Enniatin complex

Modify Date: 2025-09-09 21:00:58

Enniatin complex structure	Common Name	Enniatin complex
	CAS Number	11113-62-5	Molecular Weight	2643.441
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₃₈H₂₄₀N₁₂O₃₆	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of Enniatin complex

Enniatin complex is a mixture of cyclohexadepsipeptides isolated largely from Fusarium species of fungi, and has ionophoric, antibiotic, and in vitro hypolipidaemic properties. Enniatin complex inhibits enzymes like acyl-CoA: cholesterol acyl transferase and induces apoptosis in several cancer lines [1][2].

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-hexone;(3S,6R,9S,12R,15S,18R)-3,6,9,12,18-pentaisopropyl-4,10,16-trimethyl-15-[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone;(3S,6R,9S,12R,15S,18S)-3,6,12,18-tetraisopropyl-4,10,16-trimethyl-9,15-bis[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone;(3S,6R,9S,12R,15S,18R)-6,12,18-triisopropyl-4,10,16-trimethyl-3,9,15-tris[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

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-hexone;(3S,6R,9S,12R,15S,18R)-3,6,9,12,18-pentaisopropyl-4,10,16-trimethyl-15-[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone;(3S,6R,9S,12R,15S,18S)-3,6,12,18-tetraisopropyl-4,10,16-trimethyl-9,15-bis[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone;(3S,6R,9S,12R,15S,18R)-6,12,18-triisopropyl-4,10,16-trimethyl-3,9,15-tris[(1S)-1-methylpropyl]-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone

Description	Enniatin complex is a mixture of cyclohexadepsipeptides isolated largely from Fusarium species of fungi, and has ionophoric, antibiotic, and in vitro hypolipidaemic properties. Enniatin complex inhibits enzymes like acyl-CoA: cholesterol acyl transferase and induces apoptosis in several cancer lines [1][2].
Related Catalog	Research Areas >> Cancer Research Areas >> Infection Signaling Pathways >> Anti-infection >> Bacterial
References	[1]. Kamyar M, et al. Investigation of the electrophysiological properties of enniatins. Arch Biochem Biophys. 2004 Sep 15;429(2):215-23. [2]. Dornetshuber R, et al. Enniatin exerts p53-dependent cytostatic and p53-independent cytotoxic activities against humancancer cells. Chem Res Toxicol. 2007 Mar;20(3):465-73.

Description

Related Catalog

Research Areas >> Cancer

Research Areas >> Infection

Signaling Pathways >> Anti-infection >> Bacterial

References

[1]. Kamyar M, et al. Investigation of the electrophysiological properties of enniatins. Arch Biochem Biophys. 2004 Sep 15;429(2):215-23.

[2]. Dornetshuber R, et al. Enniatin exerts p53-dependent cytostatic and p53-independent cytotoxic activities against humancancer cells. Chem Res Toxicol. 2007 Mar;20(3):465-73.