Rubratoxin A

Product#: FNK-10663
$598.00
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Rubratoxin A

 
Cat.No.: FNK-10663
CAS#: 22467-31-8
Molecular Formula: C26 H32 O11
Molecular Weight: 520.531
Source: Penicillium sp.
Appearance: White powder
Purity: > 95% (HPLC)
Long Term Storage: at 4 C
Solubility: Soluble in DMSO, Acetone, CH3CN 
Poorly soluble in Hexane
It is recommended to avoid using alcohol such as MeOH or EtOH which esterifies Rubratoxin A.


Description

Rubratoxin A is a mycotoxin produced by Penicillium. While this compound inhibits protein phosphatase 2A (PP2A) in a competitive manner with the inhibition constant (Ki) of 28.7 nM (IC50= 6.1-15.1 nM) , it does not inhibit protein phosphatase 1, protein phosphatase 2B, protein tyrosine phosphatase 1B, alkaline phosphatase, and calf intestine phosphatase(CIP) up to 200 µM. Rubratoxin A shows cytotoxicity in cultured mammalian cells with IC50 values of around 15 µM and induces overphosphorylation of PP2A substrate proteins.

Application Notes
 

Rubratoxin A is a mycotoxin produced by Penicillium sp While this compound inhibits PP 2 A (p roteinphosphatase 2 A) in a competitive manner with the inhibition constant Ki of 28 7 nM (IC 50 6 1 15 1nM it does not inhibit PP 1 (p rotein p hosphatase 1 PP 2 B (p rotein p hosphatase 2 B PTP 1 B (proteint yrosine p hosphatase 1 B) and CIP (a lkaline p hosphatase, c alf i ntestine) up to 200 μ M Rubratoxin A shows cytotoxicity in cultured mammalian cells with IC 50 values of around 15 μ M and induces overphosphorylation in PP 2 A substrate proteins.


Reference

  1. Rubratoxin A specifically and potently inhibits protein phosphatase 2A and suppresses cancer metastasis.
    Wada S,et al. Cancer Sci. 2010 101(3) 743-50


reference by www.molview.org


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Natural macrocyclic compounds from microorganisms:
 
Structural classification Compound Name Chemical Structure Property / Biological activity Link
Bacterial proteins/Inhibition of DNA synthesis Aplasmomycin (Sodium Salt) Aplasmomycin A (sodium salt) Insecticidal, Anti-Plasmodium Antibiotic Aplasmomycin A Inhibited the growth of gram-positive bacteria including mycobacteria and showed an antimalarial activity in mice infected with Plasmodium berghei. Natural macrocyclic compounds from microorganisms, Diagnocine
Migrastatin Migrastatin Migrastatin inhibited metastasis of human esophageal cancer cells and anchorage-independent growth of human small cell lung carcinoma cells. Natural macrocyclic compounds from microorganisms, Diagnocine
Macrolactams Bisucaberin Bisucaberin Bisucaberin is a siderophore with iron-affinity and induced concentration dependent macrophage-mediated tumor cell lysis. Natural macrocyclic compounds from microorganisms, Diagnocine
Cyclic peptides Bottromycin A2 Bottromycin A2 Bottromycin A2 showed growth inhibitory activity against gram-positive bacteria, MRSA (Methicillin-resistant Staphylococcus aureus), and VRE (Vancomycin-resistant Enterococci). Natural macrocyclic compounds from microorganisms, Diagnocine
Iturin A-2 Iturin A-2 Iturin A-2 showed the control of damping-off of tomato (a seedling disease) and cytotoxicity to human breast cancer cell line BT-474. Natural macrocyclic compounds from microorganisms, Diagnocine
Plipastatin A1 Plipastatin A1 Plipastatin A1 inhibited phospholipase A2 and induced ISR (induced-systemic-resistance). Natural macrocyclic compounds from microorganisms, Diagnocine
Phepropeptin A Phepropeptin A Phepropeptin A inhibited proteasomal chymotrypsin-like activity. Natural macrocyclic compounds from microorganisms, Diagnocine
Phepropeptin B Phepropeptin B Phepropeptin B inhibited proteasomal chymotrypsin-like activity. Natural macrocyclic compounds from microorganisms, Diagnocine
Phepropeptin C Phepropeptin C Phepropeptin C inhibited proteasomal chymotrypsin-like activity. Natural macrocyclic compounds from microorganisms, Diagnocine
Phepropeptin D Phepropeptin D Phepropeptin D inhibited proteasomal chymotrypsin-like activity. Natural macrocyclic compounds from microorganisms, Diagnocine
Cycloalkenes Rubratoxin A Rubratoxin A Rubratoxin A inhibited protein phosphatase 2A (PP2A) in a competitive manner. Current Link
 

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