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BioWorld - Sunday, January 18, 2026
Home » Topics » New compound, BioWorld Science

New compound, BioWorld Science
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Illustration of tumor
Cancer

TLR7 agonist SMU-L-11 demonstrates antitumoral activity in melanoma

April 12, 2024
Recent work at Southern Medical University, Guangzhou, focused on the discovery and synthesis of imidazoquinoline-based Toll-like receptor 7 (TLR7) agonists as potential candidates for the treatment of melanoma.
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Microscope
Cancer

VB-15010, a potent and selective PARP-1 inhibitor and durable trapper, described

April 12, 2024
Previous studies have shown that targeting poly(ADP-ribose) polymerase 1 (PARP-1) demonstrated promising activity for cancer treatment.
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Cancer

Betta Pharmaceuticals reports a highly potent and selective KRAS G12D inhibitor

April 12, 2024
Results of preclinical studies with a highly potent KRAS (G12D mutant) inhibitor for the treatment of cancer were recently reported by researchers from Betta Pharmaceuticals Co. Ltd. BPI-501836 displayed higher inhibitory activity at KRAS G12D, when compared to the reference compound (IC50=0.25 and 2.4 nM, respectively) in NanoBRET assays.
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3D Rendering of tumor microenvironment
Cancer

PH027-1, a potent WRN inhibitor with a wide safety margin and efficacy against MSI-H tumors

April 10, 2024
Researchers from Puhe Biopharma Co. Ltd. presented the discovery and preclinical evaluation of PH027-1, a novel small-molecule Werner syndrome protein (WRN) inhibitor targeting microsatellite instability high (MSI-H) tumors.
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Endocrine/Metabolic

EphB tyrosine kinase inhibitor reduces whole-body weight in experimental obesity

April 9, 2024
Obesity is a chronic disorder tied to other disorders such as hyperglycemia, type 2 diabetes or cardiovascular disease, among others. Recent findings have suggested that EphB tyrosine kinase receptor and its ligand, ephrin B, may be involved in insulin signaling.
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Cancer

A potent and selective pMEK inhibitor for the treatment of pancreatic cancer

April 9, 2024
ABM Therapeutics Inc. presented a novel small-molecule, ATP-uncompetitive, phosphorylated MEK (pMEK) inhibitor – ABM-4095 – that potently prevents phosphorylation of MEK by RAF with moderate inhibition of MEK kinase activity; it is being investigated for the potential treatment of pancreatic cancer.
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Infection

Blacksmith’s new LpxC inhibitor has strong preclinical efficacy, no cardiovascular toxicity

April 5, 2024
Gram-negative bacteria require the metalloenzyme LpxC for their outer membrane biogenesis. Blacksmith Medicines Inc. has identified an LpxC inhibitor, FG-960, which has shown a robust in vitro and in vivo profile against multidrug-resistant Enterobacterales. FG-60 is currently being investigated for the treatment of urinary tract infections (UTIs).
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3D illustration of a nerve cell
Neurology/Psychiatric

MK-5661, a potent Nav1.8 inhibitor with promising safety and low oral dose predictions

April 4, 2024
Discovery of novel Nav1.8 inhibitors capable of achieving high levels of target modulation at low oral doses for the potential treatment of pain was reported by Merck & Co. Inc.
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Colorectal cancer illustration
Cancer

NCA-029, a potent HsClpP agonist with efficacy in colorectal cancer model

April 2, 2024
Researchers from West China Hospital of Sichuan University announced the discovery of homo sapiens caseinolytic protease P (HsClpP) agonists as new small-molecule candidates for the treatment of colorectal cancer.
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Concept art for blood sugar.
Gastrointestinal

Fructose metabolism inhibitor shows promise for metabolic dysfunction

March 28, 2024
Ketohexokinase (KHK) is a sugar kinase that mediates fructose metabolism.
Read More
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