26645-35-2

Phallacidin Chemical Structure
26645-35-2

Chemical Structure

Phallacidin

  • CAS No.: 26645-35-2
  • Formula:C37H50N8O13S
  • Molecular Weight:846.90

InChIKey: KUBDTFZQCYLLGC-AASPPYRUSA-N

SMILES: O=C1N[C@H](C(N[C@H](C(N[C@@]([C@H](O)C(O)=O)([H])C(N[C@@]2([H])CSC3=C(C4=C(C=CC=C4)N3)C[C@]1([H])NC([C@@H](NC([C@@]5([H])N(C[C@@H](O)C5)C2=O)=O)C)=O)=O)=O)C(C)C)=O)CC(C)(O)CO

Biological Activity: Phallacidin is a natural bicyclic heptapeptide derived from the poisonous mushroom Amanita phalloides. Phallacidin binds to filamentous actin specifically with high affinity, with a Kd of 20 nM. After binding to F-actin, Phallacidin strongly inhibits its depolymerization, stabilizes microfilament structures, and prevents their disruption by drugs such as cytochalasins. When conjugated with a fluorophore, Phallacidin serves as a specific fluorescent probe for F-actin, which is used to clearly visualize the distribution of actin in the cytoskeleton (e.g., stress fibers, cortical peripheral bands) under fluorescence microscopy[1][2].

Cat. No. Product Name Purity Description Pricing
HY-P2031
Phallacidin 92.4% Phallacidin is a natural bicyclic heptapeptide derived from the poisonous mushroom Amanita phalloides. Phallacidin binds to filamentous actin specifically with high affinity, with a Kd of 20 nM. After binding to F-actin, Phallacidin strongly inhibits its depolymerization, stabilizes microfilament structures, and prevents their disruption by drugs such as cytochalasins. When conjugated with a fluorophore, Phallacidin serves as a specific fluorescent probe for F-actin, which is used to clearly visualize the distribution of actin in the cytoskeleton (e.g., stress fibers, cortical peripheral bands) under fluorescence microscopy.
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