AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I

Base Information Edit

Chemical Name:AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I
CAS No.:56165-93-6
Molecular Formula:C₉₂H₁₅₁N₂₃O₂₄
Molecular Weight:1963.35
Hs Code.:
Mol file:56165-93-6.mol

Synonyms:

Suppliers and Price of AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
AlamethicinF50
0.5mg
$ 210.00

TRC
AlamethicinF50
1mg
$ 335.00

Cayman Chemical
Alamethicin F50 >98%
5mg
$ 318.00

Cayman Chemical
Alamethicin F50 >98%
1mg
$ 96.00

Cayman Chemical
Alamethicin F50 >98%
500μg
$ 54.00

Cayman Chemical
Alamethicin F50 >98%
10mg
$ 530.00

AK Scientific
(2S)-2-[[(2S)-2-[[2-[[(2S)-2-[[2-[[(2S)-1-(2-Acetamido-2-methylpropanoyl)pyrrolidine-2-carbonyl]amino]-2-methylpropanoyl]amino]propanoyl]amino]-2-methylpropanoyl]amino]propanoyl]amino]-N-[1-[[(2S)-1-[[1-[[2-[[(2S)-1-[[1-[(2S)-2-[[(2S)-1-[[1-[[1-[[(2R)-5-amino-1-[[(2R)-5-amino-1-[[(2S)-1-hydroxy-3-phenylpropan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-1,5-dioxopentan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamoyl]pyrrolidin-1-yl]-2-methyl-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-2-oxoethyl]amino]-2-methyl-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-2-methyl-1-oxopropan-2-yl]pentanediamide
10mg
$ 761.00

Total 8 raw suppliers

Chemical Property of AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I Edit

Chemical Property:

Purity/Quality:

>98% by HPLC ^*data from raw suppliers

AlamethicinF50 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Alamethicin F50 is a neutral linear peptaibol complex with potent antibiotic activity, containing 20 “amino acids” with an acetyl and phenylalaninol termini, produced by Trichoderma sp.. Alamethicin F50 acts an ionopohore, transporting ions through membranes and artificial lipid membranes. Alamethicin F50 forms voltage-dependent ion channels in lipid bilayer membranes. Alamethicin F50 is co-produced with an acidic linear peptaibol complex (alamethicin F30). Alamethicin itself is a variable mixture of the acidic and neutral components. In general, reports on alamethicin do not specify the ratio of F50 to F30 in the complex and comparative data between the complexes is scant.

Technology Process of AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I

There total 1 articles about AlaMethicin F, AlaMethicin Rf 50, Atroviridin A, 18-L-GlutaMine-alaMethicin I which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 45.0%

: C₉H₁₂NOPol

: 29022-11-5
N-(fluoren-9-ylmethoxycarbonyl)glycine

: 68858-20-8
Fmoc-Val-OH

: 35661-60-0
Fmoc-Leu-OH

: 35661-39-3,136132-75-7
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine

: 71989-31-6
Fmoc-Pro-OH

: 108-24-7
acetic anhydride

: 71989-20-3
N₂-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-glutamine

: 94744-50-0
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid

: 56165-93-6
alamethicin F₅₀/5

Guidance literature:: C₉H₁₂NOPol; Fmoc-Gln(Pg)-OH; With ethyl cyanoglyoxylate-2-oxime; diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 70 ℃; 2-chlorotrityl chloride resin Automated synthesizer; Microwave irradiation;

With piperidine; In N,N-dimethyl-formamide; at 33 - 70 ℃; for 0.0583333h; 2-chlorotrityl chloride resin Automated synthesizer;

N-(fluoren-9-ylmethoxycarbonyl)glycine; Fmoc-Val-OH; Fmoc-Leu-OH; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; Fmoc-Pro-OH; acetic anhydride; N₂-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-glutamine; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid; Further stages;
DOI:10.1039/c8ob00686e