
中文名称:替扎尼定
CAS号:51322-75-9
分子式: C9H8ClN5S 分子量: 253.71
产品形式: α2-adrenergic agonists
研发状态: Completed
研发用途: Malignant Melanoma Neoplasms
研究机构: Hoffmann-La Roche
研发日期: September 2 2013
研发阶段: Phase 1
Tizanidine is an imidazoline derivative and a centrally acting α2 adrenergic agonist used as a muscle relaxant for therapy of acute muscle spasms and chronic spasticity.
中文名称:盐酸异丙肾上腺素
CAS号:51-30-9
分子式: C11H17NO3.HCl 分子量: 247.72
产品形式: Hydrochloride
研发状态: Completed
研发用途: Essential Hypertension
研究机构: University of Copenhagen; University of Aarhus
研发日期: August 1 2020
研发阶段: Not Applicable
Isoprenaline HCl (NCI-c55630,Isoproterenol hydrochloride) is a non-selective beta-adrenergic receptor agonist, used for the treatment of bradycardia and heart block.
中文名称:替拉曲可
CAS号:51-24-1
分子式: C14H9I3O4 分子量: 621.93
产品形式: free base
研发状态: Recruiting
研发用途: Monocarboxylate Transporter 8 Deficiency; Allan-Herndon-Dudley Syndrome
研究机构: Rare Thyroid Therapeutics International AB; Premier Research Group plc; Egetis Therapeutics
研发日期: July 21 2023
研发阶段: Phase 3
Tiratricol (also known as TRIAC or triiodothyroacetic acid) is a thyroid hormone analogue.
中文名称:5-氟尿嘧啶
CAS号:51-21-8
分子式: C4H3FN2O2 分子量: 130.08
产品形式: free base
研发状态: Recruiting
研发用途: Pancreatic Cancer; Adjuvant Therapy
研究机构: Kuirong Jiang; CSPC Ouyi Pharmaceutical Co. Ltd.; The First Affiliated Hospital with Nanjing Medical University
研发日期: April 8 2024
研发阶段: Not Applicable
Fluorouracil (5-Fluorouracil, 5-FU, NSC 19893) is a DNA/RNA synthesis inhibitor, which interrupts nucleotide synthetic by inhibiting thymidylate synthase (TS) in tumor cells. Fluorouracil induces apoptosis and can be used in the treatment of HIV.
中文名称:醉茄素A
CAS号:5119-48-2
分子式: C28H38O6 分子量: 470.60
产品形式: free base
研发状态: Not yet recruiting
研发用途: Lynch Syndrome; Recurrent Uterine Corpus Carcinoma; Stage I Uterine Corpus Cancer; Stage II Uterine Corpus Cancer; Stage III Uterine Corpus Cancer; Stage IV Uterine Corpus Cancer
研究机构: Gynecologic Oncology Group; National Cancer Institute (NCI); GOG Foundation
研发日期: Jan-00
研发阶段: --
Withaferin A (WA, WFA) potently inhibits NF-κB activation by preventing the tumor necrosis factor-induced activation of IκB kinase β via a thioalkylation-sensitive redox mechanism. Withaferin A binds to the intermediate filament (IF) protein, vimentin with antitumor and antiangiogenesis activity. Withaferin A is a steroidal lactone isolated from Withania somnifera.
中文名称:(R)-布洛芬
CAS号:51146-57-7
分子式: C13H18O2 分子量: 206.28
产品形式: Free Base
研发状态: Recruiting
研发用途: Pain Postoperative
研究机构: B.P. Koirala Institute of Health Sciences
研发日期: August 10 2023
研发阶段: Phase 4
(R)-(-)-Ibuprofen ((R)-Ibuprofen) inhibits the activation of NF-κB in response to T-cell stimulation with IC50 of 121.8 μM, and exerts anti-inflammatory and antinociceptive effects.
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