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    <title>Patents</title>
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    <item>
      <title>Jiangsu Hengrui, Shanghai Senhui and Shanghai Shengdi patent new compounds for asthma</title>
      <description>A joint Jiangsu Hengrui Pharmaceuticals Co. Ltd., Shanghai Senhui Pharmaceutical Co. Ltd. and Shanghai Shengdi Pharmaceutical Co. Ltd. patent details new tetrahydrobenzothiazole compounds potentially useful for the treatment of allergic asthma.</description>
      <content:encoded>
        <![CDATA[A joint Jiangsu Hengrui Pharmaceuticals Co. Ltd., Shanghai Senhui Pharmaceutical Co. Ltd. and Shanghai Shengdi Pharmaceutical Co. Ltd. patent details new tetrahydrobenzothiazole compounds potentially useful for the treatment of allergic asthma.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732658</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732658-jiangsu-hengrui-shanghai-senhui-and-shanghai-shengdi-patent-new-compounds-for-asthma</link>
    </item>
    <item>
      <title>Nuoshen Pharmaceutical prepares new NLRP3 inflammasome inhibitors</title>
      <description>Nuoshen Pharmaceutical (Shanghai) Co. Ltd. has disclosed new NLRP3 inflammasome inhibitors potentially useful for the treatment of neuroinflammation, multiple sclerosis, amyotrophic lateral sclerosis, Alzheimer’s, Parkinson’s and Huntington’s disease.</description>
      <content:encoded>
        <![CDATA[Nuoshen Pharmaceutical (Shanghai) Co. Ltd. has disclosed new NLRP3 inflammasome inhibitors potentially useful for the treatment of neuroinflammation, multiple sclerosis, amyotrophic lateral sclerosis, Alzheimer’s, Parkinson’s and Huntington’s disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732657</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732657-nuoshen-pharmaceutical-prepares-new-nlrp3-inflammasome-inhibitors</link>
    </item>
    <item>
      <title>Biocytogen Pharmaceuticals discloses new anti-DLL3/B7H3 ADCs</title>
      <description>Biocytogen Pharmaceuticals (Beijing) Co. Ltd. has prepared and tested new bispecific antibody-drug conjugates (ADCs) consisting of a bispecific antibody or antigen-binding fragments targeting B7 homolog 3 (B7-H3; CD276) and delta-like protein 3 (DLL3) linked to cytotoxic drug; they are described as potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Biocytogen Pharmaceuticals (Beijing) Co. Ltd. has prepared and tested new bispecific antibody-drug conjugates (ADCs) consisting of a bispecific antibody or antigen-binding fragments targeting B7 homolog 3 (B7-H3; CD276) and delta-like protein 3 (DLL3) linked to cytotoxic drug; they are described as potentially useful for the treatment of cancer.]]>
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      <guid>http://www.bioworld.com/articles/732656</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732656-biocytogen-pharmaceuticals-discloses-new-anti-dll3-b7h3-adcs</link>
    </item>
    <item>
      <title>Nampt inhibitors reported in Alphina Therapeutics patent</title>
      <description>Alphina Therapeutics Inc. has identified new nicotinamide phosphoribosyltransferase (NAmPRTase; Nampt) inhibitors potentially useful for the treatment of autoimmune and metabolic diseases, inflammatory disorders and cancer.</description>
      <content:encoded>
        <![CDATA[Alphina Therapeutics Inc. has identified new nicotinamide phosphoribosyltransferase (NAmPRTase; Nampt) inhibitors potentially useful for the treatment of autoimmune and metabolic diseases, inflammatory disorders and cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732655</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732655-nampt-inhibitors-reported-in-alphina-therapeutics-patent</link>
    </item>
    <item>
      <title>Neolaia identifies new CD38 inhibitors</title>
      <description>Neolaia Inc. has discovered new 6,5-bicyclic compounds acting as ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 (CD38) inhibitors potentially useful for the treatment of cancer, neurodegeneration, fibrosis, renal, inflammatory, autoimmune, metabolic and cardiovascular disease, among others.</description>
      <content:encoded>
        <![CDATA[Neolaia Inc. has discovered new 6,5-bicyclic compounds acting as ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 (CD38) inhibitors potentially useful for the treatment of cancer, neurodegeneration, fibrosis, renal, inflammatory, autoimmune, metabolic and cardiovascular disease, among others.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732654</guid>
      <pubDate>Wed, 15 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732654-neolaia-identifies-new-cd38-inhibitors</link>
    </item>
    <item>
      <title>Hansoh identifies new Mat2A inhibitors</title>
      <description>A joint Hansoh Bio LLC, Jiangsu Hansoh Pharmaceutical Group Co. Ltd. and Shanghai Hansoh Biomedical Co. Ltd. patent details new S-adenosylmethionine synthase isoform type-2 (Mat2A) inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[A joint Hansoh Bio LLC, Jiangsu Hansoh Pharmaceutical Group Co. Ltd. and Shanghai Hansoh Biomedical Co. Ltd. patent details new <em>S</em>-adenosylmethionine synthase isoform type-2 (Mat2A) inhibitors potentially useful for the treatment of cancer.]]>
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      <guid>http://www.bioworld.com/articles/732640</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732640-hansoh-identifies-new-mat2a-inhibitors</link>
      <media:content url="https://www.bioworld.com/ext/resources/Stock-images/Research-and-science/Molecule-illustration.webp?t=1599684844" type="image/png" medium="image" fileSize="508796">
        <media:title type="plain">Molecule illustration</media:title>
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    </item>
    <item>
      <title>Shanghai Institute of Materia Medica patents new lipid-lowering gluconeogenesis inhibitors</title>
      <description>Shanghai Institute of Materia Medica of the Chinese Academy of Sciences has disclosed new compounds acting as lipid-lowering agents and gluconeogenesis inhibitors potentially useful for the treatment of metabolic diseases.</description>
      <content:encoded>
        <![CDATA[Shanghai Institute of Materia Medica of the Chinese Academy of Sciences has disclosed new compounds acting as lipid-lowering agents and gluconeogenesis inhibitors potentially useful for the treatment of metabolic diseases.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732639</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732639-shanghai-institute-of-materia-medica-patents-new-lipid-lowering-gluconeogenesis-inhibitors</link>
    </item>
    <item>
      <title>CNRS and collaborators discover new &lt;em&gt;Mycobacterium&lt;/em&gt; ATPase inhibitors </title>
      <description>Researchers from the Centre National de la Recherche Scientifique, the Institut National de la Santé et de la Recherche Médicale, Nanyang Technological University and the University of Montpellier have patented new Mycobacterium sp. ATP synthase (F0F1 ATPase) inhibitors potentially useful for the treatment of nontuberculous mycobacterial infections.</description>
      <content:encoded>
        <![CDATA[Researchers from the Centre National de la Recherche Scientifique, the Institut National de la Santé et de la Recherche Médicale, Nanyang Technological University and the University of Montpellier have patented new <em>Mycobacterium</em> sp. ATP synthase (F0F1 ATPase) inhibitors potentially useful for the treatment of nontuberculous mycobacterial infections.]]>
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      <guid>http://www.bioworld.com/articles/732638</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732638-cnrs-and-collaborators-discover-new-emmycobacterium-em-atpase-inhibitors</link>
    </item>
    <item>
      <title>Wuhan Createrna discloses new CFD inhibitors</title>
      <description>Wuhan Createrna Science and Technology Co. Ltd. has reported new complement factor D (CFD) inhibitors potentially useful for the treatment of cardiovascular, immunological, eye, genitourinary, renal, respiratory, neurological disorders and hematological diseases.</description>
      <content:encoded>
        <![CDATA[Wuhan Createrna Science and Technology Co. Ltd. has reported new complement factor D (CFD) inhibitors potentially useful for the treatment of cardiovascular, immunological, eye, genitourinary, renal, respiratory, neurological disorders and hematological diseases.]]>
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      <guid>http://www.bioworld.com/articles/732637</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732637-wuhan-createrna-discloses-new-cfd-inhibitors</link>
    </item>
    <item>
      <title>WRN inhibitors reported in Nutshell Therapeutics patent</title>
      <description>Nutshell Therapeutics Inc. has synthesized new nitrogen-containing heteroaryl compounds acting as Werner syndrome ATP-dependent helicase (WRN; RECQ3; RECQL2) inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Nutshell Therapeutics Inc. has synthesized new nitrogen-containing heteroaryl compounds acting as Werner syndrome ATP-dependent helicase (WRN; RECQ3; RECQL2) inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732636</guid>
      <pubDate>Tue, 14 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732636-wrn-inhibitors-reported-in-nutshell-therapeutics-patent</link>
    </item>
    <item>
      <title>Fed Circuit once again instructs on enablement of Rx claims</title>
      <description>A federal jury was wrong when it determined that Astrazeneca plc should pay Wyeth, a Pfizer Inc. unit, $107.5 million in damages for infringing two cancer patents, the U.S. Court of Appeals for the Federal Circuit said in a recent precedential decision.</description>
      <content:encoded>
        <![CDATA[A federal jury was wrong when it determined that Astrazeneca plc should pay Wyeth, a Pfizer Inc. unit, $107.5 million in damages for infringing two cancer patents, the U.S. Court of Appeals for the Federal Circuit said in a recent precedential decision.]]>
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      <guid>http://www.bioworld.com/articles/732584</guid>
      <pubDate>Mon, 13 Jul 2026 12:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732584-fed-circuit-once-again-instructs-on-enablement-of-rx-claims</link>
    </item>
    <item>
      <title>Novartis prepares new FAP-targeting radioconjugates</title>
      <description>Novartis AG has reported new drug conjugates comprising drugs targeting fibroblast activation protein α (FAP) covalently linked to a radiolabeled chelating agent through a linker potentially useful for the treatment and/or diagnosis of cancer.</description>
      <content:encoded>
        <![CDATA[Novartis AG has reported new drug conjugates comprising drugs targeting fibroblast activation protein α (FAP) covalently linked to a radiolabeled chelating agent through a linker potentially useful for the treatment and/or diagnosis of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732578</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732578-novartis-prepares-new-fap-targeting-radioconjugates</link>
    </item>
    <item>
      <title>JAK2 inhibitors reported in Prelude Therapeutics patent</title>
      <description>Prelude Therapeutics Inc. has identified new tyrosine-protein kinase JAK2 inhibitors potentially useful for the treatment of leukemia, polycythemia vera, myelofibrosis, essential thrombocythemia and graft-vs.-host disease.</description>
      <content:encoded>
        <![CDATA[Prelude Therapeutics Inc. has identified new tyrosine-protein kinase JAK2 inhibitors potentially useful for the treatment of leukemia, polycythemia vera, myelofibrosis, essential thrombocythemia and graft-vs.-host disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732577</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732577-jak2-inhibitors-reported-in-prelude-therapeutics-patent</link>
    </item>
    <item>
      <title>Shenzhen Linggene Biotechnology discloses new OGT degradation inducers</title>
      <description>Shenzhen Linggene Biotechnology Co. Ltd. has synthesized new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding agent coupled to a UDP-N-acetylglucosamine-peptide N-acetylglucosaminyltransferase (OGT)-targeting moiety acting as OGT degradation inducers.</description>
      <content:encoded>
        <![CDATA[Shenzhen Linggene Biotechnology Co. Ltd. has synthesized new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding agent coupled to a UDP-<em>N</em>-acetylglucosamine-peptide <em>N</em>-acetylglucosaminyltransferase (OGT)-targeting moiety acting as OGT degradation inducers.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732576</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732576-shenzhen-linggene-biotechnology-discloses-new-ogt-degradation-inducers</link>
    </item>
    <item>
      <title>Vastpro Pharmaceutical discovers new voltage-gated sodium channel blockers</title>
      <description>Vastpro (Shanghai) Pharmaceutical Technology Development Co. Ltd. has patented new voltage-gated sodium channel blockers potentially useful for the treatment of pain.</description>
      <content:encoded>
        <![CDATA[Vastpro (Shanghai) Pharmaceutical Technology Development Co. Ltd. has patented new voltage-gated sodium channel blockers potentially useful for the treatment of pain.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732575</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732575-vastpro-pharmaceutical-discovers-new-voltage-gated-sodium-channel-blockers</link>
    </item>
    <item>
      <title>Guangzhou Respiratory Medicine patents new cathepsin C/neutrophil elastase inhibitors</title>
      <description>Guangzhou Respiratory Medicine Engineering Technology Co. Ltd. has disclosed new cathepsin C (dipeptidyl peptidase I) and neutrophil elastase (ELANE; leukocyte elastase) inhibitors potentially useful for the treatment of asthma, diabetes, psoriasis, nasal polyps, cystic fibrosis and more.</description>
      <content:encoded>
        <![CDATA[Guangzhou Respiratory Medicine Engineering Technology Co. Ltd. has disclosed new cathepsin C (dipeptidyl peptidase I) and neutrophil elastase (ELANE; leukocyte elastase) inhibitors potentially useful for the treatment of asthma, diabetes, psoriasis, nasal polyps, cystic fibrosis and more.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732574</guid>
      <pubDate>Mon, 13 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732574-guangzhou-respiratory-medicine-patents-new-cathepsin-c-neutrophil-elastase-inhibitors</link>
    </item>
    <item>
      <title>Suzhou Puhe Biopharma discovers new KRAS mutant inhibitors</title>
      <description>Suzhou Puhe Biopharma Co. Ltd. has patented new GTPase KRAS mutant inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[Suzhou Puhe Biopharma Co. Ltd. has patented new GTPase KRAS mutant inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732559</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732559-suzhou-puhe-biopharma-discovers-new-kras-mutant-inhibitors</link>
    </item>
    <item>
      <title>NRF2 activators reported in Vailima Peninsula patent</title>
      <description>Vailima Peninsula Pty Ltd. has discovered new nuclear factor erythroid 2-related factor 2 (NFE2L2; NRF2) activators potentially useful for the treatment of neurodegeneration and inflammatory disorders.</description>
      <content:encoded>
        <![CDATA[Vailima Peninsula Pty Ltd. has discovered new nuclear factor erythroid 2-related factor 2 (NFE2L2; NRF2) activators potentially useful for the treatment of neurodegeneration and inflammatory disorders.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732558</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732558-nrf2-activators-reported-in-vailima-peninsula-patent</link>
    </item>
    <item>
      <title>Shanghai Peptidstar Therapeutics synthesizes new IL-23R antagonists</title>
      <description>Shanghai Peptidstar Therapeutics Ltd. has divulged new cyclic peptides acting as interleukin-23 receptor (IL-23R) antagonists potentially useful for the treatment of psoriasis, arthritis and inflammatory bowel disease.</description>
      <content:encoded>
        <![CDATA[Shanghai Peptidstar Therapeutics Ltd. has divulged new cyclic peptides acting as interleukin-23 receptor (IL-23R) antagonists potentially useful for the treatment of psoriasis, arthritis and inflammatory bowel disease.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732557</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732557-shanghai-peptidstar-therapeutics-synthesizes-new-il-23r-antagonists</link>
    </item>
    <item>
      <title>K2 Medicines patents EGFR mutant inhibitors</title>
      <description>K2 Medicines (Nanjing) Co. Ltd. has disclosed new epidermal growth factor receptor (EGFR; ERBB1; HER1) mutant inhibitors potentially useful for the treatment of cancer.</description>
      <content:encoded>
        <![CDATA[K2 Medicines (Nanjing) Co. Ltd. has disclosed new epidermal growth factor receptor (EGFR; ERBB1; HER1) mutant inhibitors potentially useful for the treatment of cancer.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732556</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732556-k2-medicines-patents-egfr-mutant-inhibitors</link>
    </item>
    <item>
      <title>Anew Therapeutics identifies new IL-17A/IL-17RA interaction inhibitors</title>
      <description>Anew Therapeutics Pte Ltd. has discovered new interleukin-17A (IL-17A)/interleukin-17 receptor A (IL-17RA) interaction inhibitors reported be useful for the treatment of Crohn’s disease, type 1 diabetes, dry eye and more.</description>
      <content:encoded>
        <![CDATA[Anew Therapeutics Pte Ltd. has discovered new interleukin-17A (IL-17A)/interleukin-17 receptor A (IL-17RA) interaction inhibitors reported be useful for the treatment of Crohn’s disease, type 1 diabetes, dry eye and more.]]>
      </content:encoded>
      <guid>http://www.bioworld.com/articles/732555</guid>
      <pubDate>Fri, 10 Jul 2026 09:00:00 -0400</pubDate>
      <link>https://www.bioworld.com/articles/732555-anew-therapeutics-identifies-new-il-17a-il-17ra-interaction-inhibitors</link>
    </item>
    <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>
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