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ALAMETHICIN

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
MDL Number:
MFCD00151517
MOL File:
59588-86-2.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

ALAMETHICIN Properties

Melting point 267-270℃
RTECS AY1900000
storage temp. 2-8°C
solubility Soluble in DMSO and ethanol.
form Powder
FDA UNII 0LT1I1B7S8

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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 price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Alfa Aesar J63829 Alamethicin 59588-86-2 1mg $160 2024-03-01 Buy
Alfa Aesar J63829 Alamethicin 59588-86-2 5mg $553.65 2024-03-01 Buy
Usbiological 001726 Alamethicin 59588-86-2 1mg $262 2021-12-16 Buy
Product number Packaging Price Buy
J63829 1mg $160 Buy
J63829 5mg $553.65 Buy
001726 1mg $262 Buy

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 Email Country ProdList Advantage
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15848 69
Creative Peptides info@creative-peptides.com United States 6084 56
Hunan chemfish Scientific co.,ltd 0731-85567275 19313119731 sales@chemfish.com China 4918 58
Xibao Biotechnology (Shanghai) Co., Ltd. 13761246140 58642714@qq.com China 415 58
BOC Sciences 16314854226 inquiry@bocsci.com United States 9713 58
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