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

  • Letrozole (CGS 20267)

    中文名称: 来曲唑
    CAS号:112809-51-5
    分子式: C17H11N5 分子量: 285.30
    产品形式: free base
    研发状态: Not yet recruiting
    研发用途: Leiomyoma Uterine; Leiomyoma; Fibroid; Fibroid Uterus
    研究机构: University of California San Francisco; Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    研发日期: May 13 2024
    研发阶段: Phase 4
    Letrozole (CGS 20267,Femara, Piroxicam) is a third generation inhibitor of aromatase with IC50 of 0.07-20 nM in cell-free assays.It has no effect on the plasma levels of 17α-OH progesterone, thyroid-stimulating hormone (TSH), luteinizing hormone (LH), follicle-stimulating hormone (FSH), or androstenedione and does not affect normal urine electrolyte excretion or thyroid function in clinical studies. Letrozole induces autophagy.

  • Pioglitazone HCl

    中文名称: 盐酸吡格列酮
    CAS号:112529-15-4
    分子式: C19H20N2O3S.HCl 分子量: 392.90
    产品形式: Hydrochloride
    研发状态: Not yet recruiting
    研发用途: ANCA Associated Vasculitis; Rapidly Progressive Glomerulonephritis; Crescentic Glomerulonephritis
    研究机构: Assistance Publique - Hôpitaux de Paris; Ministry of Health France
    研发日期: Jul-23
    研发阶段: Phase 3
    Pioglitazone HCl (AD-4833, U-72107E) is an inhibitor of cytochrome P450 (CYP)2C8 and CYP3A4 enzymes. Pioglitazone HCl inhibits CYP2C8, CYP3A4 and CYP2C9 with Ki of 1.7 μM, 11.8 μM and 32.1 μM, respectively. Pioglitazone HCl is also a selective peroxisome proliferator-activated receptor-gamma (PPARγ) agonist with EC50 of 0.93 μM and 0.99 μM for human PPARγ and mouse PPARγ, respectively. Pioglitazone HCl inhibits mitochondrial iron uptake, lipid peroxidation, and subsequent ferroptosis.

  • Sitravatinib (MGCD516)

    中文名称:司曲替尼
    CAS号:1123837-84-2
    分子式: C33H29F2N5O4S 分子量: 629.68
    产品形式: free base
    研发状态: Completed
    研发用途: Healthy Adults
    研究机构: Mirati Therapeutics Inc.
    研发日期: July 7 2021
    研发阶段: Phase 1
    Sitravatinib (MGCD516, MG-516) is a novel small molecule inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Kit, PDGFRβ, PDGFRα, c-Met, and Axl.

  • Quetiapine (ICI-204636) fumarate

    中文名称:富马酸喹硫平
    CAS号:111974-72-2
    分子式: C46H54N6O8S2 分子量: 883.09
    产品形式: Fumarate
    研发状态: Unknown status
    研发用途: Bipolar Disorder
    研究机构: Guangzhou Mental Hospital; First Affiliated Hospital of Jinan University; Second Affiliated Hospital of Guangzhou Medical University; Guangzhou mental Hospital Attached to Guangzhou Civil Affairs Bureau
    研发日期: Dec-08
    研发阶段: Phase 4
    Quetiapine Fumarate (ICI-204636) is an atypical antipsychotic used in the treatment of schizophrenia, bipolar I mania, bipolar II depression, bipolar I depression and shows affinity for various neurotransmitter receptors including serotonin, dopamine, histamine, and adrenergic receptors.

  • Quetiapine

    中文名称:喹硫平
    CAS号:111974-69-7
    分子式: C21H25N3O2S 分子量: 383.51
    产品形式: Free Base
    研发状态: Completed
    研发用途: Delirium
    研究机构: Ain Shams University
    研发日期: March 1 2023
    研发阶段: Phase 2
    Quetiapine(ICI204636) is an atypical antipsychotic used for the treatment of schizophrenia, bipolar disorder, and major depressive disorder.Quetiapine is a 5-HT receptors agonist with a pEC50 of 4.77 for human 5-HT1A receptor. Quetiapine is a dopamine receptor antagonist with a pIC50 of 6.33 for human D2 receptor. Quetiapine have moderate to high affinity for the human D2, HT1A, 5-HT2A, 5-HT2C receptor with pKis of 7.23, 5.74, 7.54, 5.55.

  • L-Arginine HCl (L-Arg)

    中文名称:L-精氨酸盐酸盐
    CAS号:1119-34-2
    分子式: C6H14N4O2.HCl 分子量: 210.66
    产品形式: HCl
    研发状态: Not yet recruiting
    研发用途: Chronic Obstructive Pulmonary Disease (COPD)
    研究机构: Universitätsklinikum Hamburg-Eppendorf
    研发日期: March 1 2024
    研发阶段: --
    L-Arginine(L-Arg,(S)-(+)-Arginine hydrochloride) is the nitrogen donor for synthesis of nitric oxide, a potent vasodilator that is deficient during times of sickle cell crisis.

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