Leumorphin, human
Product Specifications
UNSPSC Description
Leumorphin, human is a potent kappa opioid receptor (κ opioid receptor) agonist. Leumorphin, human inhibits the contraction of the myenteric plexus-longitudinal muscle preparation of the guinea pig ileum[1].
Target Antigen
Opioid Receptor
Type
Peptides
Related Pathways
GPCR/G Protein;Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/leumorphin-human.html
Solubility
10 mM in DMSO
Smiles
C([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC1=CC=CC=C1)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC2=CC=CC=C2)NC(CNC(CNC([C@H](CC3=CC=C(O)C=C3)N)=O)=O)=O)=O)CC(C)C)=O)CCCNC(=N)N)=O)CCCNC(=N)N)=O)CCC(N)=O)=O)=O)CCCCN)=O)C(C)C)=O)[C@H](C)C)=O)[C@@H](C)O)=O)CCCNC(=N)N)=O)CO)=O)CCC(N)=O)=O)CCC(O)=O)=O)CC(O)=O)(=O)N4[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CC5=CC=C(O)C=C5)C(N[C@H](C(NCC(N[C@H](C(N[C@H](C(N[C@@H](CC6=CC=CC=C6)C(N[C@H](C(N[C@H](C(O)=O)C)=O)CC(O)=O)=O)=O)CC(C)C)=O)CCC(O)=O)=O)=O)CO)=O)=O)C)=O)CC(N)=O)=O)CCC4
Molecular Weight
3351.64
References & Citations
[1]M Suda, K Nakao, et al. Human leumorphin is a potent, kappa opioid receptor agonist. Neurosci Lett. 1984 Sep 7;50(1-3):49-52.
Shipping Conditions
Room temperature
Product Datasheet
http://file.medchemexpress.com/batch_PDF/HY-P10006/Leumorphin-human-DataSheet-MedChemExpress.pdf
Product MSDS
http://file.medchemexpress.com/batch_PDF/HY-P10006/
Clinical Information
No Development Reported
CAS Number
88846-98-4
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