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公开(公告)号:WO2019241466A1
公开(公告)日:2019-12-19
申请号:PCT/US2019/036892
申请日:2019-06-13
Applicant: TEXAS TECH UNIVERSITY SYSTEM
Inventor: BERGESON, Susan, E. , SYAPIN, Peter , REID, Ted, W.
IPC: A61K31/65 , C07C237/26 , A61P25/32 , A61P25/36 , A61P31/00
Abstract: A method of treating Alcohol Use Disorder (AUD), Substance Use Disorder (SUD), tobacco use, pain, or proinflammatory disorders comprising: providing a subject with an effective amount of a modified tetracycline or derivative thereof to ameliorate or eliminate the AUD, SUD, tobacco use, pain, or proinflammatory disorder, and wherein the modified tetracycline or derivative thereof has reduced binding to a microbial ribosome and has the formula wherein R1 is acetyl, R2 is OH or acetyl, R3 is acetyl, R4 is H or acetyl, and R5 is acetyl.
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公开(公告)号:WO2022240936A1
公开(公告)日:2022-11-17
申请号:PCT/US2022/028695
申请日:2022-05-11
Applicant: TEXAS TECH UNIVERSITY SYSTEM
Inventor: REID, Ted, W. , FRALICK, Joe , TRAN, Phat, L. , BERFELD, Nicholas , SUNDIN, Olof
IPC: G01N33/553 , A61K31/095 , A61K33/04 , A61K33/08 , A61K33/24 , A61K47/50
Abstract: The present invention includes composition and methods for making and using a selenium-carrier conjugate for in vivo administration comprising: covalently attaching a selenium compound that reacts in vivo with naturally occurring reduced thiols and oxygen to produce superoxide, which can include a Fenton Complex that allows for a generation of hydroxyl radicals, and that wherein the selenium-carrier conjugate is stabilized against enzymatic degradation and clearance from the body and the synthetic targeting carrier binds target.
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公开(公告)号:WO2019241490A1
公开(公告)日:2019-12-19
申请号:PCT/US2019/036928
申请日:2019-06-13
Applicant: TEXAS TECH UNIVERSITY SYSTEM
Inventor: BERGESON, Susan, E. , SYAPIN, Peter , REID, Ted, W.
IPC: A61K31/65 , C07C237/26
Abstract: The present invention includes novel molecules and methods for using the same to treat Alcohol Use Disorder (AUD), Substance Use Disorder (SUD), tobacco use, pain, or proinflammatory disorders comprising: identifying a subject in need of treatment for at least one of AUD, SUD, pain, or a proinflammatory disorder; and providing the subject with an effective amount of a modified minocycline to ameliorate or eliminate the AUD, SUD, pain, or proinflammatory disorder and that has reduced, or no, antimicrobial activity, wherein the modified tetracycline has a formula, e.g., or the modified doxycycline, minocycline, and tigecycline and their tautomerized structures, where the R-groups shown in the minocycline example above could be different combination of halogen, acetyl ester, methyl ester, and diacetal.
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