Toggle Nav

Enniatin Complex

Catalog No.
C3498
ionophore
Grouped product items
SizePriceStock Qty
10mg
$355.00
Ship with 5-10 days
50mg
$1,154.00
Ship with 5-10 days

Tel: +1-832-696-8203

Email: [email protected]

Worldwide Distributors

Background

Enniatins, analogues of beauvericin, is a regular cyclic hexadepsipeptide isolated from Fusarium species of fungis, also they have been isolated from other genera, such as Verticillium and Halosarpheia [1]. They have been involved in many biological activities, such as antiinsectan, antifungal, antibiotic and cytotoxic [1].

In vitro: Fusafungine is a mixture of several enniatins with bacteriostatic activity against most micro-organisms responsible for infections and superinfections of the respiratory tract. Fusafungine has been developed for treatment of upper respiratory tract infections by oral and/or nasal inhalation. Fusafungine in low concentrations down-regulated the expression of intercellular adhesion molecule-1 (ICAM-1) by activated macrophages, inhibited the production of the proinflammatory cytokines IL-1, TNFα and IL-6 and inhibited the release of oxygen free radicals by inflammatory macrophages without altering their phagocytic activity. Fusafungine also inhibited T-cell activation and proliferation, and the synthesis of IFN-γ by activated T cells [2]. Exposure 8 h to Enniatins at nanomolar concentrations significantly stimulated cell proliferation. At low micromolar concentrations, enniatins exihibited profound apoptosis-inducing effects against various human cancer cell types. In the fluorescence-activated cell sorting analysis, Enniatins induced cell cycle arrest in the G0/G1 phase. In human cancer cells, elevated ENN concentrations induced profound p53-dependent cytostatic and p53-independent cytotoxic activities [3]. Enniatin easily incorporated into the cell membrane in which it formed cation-selective pores [4].

References:
[1] Sy-Cordero A A, Pearce C J, Oberlies N H.  Revisiting the enniatins: a review of their isolation, biosynthesis, structure determination and biological activities[J]. The Journal of antibiotics, 2012, 65(11): 541-549.
[2] German-Fattal M.  Fusafungine, an antimicrobial with anti-inflammatory properties in respiratory tract infections[J]. Clinical Drug Investigation, 2001, 21(9): 653-670.
[3] Dornetshuber R, Heffeter P, Kamyar M R, et al.  Enniatin exerts p53-dependent cytostatic and p53-independent cytotoxic activities against human cancer cells[J]. Chemical research in toxicology, 2007, 20(3): 465-473.
[4] Kamyar M, Rawnduzi P, Studenik C R, et al.  Investigation of the electrophysiological properties of enniatins[J]. Archives of biochemistry and biophysics, 2004, 429(2): 215-223.

Chemical Properties

Physical AppearanceA white powder
StorageStore at -20°C
M.Wt639.8
Cas No.11113-62-5
FormulaC33H57N3O9 (for B)
SolubilitySoluble in DMSO
Chemical Name(3S,6R,9S,12R,15S,18R)-3,6,9,12,15,18-hexaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexaone compound with (3S,6R,9S,12R,15S,18R)-3,9,15-tri((R)-sec-butyl)-6,12,18-triisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,
SDFDownload SDF
Canonical SMILESO=C(O[[email protected]](C(C)C)C(N([[email protected]](C(O[[email protected]@H](C(N([[email protected]](C(O[[email protected]@H]1C(C)C)=O)C(C)C)C)=O)C(C)C)=O)C(C)C)C)=O)[[email protected]](C(C)C)N(C)C1=O.O=C(O[[email protected]](C(C)C)C(N([[email protected]](C(O[[email protected]@H](C(N([[email protected]](C(O[[email protected]@H]2C(C)C)=O)[[email protected]@H](CC)C)C)=O)C(C)C)=O)[[email protected]](C)CC)C)=O)[[email protected]]([[email protected]@H](CC)C)N(C)C2
Shipping ConditionEvaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request
General tipsFor obtaining a higher solubility , please warm the tube at 37°C and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20°C for several months.

Quality Control

Quality Control & MSDS

View current batch:

Chemical structure

Enniatin Complex