U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C45H57N3O9
Molecular Weight 783.9488
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BEAUVERICIN

SMILES

CC(C)[C@H]1OC(=O)[C@H](CC2=CC=CC=C2)N(C)C(=O)[C@H](OC(=O)[C@H](CC3=CC=CC=C3)N(C)C(=O)[C@H](OC(=O)[C@H](CC4=CC=CC=C4)N(C)C1=O)C(C)C)C(C)C

InChI

InChIKey=GYSCAQFHASJXRS-FFCOJMSVSA-N
InChI=1S/C45H57N3O9/c1-28(2)37-40(49)46(7)35(26-32-21-15-11-16-22-32)44(53)56-39(30(5)6)42(51)48(9)36(27-33-23-17-12-18-24-33)45(54)57-38(29(3)4)41(50)47(8)34(43(52)55-37)25-31-19-13-10-14-20-31/h10-24,28-30,34-39H,25-27H2,1-9H3/t34-,35-,36-,37+,38+,39+/m0/s1

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/23877026 https://www.ncbi.nlm.nih.gov/pubmed/25178661

Beauvericin is a famous mycotoxin produced by many fungi, such as Beaveria bassiana and Fusarium spp. Beauvericin is a cyclic hexadepsipeptide (Figure 1) that belongs to the enniatin antibiotic family. It contains three D-hydroxyisovaleryl and three N-methylphenylalanyl residues in an alternating sequence. Beauvericin was first isolated from Beaveria bassiana, which is a common and commercial entomopathogenic mycoinsecticide. Beauvericin was one of the active constituents of B. bassiana and was confirmed to have antimicrobial and anti-tumor activities. Beauvericin has a strong antibacterial activity against human, animal and plant pathogenic bacteria with no selectively between Gram-positive and Gram-negative bacteria. The cytotoxicity of beauvericin to human tumor cells has been frequently reported.

Originator

Curator's Comment: The insecticidal activity of beauvericin was first discovered by Hamill et al.

Approval Year

PubMed

PubMed

TitleDatePubMed
Antimycobacterial and antiplasmodial cyclodepsipeptides from the insect pathogenic fungus Paecilomyces tenuipes BCC 1614.
2000 Dec
Block of L-type Ca2+ current by beauvericin, a toxic cyclopeptide, in the NG108-15 neuronal cell line.
2002 Jun
An investigation of the ionophoric characteristics of destruxin A.
2002 Sep 1
Presence and concentrations of the Fusarium-related mycotoxins beauvericin, enniatins and moniliformin in finnish grain samples.
2004 Aug
Fusaproliferin, beauvericin and fumonisin production by different mating populations among the Gibberella fujikuroi complex isolated from maize.
2004 Feb
Supercritical fluid extraction of Beauvericin from maize.
2004 Feb 27
Phylogenetic analyses of the Fusarium poae, Fusarium sporotrichioides and Fusarium langsethiae species complex based on partial sequences of the translation elongation factor-1 alpha gene.
2004 Sep 15
Diversity in metabolite production by Fusarium langsethiae, Fusarium poae, and Fusarium sporotrichioides.
2004 Sep 15
Occurrence of mycotoxin in Farro samples from southern Italy.
2005 Feb
Beauvericin activates Ca2+-activated Cl- currents and induces cell deaths in Xenopus oocytes via influx of extracellular Ca2+.
2005 May
Effects of beauvericin on the metabolic state and ionic homeostasis of ventricular myocytes of the guinea pig.
2005 Nov
Search for cell motility and angiogenesis inhibitors with potential anticancer activity: beauvericin and other constituents of two endophytic strains of Fusarium oxysporum.
2007 Feb
Fusarium avenaceum -- the North European situation.
2007 Oct 20
Complex etiology, prophylaxis and hygiene control in mycotoxic nephropathies in farm animals and humans.
2008 Apr
Statistical optimization of growth medium for the production of the entomopathogenic and phytotoxic cyclic depsipeptide beauvericin from Fusarium oxysporum KFCC 11363P.
2008 Jan
Diversity in Beauvericin and Enniatins H, I, and MK1688 by Fusarium oxysporum isolated from potato.
2008 Mar 20
Biosynthesis of the cyclooligomer depsipeptide beauvericin, a virulence factor of the entomopathogenic fungus Beauveria bassiana.
2008 Sep 22
Beauvericin and enniatins H, I and MK1688 are new potent inhibitors of human immunodeficiency virus type-1 integrase.
2009 Dec
LC-MS/MS multi-analyte method for mycotoxin determination in food supplements.
2009 Jun
Formation of fumonisins and other secondary metabolites by Fusarium oxysporum and F. proliferatum: a comparative study.
2010 May
Contamination by moulds of grape berries in Slovakia.
2010 May
Mycotoxin production of selected Fusarium species at different culture conditions.
2010 Sep 30
Patents

Patents

Sample Use Guides

0.2 mg/kg
Route of Administration: Oral
Incubation of H4IIE cells with beauvericin (10uM, 2 h) strongly diminished phosphorylation of the MAP kinase ERK (p44/p42) as a prerequisite of MAPK activation
Name Type Language
BEAUVERICIN
Common Name English
CYCLO((2R)-2-HYDROXY-3-METHYLBUTANOYL-N-METHYL-L-PHENYLALANYL-(2R)-2-HYDROXY-3-METHYLBUTANOYL-N-METHYL-L-PHENYLALANYL-(2R)-2-HYDROXY-3-METHYLBUTANOYL-N-METHYL-L-PHENYLALANYL)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C1976
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
Code System Code Type Description
CHEBI
3000
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID00891834
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
PRIMARY
CAS
26048-05-5
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
PRIMARY
PUBCHEM
3007984
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
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MESH
C004456
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
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FDA UNII
26S048LS2R
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
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NCI_THESAURUS
C1011
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
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WIKIPEDIA
BEAUVERICIN
Created by admin on Sat Dec 16 02:16:39 GMT 2023 , Edited by admin on Sat Dec 16 02:16:39 GMT 2023
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