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    <title>BioWorld Science</title>
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    <item>
      <title>Hexapharmatec identifies new TFEB inducers</title>
      <description>Hexapharmatec Co. Ltd. has discovered new transcription factor EB (TFEB) inducers described as potentially useful for the treatment of colitis, kidney and hepatic fibrosis.</description>
      <content:encoded>
        <![CDATA[Hexapharmatec Co. Ltd. has discovered new transcription factor EB (TFEB) inducers described as potentially useful for the treatment of colitis, kidney and hepatic fibrosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732324</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732324-hexapharmatec-identifies-new-tfeb-inducers</link>
    </item>
    <item>
      <title>Hzyg ligands disclosed in MSD patent</title>
      <description>Merck Sharp &amp; Dohme LLC (MSD) has synthesized new protein zer-1 homolog (Hzyg, ZER1) ligands potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Merck Sharp & Dohme LLC (MSD) has synthesized new protein zer-1 homolog (Hzyg, ZER1) ligands potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732323</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732323-hzyg-ligands-disclosed-in-msd-patent</link>
    </item>
    <item>
      <title>Yaoya Technology identifies new KRAS G12D mutant inhibitors</title>
      <description>Yaoya Technology (Shanghai) Co. Ltd. has discovered new pyrimidothiopyrandione GTPase KRAS G12D mutant inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Yaoya Technology (Shanghai) Co. Ltd. has discovered new pyrimidothiopyrandione GTPase KRAS G12D mutant inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732322</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732322-yaoya-technology-identifies-new-kras-g12d-mutant-inhibitors</link>
    </item>
    <item>
      <title>Blueprint Medicines reports new CDK4 degrader PROTACs</title>
      <description>Blueprint Medicines Corp. has identified new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a cyclin-dependent kinase 4 (CDK4)-targeting moiety potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Blueprint Medicines Corp. has identified new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a cyclin-dependent kinase 4 (CDK4)-targeting moiety potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732321</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732321-blueprint-medicines-reports-new-cdk4-degrader-protacs</link>
    </item>
    <item>
      <title>Sichuan Kelun-Biotech discloses new KEAP1 activators and NRF2 degradation inducers</title>
      <description>Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has synthesized new Kelch-like ECH-associated protein 1 (KEAP1) activators and nuclear factor erythroid 2-related factor 2 (NRF2) degradation inducers potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has synthesized new Kelch-like ECH-associated protein 1 (KEAP1) activators and nuclear factor erythroid 2-related factor 2 (NRF2) degradation inducers potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732320</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732320-sichuan-kelun-biotech-discloses-new-keap1-activators-and-nrf2-degradation-inducers</link>
    </item>
    <item>
      <title>Gensci-134: a long-acting growth hormone receptor agonist fusion protein</title>
      <description>Gensci-134 (Genescience Pharmaceuticals Co. Ltd.) is a growth hormone receptor (GHR) agonist fusion protein that mimics the biological activity of growth hormone (GH), does not contain GH sequence and selectively activates human GHR for the treatment of GH deficiency (GHD). It is designed to enable once-every-4-week dosing.</description>
      <content:encoded>
        <![CDATA[Gensci-134 (Genescience Pharmaceuticals Co. Ltd.) is a growth hormone receptor (GHR) agonist fusion protein that mimics the biological activity of growth hormone (GH), does not contain GH sequence and selectively activates human GHR for the treatment of GH deficiency (GHD). It is designed to enable once-every-4-week dosing.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732314</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732314-gensci-134-a-long-acting-growth-hormone-receptor-agonist-fusion-protein</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Human-growth-hormone-molecule-illustration.webp?t=1782832635" type="image/jpeg" medium="image" fileSize="522427">
        <media:title type="plain">3D illustration of human growth hormone molecules</media:title>
        <media:description type="plain">Human growth hormone.</media:description>
      </media:content>
    </item>
    <item>
      <title>CDW reports in vivo results for LNP-LANFA</title>
      <description>A Biotech Co. Ltd., a subsidiary of CDW Holding Ltd., and Neoregen Biotech Co. Ltd. have obtained promising results from in vivo murine testing of LNP-LANFA, a next-generation lipid nanoparticle (LNP) technology under joint development.</description>
      <content:encoded>
        <![CDATA[A Biotech Co. Ltd., a subsidiary of CDW Holding Ltd., and Neoregen Biotech Co. Ltd. have obtained promising results from in vivo murine testing of LNP-LANFA, a next-generation lipid nanoparticle (LNP) technology under joint development.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732313</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732313-cdw-reports-in-vivo-results-for-lnp-lanfa</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Nanoparticle-for-drug-delivery.webp?t=1678982296" type="image/png" medium="image" fileSize="1053011">
        <media:title type="plain">3D concept image of nanoparticle layers</media:title>
      </media:content>
    </item>
    <item>
      <title>Preclinical study of subpial AAV-GAD65/VGAT delivery for spinal injury-induced spasticity</title>
      <description>Spinal cord traumatic injury can lead to loss of motor function and progressive development of muscle spasticity and rigidity. Researchers from the University of California San Diego and collaborating institutions investigated a novel gene-delivery-based antispasticity strategy.</description>
      <content:encoded>
        <![CDATA[Spinal cord traumatic injury can lead to loss of motor function and progressive development of muscle spasticity and rigidity. Researchers from the University of California San Diego and collaborating institutions investigated a novel gene-delivery-based antispasticity strategy.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732312</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732312-preclinical-study-of-subpial-aav-gad65-vgat-delivery-for-spinal-injury-induced-spasticity</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Musculoskeletal/Spine-orthopedics-digital.webp?t=1645135963" type="image/png" medium="image" fileSize="386472">
        <media:title type="plain">Digital spine concept art</media:title>
      </media:content>
    </item>
    <item>
      <title>Smartbax raises additional funds to advance antibiotic pipeline</title>
      <description>Smartbax GmbH has announced the successful second closing of its pre-series A financing round for a total of €6.3 million (US$7.2 million) as it advances development of next-generation antibiotics against multidrug-resistant bacteria.</description>
      <content:encoded>
        <![CDATA[Smartbax GmbH has announced the successful second closing of its pre-series A financing round for a total of €6.3 million (US$7.2 million) as it advances development of next-generation antibiotics against multidrug-resistant bacteria.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732311</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732311-smartbax-raises-additional-funds-to-advance-antibiotic-pipeline</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/medical-research-data-rd.webp?t=1618594248" type="image/png" medium="image" fileSize="94245">
        <media:title type="plain">Illustration of medical professionals, research</media:title>
      </media:content>
    </item>
    <item>
      <title>Deerfield-backed Boulevard, Metis pen $1.6B trispecific TCE deal</title>
      <description>A U.S. biotechnology company founded by Deerfield Management Company L.P. licensed exclusive rights to Metis Techbio Co. Ltd.’s preclinical trispecific T-cell engager (TCE) for autoimmune disorders in a potential $1.62 billion deal.</description>
      <content:encoded>
        <![CDATA[A U.S. biotechnology company founded by Deerfield Management Company L.P. licensed exclusive rights to Metis Techbio Co. Ltd.’s preclinical trispecific T-cell engager (TCE) for autoimmune disorders in a potential $1.62 billion deal.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732310</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732310-deerfield-backed-boulevard-metis-pen-16b-trispecific-tce-deal</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Deals-and-MAs/Deal-merger-money-lightbulb.webp?t=1588286368" type="image/png" medium="image" fileSize="65086">
        <media:title type="plain">Handshake, businessmen holding dollar sign, lightbulb</media:title>
      </media:content>
    </item>
    <item>
      <title>Novel GPR52 agonist shows antipsychotic-like effects</title>
      <description>Predominantly expressed in the striatum, a brain region involved in cognition, motivation and motor control, G protein-coupled receptor 52 (GPR52) regulates dopaminergic and glutamatergic signaling pathways implicated in psychiatric disorders.</description>
      <content:encoded>
        <![CDATA[Predominantly expressed in the striatum, a brain region involved in cognition, motivation and motor control, G protein-coupled receptor 52 (GPR52) regulates dopaminergic and glutamatergic signaling pathways implicated in psychiatric disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732309</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732309-novel-gpr52-agonist-shows-antipsychotic-like-effects</link>
    </item>
    <item>
      <title>Antibiotics spur protein transfer that boosts bacterial survival</title>
      <description>It is known that bacterial cells exchange biological matter, but it is not clear whether bacteria can exchange functional proteins. In a recent paper published in Science on June 25, 2026, researchers from Baylor College of Medicine and their collaborators investigated horizontal protein transfer between bacteria, specifically between protein-donor Escherichia coli and protein-receiving E. coli that could turn into persister cells and tolerate lethal antibiotic doses or a stressful environment.</description>
      <content:encoded>
        <![CDATA[It is known that bacterial cells exchange biological matter, but it is not clear whether bacteria can exchange functional proteins. In a recent paper published in <em>Science</em> on June 25, 2026, researchers from Baylor College of Medicine and their collaborators investigated horizontal protein transfer between bacteria, specifically between protein-donor <em>Escherichia coli</em> and protein-receiving <em>E. coli</em> that could turn into persister cells and tolerate lethal antibiotic doses or a stressful environment.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732308</guid>
      <pubDate>Tue, 30 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732308-antibiotics-spur-protein-transfer-that-boosts-bacterial-survival</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Antibiotics-petri-dish.webp?t=1588349786" type="image/png" medium="image" fileSize="499611">
        <media:title type="plain">Petri dish and capsules</media:title>
      </media:content>
    </item>
    <item>
      <title>Celebrating recognition. Reaffirming our mission.</title>
      <author>lynn.yoffee@clarivate.com</author>
      <description>Awards are an honor, but they are not why we do what we do. That's why this year's recognition from the APEX Awards is especially meaningful. BioWorld earned seven 2026 APEX Awards, including three Grand Awards and four Awards of Excellence. Judged by publishing industry peers, these honors recognize excellence across reporting, writing, visual storytelling and editorial collaboration. While we are proud of this recognition, what makes it especially rewarding is that it reflects the work our team does every day to serve the global life sciences community.</description>
      <content:encoded>
        <![CDATA[Awards are an honor, but they are not why we do what we do. That's why this year's recognition from the APEX Awards is especially meaningful. BioWorld earned seven <a href="https://apexawards.com/winners-2026" rel="noopener noreferrer" target="_blank">2026 APEX Awards</a>, including three Grand Awards and four Awards of Excellence. Judged by publishing industry peers, these honors recognize excellence across reporting, writing, visual storytelling and editorial collaboration. While we are proud of this recognition, what makes it especially rewarding is that it reflects the work our team does every day to serve the global life sciences community.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732328</guid>
      <pubDate>Tue, 30 Jun 2026 08:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732328-celebrating-recognition-reaffirming-our-mission</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Misc/Clarivate-icon-440-gradient-award-ribbon.webp?t=1782767279" type="image/jpeg" medium="image" fileSize="151063">
        <media:title type="plain">Award ribbon icon</media:title>
      </media:content>
    </item>
    <item>
      <title>Shandong Simcere Medgenn Bio-Pharmaceutical divulges new CDK4/cyclin D1 inhibitors</title>
      <description>Shandong Simcere Medgenn Bio-Pharmaceutical Co. Ltd. has reported new CDK4/cyclin D1 inhibitors potentially useful for the treatment of breast cancer.</description>
      <content:encoded>
        <![CDATA[Shandong Simcere Medgenn Bio-Pharmaceutical Co. Ltd. has reported new CDK4/cyclin D1 inhibitors potentially useful for the treatment of breast cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732220</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732220-shandong-simcere-medgenn-bio-pharmaceutical-divulges-new-cdk4-cyclin-d1-inhibitors</link>
    </item>
    <item>
      <title>Beijing Earthwise Technology discovers new E3 ligase/VAV1 interaction inducers</title>
      <description>Beijing Earthwise Technology Co. Ltd. has patented new molecular glue degraders comprising an E3 ubiquitin-protein ligase-binding moiety acting as E3 ligase/proto-oncogene Vav (VAV1) interaction inducers and VAV1 degradation inducers.</description>
      <content:encoded>
        <![CDATA[Beijing Earthwise Technology Co. Ltd. has patented new molecular glue degraders comprising an E3 ubiquitin-protein ligase-binding moiety acting as E3 ligase/proto-oncogene Vav (VAV1) interaction inducers and VAV1 degradation inducers.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732219</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732219-beijing-earthwise-technology-discovers-new-e3-ligase-vav1-interaction-inducers</link>
    </item>
    <item>
      <title>Anti-HIV compounds reported in Boyuan Pharmaceutical patent</title>
      <description>Boyuan Pharmaceutical (Suzhou) Co. Ltd. has divulged new pyridone derivatives potentially useful for the treatment of HIV infection.</description>
      <content:encoded>
        <![CDATA[Boyuan Pharmaceutical (Suzhou) Co. Ltd. has divulged new pyridone derivatives potentially useful for the treatment of HIV infection.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732218</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732218-anti-hiv-compounds-reported-in-boyuan-pharmaceutical-patent</link>
    </item>
    <item>
      <title>Jiangxi Kerui Pharmaceutical patents new fungal GWT1 inhibitors</title>
      <description>Jiangxi Kerui Pharmaceutical Co. Ltd. has disclosed new prodrugs of fungal GPI-anchored wall transfer protein 1 (GWT1) inhibitors potentially useful for the treatment of fungal infections.</description>
      <content:encoded>
        <![CDATA[Jiangxi Kerui Pharmaceutical Co. Ltd. has disclosed new prodrugs of fungal GPI-anchored wall transfer protein 1 (GWT1) inhibitors potentially useful for the treatment of fungal infections.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732217</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732217-jiangxi-kerui-pharmaceutical-patents-new-fungal-gwt1-inhibitors</link>
    </item>
    <item>
      <title>Changchun Genescience Pharmaceuticals discloses new VAV1 degradation inducers</title>
      <description>Changchun Genescience Pharmaceuticals Co. Ltd. has synthesized new molecular glue degraders comprising E3 ubiquitin-protein ligase-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are described as potentially useful for the treatment of ulcerative colitis, Crohn’s disease, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus and myasthenia gravis.</description>
      <content:encoded>
        <![CDATA[Changchun Genescience Pharmaceuticals Co. Ltd. has synthesized new molecular glue degraders comprising E3 ubiquitin-protein ligase-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are described as potentially useful for the treatment of ulcerative colitis, Crohn’s disease, rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus and myasthenia gravis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732216</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732216-changchun-genescience-pharmaceuticals-discloses-new-vav1-degradation-inducers</link>
    </item>
    <item>
      <title>Gensci-144 shows renoprotection in CKD</title>
      <description>Genescience Pharmaceuticals Co. Ltd. has been developing an SLC6A19 inhibitor – Gensci-144 – for the potential treatment of chronic kidney disease (CKD).</description>
      <content:encoded>
        <![CDATA[Genescience Pharmaceuticals Co. Ltd. has been developing an SLC6A19 inhibitor – Gensci-144 – for the potential treatment of chronic kidney disease (CKD).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732211</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732211-gensci-144-shows-renoprotection-in-ckd</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Nephrology/Kidney-disease.webp?t=1722874886" type="image/jpeg" medium="image" fileSize="280482">
        <media:title type="plain">Illustration of diseased kidney</media:title>
      </media:content>
    </item>
    <item>
      <title>TRIP13 blockade as a therapeutic approach in prostate cancer</title>
      <description>Prostate cancer is a leading cause of cancer-related deaths among men and is a cancer type that shows genomic heterogeneity and several molecular alterations. By analyzing available microarray and next-generation transcriptome sequencing data, researchers at the University of Alabama at Birmingham found that thyroid hormone receptor-interacting protein 13 (TRIP13), a member of the AAA ATPase family, was overexpressed in prostate cancer, making it a potential therapeutic target.</description>
      <content:encoded>
        <![CDATA[Prostate cancer is a leading cause of cancer-related deaths among men and is a cancer type that shows genomic heterogeneity and several molecular alterations. By analyzing available microarray and next-generation transcriptome sequencing data, researchers at the University of Alabama at Birmingham found that thyroid hormone receptor-interacting protein 13 (TRIP13), a member of the AAA ATPase family, was overexpressed in prostate cancer, making it a potential therapeutic target.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732210</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732210-trip13-blockade-as-a-therapeutic-approach-in-prostate-cancer</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Cancer/Prostate-cancer.webp?t=1674835049" type="image/png" medium="image" fileSize="839914">
        <media:title type="plain">3D illustration showing tumor inside prostate gland and closeup view of cancer cells</media:title>
      </media:content>
    </item>
    <item>
      <title>Ext1-targeted AAV gene therapy inhibits tau propagation in model of tauopathy</title>
      <description>Neurodegenerative disorders such as Alzheimer’s disease (AD) and frontotemporal dementia are characterized by the accumulation of hyperphosphorylated tau protein, forming neurofibrillary tangles, ultimately leading to synaptic dysfunction and cognitive decline.</description>
      <content:encoded>
        <![CDATA[Neurodegenerative disorders such as Alzheimer’s disease (AD) and frontotemporal dementia are characterized by the accumulation of hyperphosphorylated tau protein, forming neurofibrillary tangles, ultimately leading to synaptic dysfunction and cognitive decline.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732209</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732209-ext1-targeted-aav-gene-therapy-inhibits-tau-propagation-in-model-of-tauopathy</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Credit-Jonathan-Bailey-NHGRI.webp?t=1708015488" type="image/jpeg" medium="image" fileSize="352743">
        <media:title type="plain">Silhouette of head and brain with DNA double helixes</media:title>
        <media:description type="plain">Credit: Jonathan Bailey, NHGR</media:description>
      </media:content>
    </item>
    <item>
      <title>IRAK4-targeting PROTAC degrader suppresses inflammatory signaling in vitro</title>
      <description>Chronic activation or upregulation of interleukin-1 receptor-associated kinase 4 (IRAK4) has been linked to several diseases, including systemic lupus erythematosus, rheumatoid arthritis, atopic dermatitis, Alzheimer’s disease and atherosclerosis. Researchers from the Ocean University of China aimed to address the limitations of traditional small-molecule inhibitors by designing novel proteolysis targeting chimeras (PROTACs) for IRAK4 degradation.</description>
      <content:encoded>
        <![CDATA[Chronic activation or upregulation of interleukin-1 receptor-associated kinase 4 (IRAK4) has been linked to several diseases, including systemic lupus erythematosus, rheumatoid arthritis, atopic dermatitis, Alzheimer’s disease and atherosclerosis. Researchers from the Ocean University of China aimed to address the limitations of traditional small-molecule inhibitors by designing novel proteolysis targeting chimeras (PROTACs) for IRAK4 degradation.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732208</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732208-irak4-targeting-protac-degrader-suppresses-inflammatory-signaling-in-vitro</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/IRAK4-protein-kinase-structure.webp?t=1782744590" type="image/jpeg" medium="image" fileSize="474262">
        <media:title type="plain">3D rendering of interleukin-1 receptor-associated kinase 4</media:title>
        <media:description type="plain">IRAK4, a protein kinase involved in signaling innate immune responses from Toll-like receptors.</media:description>
      </media:content>
    </item>
    <item>
      <title>Inhaled ALK5 inhibitor delivers lung-targeted antifibrotic effects</title>
      <description>ALK5 mediates the core profibrotic TGF-β signaling cascade that promotes fibroblast activation, myofibroblast differentiation and extracellular matrix production, ultimately leading to persistent tissue remodeling and lung fibrosis.</description>
      <content:encoded>
        <![CDATA[ALK5 mediates the core profibrotic TGF-β signaling cascade that promotes fibroblast activation, myofibroblast differentiation and extracellular matrix production, ultimately leading to persistent tissue remodeling and lung fibrosis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732207</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732207-inhaled-alk5-inhibitor-delivers-lung-targeted-antifibrotic-effects</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Therapeutic-topics/Respiratory/Lungs-wireframe-illustration.webp?t=1659647698" type="image/png" medium="image" fileSize="693657">
        <media:title type="plain">Digital lungs illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>Onco-Innovations evaluates ONC-010 in metabolism studies</title>
      <description>Onco-Innovations Ltd. has announced the initiation of hepatocyte and liver microsome metabolism studies for ONC-010, the company’s lead nanoparticle-formulated PNKP inhibitor. The studies will evaluate the metabolic stability of ONC-010 across human, rat and dog systems.</description>
      <content:encoded>
        <![CDATA[Onco-Innovations Ltd. has announced the initiation of hepatocyte and liver microsome metabolism studies for ONC-010, the company’s lead nanoparticle-formulated PNKP inhibitor. The studies will evaluate the metabolic stability of ONC-010 across human, rat and dog systems.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732206</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732206-onco-innovations-evaluates-onc-010-in-metabolism-studies</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/digital-human-body-with-molecules.webp?t=1729870096" type="image/jpeg" medium="image" fileSize="181884">
        <media:title type="plain">Illustration of human body composed of molecules</media:title>
      </media:content>
    </item>
    <item>
      <title>Sumitomo’s dual 5-HT2A/7 receptor antagonist counteracts dementia symptoms</title>
      <description>Up to 90% of people with dementia develop at least one behavioral or psychological symptom, such as psychosis, anxiety or agitation/aggression, which often overlap and worsen both patient quality of life and caregiver burden. Based on preclinical evidence, dual 5-HT2A/7 receptor antagonism may represent a rational strategy to modulate psychosis, agitation and mood-related symptoms.</description>
      <content:encoded>
        <![CDATA[Up to 90% of people with dementia develop at least one behavioral or psychological symptom, such as psychosis, anxiety or agitation/aggression, which often overlap and worsen both patient quality of life and caregiver burden. Based on preclinical evidence, dual 5-HT2A/7 receptor antagonism may represent a rational strategy to modulate psychosis, agitation and mood-related symptoms.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732205</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732205-sumitomos-dual-5-ht2a-7-receptor-antagonist-counteracts-dementia-symptoms</link>
    </item>
    <item>
      <title>CINP 2026: Gut microbiota could predict antidepressant response</title>
      <description>The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.</description>
      <content:encoded>
        <![CDATA[The gut microbiota may be altered in people with depression as a result of treatment. These microorganisms reorganize differently in individuals who respond to therapy. In a multiomics study of antidepressant-naive patients presented at the 2026 World Congress of Neuropsychopharmacology (CINP), scientists from National Taiwan University found that patients who improved after antidepressant treatment maintained a more balanced and functional microbial ecosystem, recovered beneficial metabolites, and displayed blood-based biological signals that aligned with these changes.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732204</guid>
      <pubDate>Mon, 29 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732204-cinp-2026-gut-microbiota-could-predict-antidepressant-response</link>
      <media:content url="https://www.bioworld.com/ext/resources/BWS/BWS-library/Brain-gut-axis-connection-illustration.webp?t=1782743853" type="image/jpeg" medium="image" fileSize="349828">
        <media:title type="plain">Illustration demonstrating gut-brain axis</media:title>
      </media:content>
    </item>
    <item>
      <title>Oblenio’s $62M series B for trispecific antibody in autoimmune diseases</title>
      <description>A year and a half from its formation, Oblenio Bio has generated positive nonhuman primate data for LBL-051 in chronic autoimmune diseases and closed a $62 million series B to move the trispecific T-cell engager into the clinic.</description>
      <content:encoded>
        <![CDATA[A year and a half from its formation, Oblenio Bio has generated positive nonhuman primate data for LBL-051 in chronic autoimmune diseases and closed a $62 million series B to move the trispecific T-cell engager into the clinic.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732274</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732274-oblenios-62m-series-b-for-trispecific-antibody-in-autoimmune-diseases</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Drugs/Antibodies2.webp?t=1634753068" type="image/png" medium="image" fileSize="644719">
        <media:title type="plain">Antibodies illustration</media:title>
      </media:content>
    </item>
    <item>
      <title>New WRN inhibitors reported in Laekna Pharmaceutical patent</title>
      <description>Laekna Pharmaceutical Ningbo Co. Ltd. has disclosed Werner syndrome ATP-dependent helicase (WRN; RECQ3; RECQL2) inhibitors found to be potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Laekna Pharmaceutical Ningbo Co. Ltd. has disclosed Werner syndrome ATP-dependent helicase (WRN; RECQ3; RECQL2) inhibitors found to be potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732201</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732201-new-wrn-inhibitors-reported-in-laekna-pharmaceutical-patent</link>
    </item>
    <item>
      <title>Ascentage describes new Bcl-xl degradation inducers</title>
      <description>Researchers from Ascentage Pharma Group Corp. Ltd. and Ascentage Pharma (Suzhou) Co. Ltd. have identified proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin ligase (such as Von Hippel-Lindau disease tumor suppressor [VHL]) coupled to a Bcl-2-like protein 1 (Bcl-xl; Bcl-X; BCL2L1)-targeting moiety via a linker acting as Bcl-xl degradation inducers reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Researchers from Ascentage Pharma Group Corp. Ltd. and Ascentage Pharma (Suzhou) Co. Ltd. have identified proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin ligase (such as Von Hippel-Lindau disease tumor suppressor [VHL]) coupled to a Bcl-2-like protein 1 (Bcl-xl; Bcl-X; BCL2L1)-targeting moiety via a linker acting as Bcl-xl degradation inducers reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732200</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732200-ascentage-describes-new-bcl-xl-degradation-inducers</link>
    </item>
    <item>
      <title>Shanghai Yingli Pharmaceutical identifies new KRAS mutant inhibitors</title>
      <description>Shanghai Yingli Pharmaceutical Co. Ltd. has discovered hydrazine-structured compounds as inhibitors of GTPase KRAS and its mutants. They are reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Shanghai Yingli Pharmaceutical Co. Ltd. has discovered hydrazine-structured compounds as inhibitors of GTPase KRAS and its mutants. They are reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732199</guid>
      <pubDate>Fri, 26 Jun 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732199-shanghai-yingli-pharmaceutical-identifies-new-kras-mutant-inhibitors</link>
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