发明名称 |
Efficacy in treating bacterial infections |
摘要 |
The present disclosure relates to molecules which function as selective modulators (i.e., inhibitors and agonists) of the Ras-homologous (Rho) family of small GTPases and, in particular, CDC42 GTPase, and their use to treat bacterial infection including systemic infection from sources such as Staphylococcus aureus. |
申请公布号 |
US9259415(B2) |
申请公布日期 |
2016.02.16 |
申请号 |
US201313773871 |
申请日期 |
2013.02.22 |
申请人 |
Ball State Innovation Corporation;STC.UNM |
发明人 |
McDowell Susan A.;Sammelson Robert E.;Sklar Larry A.;Haynes Mark K. |
分类号 |
A61K31/415;A61K31/63;A61K31/635 |
主分类号 |
A61K31/415 |
代理机构 |
Bingham Greenebaum Doll LLP |
代理人 |
Boots Daniel L.;Chellgren Brian W.;Bingham Greenebaum Doll LLP |
主权项 |
1. A method of suppressing bacterial infection comprising:
administering ML 141 or its analogs to a patient with Staphylococcus infection, where the analogs are defined by the following structure: where R1 is selected from the group consisting of: hydrogen, hydroxyl, halogen, methoxy, methylenedioxy (—O—CH2—O—), wherein one oxygen of the methylenedioxy (—O—CH2—O—) is bonded to a carbon on a phenyl ring and the other oxygen of the methylenedioxy (—O—CH2—O—) is bonded to an adjacent carbon on the phenyl ring, and polyethylene glycol (—(O—CH2—CH2)n—O-Me) wherein n is any integer; where R2 is selected from the group consisting of: hydrogen, methoxy, and polyethylene glycol (—(O—CH2—CH2)n—O-Me) wherein n is any integer; where R3 is selected from the group consisting of: hydrogen and methyl. |
地址 |
Muncie IN US |