
PEN (human)
CAS No. 597578-70-6
PEN (human)( —— )
Catalog No. M30581 CAS No. 597578-70-6
Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
100MG | Get Quote | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NamePEN (human)
-
NoteResearch use only, not for human use.
-
Brief DescriptionEndogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.
-
DescriptionEndogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.
-
In VitroMouse PEN (mPEN) and rat PEN (rPEN) only differ by one residue at the N-terminal end, whereas human PEN (hPEN) is more divergent and has the sequence PEG instead of PEN.PEN binds and activates a GPCR in the brain.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetGRK (GPCRK)
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number597578-70-6
-
Formula Weight2215.49
-
Molecular FormulaC97H159N27O32
-
Purity>98% (HPLC)
-
SolubilityPBS (pH 7.4):1 mg/mL
-
SMILES[H]N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Gomes et al (2016) Identification of GPR83 as the receptor for the neuroendocrine peptide PEN. Sci.Signal 9 ra43 PMID:
molnova catalog



related products
-
PEN (rat)
Endogenous peptide GPR83 agonist. ProSAAS-derived neuropeptide.
-
GRK2i
GRK2 inhibitory polypeptide that specifically inhibits Gβγ activation of GRK2. Corresponds to the Gβγ-binding domain and acts as a cellular Gβγ antagonist.
-
CCG-224406
A highly selective and potent GRK2 (G protein-coupled receptor kinase 2) inhibitor with IC50 of 130 nM.