1. MAPK/ERK Pathway
    Stem Cell/Wnt
    Apoptosis
  2. ERK
    Apoptosis
  3. Enniatin A1

Enniatin A1 

Cat. No.: HY-N6704
Handling Instructions

Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes.

For research use only. We do not sell to patients.

Enniatin A1 Chemical Structure

Enniatin A1 Chemical Structure

CAS No. : 4530-21-6

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Description

Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC50 of 49 μM in rat liver microsomes[1].

IC50 & Target[1]

ERK

 

Molecular Weight

667.87

Formula

C₃₅H₆₁N₃O₉

CAS No.

4530-21-6

SMILES

O=C([[email protected]@]([[email protected]@H](C)CC)([H])N(C)C([[email protected]@H](C(C)C)OC(C([[email protected]@H](C)CC)N(C)C([[email protected]@H](C(C)C)OC([[email protected]](C(C)C)N1C)=O)=O)=O)=O)O[[email protected]@](C(C)C)([H])C1=O

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Enniatin A1
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