(Q3637333)

image of molecular model or crystal lattice model

inferred from InChIKey

Beauvericin 3d structure.png
1,158 × 1,230; 336 KB

depicts

ball-and-stick model

0 references

mass

783.409480404 dalton

1 reference

inferred from isomeric SMILES

stereoisomer of

cyclo[D-OVal-N(Me)Phe-D-OVal-N(Me)Phe-OVal-D-N(Me)Phe]

1 reference

cyclo[D-OVal-N(Me)Phe-D-OVal-N(Me)Phe-OVal-N(Me)Phe]

inferred from InChIKey

1 reference

cyclo[OVal-D-N(Me)Phe-OVal-D-N(Me)Phe-OVal-D-N(Me)Phe]

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₄₅H₅₇N₃O₉

2 references

O=C1OC(C(=O)N(C)C(C(=O)OC(C(=O)N(C)C(C(=O)OC(C(=O)N(C)C1CC=2C=CC=CC2)C(C)C)CC=3C=CC=CC3)C(C)C)CC=4C=CC=CC4)C(C)C

0 references

isomeric SMILES

O=C1N(C)[C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O[C@@H](C(=O)N([C@H](C(=O)O[C@@H]1C(C)C)Cc2ccccc2)C)C(C)C)Cc3ccccc3)C)C(C)C)Cc4ccccc4

1 reference

Bioactive extracts and chemical constituents of two endophytic strains of Fusarium oxysporum

2 references

Search for cell motility and angiogenesis inhibitors with potential anticancer activity: beauvericin and other constituents of two endophytic strains of Fusarium oxysporum

Beauveria bassiana

4 references

Biosynthesis of the cyclooligomer depsipeptide beauvericin, a virulence factor of the entomopathogenic fungus Beauveria bassiana.

Isolation of Novel Beauvericin Analogues from the Fungus Beauveria bassiana

Synthesis of beauvericin by a multifunctional enzyme

Cell-free synthesis of the depsipeptide beauvericin

Fusarium proliferatum

1 reference

Cloning and characterization of the gene cluster required for beauvericin biosynthesis in Fusarium proliferatum.

Fusarium sporotrichioides

1 reference

Biosynthesis of beauvericin and enniatins in vitro by wheat Fusarium species and natural grain contamination in an area of central Italy

Fusarium equiseti

1 reference

Biosynthesis of beauvericin and enniatins in vitro by wheat Fusarium species and natural grain contamination in an area of central Italy

Fusarium poae

1 reference

Biosynthesis of beauvericin and enniatins in vitro by wheat Fusarium species and natural grain contamination in an area of central Italy

Fusarium avenaceum

1 reference

Biosynthesis of beauvericin and enniatins in vitro by wheat Fusarium species and natural grain contamination in an area of central Italy

Cordyceps tenuipes

2 references

Isariotins E and F, spirocyclic and bicyclic hemiacetals from the entomopathogenic fungus Isaria tenuipes BCC 12625.

Antimycobacterial and antiplasmodial cyclodepsipeptides from the insect pathogenic fungus Paecilomyces tenuipes BCC 1614.

Isaria tenuipes

1 reference

Isariotins E and F, spirocyclic and bicyclic hemiacetals from the entomopathogenic fungus Isaria tenuipes BCC 12625.

Fusarium fujikuroi

2 references

Beauvericin production by Fusarium subglutinans from different geographical areas

Isolation of beauvericin as an insect toxin from Fusarium semitectum and Fusarium moniliforme var. subglutinans

Fusarium subglutinans

1 reference

Beauvericin production by Fusarium subglutinans from different geographical areas

Paecilomyces tenuipes

1 reference

Antimycobacterial and antiplasmodial cyclodepsipeptides from the insect pathogenic fungus Paecilomyces tenuipes BCC 1614.

Fusarium incarnatum

1 reference

Isolation of beauvericin as an insect toxin from Fusarium semitectum and Fusarium moniliforme var. subglutinans

Cordyceps fumosorosea

1 reference

Incorporation of radioactive precursors into beauvericin produced by Paecilomyces fumoso-roseus

Isaria cicadae

1 reference

Involvement of Bcl-2 family, cytochrome c and caspase 3 in induction of apoptosis by beauvericin in human non-small cell lung cancer cells

Cordyceps cicadae

1 reference

Involvement of Bcl-2 family, cytochrome c and caspase 3 in induction of apoptosis by beauvericin in human non-small cell lung cancer cells

Guignardia

1 reference

Synergistic Antifungal Meroterpenes and Dioxolanone Derivatives from the Endophytic Fungus Guignardia sp.

Identifiers

InChI

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

1 reference

PubChem

2 references

PubChem

ChEBI release 2020-09-01

CAS Registry Number

26048-05-5

1 reference

Italian Wikipedia

ChemSpider ID

2277520

1 reference

English Wikipedia

PubChem CID

3007984

2 references

Italian Wikipedia

Reaxys registry number

5223711

0 references

ChEBI ID

3000

mapping relation type

exact match

2 references

English Wikipedia

International Chemical Identifier

InChI

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

0 references

2 references

inferred from InChIKey

splash10-03xr-0490110000-95ff30051844ab65a420

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-00di-0571411090-7d1587af0b3fadb364e0

0 references

splash10-001l-0690000200-3b11177db5d43f53b426

0 references

splash10-0a4i-0133001090-8c06875211838d51c481

0 references

DSSTox substance ID

DTXSID00891834

1 reference

DSSTOX compound identifier

0 references

0 references

1 reference

0 references

1 reference