enniatin A

Base Information

Chemical Name:enniatin A
CAS No.:2503-13-1
Molecular Formula:C₃₆H₆₃N₃O₉
Molecular Weight:681.911
Hs Code.:2934999090
Mol file:2503-13-1.mol

Synonyms:Enniatin A(6CI,8CI); Isoleucine, N-(D-2-hydroxy-3-methylbutyryl)-N-methyl-, trimol.cyclic ester (7CI); 1,7,13-Trioxa-4,10,16-triazacyclooctadecane, cyclic peptidederiv.; Cyclo(D-a-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-a-hydroxyisovaleryl-N-methyl-L-isoleucyl-D-a-hydroxyisovaleryl-N-methyl-L-isoleucyl)

Suppliers and Price of enniatin A

Supply Marketing:

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

Usbiological
Enniatin A
500ug
$ 426.00

TRC
EnnlatinA
25mg
$ 11815.00

Sigma-Aldrich
Enniatin A from Gnomonia errabunda, ≥95% (HPLC)
1mg
$ 183.00

ChemScene
Enniatin A
5mg
$ 1800.00

Cayman Chemical
Enniatin A ≥99%
2.5mg
$ 672.00

Cayman Chemical
Enniatin A ≥99%
500μg
$ 158.00

Adipogen Life Sciences
Enniatin A ≥98%(HPLC)
0.5 mg
$ 140.00

Total 10 raw suppliers

Chemical Property of enniatin A

Chemical Property:

Vapor Pressure:5.53E-29mmHg at 25°C
Melting Point:122-124 °C
Boiling Point:847.4°Cat760mmHg
PKA:-0.96±0.70(Predicted)
Flash Point:466.3°C
PSA：139.83000
Density:1.022g/cm³
LogP:4.13640
Storage Temp.:?20°C
Solubility.:DMSO: soluble10mg/mL

Purity/Quality:

97% ^*data from raw suppliers

Enniatin A ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 23/24/25
Safety Statements: 45

MSDS Files:: SDS file from LookChem

Useful:

Description Enniatins are cyclohexadepsipeptides commonly isolated from fungi that are known to have antibiotic properties and to induce apoptosis in several cancer lines. Many function as ionophores, forming pores in cellular membranes to allow selective ion transport. Enniatin A is one of four major analogs in the enniatin complex . It has been shown to moderately inhibit acyl-CoA:cholesterol acyltranferase activity in rat liver microsomes with an IC50 value of 22 μM. Enniatin A also demonstrates anthelmintic properties against N. brasiliensis, T. spiralis, and H. spumosa.
Uses Enniatins are a family of depsipeptide ionophores, produced by several Fusarium species. More recently, the effects of the enniatins on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumour action have received more focus. Enniatin A is one of four major analogues of the enniatin complex and has not previously been available for investigation. Enniatins are a family of depsipeptide ionophores, produced by several Fusarium species. Recently, the effects of the enniatins on acyl-CoA cholesterol transferase, transporters and the selectivity of their antitumor action have received more focus. Enniatin A is one of four major analogues of the enniatin complex. Enniatins are cyclohexadepsipeptides commonly isolated from fungi that are known to have antibiotic properties and to induce apoptosis in several cancer lines. Many function as ionophores, forming pores in cellular membranes to allow selective ion transport. Enniatin A is one of four major analogs in the enniatin complex . It has been shown to moderately inhibit acyl-CoA:cholesterol acyltranferase activity in rat liver microsomes with an IC50 value of 22 μM. Enniatin A also demonstrates anthelmintic properties against N. brasiliensis, T. spiralis, and H. spumosa.[Cayman Chemical]

Technology Process of enniatin A

There total 2 articles about enniatin A 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:

: 2503-13-1,19248-58-9
Enniatin-A

Guidance literature:: Reaktion ueber mehrere Stufen;
DOI:10.1002/hlca.19630460525

Reference yield:

: 2503-13-1,19248-58-9
Cyclohexadepsipeptid

Guidance literature:: N-Methyl-L-isoleucyl-D-α-hydroxy-isovaleryl-N-methyl-L-isoleucyl-D-α-hydroxy-isovaleryl-N-methyl-isoleucyl-D-α-hydroxy-isovaleriansaeure-hydrobromid in Bzl.d.Cyclisierung m.PCl5 <0-20grad>;
DOI:10.1002/hlca.19630460525