ALAMETHICIN

ALAMETHICIN Structure
CAS No.
59588-86-2
Chemical Name:
ALAMETHICIN
Synonyms
f-50;U-22324;ALMETHICIN;ALAMETHICIN;ALAMETHACIN;alamethicini;alamethicinf30;alamethicingamma;ANTIBIOTIC U-22324
CBNumber:
CB2423618
Molecular Formula:
C92H150N22O25
Molecular Weight:
1964.31
MOL File:
59588-86-2.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

ALAMETHICIN Properties

Melting point 267-270℃
RTECS AY1900000
storage temp. 2-8°C
solubility Soluble in DMSO and ethanol.
form Powder

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Warning
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310a-P321-P405-P501a
Hazard Codes  T
Risk Statements  25
Safety Statements  45
RIDADR  UN 3462 6.1/PG 3
WGK Germany  3
10-21
HazardClass  6.1

ALAMETHICIN Chemical Properties,Uses,Production

Uses

Alamethicin is used as a channel-forming ionophore that activates membrane enzymes, membrane channel-forming peptide. It is a 20-amino acid channel-forming peptide antibiotic that can function as a monovalent cation ionophore. Alamethicin has been used to develop methods for the routine assessment of potential new drug candidates to elicit their pharmacokinetic drug interactions.

Enzyme inhibitor

These voltage-dependent, channel-forming, peptaibol antibiotics (MWAlamethicin F-30 = 1964.40; CAS 27061-78-5) from the soil fungus Trichoderma viride NRRL 3199 are membrane-active oligopeptides isolated from that exhibit anti-bacterial and anti-fungal properties. Peptaibols are amphipathic, usually highly helical in structure, and typically form voltage dependent ion channels that uncouple oxidative phosphorylation, often attended by in bacterial and fungal cell death. Alamethicin F-30 has the sequence Ac-Aib-Pro-Aib-Ala-Aib-Ala-Gln-Aib- Val-Aib-Gly-Leu-Aib-Pro-Val-Aib-Aib-Glu-Gln-Phe-OH; Alamethicin F- 50 has the sequence Ac-Aib-Pro-Aib-Ala-Aib-Ala-Gln-Aib-Val-Aib-Gly- Leu-Aib-Pro-Val-Aib Aib-Gln-Gln-Phe-OH; and Alamethicin II has the sequence Ac-Aib-Pro-Aib-Ala-Aib-Aib-Gln-Aib-Val-Aib-Gly-Leu-Aib- Pro-Val-Aib-Aib-Glu-Gln-Phe-OH. Note: The name “peptaibol” is derived from the prefix “pep-“, the central syllable “aib”, and the suffix “-ol” to designate its peptide structure, the presence of an a-aminoisobutyryl unit, and the C-terminal alcohol.

ALAMETHICIN Preparation Products And Raw materials

Raw materials

Preparation Products

ALAMETHICIN Suppliers

Global( 43)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
Chem-Impex International, Inc. 800 869-9290 US and Canada only United States 6740 64 Inquiry
IRIS Biotech GmbH +49 9231 9619 73 Germany 4427 68 Inquiry
BIOMOL INTERNATIONAL, LP (800) 942-0430 United States 1503 77 Inquiry
Alexis Corporation +41 61 926 8989 Switzerland 3599 74 Inquiry
A.G. Scientific, Inc. 858 452 9925 United States 1066 71 Inquiry
Fluorochem Ltd. +44 1457 868921 United Kingdom 6406 74 Inquiry
SIGMA-RBI 800 736 3690 (Orders) Switzerland 6913 91 Inquiry
MP Biomedicals, Inc. 949 833 2500 United States 6566 81 Inquiry
cfm Oskar Tropitzsch +49 9231961928 Germany 1136 62 Inquiry
alamethicinf30 alamethicingamma alamethicini f-50 U-22324 ANTIBIOTIC U-22324 ALMETHICIN ALAMETHACIN ALAMETHICIN 59588-86-2 BioChemical Antibiotics Antibiotics A-F Antibiotics A to Z