TRAVEL TRAILER HAVING IMPROVED TURNING RADIUS
    3.
    发明申请
    TRAVEL TRAILER HAVING IMPROVED TURNING RADIUS 有权
    具有改进的驾驶RADIUS的旅行车

    公开(公告)号:US20060038379A1

    公开(公告)日:2006-02-23

    申请号:US11091070

    申请日:2005-03-28

    IPC分类号: B62D25/02 B62D53/06 B60J5/00

    摘要: Abstract of the DisclosureA travel trailer configured to be coupled to and towed by a vehicle is provided. The travel trailer has a compartment that is attached to a chassis which includes a front end and a rear end. A plurality of wheels are attached to the chassis adjacent the rear end, and a hitch assembly is attached to the chassis adjacent the front end. The compartment at the front end of the chassis forms first and second corners. A recess, directed inwardly toward the interior of the compartment, is located at each corner of the compartment. Cavities formed by each recess may receive a portion of the vehicle while the vehicle is engaged in a turn.

    摘要翻译: 公开摘要提供了一种被配置为联接到车辆并被拖曳的旅行拖车。 旅行拖车具有附接到包括前端和后端的底盘的隔室。 多个车轮相邻于后端附接到底盘,并且牵引组件附接到靠近前端的底盘。 底盘前端的隔间形成第一和第二个角。 向内指向隔室内部的凹槽位于隔室的每个角落处。 每个凹部形成的腔可以在车辆转弯的同时接收车辆的一部分。

    Gastrin receptor-avid peptide conjugates
    6.
    发明申请
    Gastrin receptor-avid peptide conjugates 审中-公开
    胃泌素受体 - 狂犬病肽缀合物

    公开(公告)号:US20070065362A1

    公开(公告)日:2007-03-22

    申请号:US11592864

    申请日:2006-11-03

    IPC分类号: A61K51/00 C07K14/575

    摘要: A compound for use as a therapeutic or diagnostic radiopharmaceutical includes a group capable of complexing a medically useful metal attached to a moiety which is capable of binding to a gastrin releasing peptide receptor. A method for treating a subject having a neoplastic disease includes administering to the subject an effective amount of a radiopharmaceutical having a metal chelated with a chelating group attached to a moiety capable of binding to a gastrin releasing peptide receptor expressed on tumor cells with subsequent internalization inside of the cell. A method of forming a therapeutic or diagnostic compound includes reacting a metal synthon with a chelating group covalently linked with a moiety capable of binding a gastrin releasing peptide receptor.

    摘要翻译: 用作治疗或诊断性放射性药物的化合物包括能够使与能够结合胃泌素释放肽受体的部分连接的医学上有用的金属络合的基团。 用于治疗患有肿瘤疾病的受试者的方法包括向受试者施用有效量的具有与螯合基螯合的金属的放射性药物,所述螯合基团连接到能够结合肿瘤细胞上表达的胃泌素释放肽受体的部分,随后内化 的细胞。 形成治疗或诊断化合物的方法包括使金属合成酶与能够结合胃泌素释放肽受体的部分共价连接的螯合基团反应。

    Gold-containing chemotherapeutic agents
    7.
    发明授权
    Gold-containing chemotherapeutic agents 失效
    含金化学治疗剂

    公开(公告)号:US06989158B1

    公开(公告)日:2006-01-24

    申请号:US10019192

    申请日:2000-06-23

    IPC分类号: A61K31/28 A61K33/24

    CPC分类号: A61K31/28

    摘要: There is provided a complex for use as a therapeutic pharmaceutical, the complex has a ligand containing at least one hydroxyalkyl phosphine donor group bound to a gold atom to form a stable gold-ligand complex. Also provided is a method of treating cancer by administering an effective amount of a complex having a ligand of at least one hydroxyalkyl phosphine group bound to a gold atom to form a stable gold-ligand complex. Also provided is a method of preventing the metastasis of cancer and arresting cell growth by administering an effective amount of a complex having a ligand of at least one hydroxyalkyl phosphine group bound to a gold atom to form a stable gold-ligand complex.

    摘要翻译: 提供了用作治疗药物的复合物,该配合物具有含有至少一个与金原子结合的羟烷基膦供体基团以形成稳定的金 - 配体络合物的配体。 还提供了通过施用有效量的具有与金原子结合的至少一个羟基烷基膦基团的配体的络合物以形成稳定的金 - 配体络合物来治疗癌症的方法。 还提供了通过施用有效量的具有与金原子结合的至少一个羟烷基膦基配体的配合物以形成稳定的金 - 配体络合物的方法来防止癌症转移和阻止细胞生长的方法。

    Gastrin receptor-avid peptide conjugates
    10.
    发明申请

    公开(公告)号:US20060067886A1

    公开(公告)日:2006-03-30

    申请号:US11267001

    申请日:2005-11-04

    IPC分类号: A61K51/00 C07K14/595

    CPC分类号: A61K51/088

    摘要: A compound for use as a therapeutic or diagnostic radiopharmaceutical includes a group capable of complexing a medically useful metal attached to a moiety which is capable of binding to a gastrin releasing peptide receptor. A method for treating a subject having a neoplastic disease includes administering to the subject an effective amount of a radiopharmaceutical having a metal chelated with a chelating group attached to a moiety capable of binding to a gastrin releasing peptide receptor expressed on tumor cells with subsequent internalization inside of the cell. A method of forming a therapeutic or diagnostic compound includes reacting a metal synthon with a chelating group covalently linked with a moiety capable of binding a gastrin releasing peptide receptor.