H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE is a complex chemical compound consisting of a long chain of amino acids and a trifluoroacetate group. The amino acid sequence includes various types such as glutamic acid, leucine, arginine, methionine, serine, tyrosine, proline, threonine, glycine, alanine, aspartic acid, valine, lysine, glutamine, isoleucine, and others. The trifluoroacetate group attached to this peptide sequence endows it with unique properties, making it valuable for applications in biochemical research and pharmaceutical synthesis.
166798-69-2
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Basic information
- Product Name: H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE
- Synonyms: PROADRENOMEDULLIN (45-92) (HUMAN) TRIFLUOROACETATE;H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE;H-Glu-Leu-Arg-Met-Ser-Ser-Ser-Tyr-Pro-Thr-Gly-Leu-Ala-Asp-Val-Lys-Ala-Gly-Pro-Ala-Gln-Thr-Leu-Ile-Arg-Pro-Gln-Asp-Met-Lys-Gly-Ala-Ser-Arg-Ser-Pro-Glu-Asp-Ser-Ser-Pro-Asp-Ala-Ala-Arg-Ile-Arg-Val-OH
- CAS NO:166798-69-2
- Molecular Formula: C215H359 N67 O73 S2
- Molecular Weight: 0
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE(CAS DataBase Reference)
- NIST Chemistry Reference: H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE(166798-69-2)
- EPA Substance Registry System: H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE(166798-69-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 166798-69-2(Hazardous Substances Data)
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166798-69-2 Usage
Uses
Used in Biochemical Research:H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE is used as a research tool for studying the interactions and functions of various amino acids in biological systems. The trifluoroacetate group provides a unique chemical handle for modifying and tracking the behavior of this peptide in different experimental setups.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE serves as a building block for the development of novel drug candidates. The diverse amino acid composition and the trifluoroacetate group offer opportunities for creating bioactive peptides with potential therapeutic effects.
Used in Drug Delivery Systems:
H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE can be utilized in the design of drug delivery systems, where the trifluoroacetate group may enhance the stability, solubility, or targeting of peptide-based therapeutics.
Used in Peptide Synthesis:
In the field of peptide synthesis, H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE is used as a precursor or intermediate in the synthesis of more complex peptide structures with specific biological activities.
Used in Diagnostic Applications:
H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACET
Check Digit Verification of cas no
The CAS Registry Mumber 166798-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,7,9 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.Calculate Digit Verification of CAS Registry Number 166798-69:
(8*1)+(7*6)+(6*6)+(5*7)+(4*9)+(3*8)+(2*6)+(1*9)=202
202 % 10 = 2
So 166798-69-2 is a valid CAS Registry Number.
166798-69-2Upstream product
166798-69-2Downstream Products
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H-GLU-LEU-ARG-MET-SER-SER-SER-TYR-PRO-THR-GLY-LEU-ALA-ASP-VAL-LYS-ALA-GLY-PRO-ALA-GLN-THR-LEU-ILE-ARG-PRO-GLN-ASP-MET-LYS-GLY-ALA-SER-ARG-SER-PRO-GLU-ASP-SER-SER-PRO-ASP-ALA-ALA-ARG-ILE-ARG-VAL-OH TRIFLUOROACETATE
