Patent classifications
C07C279/12
Compound for improving L-arginine bioavailability
The present application relates to a compound which may be useful for mediating NO production and improving L-arginine bioavailability in a subject. Pharmaceutical compositions comprising the compound and methods of using the compound are also provided.
Compound for improving L-arginine bioavailability
The present application relates to a compound which may be useful for mediating NO production and improving L-arginine bioavailability in a subject. Pharmaceutical compositions comprising the compound and methods of using the compound are also provided.
Non-peptidic cell-penetrating motifs
Disclosed are compounds that can penetrate the mitochondrial membrane and that are able to deliver cargo (e.g., therapeutic agents) specifically to the mitochondria.
Non-peptidic cell-penetrating motifs
Disclosed are compounds that can penetrate the mitochondrial membrane and that are able to deliver cargo (e.g., therapeutic agents) specifically to the mitochondria.
Amino acid derivatives and their uses
Provided are compounds described by the Formula I: ##STR00001##
wherein: R.sub.1 is a linear or branched, saturated or unsaturated aliphatic group having from 5 to 22 carbon atoms; R.sub.2 is selected from the group consisting of the functional groups: —NH.sub.2; ##STR00002##
and salts thereof; n is from 0 to 4; and R.sub.3 is a linear or branched, saturated or unsaturated aliphatic group having from 1 to 6 carbon atoms. Also provided are compositions comprising, and methods of use of, the compounds of the present invention.
Amino acid derivatives and their uses
Provided are compounds described by the Formula I: ##STR00001##
wherein: R.sub.1 is a linear or branched, saturated or unsaturated aliphatic group having from 5 to 22 carbon atoms; R.sub.2 is selected from the group consisting of the functional groups: —NH.sub.2; ##STR00002##
and salts thereof; n is from 0 to 4; and R.sub.3 is a linear or branched, saturated or unsaturated aliphatic group having from 1 to 6 carbon atoms. Also provided are compositions comprising, and methods of use of, the compounds of the present invention.
Methods for Detecting Symmetrical Dimethylarginine
Method of detecting Symmetrical dimethyl arginine (SDMA) in biological samples. SDMA analogs for generating anti-SDMA antibodies having little or no cross-reactivity with asymmetrical dimethyl arginine, arginine, and monomethylarginine. The analogs have a protected or free thiol (—SH) group or hydroxyl (—OH) group that allow them to be linked to a suitable conjugation target which can be, for example, a protein containing molecule of a label. The anti-SDMA antibodies can be used in diagnostic immunoassay for the diagnosis of SDMA associated disorders and/or diseases.
Methods for Detecting Symmetrical Dimethylarginine
Method of detecting Symmetrical dimethyl arginine (SDMA) in biological samples. SDMA analogs for generating anti-SDMA antibodies having little or no cross-reactivity with asymmetrical dimethyl arginine, arginine, and monomethylarginine. The analogs have a protected or free thiol (—SH) group or hydroxyl (—OH) group that allow them to be linked to a suitable conjugation target which can be, for example, a protein containing molecule of a label. The anti-SDMA antibodies can be used in diagnostic immunoassay for the diagnosis of SDMA associated disorders and/or diseases.
Capsaicinoid prodrug compounds and their use in treating medical conditions
The invention provides capsaicinoid prodrug compounds, pharmaceutical compositions, and their use in the treatment of medical conditions, such as pain, and in agonizing TRPV1 activity.
Amino Acid Derivatives and Their Uses
Provided are compounds described by the Formula I:
##STR00001##
wherein: R.sub.1 is a linear or branched, saturated or unsaturated aliphatic group having from 5 to 22 carbon atoms; R.sub.2 is selected from the group consisting of the functional groups:
##STR00002##
and salts thereof; n is from 0 to 4; and R.sub.3 is a linear or branched, saturated or unsaturated aliphatic group having from 1 to 6 carbon atoms. Also provided are compositions comprising, and methods of use of, the compounds of the present invention.