CRYSTALLINE FORM OF R)-3-(4-(2-(2-METHYLTETRAZOL-5-YL)PYRIDIN- 5-YL)-3-FLUOROPHENYL)-5-HYDROXYMETHYL OXAZOLIDIN-2-ONE DIHYDROGEN PHOSPHATE
    1.
    发明申请
    CRYSTALLINE FORM OF R)-3-(4-(2-(2-METHYLTETRAZOL-5-YL)PYRIDIN- 5-YL)-3-FLUOROPHENYL)-5-HYDROXYMETHYL OXAZOLIDIN-2-ONE DIHYDROGEN PHOSPHATE 有权
    R)-3-(4-(2-(2-甲基戊酰基-5-YL)吡啶-5-YL)-3-氟代戊烯)-5-羟基甲基氧化吡啶-2-酮二氢磷酸酯的晶体形式

    公开(公告)号:US20100227839A1

    公开(公告)日:2010-09-09

    申请号:US12699864

    申请日:2010-02-03

    摘要: A crystalline form of crystalline (R)-3-(4-(2-(2-methyltetrazol-5-yl)-pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyl oxazolidin-2-one dihydrogen phosphate, methods of making the crystalline form and pharmaceutical compositions comprising the crystalline form are useful antibiotics. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi, anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the crystalline form may be used in antibiotics.

    摘要翻译: 结晶形式的(R)-3-(4-(2-(2-甲基四唑-5-基) - 吡啶-5-基)-3-氟苯基)-5-羟基甲基恶唑烷-2-酮磷酸二氢盐, 制备结晶形式的方法和包含结晶形式的药物组合物是有用的抗生素。 此外,本发明的衍生物可以相对于各种人和动物病原体,包括葡萄球菌,肠球菌和链球菌等革兰阳性菌,拟杆菌和梭菌等厌氧菌,耐结核菌如结核分枝杆菌 和鸟分枝杆菌。 因此,包含结晶形式的组合物可以用于抗生素中。

    Crystalline form of R)-3-(4-(2-(2-methyltetrazol-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyl oxazolidin-2-one dihydrogen phosphate
    2.
    发明授权
    Crystalline form of R)-3-(4-(2-(2-methyltetrazol-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyl oxazolidin-2-one dihydrogen phosphate 有权
    R)-3-(4-(2-(2-甲基四唑-5-基)吡啶-5-基)-3-氟苯基)-5-羟基甲基恶唑烷-2-酮的结晶形式

    公开(公告)号:US08426389B2

    公开(公告)日:2013-04-23

    申请号:US12699864

    申请日:2010-02-03

    IPC分类号: A61K31/675 C07D413/14

    摘要: A crystalline form of crystalline (R)-3-(4-(2-(2-methyltetrazol-5-yl)-pyridin-5-yl)-3-fluorophenyl)-5-hydroxymethyl oxazolidin-2-one dihydrogen phosphate, methods of making the crystalline form and pharmaceutical compositions comprising the crystalline form are useful antibiotics. Further, the derivatives of the present invention may exert potent antibacterial activity versus various human and animal pathogens, including Gram-positive bacteria such as Staphylococi, Enterococci and Streptococi , anaerobic microorganisms such as Bacteroides and Clostridia, and acid-resistant microorganisms such as Mycobacterium tuberculosis and Mycobacterium avium. Accordingly, the compositions comprising the crystalline form may be used in antibiotics.

    摘要翻译: 结晶形式的(R)-3-(4-(2-(2-甲基四唑-5-基) - 吡啶-5-基)-3-氟苯基)-5-羟基甲基恶唑烷-2-酮磷酸二氢盐, 制备结晶形式的方法和包含结晶形式的药物组合物是有用的抗生素。 此外,本发明的衍生物可以相对于各种人和动物病原体,包括葡萄球菌,肠球菌和链球菌等革兰阳性菌,拟杆菌和梭菌等厌氧菌,耐结核菌如结核分枝杆菌 和鸟分枝杆菌。 因此,包含结晶形式的组合物可以用于抗生素中。

    NOVEL CRYSTALLINE SALTS OF ASENAPINE
    10.
    发明申请
    NOVEL CRYSTALLINE SALTS OF ASENAPINE 审中-公开
    ASENAPINE的新型晶体盐

    公开(公告)号:US20140163083A1

    公开(公告)日:2014-06-12

    申请号:US14116098

    申请日:2012-05-15

    IPC分类号: C07D491/22

    摘要: Crystalline Asenapine salts of tartaric acid or succinic acid, wherein the salts are e.g. selected from the group consisting of Asenapine D, L-tartrate hydrate form A, Asenapine D, L-tartrate hydrate form B, Asenapine D, L-tartrate anhydrous form, Asenapine succinate form X, Asenapine succinate form, and Asenapine succinate form II are described as well as related pharmaceutical compositions and related treatment of psychotic diseases or disorders.

    摘要翻译: 酒石酸或琥珀酸的结晶阿替那他盐,其中盐是例如。 选自阿替那丁D,L-酒石酸盐水合物形式A,阿沙那平D,L-酒石酸盐水合物形式B,阿氮平平D,L-酒石酸盐无水形式,亚甲基伞菌素琥珀酸酯形式X,阿替萘胺琥珀酸酯形式和琥珀酸阿替萘胺II型 描述以及相关的药物组合物和精神病或疾病的相关治疗。