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

  • 9-amino-CPT (9-Aminocamptothecin)

    中文名称: 9-氨基喜树碱
    CAS号:91421-43-1
    分子式: C20H17N3O4 分子量: 363.37
    产品形式: Free base
    研发状态: Unknown status
    研发用途: Traditional Chinese Medicine; Dyslipidemias; Syndrome
    研究机构: Dongzhimen Hospital Beijing
    研发日期: April 21 2021
    研发阶段: --
    9-amino-CPT (9-Aminocamptothecin, 9-AC, Aminocamptothecin, 9-amino-20(S)-camptothecin) is a Topoisomerase I inhibitor with potent anticancer activities. 9-amino-CPT (9-Aminocamptothecin) is an active, water-insoluble derivative of camptothecin.

  • Rubitecan

    中文名称: 9-硝基喜树碱
    CAS号:91421-42-0
    分子式: C20H15N3O6 分子量: 393.35
    产品形式: Free Base
    研发状态: Completed
    研发用途: Influenza
    研究机构: National Institute of Allergy and Infectious Diseases (NIAID)
    研发日期: January 8 2019
    研发阶段: Phase 1
    Rubitecan (9-NC, 9-Nitro-camptothecin, Partaject Orathecin, Partaject rubitecan, RFS 2000) is a topoisomerase I inhibitor extracted from the bark and leaves of the Camptotheca acuminata tree, which is native to China. Rubitecan is an oral camptothecin with antitumour activity.

  • Ropinirole HCl

    中文名称:盐酸罗匹尼罗
    CAS号:91374-20-8
    分子式: C16H24N2O.HCl 分子量: 296.84
    产品形式: HCl
    研发状态: Terminated
    研发用途: Restless Legs Syndrome; End Stage Renal Disease
    研究机构: University of Alberta
    研发日期: February 19 2019
    研发阶段: Phase 2
    Ropinirole (SKF-101468A) a selective dopamine D2 receptors agonist with Ki of 29 nM.

  • Onalespib (AT13387)

    中文名称:奥那司匹
    CAS号:912999-49-6
    分子式: C24H31N3O3 分子量: 409.52
    产品形式: free base
    研发状态: Completed
    研发用途: Metastatic High Grade Fallopian Tube Serous Adenocarcinoma; Metastatic Malignant Solid Neoplasm; Metastatic Primary Peritoneal Serous Adenocarcinoma; Metastatic Triple-Negative Breast Carcinoma; Platinum-Resistant Fallopian Tube Carcinoma; Platinum-Resistant Ovarian Carcinoma; Platinum-Resistant Primary Peritoneal Carcinoma; Recurrent Breast Carcinoma; Recurrent High Grade Fallopian Tube Serous Adenocarcinoma; Recurrent High Grade Ovarian Serous Adenocarcinoma; Recurrent Primary Peritoneal High Grade Serous Adenocarcinoma; Recurrent Triple-Negative Breast Carcinoma; Refractory Fallopian Tube Serous Adenocarcinoma; Refractory Ovarian Serous Adenocarcinoma; Refractory Primary Peritoneal Serous Adenocarcinoma; Refractory Triple-Negative Breast Carcinoma; Unresectable High Grade Fallopian Tube Serous Adenocarcinoma; Unresectable Malignant Solid Neoplasm; Unresectable Primary Peritoneal Serous Adenocarcinoma
    研究机构: National Cancer Institute (NCI)
    研发日期: May 19 2017
    研发阶段: Phase 1
    Onalespib (AT13387) is a selective potent Hsp90 inhibitor with IC50 of 18 nM in A375 cells, displays a long duration of anti-tumor activity. Phase 2.

  • Veliparib (ABT-888)

    中文名称:维利帕尼
    CAS号:912444-00-9
    分子式: C13H16N4O 分子量: 244.29
    产品形式: free base
    研发状态: Withdrawn
    研发用途: Cancer
    研究机构: University Medical Center Groningen; AbbVie; Dutch Cancer Society
    研发日期: Nov-19
    研发阶段: Phase 2
    Veliparib (ABT-888, NSC 737664) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM in cell-free assays, respectively. It is inactive to SIRT2. Veliparib increases autophagy and apoptosis. Phase 3.

  • Gemigliptin

    中文名称:吉格列汀
    CAS号:911637-19-9
    分子式: C18H19F8N5O2 分子量: 489.36
    产品形式: Free Base
    研发状态: Unknown status
    研发用途: Diabetes Mellitus Type 2; Dyslipidemias
    研究机构: LG Chem
    研发日期: March 21 2019
    研发阶段: Phase 1
    Gemigliptin (Zemiglo, LC15-0444) is a potent, selective and long-acting dipeptidyl peptidase 4 (DPP 4) inhibitor with a Ki of 7.25 nM. Gemigliptin shows at least >23,000-fold selectivity for DPP-4 over various proteases and peptidases, including DPP-8, DPP-9, and fibroblast activation protein (FAP)-α.

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