-phenylalkylaminobenzoic acid derivative represented by the following formula 4 comprises a step of reacting phenylalkyl methanesulfonate represented by the following formula 1 with an alkyl 5-aminosalicylate represented by the following formula 2 to form an alkyl 2-hydroxy-5-phenylalkylaminobenzoate represented by the following formula 3. In the formulae, n is an integer of 1-4; each of R1-R5 is H, halogen, C1-C4 haloalkyl, nitro, hydroxy, C1-C4 alkyl, C1-C4 alkoxy or amine; A is H or a C1-C3 alkyl; and B is H or acetyl.
    • 提供了一种制备用于治疗中枢神经系统疾病的2-羟基-5-苯基烷基氨基苯甲酸衍生物的方法,以通过包括简单纯化步骤的简单方法使目标化合物的大量产物得以实现。 由下式4表示的2-羟基-5-苯基烷基氨基苯甲酸衍生物的制备方法包括使由下式1表示的甲基磺酸苯基烷基酯与下式2表示的5-氨基水杨酸烷基酯反应形成烷基2 由下式3表示的5-羟基-5-苯基烷基氨基苯甲酸酯。在该式中,n为1-4的整数; 每个R 1 -R 5是H,卤素,C 1 -C 4卤代烷基,硝基,羟基,C 1 -C 4烷基,C 1 -C 4烷氧基或胺; A是H或C 1 -C 3烷基; B为H或乙酰基。