
Dynorphin A
CAS No. 80448-90-4
Dynorphin A( —— )
Catalog No. M30699 CAS No. 80448-90-4
Endogenous kappa receptor agonist.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 201 | Get Quote |
![]() ![]() |
10MG | 274 | Get Quote |
![]() ![]() |
100MG | Get Quote | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameDynorphin A
-
NoteResearch use only, not for human use.
-
Brief DescriptionEndogenous kappa receptor agonist.
-
DescriptionEndogenous kappa receptor agonist.
-
In VitroDynorphin 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 VivoDynorphin 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——
-
PathwayApoptosis
-
TargetCaspase
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number80448-90-4
-
Formula Weight2147.51
-
Molecular FormulaC99H155N31O23
-
Purity>98% (HPLC)
-
Solubilitywater: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℃)
-
ShippingWith 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
-
4'57-Trimethoxyflavo...
574'-Trimethoxyflavone is isolated from Kaempferia parviflora (KP) which is a medicinal plant from Thailand.
-
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.
-
Z-VAD-FMK
Z-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor, blocks all features of apoptosis.