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BioWorld - Friday, May 8, 2026
Home » Topics » New compound, BioWorld Science

New compound, BioWorld Science
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Art concept for tumor
Cancer

ETS-003, YAP/TAZ-TEAD protein-protein interaction inhibitor, shows broad antitumor activity

May 12, 2023
Researchers from Etern Biopharma (Shanghai) Co. Ltd. recently reported the discovery and preclinical characterization of ETS-003, a novel YAP/TAZ-TEAD protein-protein interaction (PPI) inhibitor, being developed for the treatment of cancer.
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Ocular

Melanocortin receptor activation with PL-9588 is promising for glaucoma as it persistently reduces intraocular pressure

May 12, 2023
Glaucoma is a complex disease characterized...
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Hands holding holographic intestine
Gastrointestinal

Researchers report discovery of ROR-107, a GPBAR1 agonist and RORγt inverse agonist for IBD

May 12, 2023
Inflammatory bowel disease (IBD) is a chronic, immunologically mediated disorder of the gastrointestinal tract in which tissue damage and sustained inflammation lead to long-term dysfunction of the gastrointestinal tract.
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Close up of man's eye
Ocular

Suprachoroidal injection of integrin inhibitor CLS-301 exhibits durable retinal compartmentalization

May 11, 2023
Diabetic macular edema (DME) is a leading contributing etiological factor for retinopathy...
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Microscope with laptop displaying histology image.
Cancer

ClpP agonist TR-107 inhibits cancer growth both in vitro and in vivo

May 11, 2023
TR-107 is a new oral ClpP agonist that targets the ClpX complex, which is responsible for the...
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Cancer

PARG inhibitor SYX-3759 shows selective and potent in vitro and in vivo cytotoxicity in HRD tumors

May 9, 2023
Data on the poly(ADP-ribose) glycohydrolase (PARG) inhibitor SYX-3759, being investigated for the treatment of homologous recombination deficient (HRD) malignancies, were recently discussed by researchers from Hangzhou Synrx Therapeutics Technology Co. Ltd.
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Microscopic image of acute myeloid leukemia (AML) cells.
Cancer

HPB-092, a potent and selective FLT3/IRAK-4 dual inhibitor, shows activity in AML models

May 5, 2023
Researchers from Hangzhou Polymed Biopharmaceuticals Inc. have reported the discovery and preclinical evaluation of HPB-092, an FMS-like tyrosine kinase 3 (FLT3) and interleukin-1 receptor-associated kinase 4 (IRAK-4) dual inhibitor, being developed for the treatment of acute myeloid leukemia (AML).
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Photomicrograph of diffuse large B-cell lymphoma
Cancer

Discovery of DW-91170, a dual EZH1/2 inhibitor with potent activity in lymphoma models

May 4, 2023
Researchers from Dong Wha Pharmaceutical Co. Ltd. presented preclinical evaluation of a newly discovered histone-lysine N-methyltransferase EZH1/2 dual inhibitor, DW-91170, being developed for the treatment of lymphoma.
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Microscopic image of Methicillin-resistant S. aureus.
Infection

Dioxane-linked optimization of the bacterial MRSA antibiotic topoisomerase inhibitor OSUAB-0284

May 4, 2023
Novel topoisomerase inhibitors that target DNA gyrase and topoisomerase IV have the potential...
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Cancer cells
Cancer

Researchers report development of HZ-R078, a novel long-acting STAT3 degrader

May 3, 2023
The Janus kinase/signal transducer and activator of transcription (JAK-STAT) pathway comprises four JAK kinases and seven STAT transcription factors. Among the latter, STAT3 is the best-known oncogene and its essential role in normal tissue makes its complete blockage useless for treatment due to severe side effects.
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