Cas no 187986-11-4 (H-Trp-Lys-Tyr-Met-Val-Met-NH2)

The hexapeptide H-Trp-Lys-Tyr-Met-Val-Met-NH2 is a synthetic peptide sequence featuring tryptophan (Trp), lysine (Lys), tyrosine (Tyr), methionine (Met), and valine (Val) residues, capped with a C-terminal amide group. This structured peptide demonstrates potential biological relevance due to its aromatic and sulfur-containing side chains, which may influence binding interactions or stability. The presence of methionine residues suggests redox-sensitive properties, while the lysine and tyrosine residues contribute to solubility and potential post-translational modifications. Its well-defined sequence allows for precise applications in biochemical research, including structure-activity relationship studies or ligand-receptor investigations. The C-terminal amidation enhances proteolytic resistance, improving utility in experimental settings.
H-Trp-Lys-Tyr-Met-Val-Met-NH2 structure
H-Trp-Lys-Tyr-Met-Val-Met-NH2 structure
Product Name:H-Trp-Lys-Tyr-Met-Val-Met-NH2
CAS No:187986-11-4
MF:C41H61N9O7S2
MW:856.10914683342
CID:138605
PubChem ID:68661247
Update Time:2025-10-31

H-Trp-Lys-Tyr-Met-Val-Met-NH2 Chemical and Physical Properties

Names and Identifiers

    • L-Methioninamide,L-tryptophyl-L-lysyl-L-tyrosyl-L-methionyl-L-valyl-
    • H-Trp-Lys-Tyr-Met-Val-Met-NH?
    • WKYMVm
    • WKYMVM trifluoroacetate salt
    • WKYMVMamide
    • W-k-y-m-v-m-nh2
    • Trp-Lys-Tyr-Met-Val-L-Met NH2 trifluoroacetate salt
    • WKYMVM-NH2
    • TRP-LYS-TYR-MET-VAL-MET-NH2
    • SCHEMBL3486226
    • Trp-Lys-Tyr-Met-Val-L-Met-NH(2)
    • W-peptide
    • AKOS024456789
    • Trp-Lys-Tyr-Met-Val-Met-NH(2)
    • (2S)-6-amino-2-[[(2S)-2-amino-3-(1H-indol-3-yl)propanoyl]amino]-N-[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-amino-4-methylsulfanyl-1-oxobutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-methylsulfanyl-1-oxobutan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]hexanamide
    • 187986-11-4
    • H-Trp-Lys-Tyr-Met-Val-Met-NH2
    • Inchi: 1S/C41H61N9O7S2/c1-24(2)35(41(57)46-31(36(44)52)16-19-58-3)50-39(55)33(17-20-59-4)48-40(56)34(21-25-12-14-27(51)15-13-25)49-38(54)32(11-7-8-18-42)47-37(53)29(43)22-26-23-45-30-10-6-5-9-28(26)30/h5-6,9-10,12-15,23-24,29,31-35,45,51H,7-8,11,16-22,42-43H2,1-4H3,(H2,44,52)(H,46,57)(H,47,53)(H,48,56)(H,49,54)(H,50,55)/t29-,31-,32-,33-,34-,35-/m0/s1
    • InChI Key: FMBGOORJEKQQLG-LXOXETEGSA-N
    • SMILES: S(C)CC[C@@H](C(N[C@H](C(N[C@H](C(N)=O)CCSC)=O)C(C)C)=O)NC([C@H](CC1C=CC(=CC=1)O)NC([C@H](CCCCN)NC([C@H](CC1=CNC2C=CC=CC1=2)N)=O)=O)=O

Computed Properties

  • Exact Mass: 855.41400
  • Monoisotopic Mass: 855.41353767g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 10
  • Hydrogen Bond Acceptor Count: 16
  • Heavy Atom Count: 59
  • Rotatable Bond Count: 31
  • Complexity: 1360
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 6
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.5
  • Topological Polar Surface Area: 327?2

Experimental Properties

  • Solubility: H2O: >2mg/mL
  • PSA: 327.25000
  • LogP: 5.24190

H-Trp-Lys-Tyr-Met-Val-Met-NH2 Pricemore >>

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H-Trp-Lys-Tyr-Met-Val-Met-NH2 Related Literature

Additional information on H-Trp-Lys-Tyr-Met-Val-Met-NH2

Introduction to H-Trp-Lys-Tyr-Met-Val-Met-NH2 (CAS No. 187986-11-4)

H-Trp-Lys-Tyr-Met-Val-Met-NH2, a synthetic peptide with the CAS number 187986-11-4, has garnered significant attention in the fields of chemical biology and pharmaceutical research. This peptide, composed of a sequence of amino acids, exhibits unique biological properties that make it a valuable tool in various scientific and medical applications. In this comprehensive introduction, we will delve into the structure, synthesis, biological activities, and potential therapeutic applications of H-Trp-Lys-Tyr-Met-Val-Met-NH2.

Structure and Synthesis

H-Trp-Lys-Tyr-Met-Val-Met-NH2 is a linear peptide consisting of six amino acids: tryptophan (Trp), lysine (Lys), tyrosine (Tyr), methionine (Met), valine (Val), and another methionine (Met). The peptide is synthesized using solid-phase peptide synthesis (SPPS) techniques, which involve the sequential addition of amino acids to a growing peptide chain anchored to a solid support. The process typically involves deprotection, coupling, and cleavage steps to yield the final product. Recent advancements in SPPS have significantly improved the efficiency and purity of synthesized peptides like H-Trp-Lys-Tyr-Met-Val-Met-NH2.

Biological Activities

The biological activities of H-Trp-Lys-Tyr-Met-Val-Met-NH2 have been extensively studied in both in vitro and in vivo models. One of the key properties of this peptide is its ability to interact with specific receptors and signaling pathways. For instance, it has been shown to modulate the activity of G-protein coupled receptors (GPCRs), which are involved in a wide range of physiological processes. This interaction can lead to various cellular responses, including changes in gene expression, cell proliferation, and apoptosis.

Recent research has also highlighted the potential of H-Trp-Lys-Tyr-Met-Val-Met-NH2 as an antioxidant and anti-inflammatory agent. Studies have demonstrated that this peptide can scavenge reactive oxygen species (ROS) and inhibit the production of pro-inflammatory cytokines such as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α). These properties make it a promising candidate for the treatment of oxidative stress-related diseases and inflammatory conditions.

Potential Therapeutic Applications

The unique biological activities of H-Trp-Lys-Tyr-Met-Val-Met-NH2 have led to its exploration in various therapeutic contexts. One area of particular interest is its potential as an anti-cancer agent. Preclinical studies have shown that this peptide can inhibit the growth and metastasis of cancer cells by targeting multiple signaling pathways involved in tumor progression. For example, it has been reported to induce cell cycle arrest and apoptosis in various cancer cell lines, including breast cancer, lung cancer, and colon cancer.

In addition to its anti-cancer properties, H-Trp-Lys-Tyr-Met-Val-Met-NH2 has also been investigated for its neuroprotective effects. Research has indicated that this peptide can protect neurons from damage caused by oxidative stress and neuroinflammation. This makes it a potential therapeutic agent for neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.

Clinical Trials and Future Directions

While preclinical studies have provided promising results, further clinical trials are necessary to fully evaluate the safety and efficacy of H-Trp-Lys-Tyr-Met-Val-Met-NH2 in human subjects. Several Phase I and Phase II clinical trials are currently underway to assess the pharmacokinetics, pharmacodynamics, and safety profile of this peptide in different patient populations.

The future directions for research on H-Trp-Lys-Tyr-Met-Val-Met-NH2 include optimizing its delivery methods to enhance bioavailability and target specificity. Additionally, efforts are being made to develop novel formulations that can improve the stability and shelf life of this peptide. These advancements are expected to broaden its therapeutic applications and bring it closer to clinical use.

Conclusion

In conclusion, H-Trp-Lys-Tyr-Met-Val-Met-NH2 (CAS No. 187986-11-4) is a multifaceted synthetic peptide with significant potential in both research and therapeutic settings. Its unique structure and biological activities make it a valuable tool for studying cellular processes and developing new treatments for various diseases. As research continues to advance, it is likely that we will uncover even more applications for this intriguing molecule.

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