Cyclopentane heptan(ENE)OIC acid, 2-heteroarylalkenyl derivatives as therapeutic agents
A compound comprising or a pharmaceutically acceptable salt or a prodrug thereof, having the groups described in detail herein is disclosed. Also disclosed herein are compounds comprising or derivatives thereof, or pharmaceutically acceptable salts, tetrazoles, or prodrugs of compounds of the structure or derivatives thereof, said derivatives being described in detail herein. Also disclosed herein are methods of treating diseases or conditions, including glaucoma and elevated intraocular pressure. Compositions and methods of manufacturing medicaments related thereto are also disclosed.
1. A compound having a formula
or a pharmaceutically acceptable salt or a prodrug thereof,
wherein
a dashed line represents the presence or absence of a bond;
A is —(CH 2 ) 6 —, or cis —CH 2 —CH═CH—(CH 2 ) 3 —, wherein 1 or 2 carbons may be substituted with S or O
B is hydrogen, —CH 3 , or ═CH 2 ;
J is —OH or ═O;
D is —(CH 2 ) n —, —X(CH 2 ) n , or —(CH 2 ) n X—, wherein n is from 0 to 3 and X is S or O; and
E is thienyl or benzothienyl, or substituted thienyl or benzothienyl having substituents comprising from 1 to 6 non-hydrogen atoms each.
2. The compound of claim 1 having a formula
or a pharmaceutically acceptable salt, a tetrazol, or a prodrug thereof.
3. The compound of claim 2 wherein E is an aromatic moiety or heteroaromatic moiety having from 1 to 3 substituents, wherein said aromatic moiety or heteroaromatic moiety is thienyl or benzothienyl and said substituents are selected from the group consisting of methyl, methoxy, bromo, chloro, and fluoro.
4. The compound of claim 2 wherein E is thienyl having from 2 to 4 substituents, said substituents comprising no more than 3 carbon atoms each.
5. The compound of claim 1 having a formula
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof.
6. The compound of claim 5 wherein E is an aromatic moiety or heteroaromatic moiety having from 1 to 3 substituents, wherein said aromatic moiety or heteroaromatic moiety is thienyl or benzothienyl and said substituents are selected from the group consisting of methyl, methoxy, bromo, chloro, and fluoro.
7. The compound of claim 5 wherein E is thienyl having from 2 to 4 substituents, said substituents comprising no more than 3 carbon atoms each.
8. The compound of claim 1 wherein A is —(CH 2 ) 6 — or cis-CH 2 —CH═CH—(CH 2 ) 3 — having no heteroatom substitution.
9. The compound of claim 1 wherein E is a thienyl having one methyl and one bromo substituent.
10. The compound of claim 1 having a formula
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof.
11. The compound of claim 10 which is not a tetrazole or a prodrug.
12. The compound of claim 1 wherein B is hydrogen.
13. The compound of claim 1 wherein B is methyl.
14. The compound of claim 1 wherein B is methylene.
15. The compound of claim 1 selected from the group consisting of
(Z)-7-{(1R,2R)-2-[(E)-(S)-5-(4-Bromo-5-methyl-thiophen-2-yl)-3-hydroxy-pent-1-enyl]-3- methyl-5-hydroxy-cyclopentyl}-hept-5-enoic acid acid;
(Z)-7-{(1R,2R)-2-[(E)-(S)-5-(4-Bromo-5-methyl-thiophen-2-yl)-3-hydroxy-pent-1-enyl]-3- ethyl-5-hydroxy-cyclopentyl}-hept-5-enoic acid acid; and
(Z)-7-{(1R,2S)-2-[(E)-(S)-5-(4-Bromo-5-methyl-thiophen-2-yl)-3-hydroxy-pent-1-enyl]-5- hydroxy-3-vinyl-cyclopentyl}-hept-5-enoic acid.
16. A method comprising administering an effective amount of
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof,
to a mammal for the prevention or treatment of glaucoma or ocular hypertension,
wherein
the dashed lines represent the presence or absence of a bond;
A is —(CH 2 ) 6 —, or cis —CH 2 —CH═CH—(CH 2 ) 3 —, wherein 1 or 2 carbons may be substituted with S or O;
B is hydrogen, —CH 3 , or ═CH 2 ;
J is —OH or ═O;
D is —(CH 2 ) n —, —X(CH 2 ) n , or —(CH 2 ) n X—, wherein n is from 0 to 3 and X is S or O; and
E is thienyl or benzothienyl, or substituted thienyl or benzothienyl having substituents comprising from 1 to 6 non-hydrogen atoms each.
17. The method of claim 16 wherein A is cis-CH 2 —CH═CH—(CH 2 ) 3 —.
18. The method of claim 16 wherein E disubstituted thienyl.
19. The method of claim 16 comprising
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof.
20. The method of claim 16 comprising
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof
wherein
E is an aromatic or a heteroaromatic moiety consisting of a single aromatic ring and one or two substituents, said ring consisting of five or six atoms, and said substituents being selected from the group consisting of bromo, chloro, flouro, methyl, and methoxy.
21. A liquid comprising
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof,
wherein said liquid is ophthalmically acceptable; and
wherein the dashed lines represent the presence or absence of a bond;
A is —(CH 2 ) 6 —, or cis —CH 2 —CH═CH—(CH 2 ) 3 —, wherein 1 or 2 carbons may be substituted with S or O;
B is hydrogen, —CH 3 , or ═CH 2 ;
J is —OH or ═O;
D is —(CH 2 ) n —, —X(CH 2 ) n , or —(CH 2 ) n X—, wherein n is from 0 to 3 and X is S or O; and
E is an aromatic or heteroaromatic moiety, or a substituted aromatic or heteroaromatic moiety having substituents comprising from 1 to 6 non-hydrogen atoms each.
22. A compound having an α and an ω chain having a formula
or a derivative thereof,
wherein B is hydrogen, —CH 3 or ═CH 2 , and
a dashed line represents the presence or absence of a bond;
wherein said derivative has a structure as shown above except that 1 or 2 alterations are made to the α chain and/or the ω chain, and
wherein an alteration consists of:
a. adding, removing, or substituting a non-hydrogen atom, or
b. changing the bond order of an existing covalent bond without adding or deleting said bond;
or a pharmaceutically acceptable salt, a tetrazole, or a prodrug thereof.
23. The compound of claim 22 wherein O or S is substituted for CH 2 .
24. The compound of claim 22 wherein no alteration is made to the α chain.
25. The compound of claim 22 wherein no alteration is made to the ω chain.
26. The compound of claim 22 having no Br.
27. The compound of claim 22 having no CH 3 .