
中文名称:磷酸奥司他韦
CAS号:204255-11-8
分子式: C16H28N2O4.H3PO4 分子量: 410.40
产品形式: Phosphate salt
研发状态: Not yet recruiting
研发用途: Severe Influenza
研究机构: Assistance Publique - Hôpitaux de Paris
研发日期: December 1 2022
研发阶段: Not Applicable
Oseltamivir Phosphate(Tamiflu) is a potent and selective inhibitor of the neuraminidase that is essential for replication of influenza A and B viruses, used to prevent influenza.
中文名称:2-(1-(4-氯苄基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
CAS号:204205-90-3
分子式: C22H16ClN3O2 分子量: 389.83
产品形式: free base
研发状态: Unknown status
研发用途: Metastatic Breast Cancer
研究机构: Alaunos Therapeutics; Memorial Sloan Kettering Cancer Center
研发日期: Mar-10
研发阶段: Phase 1 : Phase 2
Indibulin (ZIO 301, D 24851, Zybulin) is an orally applied inhibitor of tubulin assembly with potent anticancer activity. Indibulin induces mitotic arrest and apoptosis.
中文名称:1,3-二氢-3-[(3,5-二甲基-1H-吡咯-2-基)亚甲基]-2H-吲哚-2-酮
CAS号:204005-46-9
分子式: C15H14N2O 分子量: 238.28
产品形式: free base
研发状态: Terminated
研发用途: Brain and Central Nervous System Tumors
研究机构: Pediatric Brain Tumor Consortium; National Cancer Institute (NCI)
研发日期: Aug-00
研发阶段: Phase 1
Semaxanib (SU5416, semaxinib) is a potent and selective VEGFR(Flk-1/KDR) inhibitor with IC50 of 1.23 μM, 20-fold more selective for VEGFR than PDGFRβ, lack of activity against EGFR, InsR and FGFR. Phase 3.
中文名称:辛酸拉尼米韦
CAS号:203120-46-1
分子式: C21H36N4O8 分子量: 472.53
产品形式: Free base
研发状态: Completed
研发用途: Asthma
研究机构: Biota Scientific Management Pty Ltd; Department of Health and Human Services; Vaxart
研发日期: Oct-13
研发阶段: Phase 1
Laninamivir octanoate (CS-8958, R-118958, Inavir, LANI), a prodrug of Laninamivir (R-125489), is a long-acting neuraminidase (NA) inhibitor with superior anti-influenza virus activity.
中文名称:氯苯吩嗪
CAS号:2030-63-9
分子式: C27H22Cl2N4 分子量: 473.40
产品形式: free base
研发状态: Completed
研发用途: Nontuberculous Mycobacterial Diseases
研究机构: Radboud University Medical Center
研发日期: February 14 2022
研发阶段: Phase 2
Clofazimine (NSC-141046) is a rhimophenazine dye, originally developed for the treatment of tuberculosis, it has both antimicrobial and antiinflammatory activity, postulated mechanisms of action include intercalation of clofazimine with bacterial DNA and increasing levels of cellular phospholipase A2.
中文名称:比拉瑞塞
CAS号:202590-98-5
分子式: C25H22ClN5O2S 分子量: 491.99
产品形式: free base
研发状态: Terminated
研发用途: NUT Midline Carcinoma (NMC); Triple Negative Breast Cancer (TNBC); Non-small Cell Lung Cancer (NSCLC); Castration-resistant Prostate Cancer (CRPC)
研究机构: Merck Sharp & Dohme LLC
研发日期: May 4 2016
研发阶段: Phase 1
Birabresib (OTX015, MK 8628) is a potent BET bromodomain inhibitor with EC50 ranging from 10 to 19 nM for BRD2, BRD3, and BRD4 in cell-free assays. Birabresib inhibits the expression of Nuclear receptor binding SET domain protein 3 (NSD3) target genes.
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