Complement C3d-binding compounds
View Patent ↗The disclosure provides for compounds that bind with a high affinity to the C3d component of complement. The disclosure further provides for the use of the C3d-binding compounds as therapeutic and/or diagnostic agents for complement-mediated diseases or disorders.
1. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and/or diluent and a C3d-binding compound capable of complexing with complement component 3d (C3d) with a K d less than 100 μM, wherein the C3d-binding compound is selected from:
wherein,
R 1 -R 110 is independently selected from H, D, optionally substituted (C 1 -C 6 )alkyl, optionally substituted hetero-(C 1 -C 6 )alkyl, optionally substituted (C 1 -C 6 )alkenyl, optionally substituted hetero-(C 1 -C 6 )alkenyl, optionally substituted (C 1 -C 6 )alkynyl, optionally substituted hetero-(C 1 -C 6 )alkynyl, optionally substituted (C 1 -C 6 )cycloalkyl, optionally substituted (C 1 -C 6 )cycloalkenyl, optionally substituted aryl, optionally substituted heterocycle, hydroxyl, halo, imine, amine, amide, nitro, nitroso, nitrile, isocyanate, alkoxide, ester, carbonyl, carboxyl, thiol, SH, SR 1 , thionyl, sulfonyl, SiR 1 3 , PR 1 3 , and heterocycle.
2. The pharmaceutical composition of claim 1 , wherein the compound is capable of complexing with C3d with a K d less than 2 μM.
3. The pharmaceutical composition of claim 1 , wherein at least one of the 3 to 7 ring structures of the compound is heteroaromatic.
4. The pharmaceutical composition of claim 1 , wherein the compound has at least four nitrogen atoms.
5. The pharmaceutical composition of claim 1 , wherein the compound has at least 2 amide bonds.
6. The pharmaceutical composition of claim 1 , wherein the compound has florescence properties.
7. The pharmaceutical composition of claim 1 , wherein the compound has a structure selected from:
8. The pharmaceutical composition of claim 7 , wherein the derivative has substantially the same structure but 1 to 4 of the functional groups has been modified or changed, wherein the derivative is further characterized by increased binding affinity for C3d and/or improved fluorescence properties.
9. The pharmaceutical composition of claim 8 , wherein the improved fluorescent properties is exhibiting low quantum yield in its free (unbound) state, and undergoing a significant increase in quantum yield upon binding to C3d.
10. The pharmaceutical composition of claim 1 , wherein the composition is used to locate sites of complement activation, quantify the degree of complement activation, and to target therapeutic molecules to sites of complement-mediated inflammation.
11. A method of treating a complement-mediated disease or disorder in a subject, or the amelioration of the pathophysiology of diseases or disorders caused by the overactivity of the complement system in subject, comprising administering the pharmaceutical composition of claim 1 , wherein the complement-mediated disease or disorder is selected from age-related macular degeneration, systemic lupus, rheumatoid arthritis, glomerulonephritis, psoriasis, asthma, Alzheimer's disease, Huntington's disease, Parkinson's disease, age-related macular degeneration, membranoproliferative glomerulonephritis Type 2, atypical hemolytic uremic syndrome, hereditary angioedema, accelerated atherosclerosis, and paroxysmal nocturnal hemoglobinuria.
12. The method of claim 11 , wherein the complement-mediated disease or disorder is age-related macular degeneration and wherein the compound further allows for localization of C3d in a subject's eye(s) by fluorescence.
13. The method of claim 12 , where the pharmaceutical composition is formulated for intravitreal injection, subtenon injection, or topical administration.
14. A method of diagnosing or detecting a complement mediated disease or disorder, comprising administering a pharmaceutical composition of claim 1 and measuring the binding of the C3d-binding compound to C3d by detecting fluorescence wherein a localized increase in fluorescence in indicative of the complement mediated disease or disorder.
15. A C3d-binding compound selected from:
wherein,
R 1 -R 110 is independently selected from H, D, optionally substituted (C 1 -C 6 )alkyl, optionally substituted hetero-(C 1 -C 6 )alkyl, optionally substituted (C 1 -C 6 )alkenyl, optionally substituted hetero-(C 1 -C 6 )alkenyl, optionally substituted (C 1 -C 6 )alkynyl, optionally substituted hetero-(C 1 -C 6 )alkynyl, optionally substituted (C 1 -C 6 )cycloalkyl, optionally substituted (C 1 -C 6 )cycloalkenyl, optionally substituted aryl, optionally substituted heterocycle, hydroxyl, halo, imine, amine, amide, nitro, nitroso, nitrile, isocyanate, alkoxide, ester, carbonyl, carboxyl, thiol, SH, SR 1 , thionyl, sulfonyl, SiR 1 3 , PR 1 3 , and heterocycle.
16. The Cd3-binding compound of claim 15 , wherein the compound is selected form the group consisting of: