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Jun 28,2023
CAR-T疗法重要针对白血病与恶性淋巴瘤,本钻研中构建寡言PD-1的shRNA载体质粒,测序后质粒的鉴定通过南宫NG28进行
Chimeric antigen receptor T cells (CAR-T) immunotherapy has shown promising clinical results in the treatment of leukemia and lymphoma, but the effectiveness is limited for solid tumors. The shRNA vector plasmid that silences PD-1 and preparation of CAR is constructed. The plasmids sequenced were fully identified by Medicilon.
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CAR-T疗法重要针对白血病与恶性淋巴瘤,本钻研中构建寡言PD-1的shRNA载体质粒,测序后质粒的鉴定通过南宫NG28进行
Jun 28,2023
索拉非尼的无定形固体分散体用于开发改进型口服生物利用度高的快释片剂,本钻研中PK尝试通过南宫NG28进行
The SOR ASD tablets exhibited approximately 50% higher relative bioavailability in dogs than the marketed SOR tablet product, Nexavar?. The pharmacokinetic (PK) study of SOR ASD tablets and Nexavar? tablets was performed by Medicilon.
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索拉非尼的无定形固体分散体用于开发改进型口服生物利用度高的快释片剂,本钻研中PK尝试通过南宫NG28进行
Jun 28,2023
TAK-931是一种高特异性CDC7抑造剂,拥有抗肿瘤功效,本钻研中体内药效尝试通过南宫NG28进行
In vivo efficacy studies in J558 allograft models in combination with anti-mPD-1, anti-mPD-L1, and anti-mCTLA-4 antibodies were performed at Medicilon.
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TAK-931是一种高特异性CDC7抑造剂,拥有抗肿瘤功效,本钻研中体内药效尝试通过南宫NG28进行
Jun 28,2023
GS-5801是一种高效KDM5抑造剂,拥有抗HBV活性,本钻研中GS-5801通过南宫NG28合成
GS-5801, a potent inhibitor of KDM5, has antiviral activity against HBV in a primary human hepatocytes infection model, with the cellular permeability, oral bioavailability. GS-5801 was synthesized by Medicilon.
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GS-5801是一种高效KDM5抑造剂,拥有抗HBV活性,本钻研中GS-5801通过南宫NG28合成
Jun 28,2023
QF-036是一种高效的HIV-1抑造剂,拥有优良的和药代动力学个性,PK钻研通过南宫NG28进行
The favourable viral inhibitory activity and pharmacokinetic properties provide critical support for QF-036 as a promising anti-HIV therapeutic candidate. The pharmacokinetic studies were performed by Medicilon.
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QF-036是一种高效的HIV-1抑造剂,拥有优良的和药代动力学个性,PK钻研通过南宫NG28进行
Jun 28,2023
设计合成一种新型选择性的口服有效苏氨酸酪氨酸激酶 (TTK) 抑造剂,PK钻研均通过南宫NG28进行
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 carried out by Medicilon.
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设计合成一种新型选择性的口服有效苏氨酸酪氨酸激酶 (TTK) 抑造剂,PK钻研均通过南宫NG28进行
Jun 28,2023
TR-107是人类线粒体蛋白酶ClpP的有效激活剂,PK分析通过南宫NG28进行
The pharmacokinetic properties of TR‐107 were compared with other known ClpP activators including ONC201 and ONC212. TR‐107 displayed excellent exposure and serum t1/2 after oral administration. Pharmacokinetic analysis were evaluated for pharmacokinetic properties in ICR mice by Medicilon.
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TR-107是人类线粒体蛋白酶ClpP的有效激活剂,PK分析通过南宫NG28进行
Jun 28,2023
SKLB-197是一种有效且高度选择性的ATR抑造剂,PK钻研通过南宫NG28进行
SKLB-197, exhibits good pharmacokinetic properties, could be a promising lead compound for drug discovery targeting ATR. The pharmacokinetic (PK) studies were performed by Medicilon.
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SKLB-197是一种有效且高度选择性的ATR抑造剂,PK钻研通过南宫NG28进行
Jun 28,2023
H11-HLE是一种工具分子,可用于钻研Fc在介导免疫查抄点医治中的作用,拥有抗肿瘤功效
Immune checkpoint inhibition therapies have been used for multiple cancer research. H11-HLE is a tool molecule that allows the interrogation of the contribution of Fc in mediating immune checkpoint therapy. Half-life extended H11 (H11-HLE) induces potent anti-tumor efficacy in mouse syngeneic tumor models.
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H11-HLE是一种工具分子,可用于钻研Fc在介导免疫查抄点医治中的作用,拥有抗肿瘤功效
Jun 28,2023
JND003是一种新型选择性ERRα激昂剂,可缓解非酒精性脂肪肝和胰岛素抵抗,PK和组织散布测定通过南宫NG28进行
Nonalcoholic fatty liver disease (NAFLD) is one of the most prevalent forms of chronic liver diseases. Estrogen-related receptor alpha (ERRα) is a viable target for NAFLD.
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JND003是一种新型选择性ERRα激昂剂,可缓解非酒精性脂肪肝和胰岛素抵抗,PK和组织散布测定通过南宫NG28进行
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