网站主页>>>研发精选>>>临床前CDMO研发筛选相关化合物
CDMO是Contract Development and Manufacturing Organization的缩写,即合同定制研发生产组织。它是一种为制药企业及生物技术公司提供医药(特别是创新药)工艺研发及制备、工艺优化、放大生产、注册和验证批生产以及商业化生产等定制服务的机构. 在传统代工基础上增加了研发和工艺优化能力,是高技术壁垒的工艺研发能力与规模生产能力的深度结合. 1, 工艺开发与优化:创新性合成路线设计、工艺参数优化. 2, 中试放大:实验室工艺向规模化生产的转化 3, 注册批生产:支持客户新药申报的验证批生产. 4, 商业化生产:药品上市后的大规模生产供应. 全球医药CDMO行业保持较高景气度。根据弗若斯特沙利文预测:2026年全球CDMO市场规模:预计达1,189亿美元 2033年全球CDMO市场规模:预计达3,385亿美元. CDMO作为医药产业链专业化分工的产物,已经从单纯的CMO代工模式升级为"研发+生产"一体化的高附加值服务。当前,在多肽、ADC、CGT等新型药物赛道的驱动下,全球及中国CDMO市场保持高速增长。中国CDMO企业凭借完整的供应链体系、工程师红利和一体化服务能力,全球市占率有望持续提升,行业正从"成本优势"竞争迈向"体系优势"竞争的新阶段。
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临床前CDMO研发化合物筛选

  • Sildenafil Citrate

    中文名称:枸橼酸西地那非
    CAS号:171599-83-0
    分子式: C22H30N6O4S.C6H8O7 分子量: 666.70
    产品形式: Citrate
    研发状态: Completed
    研发用途: Edema Pulmonary; Immersion; Diving
    研究机构: Duke University; United States Department of Defense
    研发日期: July 15 2019
    研发阶段: Phase 2
    Sildenafil Citrate, a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5), is a well-tolerated and highly effective treatment for erectile dysfunction.

  • Tadalafil (IC351)

    中文名称:他达那非
    CAS号:171596-29-5
    分子式: C22H19N3O4 分子量: 389.40
    产品形式: free base
    研发状态: Not yet recruiting
    研发用途: Duchenne Muscular Dystrophy; Duchenne Disease; Muscular Dystrophy; Muscular Dystrophy in Children; Vasodilation; Exercise; DMD
    研究机构: University of Florida; National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
    研发日期: Mar-24
    研发阶段: Phase 2
    Tadalafil (IC351) is a PDE-5 inhibitor with IC50 of 1.8 nM in a cell-free assay. Tadalafil is at least 9000 times more selective for PDE5 than most of the other families of PDEs, with the exception of PDE11. It can partial inhibits PDE11

  • Dalbavancin

    中文名称: 达巴万星
    CAS号:171500-79-1
    分子式: C88H100Cl2N10O28 分子量: 1816.69
    产品形式: free base
    研发状态: Recruiting
    研发用途: Osteoarticular Infection
    研究机构: Centre Hospitalier Universitaire de Nice
    研发日期: March 7 2022
    研发阶段: Not Applicable
    Dalbavancin (Zeven, BI 397, MDL 63397) is a lipoglycopeptide antibiotic that has bactericidal activity against Gram-positive bacteria including various staphylococci.

  • Posaconazole (SCH 56592)

    中文名称:泊沙康唑
    CAS号:171228-49-2
    分子式: C37H42F2N8O4 分子量: 700.78
    产品形式: free base
    研发状态: Not yet recruiting
    研发用途: Acute Respiratory Tract Infection
    研究机构: European Clinical Research Alliance for Infectious Diseases (ECRAID); UMC Utrecht; University of Oxford; Universiteit Antwerpen
    研发日期: Feb-24
    研发阶段: --
    Posaconazole (SCH 56592,POS,Noxafil) is an inhibitor primarily of CYP3A4, but it does not inhibit the activity of other CYP enzymes; Also an inhibitor of sterol C14ɑ demethylase inhibitor with IC50 of 0.25 μM. Posaconazole has a median terminal elimination half-life of 15-35 hours.

  • Roblitinib (FGF401)

    中文名称:8-二氮杂萘-1(2H)-甲酰胺
    CAS号:1708971-55-4
    分子式: C25H30N8O4 分子量: 506.56
    产品形式: free base
    研发状态: Completed
    研发用途: Hepatocellular Carcinoma (HCC); Solid Malignancies
    研究机构: Novartis Pharmaceuticals; Novartis
    研发日期: December 29 2014
    研发阶段: Phase 1 : Phase 2
    Roblitinib (FGF401) is an FGFR4-selective inhibitor with an IC50 of 1.9 nM. It binds in a reversible covalent manner to the FGFR4 kinase domain and shows at least 1,000 fold selectivity against of panel of 65 kinases in biochemical assays.

  • Efaproxiral Sodium

    中文名称:乙丙昔罗钠
    CAS号:170787-99-2
    分子式: C20H23NO4.Na 分子量: 363.38
    产品形式: Sodium salt
    研发状态: Withdrawn
    研发用途: Brain and Central Nervous System Tumors
    研究机构: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins; National Cancer Institute (NCI)
    研发日期: Not Applicable
    研发阶段:
    Efaproxiral Sodium(RSR13 Sodium) is a synthetic allosteric modifier of hemoglobin, decreases Hb-oxygen (O2) binding affinity and enhances oxygenation of hypoxic tumours during radiation therapy. Efaproxiral Sodium is used for brain metastases originating from breast cancer.

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