IP Library › Granted Patent US 10,030,039
Granted Patent B2
US 10,030,039 · App. 15/468,462 · Granted Jul 24, 2018

Anti-cancer agent and cancer cell killing method

Inventors: Yoshihiro Ishikawa (Tokyo, JP); Haruki Eguchi (Tokyo, JP)
Assignees: IHI Corporation; Yoshihiro Ishikawa
C07F15/025A61K31/28A61K33/00A61K33/04A61K33/24A61K33/32
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Quick Facts
Patent No.
US 10,030,039
App. No.
15/468,462
Granted
Jul 24, 2018
Kind
B2
Abstract

[Object] An anticancer agent capable of continuously killing cancer cells in a plurality of phases is provided. [Solution] An anticancer agent contains a complex produced by making a metal-salen complex compound, which includes a central metal and (N, N, O, O) as a quadridentate ligand and is magnetic, bind to taxane molecules which are anticancerous; and the anticancer agent is to kill cancer cells regarding which phase transition of its cell cycle occurs between phases including Gap1, Synthesis, Gap2, and Mitosis and Cytokinesis. The present disclosure is suited for use to kill cancer cells of breast cancer and, particularly, cancer cells of triple-negative breast cancer. The present disclosure is designed to make the anticancer agent contact the cancer cells in two or more continuous phases selected from a group consisting of Gap1, Synthesis, Gap2, and Mitosis and Cytokinesis and kill the cancer cells.

Claims (15)

1. An anti-cancer agent, comprising:

a complex produced by making a metal-salen complex compound, which includes a central metal and N, N, O, O as a quadridentate ligand and is magnetic, the metal-salen complex compound binding to taxane molecules which are anticancerous,

wherein the anti-cancer agent is to kill cancer cells regarding which phase transition occurs between phases including Gap1, Synthesis, Gap2, and Mitosis and Cytokinesis, and

wherein the cancer cells are cancer cells of breast cancer or triple-negative breast cancer.

2. The anti-cancer agent according to claim 1 , wherein the taxane molecules are selected from either one of paclitaxel and docetaxel.

3. The anti-cancer agent according to claim 1 , wherein the metal-salen complex compound is represented by the following formula (1) bind to the taxane molecules:

wherein in formula (1), a central metal M 1 is of any one type selected from a group consisting of Fe, Cr, Mn, Co, Ni, Mo, Ru, Rh, Pd, W, Re, Os, Ir, Pt, Nd, Sm, Eu, and Gd.

4. The anti-cancer agent according to claim 1 , wherein the metal-salen complex compound is represented by the following formula (2) bind to the taxane molecules:

wherein in formula (2), a central metal M 2 and a central metal M 3 are independent of each other and are of any one type selected from a group consisting of Fe, Cr, Mn, Co, Ni, Mo, Ru, Rh, Pd, W, Re, Os, Ir, Pt, Nd, Sm, Eu, and Gd.

5. The anti-cancer agent according to claim 1 , wherein a central metal of the metal-salen complex compound is Fe.

6. The anti-cancer agent according to claim 1 , wherein the complex is represented by the following formula (3):

7. The anti-cancer agent according to claim 1 , wherein the complex is represented by the following formula (4):

8. A cancer cell killing method to kill cancer cells, the cancer cell killing method comprising:

preparing an anti-cancer agent containing a complex produced by making a metal-salen complex compound, which includes a central metal and N, N, O, O as a quadridentate ligand and is magnetic, the metal-salen complex compound binding to taxane molecules which are anticancerous that contacts the cancer cells in any two or more continuous phases selected from a group consisting of Gap1, Synthesis, Gap2, and Mitosis and Cytokinesis, wherein the cancer cells are cancer cells of breast cancer or triple-negative breast cancer.

9. The cancer cell killing method according to claim 8 , wherein the anti-cancer agent is made to contact the cancer cells by applying an external magnetic field to affected site tissues and making the anti-cancer agent indwell in the cancer cells constituting the affected site tissues.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2017
From: ISHIKAWA, YOSHIHIRO; EGUCHI, HARUKI
To: IHI CORPORATION; ISHIKAWA, YOSHIHIRO
Reel/Frame 041723/0015 →
Continuity (2)
Continuation PCTJP2014075745 · Sep 26, 2014
Related Publication 20170240581A1 · Aug 24, 2017
Cited By (2)
US 12,415,086 US 12,539,431