Dynorphin A

CAS No. 80448-90-4

Dynorphin A( —— )

Catalog No. M30699 CAS No. 80448-90-4

Endogenous kappa receptor agonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 212 In Stock
10MG 289 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
    Dynorphin A
  • Note
    Research use only, not for human use.
  • Brief Description
    Endogenous kappa receptor agonist.
  • Description
    Endogenous kappa receptor agonist.
  • In Vitro
    Dynorphin A (10 μM, 4 h/72 h) increases caspase-3 activity and the level of cytochrome c released from mitochondria in mouse striatal neurons, and induces neuronal death.dynorphin A (33 μM, 4 h) elevates [Ca2+]i and causes a significant loss of neurons.dynorphin A (1 μM) inhibits the release of vasopressin (VP) from the isolated neural lobe. Cell Viability Assay Cell Line:Mouse striatal neurons Concentration:10 μM Incubation Time:0, 24, 48, 72 h Result:Induced neuronal death (identified by the fragmentation and destruction of the cell body and neurites).
  • In Vivo
    Dynorphin A (intracerebroventricular injection, 1 μg of 2 μL, a single dose) inhibits vasopressin (VP) release in 24 h water-deprived male rats.Dynorphin A (intracerebroventricular injection, 500 pmol/5 μL per day for 4 d) alleviates stress-induced behavioral impairments in ddY mice accompanied by regulation of the 5-HTergic system in the brain. Animal Model:24 h water-deprived male rats Dosage:1 μg of 2 μL Administration: Intracerebroventricular injection Result:Inhibited vasopressin (VP) release 30 min upon injection. Animal Model:Male ddY mice Dosage:15, 150, 1500 pmol/5 μL per day for 4 days Administration:Intracerebroventricular injection Result: Attenuated the repeated stress-induced escape failures from the shock.
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    Caspase
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    80448-90-4
  • Formula Weight
    2147.51
  • Molecular Formula
    C99H155N31O23
  • Purity
    >98% (HPLC)
  • Solubility
    water:0.80 mg/mL
  • SMILES
    [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)NCC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CNC2=C1C=CC=C2)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Dhawan et al (1996) International union of pharmacology XII. Classification of opioid receptors. Pharmacol.Rev. 48 567 PMID:
molnova catalog
related products
  • PAC1

    PAC-1 is a potent procaspase-3 activator with EC50 of 0.22 μM and the first small molecule known to directly activate procaspase-3 to caspase-3.

  • Z-LEHD-fmk

    Z-LEHD-FMK is a selective and potent caspase-9 inhibitor that protects against reperfusion injury and slows apoptosis. Z-LEHD-FMK exhibits antitumor and neuroprotective activity.

  • Linderene

    Linderene, linderalactone and isolinderalactone inhibit the enzymes from both origins to the same extent.