Salinosporamides and methods for use thereof
View Patent ↗The present invention is based on the discovery that certain fermentation products of the marine actinomycete strains CNB392 and CNB476 are effective inhibitors of hyperproliferative mammalian cells. The CNB392 and CNB476 strains lie within the family Micromonosporaceae, and the generic epithet Salinospora has been proposed for this obligate marine group. The reaction products produced by this strain are classified as salinosporamides, and are particularly advantageous in treating neoplastic disorders due to their low molecular weight, low IC 50 values, high pharmaceutical potency, and selectivity for cancer cells over fungi.
1. An isolated compound of the structure (I):
wherein:
R 1 is a substituted alkyl;
R 2 is methyl;
R 3 is hydroxy;
Each R 4 is independently alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, or substituted cycloalkyl;
E 1 , E 3 , and E 4 are —O;
E 2 is —NR 5 , wherein R 5 is —H or C 1 -C 6 alkyl; and
X is 0 to 8.
2. The compound of claim 1 , wherein E 2 is —NH.
3. The compound of claim 1 , wherein R 1 is a substituted alkyl substituted with one or more substituents selected from the group consisting of halogen, cyano, oxyacyl, amino, amido, —C(O)H, acyl, carboxyl, and sulfonamide.
4. The compound of claim 3 , wherein the substituted alkyl is a halogenated alkyl.
5. The compound of claim 4 , wherein the halogenated alkyl is a chlorinated alkyl.
6. A pharmaceutical composition comprising at least one compound of claim 1 in a pharmaceutically acceptable carrier thereof.
7. The pharmaceutical composition of claim 6 , further comprising at least one anti-neoplastic agent in combination with the at least one compound of claim 1 .
8. A method of treating a human refractile cell proliferative disorder, comprising contacting human refractile cancer cells with a therapeutically effective amount of a compound of the structure (I):
wherein:
R 1 to R 3 are each independently —H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, cycloalkyl, substituted cycloalkyl, alkoxy, substituted alkoxy, thioalkyl, substituted thioalkyl, hydroxy, halogen, amino, amido, carboxyl, —C(O)H, acyl, oxyacyl, carbamate, sulfonamide, or sulfuryl;
Each R 4 is independently alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, or substituted cycloalkyl;
E 1 to E 4 are each independently —O, —NR 5 , or —S, wherein R 5 is —H or C 1 -C 6 alkyl; and
X is 0 to 8.
9. The method of claim 8 , wherein the compound is of the structure (V):
10. The method of claim 8 , wherein the human refractile cell proliferative disorder is selected from the group consisting of a mammary cancer, small-cell lung cancer, non-small-cell lung cancer, colorectal cancer, leukemia, melanoma, pancreatic adenocarcinoma, central nervous system (CNS) cancer, ovarian cancer, prostate cancer, sarcoma of soft tissue, sarcoma of bone, head cancer, neck cancer, gastric cancer, thyroid cancer, stomach cancer, myeloma, bladder cancer, renal cancer, neuroendocrine cancer, a non-Hodgkin's disease, and Hodgkin's disease.
11. The method of claim 10 , wherein the human refractile cell proliferative disorder is a sarcoma of a soft tissue or a sarcoma of a bone.
12. The method of claim 10 , wherein the human refractile cell proliferative disorder is leukemia.
13. The method of claim 10 , wherein the human refractile cell proliferative disorder is myeloma.
14. The method of claim 10 , wherein the human refractile cell proliferative disorder is ovarian cancer.
15. The method of claim 10 , wherein the human refractile cell proliferative disorder is prostate.
16. The method of claim 10 , wherein the human refractile cell proliferative disorder is non-Hodgkin's disease.
17. The method of claim 10 , wherein the human refractile cell proliferative disorder is pancreatic adenocarcinoma.
18. The method of claim 8 , wherein: R 1 is a substituted alkyl; R 2 is methyl; R 3 is hydroxy; each R 4 is independently alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, cycloalkyl, or substituted cycloalkyl; E 1 , E 4 and E 3 are —O E 2 is —NR 5 , wherein R 5 is —H or C 1 -C 6 alkyl; and X is 0 to 8.
19. The method of claim 18 , wherein R 1 is a halogenated alkyl.
20. The method of claim 8 , further comprising administering at least one anti-neoplastic agent in combination with at least one compound of the structure (I).
21. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and an effective amount of a compound of the structure:
wherein the pharmaceutical composition is in a solid form.
22. The compound of claim 1 , wherein the structure is: