Non-symmetric tripyrranes in the synthesis of novel macrocycles
View Patent ↗The present invention provides certain non-symmetric tripyrranes; that is, tripyrranes that do not contain a mirror plane of symmetry perpendicular to the plane containing the tripyrrane. Further, the invention includes texaphyrin compounds and sapphyrin compounds, as well as other polypyrrolic macrocycles, prepared using tripyrranes of Formula I as a precursor. These macrocycles are characterized by a tripyrrolic portion of the macrocyclic ring having substituents that cause the heterocycle to lack a plane of symmetry perpendicular to the plane of the macrocycle.
1. A texaphyrin of Formula II:
its hydrate, pharmaceutically acceptable salt, or a pro drug form thereof wherein,
M is a monovalent, divalent, trivalent, or tetravalent metal cation;
R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are independently chosen from the group consisting of hydrogen, halogen, hydroxyl, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted haloalkyl, nitro, acyl, optionally substituted alkoxy, saccharide, optionally substituted amino, carboxyl, optionally substituted carboxyalkyl, optionally substituted carboxyamide, optionally substituted carboxyamidealkyl, optionally substituted heterocycle, optionally substituted cycloalkyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted heterocycloalkylalkyl, and the group —X—Y, in which X is a covalent bond or a linker and Y is a catalytic group, a chemotherapeutic agent, or a
with the proviso that R 1 is different from R 6 , R 2 is different from R 5 and R 5 does not represent (CH 2 ) 2 —CO—N ((CH 2 ) 2 —OH) 2 , CH 2 CH 3 , or (CH 2 ) 2 —CO—N(CH 3 )(CH 2 —(CHOH) 4 —CH 2 —OH);
AL is an apical ligand; and
n is an integer of 1–5.
2. The texaphyrin of claim 1 , wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 11 and R 12 are independently chosen from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted alkoxy, carboxyl, and optionally substituted carboxyalkyl, and R 7 and R 8 are independently chosen from the group consisting of hydrogen, hydroxy, optionally substituted alkyl, and optionally substituted alkoxy; and R 9 and R 10 are hydrogen.
3. The texaphyrin of claim 1 , wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 11 and R 12 are independently chosen from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted alkoxy, carboxyl, and optionally substituted carboxyalkyl, R 7 is chosen from the group consisting of hydrogen, hydroxy, optionally substituted alkyl, and optionally substituted alkoxy, R 8 is a site-directing molecule or a chemotherapeutic agent; and R 9 and R 10 are hydrogen.
4. The texaphyrin of claim 2 , wherein R 1 and R 2 are ethyl; R 4 and R 6 are methyl; R 3 and R 5 are hydroxypropyl; R 7 and R 8 are independently hydrogen, hydroxy, methyl, methoxy, —OCH 2 CH 2 CH 2 OH, or —O(CH 2 CH 2 O) 3 CH 3 ; and R 9 , R 10 , R 11 and R 12 are all hydrogen.
5. A pharmaceutical composition comprising at least one pharmaceutically acceptable excipient and a therapeutically effective amount of a compound of claim 1 .