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    搜索結果包含 cancer 的內容

    Aug 21,2023
    TAK-931是一種高效的CDC7抑制劑，通過抑制CDC7來抑制DNA復制，具有抗腫瘤功效，體內藥效研究通過尊龍凱時進行
    Replication stress (RS) is a cancer hallmark; chemotherapeutic drugs targeting RS are widely used as treatments for various cancers. To develop next-generation RS-inducing anticancer drugs, cell divis
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    Jul 06,2023
    TRIM24和BRPF1是癌癥的潛在治療靶點。Y08624是一種新型TRIM24/BRPF1雙重抑制劑，具有良好的Caco-2滲透性。Caco-2 滲透性測定通過尊龍凱時進行
    TRIM24 (tripartite motif-containing protein 24) and BRPF1 (bromodomain and PHD finger containing protein 1) are epigenetics “readers”and potential therapeutic targets for cancer and other diseases. Y0
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    Jul 06,2023
    IAP蛋白是有吸引力的癌癥治療靶點。SM-406 是一種口服有效的IAP拮抗劑。SM-406 在雄性SD大鼠、比格犬和NHP中的PK研究通過尊龍凱時進行
    Apoptosis is a cellular process critical to the normal development and homeostasis of multicellular organisms.?The inhibitor of apoptosis proteins (IAPs) are a class of key apoptosis regulators.
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    Jul 06,2023
    設計合成一系列用于治療胃癌的多靶點受體酪氨酸激酶抑制劑，并進行生物學評價。其中藥代動力學分析通過尊龍凱時進行
    Gastric cancer is the second most lethal cancer across the world. Compounds 8f, inhibits FGFR1 signaling pathways as well as induces cell apoptosis, is a potential agent for the treatment of gastric c
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    Jul 06,2023
    FBPase是與腫瘤和2型糖尿病相關的一個有前景的靶點。化合物W8對FBPase表現出高選擇性。W8的藥代動力學研究通過尊龍凱時進行
    Fructose-1,6-bisphosphatase (FBPase) is a promising target associated with cancer and type 2 diabetes. Compounds W8 and W8k exhibit high selectivity against FBPase and W8 effectively reduces blood glu
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    Jul 06,2023
    PTX-HSN是一種高效納米系統，具有較高耐受劑量，可將PTX遞送至卵巢癌并增強主動腫瘤靶向性。此研究中所有體內實驗均通過尊龍凱時進行
    Paclitaxel-loaded hyaluronan solid nanoemulsions (PTX-HSNs) were successfully fabricated for the delivery of PTX to improve ovarian cancer treatment via active tumor targeting. The in vivo #toxicity,
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    Jul 06,2023
    AD80是一種多激酶抑制劑，在多種肝細胞癌臨床前動物模型中具有抗腫瘤活性，AD80在血漿中的含量通過尊龍凱時進行LC-MS/MS測定
    Liver cancer is the fourth greatest cause of cancer related mortality. AD80 is a multi-kinase inhibitor with anti-tumoral activity across a variety of hepatocellular carcinoma (HCC) preclinical models
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    Jul 06,2023
    免疫檢查點阻斷療法改變了癌癥治療的范式，此研究中通過尊龍凱時在23 個同源腫瘤模型中進行了抗PD-1抗體的體內研究
    Immune checkpoint blockade therapies have changed the paradigm of cancer therapies. Reseachers performed?in vivo?screening for anti-PD-1 therapy across 23 syngeneic tumor models and found th
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    Jul 05,2023
    研究人員設計合成STAT3和HDAC雙通路抑制劑用于治療實體腫瘤，PK實驗通過尊龍凱時進行
    The inhibition of HDACs will lead to compensated activation of a notorious cancer-related drug target, STAT3, in breast cancer through a cascade, which probably limits the anti-proliferation effect of
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    Jul 05,2023
    研究人員設計并合成了一種光籠PI3K抑制劑1，它可以通過紫外線照射激活，釋放出高效PI3K抑制劑2。化合物1和2的ADME研究通過尊龍凱時進行
    Aberrant activation of the PI3K pathway has been intensively targeted for cancer therapeutics for decades.? In this work, researchers designed and synthesized a novel photocaged PI3K inhibitor 1,
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    Jul 05,2023
    合成具有體內抗腫瘤活性的強效PD-L1抑制劑，并進行生物學評價和機制研究。PK研究通過尊龍凱時進行
    PD-1 and PD-L1 have been very successful for the treatment of various tumors, including NSCLC, urothelial cancer, melanoma, head and neck squamous cell cancer, and lymphoma. Researchers identified com
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    Jul 05,2023
    苯并咪唑衍生物XY123是一種口服有效的選擇性RORγ反向激動劑。在本研究中，所有肝微粒體測定均通過尊龍凱時進行
    Receptor-related orphan receptor γ (RORγ) has emerged as an attractive therapeutic target for the treatment of cancer and inflammatory diseases. XY123 potently inhibits the RORγ transcription activity
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    Jul 05,2023
    端錨聚合酶1/2影響WNT/β-連環蛋白和Hippo信號通路，這些信號通路涉及包括腫瘤在內的多種疾病
    Tankyrase 1 and 2 (TNKS1/2) impact the WNT/β-catenin and Hippo signaling pathways that are involved in numerous human disease conditions including cancer. OM-153 shows picomolar IC50 inhibition in a c
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    Jul 05,2023
    設計合成和評估用于治療前列腺癌的CBP溴結構域抑制劑。PK評估、肝微粒體穩定性測定和Caco-2滲透性測定通過尊龍凱時進行
    Prostate cancer (PCa) is one of the most commonly diagnosed cancers and the leading cause of cancer mortalities in men. CREB (cyclic-AMP responsive element binding protein) binding protein (CBP) is a
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    Jul 05,2023
    研究人員開發了一種高特異性的CDC7抑制劑TAK-931作為臨床腫瘤治療劑，抗腫瘤藥效研究通過尊龍凱時進行
    Cell division cycle 7 (CDC7) plays important roles in DNA replication. Researchers developed a highly specific CDC7 inhibitor, TAK-931, as a clinical cancer therapeutic agent. The antitumor efficacy s
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    Jul 05,2023
    合成一類新型選擇性TNIK抑制劑并評估其抗結直腸癌作用，PK研究通過尊龍凱時進行
    The Traf2- and Nck-interacting protein kinase (TNIK) is a downstream signal protein of the Wnt/β-catenin pathway and has been thought of as a potential target for the treatment of colorectal cancer.
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    Jul 05,2023
    選擇性小分子c-Myc降解劑可有效消退c-Myc過表達的腫瘤，表面等離子共振 (SPR) 實驗通過尊龍凱時進行
    Cancer is one of the leading causes of death worldwide. MYC oncogene is involved in the majority of human cancers and is often associated with poor outcomes. WBC100, a novel oral active molecule glue
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    Jun 28,2023
    設計合成一系列DHODH抑制劑作為潛在的類風濕性關節炎治療藥物，本研究中PK實驗通過尊龍凱時進行
    Human dihydroorotate dehydrogenase (DHODH) is a viable target for the development of therapeutics to treat cancer and immunological diseases. Herein, researchers designed and synthesized a series of acrylamide-based novel DHODH inhibitors as potential rhe
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    Jun 28,2023
    放射療法用作肺癌的主要治療方法，本研究中建立抗電離輻射肺癌細胞系的放射治療通過尊龍凱時進行
    Radiation therapy is used as the primary treatment for lung cancer. In this study, radiation therapy for establish ionizing radiation-resistant lung cancer cell lines (A549-IR/H1299-IR) was supported by Medicilon.
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    Jun 28,2023
    設計合成一種新型選擇性的口服有效蘇氨酸酪氨酸激酶 (TTK) 抑制劑，PK研究均通過尊龍凱時進行
    TTK inhibition is an attractive wide-spectrum strategy for cancer therapy. Researchers designed and synthesized a series of pyrido[2, 3-d]pyrimidin-7(8H)-ones as new selective orally bioavailable TTK inhibitors. All the pharmacokinetic studies were carrie
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