MYP_103049
Hymenochirin-1B
Anticancer
Antimicrobial
Antimicrobial
▸
Antibacterial
Antimicrobial
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Antibacterial
▸
Anti-Gram-negative
Antimicrobial
▸
Antibacterial
▸
Anti-Gram-positive
Antimicrobial
▸
Antifungal
Toxicity / Safety
▸
Blood cell toxicity
▸
Hemolysis
▸
Hemolytic
Venom / Toxin
▸
General toxin
▸
Toxic
Standard
29 amino acids
C139H251N37O37S
Standard
IKLSPETKDNLKKVLKGAIKGAIAVAKMV
3064.77 Da
10.13
4.76
4.54
0.1640
0.17
0.69
0.06
12.77
124.48
0.0000
0.00
0.00
The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.
Amino Acid Composition
1209.62
-8.69
41.0
43.0
111.0
214.0
1.0
29.0
3D PDB MODEL
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2D CHEMICAL STRUCTURE
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RECORD: Rec_0357960
VERIFIED: YES
Provenance & Taxonomy
Hymenochirus boettgeri [Animal]
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Amidation
Bio-Activity Profile
Antimicrobial
Antibacterial
L. salivarius FortaFit Ls-33 [
250 μg/mL
MIC
RECORD: Rec_0358089
VERIFIED: YES
Provenance & Taxonomy
Hymenochirus boettgeri [Animal]
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Amidation
Bio-Activity Profile
Antimicrobial
Antibacterial
L. casei Shirota [
64 μg/mL
MBC
RECORD: Rec_0376780
VERIFIED: YES
Provenance & Taxonomy
Synthetic construct [Synthetic]
32630
Structure & Mods
linear peptide [Linear]
canonical L-amino-acid peptide [L]
Amidation
C-terminal amide reported in activity study
Bio-Activity Profile
Antimicrobial
Anticancer
A549
2.5±0.2 μM
LC50
RECORD: Rec_0380381
VERIFIED: NO
Provenance & Taxonomy
Hymenochirus boettgeri [Animal]
Structure & Mods
topology not specified [Not included yet]
stereochemistry not specified [Other]
Bio-Activity Profile
Antimicrobial
Antibacterial
Anti-Gram-positive
Anti-Gram-negative
Staphylococcus epidermidis RP62A
3.1 μM
MIC
RECORD: Rec_0384813
VERIFIED: YES
Provenance & Taxonomy
synthetic construct [Synthetic]
Hymenochirin
32630
Structure & Mods
hydrocarbon-stapled side-chain cyclic peptide [Cyclic]
noncanonical stereochemical modification [Modified]
None
Amidation
The Ⓧ (position: 18 and 22) in sequence indicate (S)-N-Fmoc-2-(4'-pentenyl)alanine. Ⓧ (18) and Ⓧ (22) are cross-linked by ring-closing metathesis through an oct-4-enyl hydrocarbon staple
Bio-Activity Profile
Anticancer
A549
7.35±0.22 μM
IC50
Showing 5 records on this page · Page 10 of 13