Method for treating ovarian cancer and/or Hodgkin lymphomia with a gold(III) complex

US9782380B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9782380-B2
Application numberUS-201715496352-A
CountryUS
Kind codeB2
Filing dateApr 25, 2017
Priority dateDec 3, 2015
Publication dateOct 10, 2017
Grant dateOct 10, 2017

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A method for treating cancer and gold(III) complexes with diaminocyclohexane ligand as anticancer agents. Also described are a pharmaceutical composition incorporating the gold(III) complexes and a method of synthesizing the gold(III) complexes.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for treating cancer, comprising: administering an effective amount of at least one of a gold(III) complex represented by formula (I), a gold(III) complex represented by formula (II): a pharmaceutically acceptable salt, solvate, prodrug, or a combination thereof to a subject; wherein the cancer is ovarian cancer, Hodgkin lymphoma, or both; each of R 1 is independently selected from the group consisting of a hydrogen and a methyl group; each of R 2 is independently selected from the group consisting of a hydrogen, a halogen, a hydroxyl, an amino, a nitro, a cyano, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted arylalkyl, an optionally substituted heteroaryl, an optionally substituted alkoxyl, an optionally substituted aryl, an optionally substituted alkenyl, a N-monosubstituted amino group, and a N,N-disubstituted amino group; and X is a chloride anion. 2. The method of claim 1 , wherein R 2 is hydrogen. 3. The method of claim 1 , wherein the gold(III) complex represented by formula (I) is and the gold(III) complex represented by formula (II) is 4. The method of claim 1 , wherein the gold(III) complex represented by formula (I) and/or the gold(III) complex represented by formula (II) is administered to the subject as the pharmaceutically acceptable salt comprising at least one counterion which is at least one pharmaceutically acceptable anion selected from the group consisting of fluoride, chloride, bromide, iodide, nitrate, sulfate, phosphate, methanesulfonate, ethanesulfonate, p-toluenesulfonate, salicylate, malate, maleate, succinate, tartrate, citrate, acetate, perchlorate, trifluoromethanesulfonate, acetylacetonate, hexafluorophosphate, and hexafluoroacetylacetonate. 5. The method of claim 4 , wherein the at least one counterion is chloride. 6. The method of claim 1 , wherein the cancer is ovarian cancer, and the ovarian cancer is resistant to cisplatin. 7. The method of claim 1 , wherein the cancer is Hodgkin lymphoma and the Hodgkin lymphoma is classical Hodgkin lymphoma. 8. The method of claim 1 , further comprising measuring a concentration of a biomarker and/or detecting a mutation in the biomarker before and/or after the administering. 9. The method of claim 8 , wherein the biomarker is at least one selected from the group consisting of BRCA1, BRCA2, CCL17, CD163, CD30, NF-κB, Gal-1, CA125, HE4, mesothelin, transthyretin, ApoA1, VCAM, IL-6, IL-8, B7-H4, serum amyloid A, transferrin, osteopontin, kallikreins, OVX1, VEGF, AGR-2, inhibin, M-CSF, uPAR, EGF receptor, lysophosphatidyl acid, beta2-microglobulin, miRNA, and Epstein-Barr virus DNA. 10. The method of claim 9 , wherein the concentration of the biomarker is measured with an ELISA assay and/or the mutation in the biomarker is measured with a PCR assay. 11. The method of claim 1 , wherein the subject is a mammal. 12. The method of claim 1 , wherein the effective amount of the at least one of the gold(III) complex represented by formula (I), the gold(III) complex represented by formula (II), the pharmaceutically acceptable salt, solvate, prodrug, and a combination thereof is in a range of 1-100 mg/kg.

Assignees

Inventors

Classifications

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9782380B2 cover?
A method for treating cancer and gold(III) complexes with diaminocyclohexane ligand as anticancer agents. Also described are a pharmaceutical composition incorporating the gold(III) complexes and a method of synthesizing the gold(III) complexes.
Who is the assignee on this patent?
Univ King Fahd Pet & Minerals
What technology area does this patent fall under?
Primary CPC classification C12Q1/6886. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).