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[Leu5]-Enkephalin - 98%, high purity , CAS No.58822-25-6, Agonist of δ receptor;Agonist of κ receptor;Agonist of μ receptor

  • Moligand™
  • ≥98%
Item Number
L304070
Grouped product items
SKUSizeAvailabilityPrice Qty
L304070-10mg
10mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$58.90
L304070-25mg
25mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$117.90
L304070-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$424.90

Opioid peptide and potent δ and μ-receptor agonist

Basic Description

SynonymsLeu-enkephalin|[Leu5]-Enkephalin|leucine enkephalin|58822-25-6|Enkephalin|Tyr-Gly-Gly-Phe-Leu|Enkephalins|Enkephalin L|Leucyl-enkephalin|[Leu]enkephalin|Leucine-enkephalin|ENKEPHALIN, LEUCINE|H-Tyr-Gly-Gly-Phe-Leu-OH|[5-Leucine]Enkephalin|Leu5-Enkephalin|
Specifications & Purity98%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeAGONIST
Mechanism of actionAgonist of δ receptor;Agonist of κ receptor;Agonist of μ receptor
Product Description

Product Describtion:

[Leu5]-Enkephalin is a pentapeptide with morphine like properties. [Leu5]-Enkephalin is a five amino acid endogenous peptide that acts as an agonist at opioid receptors.

Associated Targets

OPRD1 Tclin Delta-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRK1 Tclin Kappa-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

OPRM1 Tclin Mu-type opioid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (2S)-2-[[(2S)-2-[[2-[[2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]acetyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoic acid
INCHI InChI=1S/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22-,23-/m0/s1
InChi Key URLZCHNOLZSCCA-VABKMULXSA-N
Canonical SMILES CC(C)CC(C(=O)O)NC(=O)C(CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)C(CC2=CC=C(C=C2)O)N
Isomeric SMILES CC(C)C[C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)CNC(=O)CNC(=O)[C@H](CC2=CC=C(C=C2)O)N
PubChem CID 461776
Molecular Weight 555.63

Certificates

Certificate of Analysis(COA)

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3 results found

Lot NumberCertificate TypeDateItem
G23051116Certificate of AnalysisJun 13, 2023 L304070
G23051118Certificate of AnalysisJun 13, 2023 L304070
G23051120Certificate of AnalysisJun 13, 2023 L304070

Chemical and Physical Properties

SolubilitySoluble in water (1 mg/ml ).
SensitivityMoisture sensitive

Related Documents

References

1. Lepiarczyk E et al..  (2017)  The Influence of Resiniferatoxin (RTX) and Tetrodotoxin (TTX) on the Distribution, Relative Frequency, and Chemical Coding of Noradrenergic and Cholinergic Nerve Fibers Supplying the Porcine Urinary Bladder Wall..  Toxins (Basel),  (10):   [PMID:28972567]

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