The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 07, 2017

Filed:

Dec. 11, 2013
Applicant:

Hong Kong Baptist University, Kowloon, HK;

Inventors:

Ge Zhang, Kowloon, HK;

Aiping Lu, Kowloon, HK;

Cheng Wang, Kowloon, HK;

Cheng Lu, Kowloon, HK;

Jun Lu, Kowloon, HK;

Biao Liu, Kowloon, HK;

Assignee:

HONG KONG BAPTIST UNIVERSITY, KOWLOON TONG, KOWLOON, HK;

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
C12N 15/115 (2010.01); A61K 47/48 (2006.01); A61K 31/7088 (2006.01); A61K 31/585 (2006.01); C07J 73/00 (2006.01);
U.S. Cl.
CPC ...
C12N 15/115 (2013.01); A61K 31/585 (2013.01); A61K 31/7088 (2013.01); A61K 47/48092 (2013.01); C07J 73/003 (2013.01); C12N 2310/16 (2013.01); C12N 2310/351 (2013.01); C12N 2320/30 (2013.01);
Abstract

Tripyolide-nucleic acid aptamer derivatives, a preparation method and use thereof are shown. The structure of the triptolide-nucleic acid aptamer derivatives is as shown by formula I, wherein the definitions of R-R, G, A, B, M, Z and X are described. The present invention uses a nucleic acid aptamer and triptolide or modified compounds thereof as the starting materials, and introduces a linking group A at the C-14 hydroxyl group, epoxy groups and five-membered ring lactones in triptolide, then connects it to a nucleic acid aptamer B, and obtains the triptolide-nucleic acid aptamer derivatives. The triptolide-nucleic acid aptamer derivatives of the present invention have the characteristics of good targeting, a high anti-cancer activity, low toxicity and side effects, good water solubility and high bioavailability, and the preparation method of the present invention is scientific and reasonable and has a controllable quality and good repeatability, and is thereby suitable for production.


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