摘要:
The present invention concerns compounds of formula (I):their process of preparation and compositions thereof. The present invention also concerns their use as diagnostic agent in PET imaging.
摘要:
Composition containing a microorganism, preferably an Archaea , expressing a TMA methyltransferase and a TMA methyl group acceptor corrinoid protein, capable of metabolizing trimethylamine (TMA) in the presence of hydrogen in a human cavity, such as the intestine or the vagina, for use as a medicament for treating, reducing or eliminating TMA at the level of the human cavity. In addition, a composition containing a TMA methyltransferase and a TMA methyl group acceptor corrinoid protein. These compositions are of use for treating trimethylaminuria, for treating vaginal fluids in the case of bacterial vaginosis and for reducing or eliminating odours due to TMA. These compositions are also of use for reducing the level of plasma TMAO, for preventing the formation of atheroma plaques and/or for preventing cardiovascular diseases.
摘要:
The present invention relates to the compound of formula (I), in which R1 represents Sn(R) 3 , B(OH) 2 , B(OR) 2 , a halogen atom, NO 2 , a radionuclide or a -N + (R) 3 group, where R is a (C 1 -C 6 ) alkyl group, R2 represents a hydrogen atom or a (C 1 -C 6 )alkyl group, R3 represents: - a -(CH 2 CH 2 O) n2 -(CH 2 ) n3 -X group, or - a –(CH 2 CH 2 O) n4 -(CH 2 )n 5 -Y group with Y representing a -C=C-H, a -N 3 or a -Ar-(CH 2 ) n6 -(OCH 2 CH 2 ) n7 -X group, and X represents a halogen atom, a radionuclide or a -OSO 2 R' group, where R' is a CF 3 , CH 3 , t -Bu, Ph, p -NO 2 Ph, p -BrPh or p -CH 3 Ph group, and their addition salts with pharmaceutically acceptable acids, The present invention also relates to pharmaceutical compositions comprising them and to their use in diagnosis, in particular with SPECT or PET imaging and in therapy of melanoma, via targeted radionuclide therapy.
摘要:
The present invention relates to the use of compounds for the treatment or prevention of pain in mammals, in particularly in human beings, and also to a process for preparing these compounds.
摘要:
An antagonist of the interaction between the Gp96 receptor and E. coli AIEC strains, for the prevention or treatment of inflammatory bowel disease. The antagonist is for specifically blocking or reducing the interaction between Gp96 receptor and the outer membrane vesicles (OMVs), typically the outer protein membrane OmpA of E. coli AIEC strains. The inventions provides for pharmaceutical compositions containing such an antagonist, which may be an antibody against gp96 or OmpA, or a gp96 or OmpA polypeptide. It may be combined to an antagonist of the interaction between the CEACAM6 receptor and E. coli AIEC strains, such as an anti-CEACAM6 antibody, a CEACAM6 polypeptide, or a mannoside or particle having a mannose unit. The invention also relates to a method for the diagnosis of inflammatory bowel disease, or of the determination of a predisposition of a person to develop inflammatory bowel disease.
摘要:
The present invention relates to a combination of a curcuminoid and a taxane for use in the treatment of a hormone-refractory prostate cancer (HRPC) in a patient in need thereof.
摘要:
The present invention relates to a process for manufacturing a fuse, comprising a step of defining the geometry of at least one fusible strip (16) employed in the fuse, in which step the following parameters are considered: a nominal current density (i16) conducted by the fusible strip (16); a nominal operating voltage of the fuse; a Joule integral corresponding, in the pre-arcing regime, to at least one part (18) of the fusible strip; and a Joule integral corresponding, in the arcing regime, to this part (18) of the fusible strip. The process is characterized in that, in this defining step, the Lorentz forces (F21-F25) acting on at least this part (18) of the fusible strip are also taken into consideration. The invention also relates to a fuse, comprising a ceramic casing and at least one fusible strip (16) placed in this casing, characterized in that it also comprises means for controlling the electromagnetic environment of the fusible strip (16) in a pre-arcing and/or a pre-arcing/arcing transition regime by amplifying or attenuating the Lorentz forces acting on at least one part of the fusible strip (16).
摘要:
The present invention relates to the use of riluzole for treating or preventing the adverse effects linked to the delivery of anti-neoplastic agents that have neurotoxic effects, for example such as platinum salts, taxanes and periwinkle alkaloids.