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Alamethicin

LS-1075

Almethicin, Antibiotic U-22324; Ac-Aib-Pro-Aib-Ala-Aib-Ala-Gln-Aib-Val-Aib-Gly-Leu-Aib-Pro-Val-Aib-Aib-Glu-Gln-Phenylalaninol

CAS-NO

27061-78-5

FORMULA

C92H150N22O25

MOLECULAR WEIGHT

1964,3 g/mole

ART-NO PRODUCT NAME QUANTITY PRICE  
LS-1075.0000 Alamethicin 0 inquire

Further Information

Alpha-helical peptide antibiotic produced by the fungus Trichoderma viride. It forms tetra- and hexameric voltage gated ion channels in membranes and can mimic nerve action potential across artificial membrandes. 1. Fox, R.O. Jr, Richards, F.M., A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-A resolution. Nature. 1982; 300(5890):325-30. 2. Mathew, M.K., Balaram P., Alamethicin and related membrane channel forming polypeptides. Mol Cell Biochem. 1983; 50(1):47-64. 3. Stella, L., et al., Alamethicin interaction with lipid membranes: a spectroscopic study on synthetic analogues. Chem Biodivers. 2007; 4(6):1299-312.

Details

Alpha-helical peptide antibiotic produced by the fungus Trichoderma viride. It forms tetra- and hexameric voltage gated ion channels in membranes and can mimic nerve action potential across artificial membrandes. 1. Fox, R.O. Jr, Richards, F.M., A voltage-gated ion channel model inferred from the crystal structure of alamethicin at 1.5-A resolution. Nature. 1982; 300(5890):325-30. 2. Mathew, M.K., Balaram P., Alamethicin and related membrane channel forming polypeptides. Mol Cell Biochem. 1983; 50(1):47-64. 3. Stella, L., et al., Alamethicin interaction with lipid membranes: a spectroscopic study on synthetic analogues. Chem Biodivers. 2007; 4(6):1299-312.

Additional Information

ART-NO LS-1075
CAS-NO 27061-78-5
DETAIL NAME Almethicin, Antibiotic U-22324; Ac-Aib-Pro-Aib-Ala-Aib-Ala-Gln-Aib-Val-Aib-Gly-Leu-Aib-Pro-Val-Aib-Aib-Glu-Gln-Phenylalaninol
FORMULA C92H150N22O25
MOLECULAR WEIGHT 1964,3
Bezeichnung Mol Ge g/mole
QUANTITY 0
neu N

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