Syringomycin E

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Syringomycin E
Details
Product Name:D-K6L9 (D-amino-acid-modified K6L9 antimicrobial peptide)
CAS No.:426264-61-1
Synonyms:D-K6L9; K6L9 D-enantiomer; LK-{d-Leu}-LK-{d-Lys}-L-{d-Leu}-{d-Lys}-KLL-{d-Lys}-LL-NH2
Sequence:Leu-Lys-{d-Leu}-Leu-Lys-{d-Lys}-Leu-{d-Leu}-{d-Lys}-Lys-Leu-Leu-{d-Lys}-Leu-Leu-NH2 (one-letter: LK{dL}LK{dK}L{dL}{dK}KLL{dK}LL-NH2, C-terminally amidated)
Length:15 amino acid residues (6 lysines + 9 leucines)
Purity (HPLC):≥95%
Related Documents
• Certificate of Analysis (COA)
• Mass Spectrometry (MS) Report
• HPLC Purity Report
• Peptide Solubility and Storage Guide
Category
Antimicrobial Peptides
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Description

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Description D-K6L9 is a host-defense-like peptide composed of six lysines and nine leucines (K6L9), modified by the inclusion of D-amino acids to improve antimicrobial activity and resistance to degradation by proteases (Isca Biochemicals/MCE). Several L-residues are replaced by their D-enantiomers (Leu-Lys-{d-Leu}-Leu-Lys-{d-Lys}-Leu-{d-Leu}-{d-Lys}-Lys-Leu-Leu-{d-Lys}-Leu-Leu-NH2, 15 aa, C-terminally amidated), conferring stability against degradation by cystic fibrosis (CF) sputum proteases. D-K6L9 shows antimicrobial and antibiofilm activities against multidrug-resistant P. aeruginosa from CF patients without inducing bacterial resistance (J Med Chem 2022); in addition, in animal models it targets and arrests the growth of aggressive, hormone-resistant primary tumors (PMC5542299). Molecular formula C90H174N22O15, molecular weight 1804.48 Da (MCE). Widely used in cystic fibrosis infection therapy, D-peptide design, and antibiofilm research.
Molecular formula C₉₀H₁₇₄N₂₂O₁₅
Molecular weight (Da) 1804.48
Structure type Cationic amphipathic α-helical peptide (D-amino-acid-modified)
Solubility Freely soluble in water, PBS, DMSO
Storage -20°C, dry, protected from light

 

Product Basic Information Table

 

Product Standard English Name Product Abbreviation / Alias Function Tags (comma-separated) Core Structure Molecular Formula Exact Mass (Da) Average MW (Da) Salt Form Length (aa)
Syringomycin E Syringomycin E; Pseudomonas-derived lipopeptide antibiotic Antifungal lipopeptide, plant disease control, biopesticide, membrane pore-forming agent, phytopathogenic fungi Lipopeptide antibiotic from Pseudomonas syringae, consisting of a cyclic nonapeptide backbone and a fatty acid side chain; forms ion channels in fungal cell membranes to disrupt membrane potential and integrity, potent against various crop pathogenic fungi C₅₄H₈₇N₉O₁₇ 1109.62 ~1110.4 Free peptide 9 (cyclic lipopeptide)

 

Physicochemical Solubility & Storage Parameters

 

Product Code Appearance Long-term Storage Short-term Storage Solution Stability Solid Powder Stability
PEP-SYRE White to off-white crystalline powder Store at -20°C, sealed, dry and protected from light. Aliquot for storage. Stable for 1 month at 2–8°C in sealed dry condition; stable for shipping at ambient temperature. Stable for 7 days at 4°C. Soluble in methanol, DMSO and dilute ethanol. Lipopeptide structure is sensitive to strong oxidants; prone to aggregation in aqueous solution. Prepare fresh before use. Stable for 2 years at -20°C, dry and protected from light.

Functional Description

 

Product Code Frontend Short Summary (for search list display) Detailed Biological Function Description Applicable Research Areas (comma-separated) Targets / Pathways
PEP-SYRE Syringomycin E lipopeptide with membrane pore-forming antifungal activity Syringomycin E is a lipopeptide antibiotic secreted by Pseudomonas syringae, consisting of a cyclic nonapeptide scaffold linked to a fatty acid tail to form an amphipathic structure. It assembles into voltage-gated ion channels in fungal membranes, causing ion leakage and membrane potential collapse, with potent activity against crop pathogenic fungi. Plant fungal disease control, biopesticide development, lipopeptide antibiotics, membrane channel formation, phytopathology Fungal membrane ion channel formation; membrane potential collapse; phytopathogen killing

 

 

 

 

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