Tetrazole derivatives
US-2024382468-A2 · Nov 21, 2024 · US
US10245261B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10245261-B2 |
| Application number | US-201615379696-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 15, 2016 |
| Priority date | Mar 15, 2013 |
| Publication date | Apr 2, 2019 |
| Grant date | Apr 2, 2019 |
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.
The present invention relates generally to the use of compounds to treat a variety of disorders, diseases and pathologic conditions and more specifically to the use of substituted indol-5-ol derivatives to modulate protein kinases and for treating protein kinase-mediated diseases.
Opening claim text (preview).
The invention claimed is: 1. A method of treating cancer in a mammal, wherein the cancer is selected from the group consisting of Chronic Myelogenous Leukemia (CIVIL), Acute Myelogenous Leukemia (AML) and thyroid, endometrial, gastric, breast and pancreatic carcinoma, and wherein the method comprises administering to the mammal a therapeutically effective amount of a composition comprising NTW-3475, wherein NTW-3475 is the compound having the structure: 2. The method of claim 1 , wherein NTW-3475 is administered with other active agents. 3. The method of claim 1 , wherein NTW-3475 is administered with a carrier. 4. The method of claim 1 wherein the cancer is pancreatic carcinoma. 5. The method of claim 1 , wherein the administration of the composition results in reduced signal transduction by the pERK pathway. 6. The method of claim 1 , wherein the administration of the composition results in reduced signal transduction by the pERK pathway. 7. The method of claim 1 , wherein the mammal is human. 8. A method for reducing signal transduction by the pERK pathway in cells comprising contacting the cells with NTW-3475, wherein the cells are MiaPaCa-2 cells or BxPC3 cells, and wherein NTW-3475 is the compound having the structure: 9. The method of claim 8 , wherein the cells are in vivo. 10. The method of claim 8 , wherein the cells are human. 11. The method of claim 1 , wherein the cancer is CML. 12. The method of claim 1 , wherein the cancer is AML. 13. The method of claim 1 , wherein the cancer is thyroid carcinoma. 14. The method of claim 1 , wherein the cancer is endometrial carcinoma. 15. The method of claim 1 , wherein the cancer is gastric carcinoma. 16. The method of claim 1 , wherein the cancer is breast carcinoma.
Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title
Immunosuppressants, e.g. drugs for graft rejection · CPC title
Immunostimulants · CPC title
Drugs for immunological or allergic disorders · CPC title
Antihypertensives · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.