<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:media="http://search.yahoo.com/mrss/" xmlns:content="http://purl.org/rss/1.0/modules/content/">
  <channel>
    <title>Patents</title>
    <description></description>
    <link>https://www.bioworld.com/rss</link>
    <language>en-us</language>
    <item>
      <title>Apolin Bio and Viva Biotech present new ApoA/APOB interaction inhibitors</title>
      <description>Apolin Bio Ltd. and Shanghai Viva Dancheng Entrepreneurship Incubator Management Ltd. have detailed polycyclic compounds acting as apolipoprotein A (ApoA; LPA)/apolipoprotein B-100 (APOB) interaction inhibitors that are potentially useful for the treatment of cardiovascular disorders.</description>
      <content:encoded>
        <![CDATA[Apolin Bio Ltd. and Shanghai Viva Dancheng Entrepreneurship Incubator Management Ltd. have detailed polycyclic compounds acting as apolipoprotein A (ApoA; LPA)/apolipoprotein B-100 (APOB) interaction inhibitors that are potentially useful for the treatment of cardiovascular disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732513</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732513-apolin-bio-and-viva-biotech-present-new-apoa-apob-interaction-inhibitors</link>
    </item>
    <item>
      <title>Nuvalent discloses new AKT1 inhibitors</title>
      <description>Nuvalent Inc. has described RAC-α serine/threonine-protein kinase (AKT1; PKBα) E17K mutant inhibitors reported to be useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Nuvalent Inc. has described RAC-α serine/threonine-protein kinase (AKT1; PKBα) E17K mutant inhibitors reported to be useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732512</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732512-nuvalent-discloses-new-akt1-inhibitors</link>
    </item>
    <item>
      <title>U&amp;S Bio identifies new H+/K+-ATPase inhibitors</title>
      <description>U&amp;S Bio Co. Ltd. has divulged H+/K+-ATPase inhibitors with improved stability found to be potentially useful for the treatment of gastrointestinal disorders, cancer, Helicobacter pylori infection, sialorrhea, asthma and airways obstruction, among others.</description>
      <content:encoded>
        <![CDATA[U&S Bio Co. Ltd. has divulged H+/K+-ATPase inhibitors with improved stability found to be potentially useful for the treatment of gastrointestinal disorders, cancer, <em>Helicobacter pylori</em> infection, sialorrhea, asthma and airways obstruction, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732511</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732511-u-and-s-bio-identifies-new-h-k-atpase-inhibitors</link>
    </item>
    <item>
      <title>Prelude Therapeutics patents new KAT6A-targeting PROTACs</title>
      <description>Prelude Therapeutics Inc. has synthesized proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin-protein ligase (CRBN)-binding moiety coupled to a histone acetyltransferase KAT6A (MOZ; MYST-3)-targeting moiety that are potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Prelude Therapeutics Inc. has synthesized proteolysis targeting chimeras (PROTACs) comprising an E3 ubiquitin-protein ligase (CRBN)-binding moiety coupled to a histone acetyltransferase KAT6A (MOZ; MYST-3)-targeting moiety that are potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732510</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732510-prelude-therapeutics-patents-new-kat6a-targeting-protacs</link>
    </item>
    <item>
      <title>Promomed Rus discovers new JAK inhibitors</title>
      <description>Promomed Rus LLC has identified Janus kinase (JAK) inhibitors reported to be useful for the treatment of alopecia, atopic dermatitis, juvenile arthritis, rheumatoid arthritis, systemic lupus erythematosus and psoriatic arthritis.</description>
      <content:encoded>
        <![CDATA[Promomed Rus LLC has identified Janus kinase (JAK) inhibitors reported to be useful for the treatment of alopecia, atopic dermatitis, juvenile arthritis, rheumatoid arthritis, systemic lupus erythematosus and psoriatic arthritis.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732509</guid>
      <pubDate>Thu, 09 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732509-promomed-rus-discovers-new-jak-inhibitors</link>
    </item>
    <item>
      <title>Beijing Mabworks Biotech discloses new DLL3-targeting ADCs</title>
      <description>A Beijing Mabworks Biotech Co. Ltd. patent describes new antibody-drug conjugates (ADCs) comprising antigen-binding fragments or antibodies targeting delta-like protein 3 (DLL3) linked to a cytotoxic drug potentially useful for the treatment of small-cell lung cancer (SCLC).</description>
      <content:encoded>
        <![CDATA[A Beijing Mabworks Biotech Co. Ltd. patent describes new antibody-drug conjugates (ADCs) comprising antigen-binding fragments or antibodies targeting delta-like protein 3 (DLL3) linked to a cytotoxic drug potentially useful for the treatment of small-cell lung cancer (SCLC).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732495</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732495-beijing-mabworks-biotech-discloses-new-dll3-targeting-adcs</link>
    </item>
    <item>
      <title>Beijing Jingwei-Yankang Biomedical divulges new RBP4 inhibitors</title>
      <description>Beijing Jingwei-Yankang Biomedical Co. Ltd. has reported new phenyl-substituted heterocyclic compounds acting as retinol-binding protein 4 (RBP4) inhibitors with potential in the treatment of age-related macular degeneration (AMD).</description>
      <content:encoded>
        <![CDATA[Beijing Jingwei-Yankang Biomedical Co. Ltd. has reported new phenyl-substituted heterocyclic compounds acting as retinol-binding protein 4 (RBP4) inhibitors with potential in the treatment of age-related macular degeneration (AMD).]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732494</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732494-beijing-jingwei-yankang-biomedical-divulges-new-rbp4-inhibitors</link>
    </item>
    <item>
      <title>KU Leuven and Universität Zürich describe new PTPN1/PTPN2 inhibitors</title>
      <description>KU Leuven and Universität Zürich have discovered new tyrosine-protein phosphatase non-receptor type 1 (PTPN1; PTP-1B) and/or tyrosine-protein phosphatase non-receptor type 2 (PTPN2; TCPTP) inhibitors potentially useful for the treatment of cancer and metabolic diseases.</description>
      <content:encoded>
        <![CDATA[KU Leuven and Universität Zürich have discovered new tyrosine-protein phosphatase non-receptor type 1 (PTPN1; PTP-1B) and/or tyrosine-protein phosphatase non-receptor type 2 (PTPN2; TCPTP) inhibitors potentially useful for the treatment of cancer and metabolic diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732493</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732493-ku-leuven-and-universitat-zurich-describe-new-ptpn1-ptpn2-inhibitors</link>
    </item>
    <item>
      <title>Pikavation Therapeutics identifies new PI3Kα inhibitors</title>
      <description>Pikavation Therapeutics Inc. has patented new phosphatidylinositol 3-kinase α (PI3Kα) inhibitors potentially useful for the treatment of cancer, congenital lipomatous overgrowth, vascular malformations, epidermal naevi and skeletal abnormalities and PIK3CA-related overgrowth spectrum.</description>
      <content:encoded>
        <![CDATA[Pikavation Therapeutics Inc. has patented new phosphatidylinositol 3-kinase α (PI3Kα) inhibitors potentially useful for the treatment of cancer, congenital lipomatous overgrowth, vascular malformations, epidermal naevi and skeletal abnormalities and PIK3CA-related overgrowth spectrum.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732492</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732492-pikavation-therapeutics-identifies-new-pi3k-inhibitors</link>
    </item>
    <item>
      <title>Nurix Therapeutics patents new SMARCA2-targeting PROTACs</title>
      <description>Nurix Therapeutics Inc. has disclosed new proteolysis targeting chimera (PROTAC) compounds potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Nurix Therapeutics Inc. has disclosed new proteolysis targeting chimera (PROTAC) compounds potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732491</guid>
      <pubDate>Wed, 08 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732491-nurix-therapeutics-patents-new-smarca2-targeting-protacs</link>
    </item>
    <item>
      <title>Wigen Biomedicine Technology identifies new PI3Kα modulators</title>
      <description>Wigen Biomedicine Technology (Shanghai) Co. Ltd. has synthesized new phosphatidylinositol 3-kinase α (PI3Kα) modulators potentially useful for the treatment of solid tumors and hematological cancers.</description>
      <content:encoded>
        <![CDATA[Wigen Biomedicine Technology (Shanghai) Co. Ltd. has synthesized new phosphatidylinositol 3-kinase α (PI3Kα) modulators potentially useful for the treatment of solid tumors and hematological cancers.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732466</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732466-wigen-biomedicine-technology-identifies-new-pi3k-modulators</link>
    </item>
    <item>
      <title>China Pharmaceutical University discovers new PCSK9 inhibitors</title>
      <description>China Pharmaceutical University has patented new isochromanone compounds acting as proprotein convertase subtilisin/kexin-type 9 (PCSK9) inhibitors. As such, they are described as potentially useful for the treatment of atherosclerosis, obesity, hepatic steatosis, hypercholesterolemia, hyperlipidemia and hypertriglyceridemia.</description>
      <content:encoded>
        <![CDATA[China Pharmaceutical University has patented new isochromanone compounds acting as proprotein convertase subtilisin/kexin-type 9 (PCSK9) inhibitors. As such, they are described as potentially useful for the treatment of atherosclerosis, obesity, hepatic steatosis, hypercholesterolemia, hyperlipidemia and hypertriglyceridemia.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732465</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732465-china-pharmaceutical-university-discovers-new-pcsk9-inhibitors</link>
    </item>
    <item>
      <title>STING agonists disclosed in Spark Biopharma patent </title>
      <description>Spark Biopharma Inc. has identified new stimulator of interferon genes protein (STING; TMEM173) agonists potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Spark Biopharma Inc. has identified new stimulator of interferon genes protein (STING; TMEM173) agonists potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732464</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732464-sting-agonists-disclosed-in-spark-biopharma-patent</link>
    </item>
    <item>
      <title>Gilead Sciences patents new TIPARP inhibitors</title>
      <description>Gilead Sciences Inc. has described new protein mono-ADP-ribosyltransferase TIPARP (PARP-7; ARTD14) inhibitors potentially useful for the treatment of cancer. 100% 10 mM HCl formulation suspension form of an exemplified compound (Ex 13 pg 135, claim 42) exhibited bioavailability (F) of 48% in beagle dog plasma at 30 mg (equiv.)/kg p.o.</description>
      <content:encoded>
        <![CDATA[Gilead Sciences Inc. has described new protein mono-ADP-ribosyltransferase TIPARP (PARP-7; ARTD14) inhibitors potentially useful for the treatment of cancer. 100% 10 mM HCl formulation suspension form of an exemplified compound (Ex 13 pg 135, claim 42) exhibited bioavailability (F) of 48% in beagle dog plasma at 30 mg (equiv.)/kg p.o.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732463</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732463-gilead-sciences-patents-new-tiparp-inhibitors</link>
    </item>
    <item>
      <title>Ono Pharmaceutical and Vanderbilt University detail new TREK1/2 inhibitor prodrugs</title>
      <description>Ono Pharmaceutical Co. Ltd. and Vanderbilt University have prepared and tested new prodrugs of potassium channel subfamily K member 10 (TREK2; KCNK10) and member 2 (TREK-1; KCNK2) inhibitors potentially useful for the treatment of cancer, pulmonary fibrosis, neurological disorders and more.</description>
      <content:encoded>
        <![CDATA[Ono Pharmaceutical Co. Ltd. and Vanderbilt University have prepared and tested new prodrugs of potassium channel subfamily K member 10 (TREK2; KCNK10) and member 2 (TREK-1; KCNK2) inhibitors potentially useful for the treatment of cancer, pulmonary fibrosis, neurological disorders and more.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732462</guid>
      <pubDate>Tue, 07 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732462-ono-pharmaceutical-and-vanderbilt-university-detail-new-trek1-2-inhibitor-prodrugs</link>
    </item>
    <item>
      <title>Chinese, Australian researchers disclose GD2 ganglioside-targeting ADCs</title>
      <description>Children’s Hospital of Fudan University, Sydney Children’s Hospital and the University of Sydney have jointly patented new antibody-drug conjugates comprising an antibody targeting GD2 ganglioside covalently linked to cytotoxic drugs potentially useful for the treatment of osteosarcoma.</description>
      <content:encoded>
        <![CDATA[Children’s Hospital of Fudan University, Sydney Children’s Hospital and the University of Sydney have jointly patented new antibody-drug conjugates comprising an antibody targeting GD2 ganglioside covalently linked to cytotoxic drugs potentially useful for the treatment of osteosarcoma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732411</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732411-chinese-australian-researchers-disclose-gd2-ganglioside-targeting-adcs</link>
    </item>
    <item>
      <title>Beijing Double-Crane Runchuang identifies new TLR7/8 antagonists</title>
      <description>Beijing Double-Crane Runchuang Technology Co. Ltd. has discovered new Toll-like receptor 7 (TLR7) and/or TLR8 antagonists potentially useful for the treatment of rheumatoid arthritis, systemic lupus erythematosus, cutaneous lupus erythematosus, dermatomyositis, hidradenitis suppurativa, polymyositis, psoriasis and Sjogren’s syndrome, among others.</description>
      <content:encoded>
        <![CDATA[Beijing Double-Crane Runchuang Technology Co. Ltd. has discovered new Toll-like receptor 7 (TLR7) and/or TLR8 antagonists potentially useful for the treatment of rheumatoid arthritis, systemic lupus erythematosus, cutaneous lupus erythematosus, dermatomyositis, hidradenitis suppurativa, polymyositis, psoriasis and Sjogren’s syndrome, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732410</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732410-beijing-double-crane-runchuang-identifies-new-tlr7-8-antagonists</link>
    </item>
    <item>
      <title>Inventisbio patents new STAT6-targeting PROTAC compounds</title>
      <description>Inventisbio Co. Ltd. and Inventisbio LLC have disclosed new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety coupled to a signal transducer and activator of transcription 6 (STAT6)-targeting moiety potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Inventisbio Co. Ltd. and Inventisbio LLC have disclosed new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety coupled to a signal transducer and activator of transcription 6 (STAT6)-targeting moiety potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732409</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732409-inventisbio-patents-new-stat6-targeting-protac-compounds</link>
    </item>
    <item>
      <title>Shanghai Aryl Pharmtech, Zhejiang Hisun report new CTPS1 inhibitors</title>
      <description>Shanghai Aryl Pharmtech Co. Ltd. and Zhejiang Hisun Pharmaceutical Co. Ltd. have identified new CTP synthase 1 (CTPS1) inhibitors potentially useful for the treatment of lymphoma and solid tumors.</description>
      <content:encoded>
        <![CDATA[Shanghai Aryl Pharmtech Co. Ltd. and Zhejiang Hisun Pharmaceutical Co. Ltd. have identified new CTP synthase 1 (CTPS1) inhibitors potentially useful for the treatment of lymphoma and solid tumors.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732408</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732408-shanghai-aryl-pharmtech-zhejiang-hisun-report-new-ctps1-inhibitors</link>
    </item>
    <item>
      <title>Genfleet Therapeutics synthesizes new PI3K inhibitors</title>
      <description>Genfleet Therapeutics (Shanghai) Co. Ltd. has divulged new phosphatidylinositol 3-kinase (PI3K) inhibitors potentially useful for the treatment of cancer, Alzheimer’s disease, aging, diabetes, Parkinson’s disease, asthma, cardiovascular disease and allergy, among others.</description>
      <content:encoded>
        <![CDATA[Genfleet Therapeutics (Shanghai) Co. Ltd. has divulged new phosphatidylinositol 3-kinase (PI3K) inhibitors potentially useful for the treatment of cancer, Alzheimer’s disease, aging, diabetes, Parkinson’s disease, asthma, cardiovascular disease and allergy, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732407</guid>
      <pubDate>Mon, 06 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732407-genfleet-therapeutics-synthesizes-new-pi3k-inhibitors</link>
    </item>
    <item>
      <title>Brightgene Bio-Medical discovers new calcitonin/AMY3 receptor agonists</title>
      <description>Brightgene Bio-Medical Technology Co. Ltd. has patented new calcitonin receptor (CALCR; CT-R) and amylin AMY3 receptor agonists potentially useful for the treatment of obesity and metabolic disorders.</description>
      <content:encoded>
        <![CDATA[Brightgene Bio-Medical Technology Co. Ltd. has patented new calcitonin receptor (CALCR; CT-R) and amylin AMY3 receptor agonists potentially useful for the treatment of obesity and metabolic disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732390</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732390-brightgene-bio-medical-discovers-new-calcitonin-amy3-receptor-agonists</link>
    </item>
    <item>
      <title>Beijing Avistone Pharmaceuticals prepares new KRAS mutant inhibitors</title>
      <description>Beijing Avistone Pharmaceuticals Biotechnology Co. Ltd. has reported new GTPase KRAS mutant inhibitors potentially useful for the treatment of cancer, immunological and inflammatory disorders.</description>
      <content:encoded>
        <![CDATA[<p>Beijing Avistone Pharmaceuticals Biotechnology Co. Ltd. has reported new GTPase KRAS mutant inhibitors potentially useful for the treatment of cancer, immunological and inflammatory disorders.</p>]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732389</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732389-beijing-avistone-pharmaceuticals-prepares-new-kras-mutant-inhibitors</link>
    </item>
    <item>
      <title>Duke Street Bio reports new PARP-1 inhibitors</title>
      <description>Duke Street Bio Ltd. has identified new poly(ADP-ribose) polymerase 1 (PARP-1; ARTD1) inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Duke Street Bio Ltd. has identified new poly(ADP-ribose) polymerase 1 (PARP-1; ARTD1) inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732388</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732388-duke-street-bio-reports-new-parp-1-inhibitors</link>
    </item>
    <item>
      <title>University of Edinburgh patents new mTOR inhibitors</title>
      <description>The University of Edinburgh has disclosed new benzoxazol mammalian target of rapamycin (mTOR; FRAP1) inhibitors potentially useful for the treatment of cancer, autoimmune, metabolic diseases, fibrosis, parasitic infections, genetic, inflammatory and neurological disorders.</description>
      <content:encoded>
        <![CDATA[The University of Edinburgh has disclosed new benzoxazol mammalian target of rapamycin (mTOR; FRAP1) inhibitors potentially useful for the treatment of cancer, autoimmune, metabolic diseases, fibrosis, parasitic infections, genetic, inflammatory and neurological disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732387</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732387-university-of-edinburgh-patents-new-mtor-inhibitors</link>
    </item>
    <item>
      <title>NLRP3 inflammasome inhibitors disclosed in MSD patent</title>
      <description>Merck Sharp &amp; Dohme LLC (MSD) has synthesized new benzimidazole derivatives acting as NLRP3 inflammasome inhibitors. As such, they are potentially useful for the treatment of atherosclerosis, metabolic dysfunction-associated steatohepatitis (MASH), neuroinflammation, inflammatory skin, inflammatory joint and autoimmune disease, Alzheimer’s and Parkinson’s disease, among others.</description>
      <content:encoded>
        <![CDATA[Merck Sharp & Dohme LLC (MSD) has synthesized new benzimidazole derivatives acting as NLRP3 inflammasome inhibitors. As such, they are potentially useful for the treatment of atherosclerosis, metabolic dysfunction-associated steatohepatitis (MASH), neuroinflammation, inflammatory skin, inflammatory joint and autoimmune disease, Alzheimer’s and Parkinson’s disease, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732386</guid>
      <pubDate>Fri, 03 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732386-nlrp3-inflammasome-inhibitors-disclosed-in-msd-patent</link>
    </item>
    <item>
      <title>Ontrack Therapeutics divulges compounds for neurodegenerative diseases</title>
      <description>Ontrack Therapeutics Ltd. has reported new heterotricyclic compounds potentially useful for the treatment of neurodegenerative diseases.</description>
      <content:encoded>
        <![CDATA[Ontrack Therapeutics Ltd. has reported new heterotricyclic compounds potentially useful for the treatment of neurodegenerative diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732372</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732372-ontrack-therapeutics-divulges-compounds-for-neurodegenerative-diseases</link>
    </item>
    <item>
      <title>Aigen Sciences discovers new USP1 inhibitors</title>
      <description>Aigen Sciences Inc. has patented new ubiquitin carboxyl-terminal hydrolase 1 (USP1) inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Aigen Sciences Inc. has patented new ubiquitin carboxyl-terminal hydrolase 1 (USP1) inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732371</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732371-aigen-sciences-discovers-new-usp1-inhibitors</link>
    </item>
    <item>
      <title>Primo Thera synthesizes new IL-6Rβ inhibitors</title>
      <description>Primo Thera Co. Ltd. has divulged new interleukin-6 receptor subunit β (IL-6Rβ; gp130) inhibitors potentially useful for the treatment of autoimmune disease.</description>
      <content:encoded>
        <![CDATA[Primo Thera Co. Ltd. has divulged new interleukin-6 receptor subunit β (IL-6Rβ; gp130) inhibitors potentially useful for the treatment of autoimmune disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732370</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732370-primo-thera-synthesizes-new-il-6r-inhibitors</link>
    </item>
    <item>
      <title>Reunion Neuroscience reports new 5-HT2A partial agonists and/or 5-HT2B antagonists</title>
      <description>Reunion Neuroscience Inc. has identified new 5-HT2A receptor partial agonists and/or 5-HT2B receptor antagonists potentially useful for the treatment of psychiatric and neurological disorders.</description>
      <content:encoded>
        <![CDATA[Reunion Neuroscience Inc. has identified new 5-HT2A receptor partial agonists and/or 5-HT2B receptor antagonists potentially useful for the treatment of psychiatric and neurological disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732369</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732369-reunion-neuroscience-reports-new-5-ht2a-partial-agonists-and-or-5-ht2b-antagonists</link>
    </item>
    <item>
      <title>Recurium patents new Wee1 inhibitors</title>
      <description>Recurium IP Holdings LLC has disclosed new Wee1-like protein kinase (Wee1) inhibitors and/or degradation inducers potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Recurium IP Holdings LLC has disclosed new Wee1-like protein kinase (Wee1) inhibitors and/or degradation inducers potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732368</guid>
      <pubDate>Thu, 02 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732368-recurium-patents-new-wee1-inhibitors</link>
    </item>
  </channel>
</rss>
