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MYP_027549
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Basic Information
Entry 28
Anticancer ▸ Cytotoxic anticancer activity ▸ Cytotoxic
Antimicrobial
Antiviral
Antiviral ▸ Anti-Flavivirus ▸ Anti-Dengue virus
Antiviral ▸ Antiviral mechanism ▸ Viral replication inhibition
Toxicity / Safety ▸ Cytotoxicity ▸ Cytotoxic
Venom / Toxin ▸ General toxin ▸ Cytotoxic
not Standard
8 amino acids
-
contains X representing unresolved or non-standard residue
Sequence
RRRKSXXF
Physicochemical Analysis
0.00 Da
0.00
0.00
0.00
0.00
0.00
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Residue Composition
Amino Acid Composition
Chemical Descriptors
Structural Visualization
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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Experimental Records
RECORD: Rec_0003987 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
head-to-tail cyclic peptide with noncanonical residue [Cyclic]
mixed L/D amino-acid peptide (D-Arg1, Phe8) [Mixed]
not reported
not reported
The 'X' at position 6 indicates homophenylalanine(hPhe), position 7 indicates L-1-naphthylalanine(L-1Nal). The N-terminal and C-terminal cyclized by a amide bond
Bio-Activity Profile
Antimicrobial Antiviral
dengue virus 2(DENV2):inhibition of the activity of NS2B-NS3 protease
1.6 μM
IC50
PaperPubMed PMID: 28539222 PMID28539222 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/28539222/
RECORD: Rec_0022843 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Synthetic peptide
32630
Structure & Mods
cyclic peptide [Cyclic]
mixed L/D amino-acid peptide [Mixed]
No specific N-terminal
No specific C-terminal
The 'X' at position 6 indicates homophenylalanine(hPhe), position 7 indicates L-1-naphthylalanine(L-1Nal). The N-terminal and C-terminal cyclized by a amide bond.
Bio-Activity Profile
Antiviral Anti-DENV Replication inhibition
Dengue virus 2(DENV2) | BHK-21 cells
23.2 μM
EC50
PaperDiscovery of novel cyclic peptide inhibitors of dengue virus NS2B-NS3 protease with antiviral activity. | Takagi Y, Matsui K, Nobori H, Maeda H, Sato A, Kurosu T, Orba Y, Sawa H, Hattori K, Higashino K, Numata Y, Yoshida Y. | Bioorg Med Chem Lett. 2017 Aug 1;27(15):3586-3590. | DOI:10.1016/j.bmcl.2017.05.027 | PMID:28539222 PMID28539222 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/28539222/
RECORD: Rec_0043370 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
head-to-tail cyclic peptide with noncanonical residue [Cyclic]
mixed L/D amino-acid peptide (D-Arg1, Phe8) [Mixed]
not reported
not reported
The 'X' at position 6 indicates homophenylalanine(hPhe), position 7 indicates L-1-naphthylalanine(L-1Nal). The N-terminal and C-terminal cyclized by a amide bond
Bio-Activity Profile
Antimicrobial Antiviral Cytotoxic
BHK-21 cells
233 μM
CC50
PaperPubMed PMID: 28539222 PMID28539222 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/28539222/
RECORD: Rec_0080988 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Synthetic peptide
32630
Structure & Mods
cyclic peptide [Cyclic]
mixed L/D amino-acid peptide [Mixed]
No specific N-terminal
No specific C-terminal
The 'X' at position 6 indicates homophenylalanine(hPhe), position 7 indicates L-1-naphthylalanine(L-1Nal). The N-terminal and C-terminal cyclized by a amide bond.
Bio-Activity Profile
Antiviral Anti-DENV Replication inhibition
Dengue virus 2(DENV2)
1.6 μM
IC50
PaperDiscovery of novel cyclic peptide inhibitors of dengue virus NS2B-NS3 protease with antiviral activity. | Takagi Y, Matsui K, Nobori H, Maeda H, Sato A, Kurosu T, Orba Y, Sawa H, Hattori K, Higashino K, Numata Y, Yoshida Y. | Bioorg Med Chem Lett. 2017 Aug 1;27(15):3586-3590. | DOI:10.1016/j.bmcl.2017.05.027 | PMID:28539222 PMID28539222 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/28539222/
RECORD: Rec_0178010 VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
head-to-tail cyclic peptide with noncanonical residue [Cyclic]
mixed L/D amino-acid peptide (D-Arg1, Phe8) [Mixed]
not reported
not reported
The 'X' at position 6 indicates homophenylalanine(hPhe), position 7 indicates L-1-naphthylalanine(L-1Nal). The N-terminal and C-terminal cyclized by a amide bond
Bio-Activity Profile
Antimicrobial Antiviral Cytotoxic
PaperPubMed PMID: 28539222 PMID28539222 Evidence URLhttps://pubmed.ncbi.nlm.nih.gov/28539222/
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