H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH
H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH Basic information
- Product Name:
- H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH
- Synonyms:
-
- H-RRRRRRRRR-NH2
- RRRRRRRRR
- (ARG)9
- H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH
- Nonaarginine
- H(-Arg)9-OH, Nonaarginine
- (Arg)9 peptide
- Arg-Arg-Arg-Arg-Arg-Arg-Arg-Arg-Arg
- CAS:
- 143413-47-2
- MF:
- C54H110N36O10
- MW:
- 1423.69
- Product Categories:
-
- peptide
- Mol File:
- 143413-47-2.mol
H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH Chemical Properties
- Density
- 1.60±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- Sequence
- H-Arg-Arg-Arg-Arg-Arg-Arg-Arg-Arg-Arg-OH
H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH Usage And Synthesis
Uses
(Arg)9 (Nona-L-arginine) is a cell-penetrating peptide (CPP) made up of 9 arginine residues, which is an inhibitor of serine endoprotease Furin. (Arg)9 has neuroprotective property, exhibits neuroprotective activity with an IC50 of 0.78 μM in the glutamic acid model[1][2].
Biological Activity
(Arg)9 (Nona-L-arginine; Peptide R9) is a cell-permeable polypeptide with IC50 value of 0.78 μM for neuroprotection in a glutamate model experimental model.
in vitro
Poly-arginine (eg (Arg)9) and arginine-rich peptides (eg TAT, penetratin), which belong to a class of peptides with cell-penetrating properties are neuroprotective. It provides significant neuroprotection in a dose–response manner following glutamic acid exposure (IC 50 =0.78 μM). Following kainic acid exposure, (Arg)9 is neuroprotective, but less effective than in the glutamic acid model (IC 50 =0.81 μM). (Arg)9 also shows neuroprotection following in vitro ischemia (IC 50 =6 μM).
in vivo
(Arg)9) (D-isoform) is neuroprotective in rat stroke models. (Arg)9) is highly neuroprotective, with efficacy increasing with increasing arginine content, has the capacity to reduce glutamic acid-induced neuronal calcium influx and requires heparan sulfate preotoglycan-mediated endocytosis to induce a neuroprotective effect. (Arg)9) (D-isoform) administered intravenously at a dose of 1000 nmol/kg 30 min after reduces permanent middle cerebral artery occlusion (MCAO) infarct volume .
target
IC50: 0.78 μM (neuroprotection)
References
[1] Cameron A, et al. Polyarginines are potent furin inhibitors. J Biol Chem. 2000 Nov 24;275(47):36741-9. DOI:10.1074/jbc.M003848200
[2] Meloni BP, et, al. The neuroprotective efficacy of cell-penetrating peptides TAT, penetratin, Arg-9, and Pep-1 in glutamic acid, kainic acid, and in vitro ischemia injury models using primary cortical neuronal cultures. Cell Mol Neurobiol. 2014 Mar;34(2):173-81. DOI:10.1007/s10571-013-9999-3
[3] Meloni BP, et, al. Poly-arginine and arginine-rich peptides are neuroprotective in stroke models. J Cereb Blood Flow Metab. 2015 Jun;35(6):993-1004. DOI:10.1038/jcbfm.2015.11
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H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH(143413-47-2)Related Product Information
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- GIP (1-39)
- H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH
- (ARG)9, TAMRA-LABELED
- (ARG)9, FAM-LABELED
- H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-OH
- H-ARG-ARG-ARG-ARG-OH