Date published: 2026-5-1

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Pyridoxatin (CAS 135529-30-5)

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Alternate Names:
Tolypocin
Application:
Pyridoxatin is a MMP-2 (Gelatinase A) inhibitor with antibiotic and anticancer properties
CAS Number:
135529-30-5
Purity:
≥95%
Molecular Weight:
263.33
Molecular Formula:
C15H21NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Pyridoxatin, a fungal metabolite found in Acremonium, displays a wide range of biological activities, making it a versatile compound of research interest. With its free radical scavenging properties, it counteracts the damaging effects of free radicals, exhibiting an IC50 of 8 μM. As an inhibitor of matrix metalloproteinase-2 (MMP-2), it demonstrates its ability to impede the activity of this enzyme. Moreover, pyridoxatin showcases inhibitory effects on lipid peroxidation and DNA synthesis, further solidifying its multifaceted nature.


Pyridoxatin (CAS 135529-30-5) References

  1. Differential analysis of 2D NMR spectra: new natural products from a pilot-scale fungal extract library.  |  Schroeder, FC., et al. 2007. Angew Chem Int Ed Engl. 46: 901-4. PMID: 17183517
  2. Isolation and structural elucidation of pyridoxatin, a free radical scavenger of microbial origin.  |  Teshima, Y., et al. 1991. J Antibiot (Tokyo). 44: 685-7. PMID: 2071495
  3. Two new antibiotic pyridones produced by a marine fungus, Trichoderma sp. strain MF106.  |  Wu, B., et al. 2014. Mar Drugs. 12: 1208-19. PMID: 24663111
  4. Lichen endophyte derived pyridoxatin inactivates Candida growth by interfering with ergosterol biosynthesis.  |  Chang, W., et al. 2015. Biochim Biophys Acta. 1850: 1762-71. PMID: 25960388
  5. New PKS-NRPS tetramic acids and pyridinone from an Australian marine-derived fungus, Chaunopycnis sp.  |  Shang, Z., et al. 2015. Org Biomol Chem. 13: 7795-802. PMID: 26107107
  6. Tetramic Acids and Pyridone Alkaloids from the Endolichenic Fungus Tolypocladium cylindrosporum.  |  Li, XB., et al. 2015. J Nat Prod. 78: 2155-60. PMID: 26356746
  7. Establishing the Secondary Metabolite Profile of the Marine Fungus: Tolypocladium geodes sp. MF458 and Subsequent Optimisation of Bioactive Secondary Metabolite Production.  |  Kebede, B., et al. 2017. Mar Drugs. 15: PMID: 28333084
  8. Isolation and Characterization of Aphidicolin Derivatives from Tolypocladium inflatum.  |  Lin, J., et al. 2017. Molecules. 22: PMID: 28704971
  9. Antioxidant activity and cellular uptake of the hydroxamate-based fungal iron chelators pyridoxatin, desferriastechrome and desferricoprogen.  |  da Silva, GS., et al. 2019. Biometals. 32: 707-715. PMID: 31152280
  10. Screening of tenuazonic acid production-inducing compounds and identification of NPD938 as a regulator of fungal secondary metabolism.  |  Motoyama, T., et al. 2021. Biosci Biotechnol Biochem. 85: 2200-2208. PMID: 34379730
  11. Identification, Characterization, and Evaluation of Nematophagous Fungal Species of Arthrobotrys and Tolypocladium for the Management of Meloidogyne incognita.  |  Kassam, R., et al. 2021. Front Microbiol. 12: 790223. PMID: 34956156
  12. Lipopolysaccharide acting via toll-like receptor 4 transactivates the TGF-β receptor in vascular smooth muscle cells.  |  Afroz, R., et al. 2022. Cell Mol Life Sci. 79: 121. PMID: 35122536
  13. Liver-cell protective pyridones from the fungi Tolypocladium album dws120.  |  Wu, XQ., et al. 2023. Phytochemistry. 212: 113730. PMID: 37220864
  14. What was old is new again: Phenotypic screening of a unique fungal library yields pyridoxatin, a promising lead against extensively resistant Acinetobacter baumannii (AB5075).  |  Winter, HL., et al. 2023. Phytochem Lett. 55: 88-96. PMID: 37252254

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Pyridoxatin, 1 mg

sc-391043
1 mg
$163.00