tricoumaroyl spermidine

CAS No. 131086-78-7

tricoumaroyl spermidine( N1,N5,N10-(Z)-tri-p-coumaroylspermidine )

Catalog No. M23469 CAS No. 131086-78-7

Tricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 203 In Stock
5MG 294 In Stock
10MG 446 In Stock
25MG 712 In Stock
50MG 1008 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    tricoumaroyl spermidine
  • Note
    Research use only, not for human use.
  • Brief Description
    Tricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
  • Description
    Tricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    N1,N5,N10-(Z)-tri-p-coumaroylspermidine
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    131086-78-7
  • Formula Weight
    583.67
  • Molecular Formula
    C34H37N3O6
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Oc1ccc(/C=C/C(NCCCCN(CCCNC(/C=C/c(cc2)ccc2O)=O)C(/C=C/c(cc2)ccc2O)=O)=O)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Yang Z, et al. Isolation and identification of spermidine derivatives in tea (Camellia sinensis) flowers and their distribution in floral organs. J Sci Food Agric. 2012 Aug 15;92(10):2128-32.
molnova catalog
related products
  • PRX-07034

    PRX-07034 is a selective antagonist of 5-HT6 receptor. It has cognition and memory-enhancing properties and potently decreases food intake and body weight in rodents.?PRX-07034 is both a potent (Ki = 4-8 nM) and highly selective 5-HT(6) receptor antagonist (≥100-fold selectivity for the 5-HT(6) receptor compared to 68 other GPCRs, ion channels, and transporters, except D(3) (Ki = 71 nM) and 5-HT(1B) (Ki = 260 nM) receptors.

  • DSP-6952 hydrobromid...

    DSP-6952 is a novel potent, selective, orally active 5-HT4 receptor partial agonist with Ki of 50-100 nM for human 5-HT4a/4b/4c.

  • Pindolol

    Pindolol is a nonselective β-blocker with partial beta-adrenergic receptor agonist activity, also functions as a 5-HT1A receptor weak partial agonist / antagonist (Ki=33nM).