AMI-1

CAS No. 20324-87-2

AMI-1( AMI-1 | AMI 1 | AMI1 | AMI-1 disodium salt. )

Catalog No. M13165 CAS No. 20324-87-2

A specific inhibitor of PRMTs (protein arginine methyltransferases), but not lysine methyltransferases.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 39 In Stock
10MG 58 In Stock
25MG 115 In Stock
50MG 170 In Stock
100MG 267 In Stock
500MG 646 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    AMI-1
  • Note
    Research use only, not for human use.
  • Brief Description
    A specific inhibitor of PRMTs (protein arginine methyltransferases), but not lysine methyltransferases.
  • Description
    A specific inhibitor of PRMTs (protein arginine methyltransferases), but not lysine methyltransferases; inhibits PRMT1 and Hmt1p with IC50s of 8.81 uM and 3.03 uM respectively; increases the ratio of Bax/Bcl-2, and leads to apoptosis and loss of migratory activity in several HCC cells,decreases the expression levels of H4R3me2s; strongly inhibits HCC growth in vivo.
  • In Vitro
    AMI-1 can inhibit the in vitro methylation reactions performed by all five recombinantly active PRMTs (PRMT1, -3, -4, and -6 and Hmt1p).AMI-1 not only inhibits type I PRMTs (PRMT1, 3, 4 and 6) but also type II PRMT5. AMI-1 specifically inhibits arginine, but not lysine, methyltransferase activity in vitro and does not compete for the AdoMet binding site. AMI-1 inhibits methylation of GFP-Npl3 and cellular proteins.AMI-1 (0.6-2.4 mM; 48-96 hours) inhibits the cell viability of sarcoma in S180 and U2OS cells in a time-dependent and dose-dependent manner in vitro.AMI-1 (1.2-2.4 mM; 48-72 hours) reduces S180 cell viability through the induction of cell apoptosis. Cell Viability Assay Cell Line:S180 cells, U2OS cells Concentration:0.6 mM, 1.2 mM, 2.4 mM Incubation Time:48 hours, 72 hours, 96 hours Result:Inhibited the cell viability.Apoptosis AnalysisCell Line:S180 cellsConcentration:1.2 mM, 2.4 mM Incubation Time:48 hours, 72 hours Result:Increased the percentages of cells undergoing apoptosis.
  • In Vivo
    AMI-1 (0.5 mg; intratumorally; daily; for 7 days) inhibits S180 viability in vivo.AMI-1 (0.5 mg; intratumorally; daily; for 7 days) downregulates PRMT5 but does not regulate the expression of PRMT7 in a tumor xenograft model.AMI-1 (0.5 mg; intratumorally; daily; for 7 days) decreases the levels of H4R3me2s and H3R8me2s in a tumor xenograft model. Animal Model:6-7 weeks old male Kunming mice (18-22 g), with S180 cells xenograft Dosage:0.5 mg Administration:Intratumorally, daily, for 7 days Result:Decreased tumor weight.
  • Synonyms
    AMI-1 | AMI 1 | AMI1 | AMI-1 disodium salt.
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    PRMT1|yeastHmt1p
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    20324-87-2
  • Formula Weight
    548.4534
  • Molecular Formula
    C21H14N2Na2O9S2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 46 mg/mL
  • SMILES
    O=C(NC1=CC2=CC(S(=O)([O-])=O)=CC(O)=C2C=C1)NC3=CC4=CC(S(=O)([O-])=O)=CC(O)=C4C=C3.[Na+].[Na+]
  • Chemical Name
    2-Naphthalenesulfonic acid, 7,7'-(carbonyldiimino)bis[4-hydroxy-, sodium salt (1:2)

Shipping & Storage Information

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

Reference

1. Cheng D, et al. J Biol Chem. 2004 Jun 4;279(23):23892-9. 2. Zhang B, et al. Oncotarget. 2015 Sep 8;6(26):22799-811. 3. Zhang B, et al. J Transl Med. 2015 Nov 5;13:349.
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