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BioWorld - Saturday, July 18, 2026
Home » Shanghai Hengrui Pharmaceutical Co. Ltd.

Articles Tagged with ''Shanghai Hengrui Pharmaceutical Co. Ltd.''

Concept art for cells receptors, inhibitors
Cancer

HRS-4642 is highly active against KRAS G12D-mutated tumors

July 19, 2024
The development of KRAS G12D inhibitors has proven challenging to date and, different from anti-KRAS G12C strategies, no compound targeting KRAS G12D mutation has been approved so far.
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Cancer

Hengrui scientists patent new PARP-1 inhibitors

March 20, 2024
Scientists at Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have disclosed poly(ADP-ribose) polymerase 1 (PARP-1; ARTD1) inhibitors reported to be useful for the treatment of cancer.
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Neurology/Psychiatric

Chinese scientists describe new Nav1.8 channel blockers

March 19, 2024
Scientists at Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have identified sodium channel protein type 10 subunit α (Nav1.8) channel blockers reported to be useful for the treatment of treatment of pain, Charcot-Marie-Tooth disease, urinary incontinence, multiple sclerosis and arrhythmia.
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Cancer

Chinese scientists discover new EGFR degradation inducers

Feb. 29, 2024
Scientists at Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have described proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to an EGFR targeting moiety reported to be useful for the treatment of cancer particularly, non-small-cell lung cancer (NSCLC).
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Cancer

Chinese researchers patent new HER2 inhibitors for cancer

Oct. 31, 2023
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have disclosed HER2 (erbB2) and/or HER2 (erbB2) mutant inhibitors reported to be useful for the treatment of cancer.
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Cancer

Hengrui reports YAP1/TEAD interaction inhibitors for cancer

Oct. 30, 2023
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have patented transcriptional coactivator YAP1/transcriptional enhancer factor (TEAD) interaction inhibitors reported to be useful for the treatment of cancer.
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Inflammatory

Jiangsu Hengrui Medicine and Shanghai Hengrui Pharmaceutical prepare and test RIPK1 inhibitors

Oct. 13, 2023
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have described fused heterocyclic compounds acting as receptor-interacting serine/threonine-protein kinase 1 (RIPK1; RIP-1) inhibitors.
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Dividing breast cancer cell.
Cancer

Novel CDK7 inhibitor SHR-5428 is effective in breast cancer models

Sep. 21, 2023
Cyclin-dependent kinase 7 (CDK7) regulates both cell cycle and global transcription and is a validated therapeutic target in cancer. Researchers from Shanghai Hengrui Pharmaceutical Co. Ltd. reported on the discovery and preclinical evaluation of SHR-5428, a noncovalent CDK7 inhibitor.
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Respiratory

Jiangsu Hengrui and Shanghai Hengrui patent describes new sGC activators

Sep. 14, 2023
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have divulged new soluble guanylate cyclase (sGC) activators reported to be useful for the treatment of chronic obstructive pulmonary disease, fibrosis, psoriasis, erectile dysfunction, multiple sclerosis, heart failure, overactive bladder and neuropathic pain, among others.
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Cancer

Jiangsu Hengrui Medicine and Shanghai Hengrui Pharmaceutical patent new RIPK1 inhibitors

Aug. 24, 2023
Jiangsu Hengrui Medicine Co. Ltd. and Shanghai Hengrui Pharmaceutical Co. Ltd. have disclosed fused heterocyclic compounds acting as receptor-interacting serine/threonine-protein kinase 1 (RIPK1; RIP-1) inhibitors reported to be useful for the treatment of cancer, amyotrophic lateral sclerosis and inflammatory disorders, among others.
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