Compounds and compositions for inhibiting the activity of ABL1, ABL2 and BCR-ABL1
US-9458112-B2 · Oct 4, 2016 · US
US9896475B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9896475-B2 |
| Application number | US-201515505327-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 26, 2015 |
| Priority date | Aug 26, 2014 |
| Publication date | Feb 20, 2018 |
| Grant date | Feb 20, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Pyridyl analogs of 1-(2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl) imidazole and pharmaceutical compositions containing the same are provided. The present invention is a tnterpenoid compound of Formula I, or a hydrate, isomer, prodrug or pharmaceutically acceptable salt thereof: wherein one or more of R, R or R is independently a substituted or unsubstituted aryl group, heteroaryl group, cycloalkyl group or heterocyclyl group, and the remaining R groups are hydrogen. The pyridyl analogs of CD-DO-1m 1 have been developed, which are more stable in human plasma and achieve a higher concentration in target tissues such as liver, pancreas, kidney and lungs.
Opening claim text (preview).
What is claimed is: 1. A triterpenoid compound having the structure of Formula I, or a hydrate, isomer, prodrug or pharmaceutically acceptable salt thereof: wherein one or more of R 1 , R 2 or R 3 is independently a substituted or unsubstituted heteroaryl group, cycloalkyl group or heterocyclyl group, and the remaining R groups are hydrogen. 2. The triterpenoid compound of claim 1 , wherein R 2 is a substituted or unsubstituted heteroaryl group, cycloalkyl group or heterocyclyl group, and R 1 and R 3 are hydrogen. 3. A pharmaceutical composition comprising the compound of claim 1 in admixture with a pharmaceutically acceptable carrier.
having two double bonds between ring members or between ring members and non-ring members · CPC title
Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by contraction of only one ring by one or two atoms · CPC title
directly linked by a ring-member-to-ring-member bond · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.