Asgpr-binding compounds for the degradation of extracellular proteins
US-2024424108-A1 · Dec 26, 2024 · US
US2016016941A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016016941-A1 |
| Application number | US-201414774961-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 11, 2014 |
| Priority date | Mar 11, 2013 |
| Publication date | Jan 21, 2016 |
| Grant date | — |
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Pharmaceutical compositions of the invention comprise functionalized lactone derivatives having a disease-modifying action in the treatment of diseases associated with dysregulation of 5-hydroxytryptamine receptor 7 activity.
Opening claim text (preview).
What is claimed is: 1 . A compound having formula (I): Including hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, wherein: A is selected from a group consisting of R 1a and R 1b are independently selected from a group consisting of hydrogen, C 1-6 linear alkyl, C 1-6 branched alkyl, and optionally substituted aryl; R 1a and R 1b are taken together with the atom to which they are bound to form a ring having from 3 to 7 ring atoms; R 2a and R 2b are independently selected from a group consisting of hydrogen, C 1-6 linear alkyl, C 1-6 branched alkyl, and optionally substituted aryl; R 2a and R 2b are taken together with the atom to which they are bound to form a ring having from 3 to 7 ring atoms; R 3 is selected from a group consisting of C 1-6 linear alkyl, C 1-6 branched alkyl, C 3-7 cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, R 4 is optionally substituted aryl; R 5a and R 5b are each independently optionally substituted aryl; R 6a , R 6b , R 6c , and R 6d are each independently selected from a group consisting of hydrogen, halogen, OH, C 1-6 linear alkyl, C 1-6 branched alkyl, C 1-6 alkoxy, C 1-6 haloalkyl, C 1-6 haloalkoxy, cyano, NH(C 1-6 alkyl), N(C 1-6 alkyl) 2 , NHC(O)R 7 , C(O)NHR 7 , C(O)N(R 7 ) 2 , SH, SC 1-6 alkyl, SO 2 NH 2 , SO 2 NHR 7 , SO 2 R 7 , and NHSO 2 R 7 ; R 7 is independently selected at each occurrence from a group consisting of C 1-6 linear alkyl, C 1-6 branched alkyl, and C 3-7 cycloalkyl; HetAr is optionally substituted heteroaryl; n is 1, 2, or 3; and m is 1 or 2. 2 . The compound of claim 1 , having the formula (XXXXII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 3 . The compound of claim 1 , having the formula (XXXXIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 4 . The compound of claim 1 , having the formula (XXXXIV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 5 . The compound of claim 1 , having the formula (XXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 6 . The compound of claim 1 , having the formula (XXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 7 . The compound of claim 1 , having the formula (XXXXVII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 8 . The compound of claim 1 , having the formula (XXXXVIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 9 . The compound of claim 1 , having the formula (XXXXIX): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 10 . The compound of claim 1 , having the formula (XXXXX): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 11 . The compound of claim 1 , having the formula (XXXXXI): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 12 . The compound of claim 1 , having the formula (XXXXXII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 13 . The compound of claim 1 , having the formula (XXXXXIII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 14 . The compound of claim 1 , having the formula (XXXXXIV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 15 . The compound of claim 1 , having the formula (XXXXXV): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 16 . The compound of claim 1 , having the formula (XXXXXVI): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 17 . The compound of claim 1 , having the formula (XXXXXVII): Including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 18 . The compound of claim 1 , having the formula (XXXXXVIII): including hydrates, solvates, enantiomers, diasteromers, pharmaceutically acceptable salts, prodrugs and complexes thereof. 19 . A compound of claim 1 , comprising: 2-(4-(2-(4,4-diethyl-5-oxotetrahydrofuran-2-yl)ethyl)piperazin-1-yl)benzonitrile; 3,3-diethyl-5-(2-(4-(4-methoxyphenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(4-hydroxyphenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(4-nitrophenyl)piperazin-1-yl)ethyl)dihydrofuran-2(3H)-one; 3,3-diethyl-5-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth
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