Enniatin A1
| Code | Size | Price |
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| TAR-T11201-5mg | 5mg | Enquire | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Quantity:
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Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Documents
Further Information
Bioactivity:
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. Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids.
CAS:
4530-21-6
Formula:
C35H61N3O9
Molecular Weight:
667.885
Pathway:
MAPK
Purity:
0.98
SMILES:
[H][C@@]1(OC(=O)[C@]([H])([C@@H](C)CC)N(C)C(=O)[C@H](OC(=O)C([C@@H](C)CC)N(C)C(=O)[C@H](OC(=O)[C@H](C(C)C)N(C)C1=O)C(C)C)C(C)C)C(C)C
Target:
ERK
References
1. W?tjen W, et al. Enniatins A1, B and B1 from an endophytic strain of