YM 511

CAS No. 148869-05-0

YM 511( —— )

Catalog No. M27743 CAS No. 148869-05-0

aromatase (CYP19) inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 73 In Stock
10MG 122 In Stock
25MG 259 In Stock
50MG 406 In Stock
100MG 551 In Stock
200MG 728 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    YM 511
  • Note
    Research use only, not for human use.
  • Brief Description
    aromatase (CYP19) inhibitor.
  • Description
    aromatase (CYP19) inhibitor.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    148869-05-0
  • Formula Weight
    354.211
  • Molecular Formula
    C16H12BrN5
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (705.82 mM)
  • SMILES
    Brc1ccc(CN(c2ccc(cc2)C#N)n2cnnc2)cc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Ke Fang, et al. [Advances on the profiling of 5-hydroxymethylcytosine]. Yi Chuan. 2016 Mar;38(3):206-16.
molnova catalog
related products
  • E-3030

    E-3030 free acid is a potent dual activator of peroxisome proliferator-activated receptor (PPAR) alpha and PPARgamma, exhibiting significant antidiabetic and lipid-modulating effects. E-3030 decreases blood glucose, triglyceride, non-esterified fatty acids, and insulin levels, while increasing blood adiponectin levels. E-3030 improves glucose tolerance and shows remarkable triglyceride- and non-high-density lipoprotein cholesterol-lowering effects in animal models.

  • Tenuifolin

    Tenuifolin has no inherent toxicity to either the transfected or wild type cells at the effective concentrations, it inhibits amyloid-β secretion in vitro.

  • Boc-Lys(Ac)-AMC

    Commendamide (N-acyl-3-hydroxypalmitoyl-glycine) is a newly discovered GPCR G2A/GPR132 agonist (EC50=11.8 μM) that isolated from Bacteroides vulgatus.