Tetracyclic anthraquinone derivatives
AssigneeTianjin Hemay Oncology Pharmaceutical Co., Ltd.
InventorsHesheng Zhang, Aihong Huo, Zhenzhong Li
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Abstract
Disclosed are a compound represented by formula (I) and a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, W, n are defined as in the present application. Also disclosed is a method for treating cancer, comprising administering to a subject in need thereof a therapeutically effective amount of the compound represented by formula (I) or a pharmaceutically acceptable salt thereof. The compound and a salt thereof according to the present application possess good anticancer and/or antitumor activity, and good water solubility and stability, as well as good tolerance in animal bodies. Also disclosed is a process for preparing a compound represented by formula (I) of the present application.
Claims10
A method for treating-tumor and/or cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a compound represented by formula (I) or a pharmaceutically acceptable salt thereof, or a formulation comprising a compound represented by formula (I) or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier,
- wherein:
- R1 is selected from the group consisting of H, optionally substituted alkyl, and optionally substituted alkoxy;
- R2 is selected from the group consisting of H, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted (alkyleneoxy)malkyl, optionally substituted heterocyclyl, optionally substituted alkyl, and optionally substituted —S(═O)2R;
- R3 is selected from the group consisting of H, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted (alkyleneoxy)malkyl, optionally substituted heterocyclyl, optionally substituted alkyl, and optionally substituted —S(═O)2R;
- or NR2R3 represents optionally substituted heterocyclyl;
- wherein R comprises optionally substituted alkyl, optionally substituted cyclohydrocarbyl, optionally substituted heterocyclyl, optionally substituted aryl, or optionally substituted heteroaryl;
- m is selected from the group consisting of 0, 23, 2, 3, 4, 5, 6, 7, 8, 9, 10, and 11;
- W is selected from the group consisting of O and NH;
- R4 is selected from the group consisting of H, F, and optionally substituted alkyl;
- R5 is selected from the group consisting of H, F, optionally substituted alkyl and OR6, wherein R6 is selected from the group consisting of H and tetrahydropyran-2-yl;
- and
- n is selected from the group consisting of 23, 2 and 3;
- wherein the tumor and/or cancer is selected from the group consisting of gastric cancer, intestine cancer, head and neck cancer, cervical cancer, brain glioma, various leukemia, lymphoma, and multiple bone marrow cancer.
Dependencies are inferred from the claim text.