Date published: 2026-4-24

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N-Deacetylcolchiceine (CAS 3482-37-9)

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Alternate Names:
(7S)-7-Amino-6,7-dihydro-10-hydroxy-1,2,3-trimethoxy-benzo[a]heptalen-9(5H)-one
CAS Number:
3482-37-9
Molecular Weight:
343.37
Molecular Formula:
C19H21NO5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Antimitotic agent disrupting microtubule action through the binding of tubulin and preventing polymerization. Has been shown to stimulate the intrinsic GTPase activity of tubulin. Induces apoptosis and activates the JNK/SAPK signals.


N-Deacetylcolchiceine (CAS 3482-37-9) References

  1. Effect of colchicine and its derivatives on the expression of selected isoforms of cytochrome P450 in primary cultures of human hepatocytes.  |  Dvorák, Z., et al. 2000. Acta Univ Palacki Olomuc Fac Med. 143: 47-50. PMID: 11144118
  2. Anti-/pro-oxidant effects of phenolic compounds in cells: are colchicine metabolites chain-breaking antioxidants?  |  Modriansky, M., et al. 2002. Toxicology. 177: 105-17. PMID: 12126799
  3. Tubulin structure and biochemistry.  |  Ludueña, RF., et al. 1992. Curr Opin Cell Biol. 4: 53-7. PMID: 1558754
  4. The effect of N-deacetylcolchiceine on serum lipoproteins in rats.  |  Skottová, N., et al. 1992. Planta Med. 58: 26-30. PMID: 1620740
  5. Behavior of drug excited states within macromolecules: binding of colchicine and derivatives to albumin.  |  Bosca, F. and Tormos, R. 2013. J Phys Chem B. 117: 7528-34. PMID: 23730875
  6. Apoptosis in rat hippocampal dentate gyrus after intraventricular colchicine.  |  Ceccatelli, S., et al. 1997. Neuroreport. 8: 3779-83. PMID: 9427370
  7. Microtubule-interfering agents activate c-Jun N-terminal kinase/stress-activated protein kinase through both Ras and apoptosis signal-regulating kinase pathways.  |  Wang, TH., et al. 1998. J Biol Chem. 273: 4928-36. PMID: 9478937
  8. Role of the colchicine ring A and its methoxy groups in the binding to tubulin and microtubule inhibition.  |  Andreu, JM., et al. 1998. Biochemistry. 37: 8356-68. PMID: 9622487
  9. Simple conversion of colchicine into demecolcine  |  Capraro, H. G., & Brossi, A. 1979. Helvetica Chimica Acta. 62(4): 965-970.
  10. The reasons for fluorescence emitting from the mixture of colchicine and H2SO4  |  Hui, W., Leilei, L., Shuqin, L., & Yu, W. 2005. Analytical letters. 38(12): 1967-1973.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Deacetylcolchiceine, 100 mg

sc-208016
100 mg
$345.00