Abstract: 10-oxo-6,1-dihydrobenzo[e]pyrido[1,2-c][1,3]oxazine-9-carboxylic acid derivatives of formula (I) as hepatitis B surface antigen inhibitors or pharmaceutically acceptable salts thereof, and uses of a compound of formula (I) or pharmaceutically acceptable salts thereof and pharmaceutical compositions thereof in preparation of medicaments for treatment of viral hepatitis B.
Type:
Application
Filed:
March 9, 2018
Publication date:
February 6, 2020
Applicants:
FUJIAN COSUNTER PHARMACEUTICAL CO., LTD., MEDSHINE DISCOVERY INC.
Inventors:
Fei SUN, Jinhua DU, Yanbin HU, Lili ZHOU, Charles Z. DING, Shuhhui CHEN
Abstract: A benzotriazole-derived ? and ?-unsaturated amide compound used as TGF-?R1 inhibitor or a pharmaceutically acceptable salt thereof, the structure of the compound being as shown in formula (I).
Type:
Grant
Filed:
June 8, 2017
Date of Patent:
February 4, 2020
Assignees:
Genfleet Therapeutics (Shanghai) Inc., Medshine Discovery Inc.
Inventors:
Fei Sun, Lifang Wu, Charles Z. Ding, Guoping Hu, Jian Li, Shuhui Chen, Jianyu Lu
Abstract: Provided are a phosphodiesterase-4 (PDE4) inhibitor and application thereof in preparation of a medication for treating a disease related to PDE4. Specifically disclosed is a compound as shown in formula (I) and a pharmaceutically acceptable salt thereof.
Abstract: Disclosed in the present invention is a type of novel ?-lactamase inhibitors, and specifically disclosed are a compound represented by formula (I) or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
June 2, 2017
Publication date:
January 9, 2020
Applicant:
MEDSHINE DISCOVERY INC.
Inventors:
Boyu HU, Charles Z. DING, Zhigang HUANG, Ruibin LIN, Minliang XIAO, Jinsheng XIE, Shuhui CHEN, Cheng LI
Abstract: FGFR and VEGFR inhibitors are provided, and compounds represented by formula (1) or formula (II) as FGFR and VEGFR inhibitors, pharmaceutically acceptable salts or tautomers thereof are specifically disclosed.
Abstract: The present invention discloses a benzimidazole-linked indole compound acting as novel divalent IAP antagonist, specifically disclosing the compound shown in formulas (I) or a pharmaceutically acceptable salt thereof.
Type:
Grant
Filed:
April 27, 2017
Date of Patent:
December 17, 2019
Assignee:
MEDSHINE DISCOVERY INC.
Inventors:
Fei Sun, Charles Z. Ding, Zhe Cai, Wenyuan Qian, Guoping Hu, Jian Li, Shuhui Chen
Abstract: Provided are compounds of formula I and formula II or pharmaceutically acceptable salts of the compounds and pharmaceutical compositions thereof. The compounds of formula I and formula II or the pharmaceutically acceptable salts of the compounds provide indole 2,3-dioxygenase (IDO) inhibitory activity and are capable of treating IDO-mediated immunosuppressive diseases, such as infectious diseases or cancer.
Type:
Grant
Filed:
February 20, 2017
Date of Patent:
November 26, 2019
Assignees:
Chia Tai Tianqing Pharmaceutical Group Co., Ltd., Medshine Discovery Inc.
Abstract: The present invention discloses a crystal form and salt of a nitroimidazole compound, and a manufacturing method thereof. The invention further comprises an application of the crystal form and salt in preparing a pharmaceutical product for preventing and treating an infection caused by Mycobacterium tuberculosis or another microbe.
Type:
Application
Filed:
July 21, 2017
Publication date:
September 12, 2019
Applicant:
Medshine Discovery Inc.
Inventors:
Wei LUO, Charles Z. DING, Zhigang HUANG, Yinghu HU, Zongbin LI, Qingqing LU
Abstract: The present invention relates to linkers, containing amide surrogates with a regular or a novel lysosomal enzymatic cleavable dipeptidic unit, to connect cytotoxic drugs to antibodies. The present invention also relates to ADCs (antibody-drug conjugates) derived from these amide surrogate linkers for the treatment of cancers.
Type:
Grant
Filed:
July 13, 2015
Date of Patent:
May 7, 2019
Assignee:
MEDSHINE DISCOVERY INC.
Inventors:
Chun Sing Li, Jian Li, Yong Cang, Shuhui Chen, Gang Li, Xiongbin Xu, Lun Lu
Abstract: Disclosed is a substituted nitroimidazole derivative, which is mainly used for treating related diseases caused by mycobacterial infections, such as Mycobacterium tuberculosis, especially being suitable for diseases caused by resistant Mycobacterium tuberculosis.
Type:
Grant
Filed:
January 28, 2016
Date of Patent:
March 12, 2019
Assignee:
MEDSHINE DISCOVERY INC.
Inventors:
Wei Luo, Charles Z. Ding, Zhigang Huang, Shuhui Chen
Abstract: Disclosed are two axially chiral isomers and pharmaceutically available salts thereof, preparation method therefor, and pharmaceutical use of the two axially chiral isomers or pharmaceutical compositions thereof.
Type:
Grant
Filed:
April 1, 2016
Date of Patent:
January 22, 2019
Assignee:
MEDSHINE DISCOVERY INC.
Inventors:
Jianfei Wang, Jing Zhang, Long Zhang, Yang Zhang, Jian Li, Shuhui Chen
Abstract: Disclosed is a substituted nitroimidazole derivative, which is mainly used for treating related diseases caused by mycobacterial infections, such as Mycobacterium tuberculosis, especially being suitable for diseases caused by resistant Mycobacterium tuberculosis.
Type:
Application
Filed:
January 28, 2016
Publication date:
June 14, 2018
Applicant:
MEDSHINE DISCOVERY INC.
Inventors:
Wei LUO, Charles Z. DING, Zhigang HUANG, Shuhui CHEN
Abstract: Disclosed are a novel pyrrolopyrimidine ring compound as a TLR7 agonist or a pharmaceutically acceptable salt thereof, used for preventing or treating allergic rhinitis and asthma. In particular, disclosed is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
December 29, 2015
Publication date:
May 31, 2018
Applicant:
MEDSHINE DISCOVERY INC.
Inventors:
Charles Z. DING, Fei SUN, Lifang WU, Jinhua DU, Yasuhiro KATSU, Guoping HU, Jian LI
Abstract: Disclosed is a substituted 2H-pyrazole derivative serving as a selective CDK4/6 inhibitor. Specifically, disclosed is a compound of formula (I) or a pharmaceutically acceptable salt thereof which serves as a selective CDK4/6 inhibitor.
Type:
Grant
Filed:
March 10, 2016
Date of Patent:
May 15, 2018
Assignees:
CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD., MEDSHINE DISCOVERY INC.
Inventors:
Charles Z. Ding, Shuhui Chen, Baoping Zhao, Zhaobing Xu, Yingchun Liu, Ruibin Lin, Fei Wang, Jian Li
Abstract: The present invention discloses a class of isoquinolinesulfonyl derivatives as RHO kinase inhibitors, and pharmaceutical compositions thereof, and relates to pharmaceutically acceptable uses thereof. Specifically, the present invention relates to a compound as represented by formula (I), or a pharmaceutically acceptable salt thereof.
Abstract: Disclosed is a series of analogs of 4H-pyrazolo[1,5-?]benzimidazole compound as PARP inhibitors. In particular, disclosed in the invention is a compound as shown by formula (I) or a pharmaceutically acceptable salt thereof as a PARP inhibitor.
Type:
Grant
Filed:
March 30, 2015
Date of Patent:
January 2, 2018
Assignees:
Hubei Bio-Pharmaceutical Industrial Technological Institute Inc., Humanwell Healthcare (Group) Co., Ltd., Medshine Discovery Inc.
Inventors:
Xuehai Wang, Zhaozhong Ding, Yong Xu, Shuhui Chen, Lie Li, Gang Li, Ronghua Tu, Cailin Wang, Yang Yue, Zhibo Zhang, Hailiang Chen, Wenjie Sun, Lu Huang
Abstract: Hydroxyl purine compounds represented by formula (I), tautomers or pharmaceutically acceptable salts thereof, and applications thereof as PDE2 or TNF-? inhibitors.
Type:
Application
Filed:
September 22, 2015
Publication date:
November 16, 2017
Applicants:
GUANGDONG ZHONGSHENG PHARMACEUTICAL CO., LTD, MEDSHINE DISCOVERY INC.
Abstract: The present invention discloses a novel DGAT1 inhibitor, especially the compound of formula (I) or a pharmaceutically acceptable salt thereof, preparation and pharmaceutical composition thereof, as well as their uses in the preparation of a medicament for the prevention and treatment of Familial hyperchylomicronemia (FCS), obesity, hyperlipoproteinemia or hypertriglyceridemia.
Type:
Grant
Filed:
August 18, 2014
Date of Patent:
November 7, 2017
Assignees:
Qingdao Huanghai Pharmaceutical Co., Ltd., Medshine Discovery Inc.
Abstract: The present invention relates to linkers, containing amide surrogates with a regular or a novel lysosomal enzymatic cleavable dipeptidic unit, to connect cytotoxic drugs to antibodies. The present invention also relates to ADCs (antibody-drug conjugates) derived from these amide surrogate linkers for the treatment of cancers.
Type:
Application
Filed:
July 13, 2015
Publication date:
July 20, 2017
Applicant:
MEDSHINE DISCOVERY INC.
Inventors:
Chun Sing LI, Jian LI, Yong CANG, Shuhui CHEN, Gang LI, Xiongbin XU, Lun LU
Abstract: Disclosed is a dihydropyrimido fused ring derivative as a HBV inhibitor, and in particular relates to a compound shown as formula (I) or a pharmaceutically acceptable salt thereof.