US2015306077A1PendingUtilityA1
Novel Compositions and Methods for Treating Cancer
Est. expiryOct 28, 2031(~5.2 yrs left)· nominal 20-yr term from priority
C07D 471/14C07D 403/12A61P 35/00A61K 45/06A61K 31/404C07D 471/04C07D 209/18C07D 209/14C07D 209/20A61K 31/437
40
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Provided herein are methods and compositions inter alia for treating diseases, including hyperproliferative diseases, migraine headaches, and depression.
Claims
exact text as granted — not AI-modified1 .- 20 . (canceled)
21 . A method of treating cancer in a patient in need of such treatment, said method comprising administering a therapeutically effective amount of a compound having the formula:
wherein
R 1A is independently hydrogen,
halogen, —CX 1A 3 , —C(O)R 7A , —C(O)—OR 7A , —C(O)NR 7A R 8A , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R 2A is independently hydrogen,
halogen, —CX 2A 3 , —C(O)R 9A , —C(O)—OR 9A , —C(O)NR 9A R 10A , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R 1A and R 2A are optionally joined to form a substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl;
R 3 is independently hydrogen, halogen, —CX 3 3 , —CN, —SO 2 Cl, —SO 1 R 14 , —SO k NR 11 R 12 , —NHNH 2 , —ONR 11 R 12 , —NHC═(O)NHNH 2 ,
—NHC═(O)NR 11 R 12 , —N(O) m , —NR 11 R 12 , —C(O)R 13 , —C(O)—OR 13 , —O—C(O)—R 13 , —C(O)NR 11 R 12 , —NR 11 C(O)R 13 , —OR 14 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
R 7A , R 8A , R 9A , R 10A , R 11 , R 12 , R 13 , and R 14 are independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl;
A 1 is independently ═N— or ═CR 3 —;
k and m are independently 1 or 2;
n is independently an integer from 0 to 4;
z1 is independently an integer from 0 to 3; and
X 1A , X 2A , and X 3 are independently —Cl, —Br, —I, or —F.
22 . The method of claim 21 having the formula:
23 . The method of claim 21 having the formula:
24 . The method of claim 21 , wherein
R 1A is independently hydrogen, unsubstituted alkyl, —C(O)R 7A or —C(O)—OR 7A ; and R 7A is independently hydrogen, substituted or unsubstituted C 1 -C 20 alkyl, substituted or unsubstituted 2 to 20 membered heteroalkyl, substituted or unsubstituted C 3 -C 8 cycloalkyl, substituted or unsubstituted 3 to 8 membered heterocycloalkyl, substituted or unsubstituted C 6 -C 10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl.
25 . The method of claim 21 , wherein
R 2A is independently hydrogen, unsubstituted alkyl, —C(O)R 9A or —C(O)—OR 9A ; and R 9A is independently hydrogen, substituted or unsubstituted C 1 -C 20 alkyl, substituted or unsubstituted 2 to 20 membered heteroalkyl, substituted or unsubstituted C 3 -C 8 cycloalkyl, substituted or unsubstituted 3 to 8 membered heterocycloalkyl, substituted or unsubstituted C 6 -C 10 aryl, or substituted or unsubstituted 5 to 10 membered heteroaryl.
26 . The method of claim 21 , wherein R 3 is independently hydrogen, halogen, —C(O)R 13 , —O—C(O)—R 13 , —C(O)—OR 13 , —OR 14 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
27 . The method of claim 21 , wherein
R 3 is independently hydrogen or —OR 14 ; and R 14 is independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.
28 . The method of claim 27 , wherein R 14 is independently hydrogen, substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl.
29 . The method of claim 27 , wherein R 14 is independently substituted or unsubstituted alkyl.
30 . The method of claim 27 , wherein R 14 is independently substituted or unsubstituted C 1 -C 20 alkyl.
31 . The method of claim 27 , wherein R 14 is independently substituted or unsubstituted C 6 -C 16 alkyl.
32 . The method of claim 27 , wherein R 14 is independently unsubstituted C 6 -C 16 alkyl.
33 . The method of claim 21 , wherein A 1 is ═CR 3 —.
34 . The method of claim 21 , wherein A 1 is ═N—.
35 . The method of claim 21 , wherein A 1 is ═CH—.
36 . The method of claim 21 , wherein the compound is:
37 . The method of claim 21 , wherein said cancer is breast cancer, ovarian cancer, pancreatic cancer, liver cancer, glioblastoma, glioma, lung cancer, prostate cancer, leukemia, or melanoma.
38 . The method of claim 21 , wherein said cancer is breast cancer.
39 . The method of claim 21 , wherein said cancer is metastatic cancer.
40 . The method of claim 21 , wherein said compound is co-administered with a chemotherapeutic agent.Join the waitlist — get patent alerts
Track US2015306077A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.