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BioWorld - Thursday, April 2, 2026
Breaking News: Best of BioWorld Science: Q1Breaking News: Best of BioWorld Science: Q1Breaking News: Best of BioWorld Science: Q1
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3D illustration of a chain of amino acid or biomolecules called protein
Drug design, drug delivery & technologies

Omnigeniq’s journey from space science to drug design

Feb. 18, 2026
By Tamra Sami
No Comments
A project that started as a bioreactor to assist astronauts in deep space to keep medications safe in a microgravity environment could help pharma companies model how drugs behave in the human body. Omnigeniq unveiled at the J.P. Morgan Healthcare conference the first computer model of a human protein as it exists in the body, confirming that native protein topology can be calculated directly from physics.
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Cancer

Shenzhen Targetrx reports EGFR-targeted PROTACs

Feb. 18, 2026
Shenzhen Targetrx Inc. has designed new proteolysis targeting chimeric (PROTACs) compounds comprising cereblon (CRBN) ligands covalently bonded to an EGFR L858R-, L858R/T790M double mutant- and L858R/T790M/C797S triple mutant-targeting moiety through a linker reported to useful for the treatment of non-small-cell lung cancer.
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Endocrine/metabolic

Deeplake Pharmaceuticals divulges new dual XOR/URAT1 inhibitors

Feb. 18, 2026
Deeplake Pharmaceuticals (Shandong) Co. Ltd. has patented oxazolo- or thiazolo-indole compounds acting as xanthine dehydrogenase/oxidase (XDH; XOR) and/or solute carrier family 22 member 12 (SLC22A12; URAT1) dual inhibitors. They are reported to be useful for the treatment of gout and hyperuricemia.
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Neurology/psychiatric

5-HT2A receptor agonists divulged in University of California patent

Feb. 18, 2026
The University of California has reported new azocino[4,5,6-cd]indoles acting as 5-HT2A receptor agonists and thus potentially useful for the treatment of neurological and psychiatric disorders.
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Cancer

Tyra Biosciences patents new FGFR inhibitors

Feb. 18, 2026
Tyra Biosciences Inc. has disclosed new indazole compounds acting as fibroblast growth factor receptor (FGFR) inhibitors. They are reported to be useful for the treatment of cancer and developmental disorders.
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Cardiovascular

China Pharmaceutical University identifies sphingomyelin phosphodiesterase inhibitors

Feb. 18, 2026
No Comments
China Pharmaceutical University has prepared and tested sphingomyelin phosphodiesterase (SMPD1; aSMase) inhibitors potentially useful for the treatment of cancer, autoimmune disease, chronic obstructive pulmonary disease (COPD), Alzheimer’s disease, depression, diabetes, hepatic steatosis and stroke, among others.
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Melanoma cells stained with an H & E stain and magnified to 320x.
Cancer

HOXD13 drives angiogenesis and immune evasion in melanoma

Feb. 18, 2026
No Comments
Although physiological immune responses require increased tissue vasculature, many solid tumors simultaneously activate angiogenesis to meet the increasing demand for oxygen and nutrients while excluding immune cells. The exact molecular mechanisms by which cancer cells control this immune-refractory angiogenic process remain widely unclear.
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Klebsiella pneumoniae colonies in petri dish
Infection

First-in-class non-β-lactam targeting AMR gram-negative pathogens

Feb. 18, 2026
No Comments
Antimicrobial resistance (AMR) is increasingly compromising the effectiveness of essential antibiotics, resulting in higher global mortality and morbidity rates. Despite this urgent need, few new antibiotics, particularly against gram-negative bacteria, are in development.
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Dollar sign droplet above test tube
Ocular

Financing at Gelmedix supports GMX-101 for geographic atrophy

Feb. 18, 2026
No Comments
Gelmedix Inc. has completed a $13 million seed financing to support progression of the company’s lead program, GMX-101, a retinal pigment epithelial (RPE) cell therapy to treat late-stage geographic atrophy.
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Cancer

New compound against tumors with aberrant FGFR2 signaling

Feb. 18, 2026
No Comments
Fibroblast growth factor receptor 2 (FGFR2) is a transmembrane tyrosine kinase that regulates signaling pathways controlling cell survival and proliferation. Dysregulation of FGFR2, through amplification or activating mutations, contributes to tumor development, making it an attractive target for therapeutic intervention in oncology.
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