Date published: 2025-12-15

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Actinomycin C (CAS 8052-16-2)

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Application:
Actinomycin C is an antibiotic produced by Streptomyces chrysomallus that intercalates DNA
CAS Number:
8052-16-2
Molecular Weight:
1269.4
Molecular Formula:
C63H88N12O16
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Actinomycin C, with the CAS number 8052-16-2, is a member of the actinomycin group of compounds, which are chromopeptide lactones produced by various species of the bacterium Streptomyces. This compound is particularly noted for its role in binding to DNA, where it intercalates between specific guanine-cytosine base pairs, thereby inhibiting the transcription process. By inserting itself into the DNA double helix, actinomycin C disrupts the elongation phase of RNA synthesis, preventing RNA polymerase from advancing along the DNA template to transcribe genes. This unique mechanism makes it a powerful tool in molecular biology research for studying gene expression and the effects of transcription inhibition on cellular processes. Researchers utilize actinomycin C to understand the dynamics of gene regulation, to dissect the pathways involved in cellular response to transcription stress, and to explore the complex relationship between DNA structure and function. Additionally, its ability to halt RNA synthesis allows scientists to use actinomycin C in experiments designed to measure rates of RNA synthesis and decay, providing valuable insights into the stability and lifespan of various RNA molecules within cells. Through these applications, actinomycin C enhances our understanding of cellular biochemistry and the genetic mechanisms that underpin cellular function and response.


Actinomycin C (CAS 8052-16-2) References

  1. The cytoprotective properties of prostaglandin E2 against the toxic effects of actinomycin C on embryonic neural retina cells.  |  Dymond, JB. and Kalmus, GW. 1992. Prostaglandins. 44: 129-34. PMID: 1279745
  2. Proliferation of antibiotic-producing bacteria and concomitant antibiotic production as the basis for the antibiotic activity of Jordan's red soils.  |  Falkinham, JO., et al. 2009. Appl Environ Microbiol. 75: 2735-41. PMID: 19286796
  3. Genetics of actinomycin C production in Streptomyces chrysomallus.  |  Haese, A. and Keller, U. 1988. J Bacteriol. 170: 1360-8. PMID: 2449423
  4. Genetic interrelations in the actinomycin biosynthetic gene clusters of Streptomyces antibioticus IMRU 3720 and Streptomyces chrysomallus ATCC11523, producers of actinomycin X and actinomycin C.  |  Crnovčić, I., et al. 2017. Adv Appl Bioinform Chem. 10: 29-46. PMID: 28435299
  5. Review of xenografts in organ transplantation.  |  Deodhar, SD. 1986. Transplant Proc. 18: 83-7. PMID: 3521004
  6. Actinomycin C and antibody biosynthesis in vitro.  |  Stanchev, BD. 1970. Nauchni Tr Vissh Med Inst Sofiia. 49: 37-42. PMID: 4103376
  7. Effect of actinomycin C and ALS on the production of cytophilic and haemolytic antibodies against sheep erythrocytes in guinea pigs.  |  Rudnicka, W., et al. 1974. Bull Acad Pol Sci Biol. 22: 85-9. PMID: 4132386
  8. Origin of the sarcosine molecules of actinomycins.  |  Ciferri, O., et al. 1965. Biochem J. 96: 853-61. PMID: 4159551
  9. [Biologically active substances formed by a number of strains of the actinomycin C producer--Streptomyces chrysomallus].  |  Konoshenko, GI., et al. 1994. Antibiot Khimioter. 39: 22-5. PMID: 7526813
  10. Binding of biologically important molecules to DNA, probed using electro-fluorescence polarization spectroscopy.  |  Windsor, SA. and Tinker, MH. 1996. Biophys Chem. 58: 141-50. PMID: 8679917

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Actinomycin C, 1 mg

sc-202905
1 mg
$500.00

Actinomycin C, 25 mg

sc-202905A
25 mg
$2150.00