Suramin sodium salt

CAS No. 129-46-4

Suramin sodium salt( Suramin hexasodium salt | BAY-205 | NF-060 )

Catalog No. M11191 CAS No. 129-46-4

Suramin sodium salt (BAY-205, NF-060) is an antitrypansomal drug that also possesses antitumor activity; inhibits CRL (Cullin-RING E3 ubiquitin ligases) activity by disrupting its ability to recruit Cdc34.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 87 In Stock
10MG 131 In Stock
25MG 222 In Stock
50MG 332 In Stock
100MG 499 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Suramin sodium salt
  • Note
    Research use only, not for human use.
  • Brief Description
    Suramin sodium salt (BAY-205, NF-060) is an antitrypansomal drug that also possesses antitumor activity; inhibits CRL (Cullin-RING E3 ubiquitin ligases) activity by disrupting its ability to recruit Cdc34.
  • Description
    Suramin sodium salt (BAY-205, NF-060) is an antitrypansomal drug that also possesses antitumor activity; inhibits CRL (Cullin-RING E3 ubiquitin ligases) activity by disrupting its ability to recruit Cdc34; induces accumulation of CRL substrates; also inhibits multiple viruses (ZIKVs, EV71).Parasite Infection Approved.
  • In Vitro
    Cell Proliferation Assay Cell Line:HO-8910 PM ovarian and Hela cervical cancer cells Concentration:50, 100, 200, 300, 400, 500 and 600 μg/mL.Incubation Time:For 24, 48, 72 and 96 hoursResult:Inhibited cells proliferation in a dose-dependent and time-dependent manner.Apoptosis Analysis Cell Line:HeLa cells Concentration:300 μg/mL .Incubation Time:For 48 hours Result:Induced cells apoptosis.Western Blot Analysis Cell Line:PA-SMCs cells. Concentration:1 mg/mL Incubation Time:For 1 hour Result:Significantly suppressed the phosphorylated ERK1/2.
  • In Vivo
    Animal Model:Adult male Wistar rats (200-225 g )Dosage:10 mg/kg Administration:IV; twice weekly for 3 weeks Result:Reversed established PH, thereby normalizing the pulmonary artery pressure values and vessel structure.
  • Synonyms
    Suramin hexasodium salt | BAY-205 | NF-060
  • Pathway
    Proteasome/Ubiquitin
  • Target
    E3 Ubiquitin Ligase
  • Recptor
    TopoII
  • Research Area
    Infection
  • Indication
    Parasite Infection

Chemical Information

  • CAS Number
    129-46-4
  • Formula Weight
    1429.171
  • Molecular Formula
    C51H34N6Na6O23S6
  • Purity
    >98% (HPLC)
  • Solubility
    H2O: ≥ 200 mg/mL; DMSO: 5.6 mg/mL (Need warming)
  • SMILES
    O=C(C1=CC=C(C)C(NC(C2=CC(NC(NC3=CC(C(NC4=C(C)C=CC(C(NC5=C(C(S(=O)([O-])=O)=CC(S(=O)([O-])=O)=C6)C6=C(S(=O)([O-])=O)C=C5)=O)=C4)=O)=CC=C3)=O)=CC=C2)=O)=C1)NC7=CC=C(S(=O)([O-])=O)C8=C7C(S(=O)([O-])=O)=CC(S(=O)([O-])=O)=C8.[Na+].[Na+].[Na+].[Na+].[Na+].
  • Chemical Name
    1,3,5-Naphthalenetrisulfonic acid, 8,8'-[carbonylbis[imino-3,1-phenylenecarbonylimino(4-methyl-3,1-phenylene)carbonylimino]]bis-, sodium salt (1:6)

Shipping & Storage Information

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

Reference

1. Wu K, et al. Proc Natl Acad Sci U S A. 2016 Apr 5;113(14):E2011-8. 2. Ren P, et al. Sci Rep. 2017 Feb 20;7:42902. 3. Albulescu IC, et al. Antiviral Res. 2017 Jul;143:230-236.
molnova catalog
related products
  • BRD5529

    BRD5529 is a small-molecule inhibitor that disrupts the interaction of CARD9-E3 ubiquitin ligase TRIM62 with IC50 of 8.6 uM.

  • VHL-IN-15

    VHL-IN-15 is a potent (IC50=4.1 uM) von Hippel–Lindau protein (VHL) ligand that disrupts the VHL/HIF-1α interaction.

  • cIAP1 E3 ligase inhi...

    cIAP1 E3 ligase inhibitor D19 (cIAP1 inhibitor D19) is a small-molecule inhibitor of E3 ligase activity of cIAP1, inhibits cIAP1 auto-ubiquitination with IC50 of 14.1 uM.