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

  • Cenicriviroc (TAK-652)


    CAS号:497223-25-3
    分子式: C41H52N4O4S 分子量: 696.94
    产品形式: free base
    研发状态: Not yet recruiting
    研发用途: End Stage Renal Disease
    研究机构: Xeltis
    研发日期: Jul-24
    研发阶段: Not Applicable
    Cenicriviroc (CVC, TAK-652, TBR-652) is a potent, orally active dual inhibitor of CC chemokine receptor 2 (CCR2) and CCR5. Cenicriviroc also inhibits HIV-1 and HIV-2 with potent anti-inflammatory and antiinfective activity.

  • Eltrombopag (SB497115) Olamine

    中文名称:艾曲波帕乙醇胺
    CAS号:496775-62-3
    分子式: C29H36N6O6 分子量: 564.63
    产品形式: diolamine
    研发状态: Terminated
    研发用途: Adult Acute Basophilic Leukemia; Adult Acute Eosinophilic Leukemia; Adult Acute Megakaryoblastic Leukemia (M7); Adult Acute Minimally Differentiated Myeloid Leukemia (M0); Adult Acute Monoblastic Leukemia (M5a); Adult Acute Monocytic Leukemia (M5b); Adult Acute Myeloblastic Leukemia With Maturation (M2); Adult Acute Myeloblastic Leukemia Without Maturation (M1); Adult Acute Myeloid Leukemia With 11q23 (MLL) Abnormalities; Adult Acute Myeloid Leukemia With Del(5q); Adult Acute Myeloid Leukemia With Inv(16)(p13;q22); Adult Acute Myeloid Leukemia With t(16;16)(p13;q22); Adult Acute Myeloid Leukemia With t(8;21)(q22;q22); Adult Acute Myelomonocytic Leukemia (M4); Adult Erythroleukemia (M6a); Adult Pure Erythroid Leukemia (M6b); Recurrent Adult Acute Myeloid Leukemia
    研究机构: Roswell Park Cancer Institute; GlaxoSmithKline
    研发日期: May-12
    研发阶段: Phase 1
    Eltrombopag Olamine (SB-497115-GR, Revolade, Promacta,Promacta Olamine) is a member of the biarylhydrazone class, which is a nonpeptide agonist of the thrombopoietin receptor (TpoR).

  • Eltrombopag

    中文名称:伊屈泼帕
    CAS号:496775-61-2
    分子式: C25H22N4O4 分子量: 442.47
    产品形式: Free Base
    研发状态: Recruiting
    研发用途: Lymphoma; Peripheral Blood Stem Cell Transplantation
    研究机构: National Taiwan University Hospital; Novartis
    研发日期: August 15 2023
    研发阶段: Phase 2
    Eltrombopag (SB-497115), a member of the biarylhydrazone class, is a nonpeptide agonist of the thrombopoietin receptor (TpoR), used to treat chronic hepatitis C-associated thrombocytopenia and chronic immune (idiopathic) thrombocytopenia (ITP).

  • Hippuric acid

    中文名称:马尿酸
    CAS号:495-69-2
    分子式: C9H9NO3 分子量: 179.17
    产品形式: free base
    研发状态: Recruiting
    研发用途: Renal Insufficiency Chronic; Kidney Failure Chronic; Chronic Kidney Diseases
    研究机构: UMC Utrecht; European Commission Horizon 2020; Dutch Kidney Foundation; Health Holland; Nanodialysis Ltd; Università degli studi di Modena e Reggio Emilia (UNIMORE); Servicio Madrileno De Salud (SERMAS); PPI Healthcare Consulting Ltd
    研发日期: January 22 2024
    研发阶段: Not Applicable
    Hippuric Acid (2-Benzamidoacetic acid, Benzoylglycine) is an acyl glycine produced by the conjugation of benzoic acid and glycine, found as a normal component in urine as a metabolite of aromatic compounds from food.

  • Fenofibrate (NSC-281319)

    中文名称:非诺贝特
    CAS号:49562-28-9
    分子式: C20H21ClO4 分子量: 360.83
    产品形式: free base
    研发状态: Recruiting
    研发用途: Liver Transplant
    研究机构: Mayo Clinic
    研发日期: August 17 2022
    研发阶段: Phase 2
    Fenofibrate (NSC-281319) is a compound of the fibrate class and fibric acid derivative. Fenofibrate is a selective agonist of PPARα with EC50 of 30 μM. Fenofibrate binds to and inhibits cytochrome P450 epoxygenase (CYP)2C with IC50 of 0.2 μM, 0.7 μM and 9.7 μM for CYP2C19, CYP2B6 and CYP2C9, respectively. Fenofibrate induces autophagy.

  • Saroglitazar

    中文名称:萨格列扎
    CAS号:495399-09-2
    分子式: C25H29NO4S 分子量: 439.57
    产品形式: Free Base
    研发状态: Recruiting
    研发用途: Nonalcoholic Steatohepatitis
    研究机构: Zydus Therapeutics Inc.
    研发日期: September 26 2022
    研发阶段: Phase 2
    Saroglitazar (Lipaglyn, ZYH1) is an agonist of peroxisome proliferator-activated receptor (PPAR) with EC50 of 0.65 pM and 3 nM for hPPARα and hPPARγ in HepG2 cells, respectively.

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