5-bromo-indirubins
US-11306072-B2 · Apr 19, 2022 · US
US2022274964A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022274964-A1 |
| Application number | US-202217690323-A |
| Country | US |
| Kind code | A1 |
| Filing date | Mar 9, 2022 |
| Priority date | Mar 14, 2013 |
| Publication date | Sep 1, 2022 |
| Grant date | — |
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Disclosed herein inter alia are compositions and methods for treating cancer using 5-Br-indirubin derivatives.
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1 . A compound, or pharmaceutically acceptable salt thereof, having the formula: wherein L is an unsubstituted alkylene; R 1 is —NR 2 R 3 ; R 2 and R 3 are joined together to forma substituted or unsubstituted heterocycloalkyl or substituted or unsubstituted heteroaryl; R 5 and R 6 are independently hydrogen. 2 .- 5 . (canceled) 6 . The compound of claim 1 , wherein L is unsubstituted C 2 alkylene. 7 .- 17 . (canceled) 18 . The compound of claim 1 , wherein R 2 and R 3 are joined together to form a substituted or unsubstituted C 5 -C 7 heterocycloalkyl. 19 . The compound of claim 18 , wherein R 2 and R 3 are joined together to form a substituted C 5 -C 7 heterocycloalkyl. 20 . The compound of claim 19 , wherein R 2 and R 3 are joined together to form an R 23 -substituted C 5 -C 7 heterocycloalkyl, wherein R 23 is independently a substituted or unsubstituted alkyl or substituted or unsubstituted heteroalkyl. 21 . The compound of claim 20 , wherein R 23 is independently a substituted or unsubstituted C 1 -C 8 alkyl or substituted or unsubstituted 2 to 8 membered heteroalkyl. 22 . The compound of claim 16 , wherein R 2 and R 3 are joined together to form a substituted or unsubstituted pyrrolidinyl. 23 . The compound of claim 16 , wherein R 2 and R 3 are joined together to form a substituted or unsubstituted piperazinyl. 24 . The compound of claim 1 comprising a protonated nitrogen cation or a plurality of protonated nitrogen cations. 25 . (canceled) 26 . (canceled) 27 . The compound of claim 1 having formula: including pharmaceutical salts thereof. 28 . A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of claim 1 . 29 . The compound of claim 1 for use in treating cancer in a subject in need thereof. 30 . The compound of claim 29 , wherein said compound is administered in an effective amount to said subject. 31 . The compound of claim 29 , wherein said compound is in a pharmaceutical composition comprising a pharmaceutically acceptable excipient. 32 . The compound of claim 29 , wherein said cancer is lung cancer, breast cancer, ovarian cancer, leukemia, lymphoma, melanoma, pancreatic cancer, sarcoma, bladder cancer, bone cancer, brain cancer, cervical cancer, colon cancer, esophageal cancer, gastric cancer, liver cancer, head and neck cancer, kidney cancer, myeloma, thyroid cancer, or prostate cancer. 33 . The compound of claim 29 , wherein said compound is co-administered with an effective amount of an anti-cancer agent. 34 . A method of modulating a kinase, a JAK, JAK2, TYK2, Src, c-Src, ABL1, ABL1 T315I, an Aurora kinase, Aurora A, GSK-3β, a CDK, a STAT, or STAT3, said method comprising contacting the protein with the compound of claim 1 . 35 . The method of claim 34 , wherein the compound is in a pharmaceutical composition comprising a pharmaceutically acceptable excipient. 36 . A method of modulating a Janus kinase, said method comprising contacting said Janus kinase with the compound of claim 1 . 37 . The method of claim 36 , wherein the compound is in a pharmaceutical composition comprising a pharmaceutically acceptable excipient.
directly linked by a ring-member-to-ring-member bond · CPC title
containing three or more hetero rings · CPC title
containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole (nicotine A61K31/465) · CPC title
Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin · CPC title
specific for leukemia · CPC title
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