Cart
sales@molnova.com
Home - Products - Membrane Transporter/Ion Channel - Sodium Channel - N-Me-aminopyrimidinone9

N-Me-aminopyrimidinone9

CAS No. 1356834-62-2

N-Me-aminopyrimidinone9( —— )

Catalog No. M21974 CAS No. 1356834-62-2

N-Me-aminopyrimidinone9 is a sodium channel antagonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 119 In Stock
5MG 119 In Stock
10MG 181 In Stock
25MG 297 In Stock
50MG 410 In Stock
100MG 554 In Stock
200MG 736 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    N-Me-aminopyrimidinone9
  • Note
    Research use only, not for human use.
  • Brief Description
    N-Me-aminopyrimidinone9 is a sodium channel antagonist.
  • Description
    N-Me-aminopyrimidinone9 is a sodium channel antagonist.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Sodium Channel
  • Recptor
    Sodium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1356834-62-2
  • Formula Weight
    303.4
  • Molecular Formula
    C16H21N3OS?
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Cn1c(SCc2ccc(cc2)C(C)(C)C)nc(N)cc1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • Huwentoxin IV

    Selective NaV1.7 channel blocker. Preferentially inhibits neuronal NaV1.7, 1.2 and 1.3 (IC50 values are 26, 150 and 338 nM respectively), compared to muscle subtypes NaV1.4 and 1.5 (IC50 = >10 μM). Inhibits the channel by binding at the neurotoxin receptor site 4 in the S3-S4 linker of domain II, trapping the voltage sensor in the inward, closed configuration.

  • SM-6586

    SM-6586 is a potent calcium channel antagonist with inhibitory effects on Na+/H+ and Na+/Ca2+ exchange channels, and can be used in the study of cerebrovascular disease and hypertension, among other diseases.

  • Nav1.8-IN-4

    Nav1.8-IN-4 is a potent Nav1.8 channel inhibitor with potential analgesic activity.Nav1.8-IN-4 can be used for pain and neurological related disorders.

Sign In Join Free