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Chemical structure of Cecropin A (1-7)-Melittin A (2-9) amide

GA21254

Cecropin A (1-7)-Melittin A (2-9) amide

Also known as (2S)-2,6-diamino-N-[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-6-amino-1-[[(2S,3S)-1-[[2-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-6-amino-1-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxohexan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-1-oxohexan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxohexan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]hexanamide

Cecropin A (1-7)-Melittin A (2-9) amide, also referred to as CAMEL0, is a synthetic hybrid peptide that is composed of portions of the naturally occurring antibiotic peptide cecropin A and melittin· CAMEL0 shows a better antimicrobial activity than the native molecules, but lacks the hemolytic properties of melittin· Studies revealed that the range of its antimicrobial activity is not only restricted to aerobic microorganisms but also included several gram-negative and gram-positive anaerobic microorganisms· Through its ascertained broad spectrum of antibiotic activity, this hybrid peptide may also represent an effective substitute for ciprofloxacin in the treatment of anthrax infections

ChemicalCAS157606-25-2MW1770.33FormulaC89H152N22O15
CAS number
157606-25-2
Molecular weight
1770.33
Formula
C89H152N22O15
Solubility
Soluble in DMSO
InChIKey
WMTUWZOBAVPERW-VZYQMWHSSA-N
Catalogue number
GA21254
Brand
GLPBIO
Computed properties PubChem CID 9833894 · XLogP 3.7 · TPSA 622 Ų · H-bond donors 22
XLogP
3.7
TPSA
622 Ų
H-bond donors
22
H-bond acceptors
21
Rotatable bonds
63
Heavy atoms
126

SMILES CC[C@H](C)[C@@H](C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC2=CNC3=CC=CC=C32)NC(=O)[C@H](CCCCN)N

Computed descriptors from PubChem (CID 9833894), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

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