MYP_113264
15
Anticancer
Anticancer
▸
Cytotoxic anticancer activity
▸
Cytotoxic
Antimicrobial
Toxicity / Safety
▸
Blood cell toxicity
▸
Hemolysis
▸
Hemolytic
Toxicity / Safety
▸
Cytotoxicity
▸
Cytotoxic
Venom / Toxin
▸
General toxin
▸
Cytotoxic
not Standard
3 amino acids
-
contains X representing unresolved or non-standard residue
YXG
0.00 Da
0.00
0.00
0.00
0.00
0.00
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Amino Acid Composition
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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RECORD: Rec_0348973
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
X=Cα -dialkylated glycine (Aaa2,S )
Bio-Activity Profile
Antimicrobial
Anticancer
CaCo-2 , 6.9% inhibition at 10μM, 8.1% inhibition at 100μM, 8.6% inhibition at 1000μM
8.1 %
Inhibition
RECORD: Rec_0373054
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
X=Cα -dialkylated glycine (Aaa2,S )
Bio-Activity Profile
Antimicrobial
Anticancer
Hemolytic
RECORD: Rec_0376730
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
X=Cα -dialkylated glycine (Aaa2,R )
Bio-Activity Profile
Antimicrobial
Anticancer
HEp-2 , 4.9% inhibition at 10μM, 12.6% inhibition at 100μM, 26.4% inhibition at 1000μM
4.6 %
Inhibition
RECORD: Rec_0390439
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
X=Cα -dialkylated glycine (Aaa2,R )
Bio-Activity Profile
Antimicrobial
Anticancer
13.5% inhibition at 10μM, 13.5% inhibition at 100μM, 25.3% inhibition at 1000μM
17 %
Inhibition
RECORD: Rec_0400375
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
None
None
X=Cα -dialkylated glycine (Aaa2,R )
Bio-Activity Profile
Antimicrobial
Anticancer
MCF-7
21.2 %
Inhibition
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