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    • 52. 发明公开
    • 창이자, 숙지황 및 오가피의 혼합 생약재 추출물을함유하는 관절염 예방 및 치료용 조성물
    • 用于预防和治疗包含XINTHIUM STRUMARIUM LINNE,REHMANNIAE RADIX PREPARATA和ACANTHOPANACIS CORTEX的草药混合物的芽孢杆菌的组合物
    • KR1020090011140A
    • 2009-02-02
    • KR1020070074437
    • 2007-07-25
    • 주식회사 오스코텍
    • 김정근김세원장순화
    • A61K36/28A61K36/804A61K36/254A61P19/02
    • A composition for treating and preventing arthritis is provided to suppress ruin of cartilage and bone, to be used widely as Arthritis curing agent or Arthritis prevention agent or health food by using extract of herbal mixture of Acanthopanacis Cortex, Xanthii Fructus and Rehmanniae Radix Preparata. A composition for treating and preventing arthritis contains extract of herbal mixture of Acanthopanacis Cortex, Xanthii Fructus and Rehmanniae Radix Preparata extracted by a solvent such as water, alcohol or their mixture. The Acanthopanacis Cortex originates from one selected from a group consisting of timber of Acanthopanacis Cortex Radicis grown or cultivated in China and acanthopanax sessiliflorus, acanthopanax chilsanensis, acanthopanax Koreanm, acanthopanax rufinerve, Acanthopanax Seoulensis, Eleutherococcus senticosus Maxim and auger drill timber cultivated or grown in Korea.
    • 提供用于治疗和预防关节炎的组合物,以通过使用刺五加皮草,Xanthii Fructus和地黄地黄的草药混合物的提取物来广泛用作关节炎固化剂或关节炎预防剂或保健食品广泛使用的软骨和骨的破坏。 用于治疗和预防关节炎的组合物含有通过溶剂如水,醇或它们的混合物提取的刺五加皮质,Xanthii Fructus和地黄提取物的草药混合物的提取物。 刺五加皮质起源于中国生长或栽培的刺五加皮科植物,刺五加,刺五加,刺五加,刺五加,南极刺五加,韩国Ele er drill drill Korea Korea Korea from from from Korea Korea Korea Korea Korea Korea 。
    • 54. 发明公开
    • OPG 분비를 촉진하는 대사성 골 질환의 예방 및 치료제
    • 用于预防和治疗代谢性骨髓疾病的OPG秘密
    • KR1020070100072A
    • 2007-10-10
    • KR1020060031655
    • 2006-04-06
    • 주식회사 오스코텍
    • 김정근김세원심성보고선일장순화이재상강대필성하창박정애
    • C07D215/48C07D215/18
    • C07D215/48C07D401/04C07D401/12C07D401/14C07D413/12C07D413/14
    • A novel quinoline ester derivative is provided to promote the secretion of OPG from osteoblast and inhibit the differentiation of osteoclast, thereby being usefully used as an agent for preventing and treating metabolic bone diseases such as osteoporosis and osteoarthritis. A method for preparing the same is provided to produce the desired product at relatively cheap cost due to be manufactured from a low molecular material which is able to be synthesized easily. A quinoline ester derivative is represented by the formula(1), wherein X is H or halogen; Z is H, halogen, unsubstituted or substituted linear or branched C1-10 alkyl, C5-10 aryl, C2-8 heterocycliyl, C1-10 alkylamine, C1-10 alkenylamine, C5-10 aryl, C1-10 alkylamine, C5-10 cycloalkylamine or C1-10 hydroxyalkylamine; R is phenyl carboxyl substituted by U and Y represented by the formula(2). In the formula(2), U is -O-(CH2)m-V or -CH2-O-(CH2)m-V(wherein m is an integer from 0 to 10; V is H, C5-10 aryl substituted by R1(which is selected from the group consisting of H, halogen, nitro, cyano, C2-8 heteroaryl and C2-8 heterocyclo C1-10 alkyloxy), C2-8 heterocyclyl, C5-10 aryloxy or C5-10 arylamine); and Y is H, halogen, hydroxy, amino, nitro, unsubstituted or substituted linear or branched C1-10 alkyl, C2-8 heterocyclyl, C1-10 alkyl, C5-10 aryl or C2-8 heteroaryl, provided that the heterocyclyl, heteroaryl or heterocycloalkyloxy includes at least one hetero atom. A method for preparing the quinoline ester derivative comprises the steps of: (a) dissolving a compound represented by the formula(3) in a proper solvent to prepare a starting material; and (b) reacting the starting material with at least one compound selected from the group consisting of catechol, alkyl bromide and heterocycle compounds(V-H) to prepare the compound of the formula(1), wherein A is H or C1-10 halogenated alkyl; each R, X, Z and V is same as defined above. An agent for preventing and treating a metabolic bone disease comprises the quinoline derivative as an effective ingredient.
    • 提供了一种新型喹啉酯衍生物,用于促进成骨细胞分泌OPG,抑制破骨细胞的分化,从而有效地用作预防和治疗骨质疏松症和骨关节炎等代谢骨疾病的药剂。 提供了制备该方法的方法,由于能够容易地合成的低分子材料制造,以相对便宜的成本制造所需产品。 喹啉酯衍生物由式(1)表示,其中X为H或卤素; Z是H,卤素,未取代或取代的直链或支链C 1-10烷基,C 5-10芳基,C 2-8杂环基,C 1-10烷基胺,C 1-10烯基胺,C 5-10芳基,C 1-10烷基胺,C 5-10 环烷基胺或C1-10羟烷基胺; R是由式(2)表示的U和Y取代的苯基羧基。 式(2)中,U为-O-(CH2)mV或-CH2-O-(CH2)mV(其中,m为0〜10的整数,V为H,被R 1取代的C5-10芳基 选自H,卤素,硝基,氰基,C 2-8杂芳基和C 2-8杂环C 1-10烷氧基),C 2-8杂环基,C 5-10芳氧基或C 5-10芳基胺); 并且Y是H,卤素,羟基,氨基,硝基,未取代或取代的直链或支链C 1-10烷基,C 2-8杂环基,C 1-10烷基,C 5-10芳基或C 2-8杂芳基,条件是杂环基,杂芳基 或杂环烷氧基包括至少一个杂原子。 制备喹啉酯衍生物的方法包括以下步骤:(a)将由式(3)表示的化合物溶于适当的溶剂中以制备原料; 和(b)使起始材料与选自由儿茶酚,烷基溴和杂环化合物(VH)组成的组中的至少一种化合物反应以制备式(1)化合物,其中A为H或C 1-10卤代烷基 ; 每个R,X,Z和V与上述定义相同。 用于预防和治疗代谢性骨病的药剂包含喹啉衍生物作为有效成分。