Cas no 78761-61-2 (Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2)

Met-Enkephalin-Arg-Phe amide (H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH?) is a synthetic heptapeptide and an analog of endogenous Met-enkephalin, extended with Arg-Phe residues at the C-terminus and amidated for enhanced stability. This modification improves receptor binding affinity and resistance to enzymatic degradation compared to native enkephalins. It exhibits selective activity at opioid receptors, particularly the μ and δ subtypes, making it valuable for neuropharmacological research. The peptide’s structure allows for studies on pain modulation, neurotransmitter release, and receptor signaling pathways. Its high purity and well-defined sequence ensure reproducibility in experimental applications, supporting investigations into opioid peptide function and potential therapeutic mechanisms.
Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2 structure
78761-61-2 structure
Product Name:Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2
CAS No:78761-61-2
MF:C42H57N11O8S
MW:876.035887479782
CID:564157
Update Time:2025-10-19

Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2 Chemical and Physical Properties

Names and Identifiers

    • L-Phenylalaninamide,L-tyrosylglycylglycyl-L-phenylalanyl-L-methionyl-L-arginyl- (9CI)
    • H-TYR-GLY-GLY-PHE-MET-ARG-PHE-NH2
    • Meapaa
    • Tyr-Gly-Gly-Phe-Met-Arg-Phe-amide
    • Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2
    • Yggfmrf amide
    • L-Phenylalaninamide, L-tyrosylglycylglycyl-L-phenylalanyl-L-methionyl-L-arginyl-
    • Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2
    • Inchi: 1S/C42H57N11O8S/c1-62-20-18-32(40(60)51-31(13-8-19-47-42(45)46)39(59)53-33(37(44)57)22-26-9-4-2-5-10-26)52-41(61)34(23-27-11-6-3-7-12-27)50-36(56)25-48-35(55)24-49-38(58)30(43)21-28-14-16-29(54)17-15-28/h2-7,9-12,14-17,30-34,54H,8,13,18-25,43H2,1H3,(H2,44,57)(H,48,55)(H,49,58)(H,50,56)(H,51,60)(H,52,61)(H,53,59)(H4,45,46,47)/t30-,31-,32-,33-,34-/m0/s1
    • InChI Key: DIESNRFJUNWWPJ-LJADHVKFSA-N
    • SMILES: S(C)CC[C@@H](C(N[C@H](C(N[C@H](C(N)=O)CC1C=CC=CC=1)=O)CCC/N=C(\N)/N)=O)NC([C@H](CC1C=CC=CC=1)NC(CNC(CNC([C@H](CC1C=CC(=CC=1)O)N)=O)=O)=O)=O

Computed Properties

  • Hydrogen Bond Donor Count: 11
  • Hydrogen Bond Acceptor Count: 11
  • Heavy Atom Count: 62
  • Rotatable Bond Count: 26
  • Complexity: 1480
  • Topological Polar Surface Area: 354

Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2 Pricemore >>

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Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2 Related Literature

Additional information on Met-Enkephalin-Arg-Phe amide H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2

Met-Enkephalin-Arg-Phe Amide (CAS No. 78761-61-2): A Comprehensive Overview

Met-enkephalin-arg-phe amide, also known as H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2, is a synthetic peptide that has garnered significant attention in the fields of neuroscience and pharmacology. This compound, identified by the CAS registry number 78761-61-2, is a derivative of the naturally occurring enkephalins, which are endogenous opioid peptides involved in pain modulation and neurotransmission. The addition of arginine and phenylalanine residues to the N-terminal of the peptide enhances its bioactivity and stability, making it a promising candidate for therapeutic applications.

The structure of met-enkephalin-arg-phe amide consists of seven amino acids: histidine (H), tyrosine (Tyr), glycine (Gly), phenylalanine (Phe), methionine (Met), arginine (Arg), and another phenylalanine (Phe), terminated by an amide group (-NH2). This specific sequence allows the peptide to interact with opioid receptors, particularly the μ-opioid receptor (MOR), which is central to its analgesic effects. Recent studies have highlighted the potential of this compound in treating chronic pain conditions, such as neuropathic pain and inflammatory arthritis, due to its ability to modulate both acute and persistent pain pathways.

One of the most notable advancements in research involving CAS No. 78761-61-2 is its role in neuroprotection. Preclinical studies have demonstrated that this peptide can mitigate neuronal damage caused by ischemia-reperfusion injury, a condition often observed in stroke patients. The neuroprotective effects are attributed to its ability to reduce oxidative stress and inhibit pro-inflammatory cytokines, thereby preserving neuronal integrity. These findings suggest that met-enkephalin-arg-phe amide could be a novel therapeutic agent for neurodegenerative diseases such as Alzheimer's and Parkinson's.

In addition to its therapeutic potential, CAS No. 78761-61-2 has been extensively studied for its pharmacokinetic properties. Research indicates that the peptide exhibits good bioavailability when administered via certain routes, such as subcutaneous injection or nasal delivery. However, challenges remain in optimizing its delivery methods to enhance efficacy and reduce systemic side effects. Recent innovations in drug delivery systems, including lipid nanoparticles and polymeric micelles, are being explored to address these limitations.

The latest research on H-Tyr-Gly-Gly-Phe-Met-Arg-Phe-NH2 also points to its potential as an anti-addictive agent. By selectively targeting certain opioid receptor subtypes, this compound may offer a safer alternative to traditional opioids, which are associated with high risks of dependence and overdose. Clinical trials are currently underway to evaluate its safety profile and efficacy in managing opioid use disorder.

In conclusion, CAS No. 78761-61-2, or met-enkephalin-arg-phe amide, represents a significant advancement in peptide-based drug development. Its dual roles as an analgesic and neuroprotective agent make it a versatile compound with broad therapeutic applications. As research continues to uncover its mechanisms of action and optimize its delivery methods, this peptide holds great promise for addressing unmet medical needs in pain management and neurodegenerative diseases.

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