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172 条记录 (耗时 0.043 秒)

    5-nitro-furfurylidene antimicrobic agents
    23.
    发明授权
    5-nitro-furfurylidene antimicrobic agents 失效
    5-NITRO-FURFURYLIDENE抗菌剂

    公开(公告)号：US3716531A

    公开(公告)日：1973-02-13

    申请号：US3716531D

    申请日：1968-10-31

    申请人： SCHERING AG ,  SCHROEDER E ,  ALBRECHT R

    发明人： ALBRECHT R ,  SCHRODER E ,  MUFTIC M

    IPC分类号： C07D207/42 ,  C07D307/71 ,  C07D333/44 ,  C07D5/30

    CPC分类号： C07D207/42 ,  C07D307/71 ,  C07D333/44

    摘要： For combating and preventing infections caused by a variety of microbes such as bacteria and Trichomonas vaginalis, new compounds of the formula
    WHEREIN X is O, S or NH; Y is O; S; -CH2-O-; -S-CH2-; -CH2-S-; -O-CH2-; -SO-; -SO-CH2-; CH2-SO-; -CH2-SO2-; -SO2-CH2- or -CA2-, A being H, methyl, ethyl or phenyl; and R1, R2 and R3 each represents alkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyalkoxy, mono- or dialkylaminoalkyl, dialkylaminoalkoxy, amino, acylamino, mono- or dialkylamino, alkylsulfonylamino, acyloxy, alkylsulfonyloxy, benzyloxy groups wherein each alkyl, alkoxy or acyl residue is not more than five carbon atoms and acyl is derived from a carboxylic acid; halogen; or hydrogen with the provision that when Y represents -CH2-, at least one of R1, R2, and R3 is other than hydrogen.

    摘要翻译： 为了防治由各种微生物（如细菌和阴道毛滴虫）引起的感染，式WHEREIN X的新化合物是O，S或NH; Y是O; S; -CH 2 -O-; -S-CH 2 - ; -CH 2 -S-; -O-CH 2 - ; -所以-; -SO-CH 2 - ; -CH 2 -SO-; -CH 2 -SO 2 - ; -SO 2 -CH 2 - 或-CA 2 - ，A为H，甲基，乙基或苯基; R1，R2和R3各自表示烷基，羟基，羟烷基，烷氧基，烷氧基烷基，烷氧基烷氧基，一或二烷基氨基烷基，二烷基氨基烷氧基，氨基，酰氨基，一烷基氨基或二烷基氨基，烷基磺酰氨基，酰氧基，烷基磺酰氧基，苄氧基，其中各烷基，烷氧基或 酰基残基不超过5个碳原子，酰基衍生自羧酸; 卤素; 或氢，条件是当Y表示-CH 2 - 时，R 1，R 2和R 3中的至少一个不是氢。

    Inhibitors of c-fms kinase
    29.
    发明申请
    Inhibitors of c-fms kinase 有权
    c-fms激酶抑制剂

    公开(公告)号：US20060148812A1

    公开(公告)日：2006-07-06

    申请号：US11254276

    申请日：2005-10-20

    申请人： Carl Illig ,  Shelley Ballentine ,  Jinsheng Chen ,  Sanath Meegalla ,  M. Rudolf ,  Mark Wall ,  Ken Wilson ,  Renee Desjarlais ,  Carl Manthey ,  Christopher Flores ,  Chris Molloy

    发明人： Carl Illig ,  Shelley Ballentine ,  Jinsheng Chen ,  Sanath Meegalla ,  M. Rudolf ,  Mark Wall ,  Ken Wilson ,  Renee Desjarlais ,  Carl Manthey ,  Christopher Flores ,  Chris Molloy

    IPC分类号： A61K31/496 ,  A61K31/4545 ,  C07D409/14 ,  A61K31/4178

    CPC分类号： C07D307/71 ,  C07D401/12 ,  C07D401/14 ,  C07D407/12 ,  C07D409/12 ,  C07D409/14

    摘要： The invention is directed to compounds of Formula I: wherein A, X, R2 and W are set forth in the specification, as well as solvates, hydrates, tautomers and pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, especially c-fms kinase. Methods of treating autoimmune diseases; and diseases with an inflammatory component; treating metastasis from ovarian cancer, uterine cancer, breast cancer, colon cancer, stomach cancer, hairy cell leukemia and non-small lung carcinoma; and treating pain, including skeletal pain caused by tumor metastasis or osteoarthritis, or visceral, inflammatory, and neurogenic pain; as well as osteoporosis, Paget's disease, and other diseases in which bone resorption mediates morbidity including arthritis, prosthesis failure, osteolytic sarcoma, myeloma, and tumor metastasis to bone with the compounds of Formula I, are also provided.

    摘要翻译： 本发明涉及式I化合物：其中A，X，R 2和W在本说明书中列出，以及其抑制蛋白质的溶剂合物，水合物，互变异构体和药学上可接受的盐 酪氨酸激酶，特别是c-fms激酶。 治疗自身免疫性疾病的方法 和具有炎症成分的疾病; 治疗卵巢癌，子宫癌，乳腺癌，结肠癌，胃癌，毛细胞白血病和非小细胞肺癌的转移; 并治疗疼痛，包括由肿瘤转移或骨关节炎引起的骨骼疼痛，或内脏，炎症和神经源性疼痛; 还提供了骨质疏松症，佩吉特氏病和其它骨吸收介导包括关节炎，假体失败，溶骨性骨肉瘤，骨髓瘤以及与式I化合物对骨的肿瘤转移的其它疾病。