
中文名称:替诺福韦艾拉酚胺
CAS号:379270-37-8
分子式: C21H29N6O5P 分子量: 476.47
产品形式: free base
研发状态: Unknown status
研发用途: HIV-1-infection
研究机构: ANRS Emerging Infectious Diseases; Gilead Sciences
研发日期: February 1 2022
研发阶段: Not Applicable
Tenofovir Alafenamide (GS-7340) is a prodrug of tenofovir, which is a reverse transcriptase inhibitor, used to treat HIV and Hepatitis B.
中文名称:萨拉卡蒂尼(AZD0530)
CAS号:379231-04-6
分子式: C27H32ClN5O5 分子量: 542.03
产品形式: free base
研发状态: Active not recruiting
研发用途: Idiopathic Pulmonary Fibrosis (IPF)
研究机构: National Jewish Health; Yale University; Icahn School of Medicine at Mount Sinai; AstraZeneca; National Center for Advancing Translational Sciences (NCATS); Baylor University; International Center for Health Outcomes and Innovation Research
研发日期: November 12 2020
研发阶段: Phase 1 : Phase 2
Saracatinib (AZD0530) is a potent Src inhibitor with IC50 of 2.7 nM in cell-free assays, and potent to c-Yes, Fyn, Lyn, Blk, Fgr and Lck; less active for Abl and EGFR (L858R and L861Q). Saracatinib induces autophagy. Phase 2/3.
中文名称:倍他米松
CAS号:378-44-9
分子式: C22H29FO5 分子量: 392.46
产品形式: Free Base
研发状态: Recruiting
研发用途: Sacral Myelomeningocele; Neural Tube Defects; Spina Bifida
研究机构: Assistance Publique - Hôpitaux de Paris
研发日期: April 16 2021
研发阶段: Not Applicable
Betamethasone (NSC-39470, SCH-4831) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties.
中文名称: 异环磷酰胺
CAS号:3778-73-2
分子式: C7H15Cl2N2O2P 分子量: 261.09
产品形式: free base
研发状态: Recruiting
研发用途: Leiomyosarcoma
研究机构: University of Michigan Rogel Cancer Center; National Cancer Institute (NCI)
研发日期: April 26 2023
研发阶段: --
Ifosfamide (Mitoxana, Ifex,Isophosphamide,NSC109724) is a nitrogen mustard alkylating agent used in the treatment of cancer.
中文名称:瑞德南特
CAS号:377727-87-2
分子式: C25H29N9O3 分子量: 503.56
产品形式: free base
研发状态: Completed
研发用途: Chronic Hepatic Impairment
研究机构: Merck Sharp & Dohme LLC
研发日期: November 10 2011
研发阶段: Phase 1
Preladenant (Privadenant, SCH 420814, MK-3814) is a potent, competitive and selective antagonist of the human adenosine A2A receptor with Ki of 1.1 nM.
中文名称: 马拉维若
CAS号:376348-65-1
分子式: C29H41F2N5O 分子量: 513.67
产品形式: free base
研发状态: Recruiting
研发用途: Post Stroke Cognitive Impairment
研究机构: Tel-Aviv Sourasky Medical Center; Hadassah Medical Organization; Soroka University Medical Center
研发日期: May 1 2021
研发阶段: Phase 2
Maraviroc (Celsentri,UK-427857) is a CCR5 antagonist for MIP-1α, MIP-1β and RANTES with IC50 of 3.3 nM, 7.2 nM and 5.2 nM in cell-free assays, respectively. Maraviroc is used in the treatment of HIV infection.
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