Date published: 2026-3-19

1-800-457-3801

SCBT Portrait Logo
Seach Input

Spiramycin I (CAS 24916-50-5)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Foromacidin A; Spiramycin A
Application:
Spiramycin I is an antibiotic from the erythromycin-carbomycin group
CAS Number:
24916-50-5
Purity:
≥98%
Molecular Weight:
843.05
Molecular Formula:
C43H74N2O14
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Connexin 46 inhibitors are a class of chemical compounds that specifically target and inhibit the function of connexin 46, a protein encoded by the GJA3 (gap junction protein alpha 3) gene. Connexin 46 is a member of the connexin family of proteins, which are integral components of gap junctions. These gap junctions are specialized intercellular channels that allow for direct communication between adjacent cells by facilitating the passage of ions, metabolites, and other small molecules. Connexin 46, in particular, is predominantly expressed in the lens of the eye, where it plays a crucial role in maintaining lens transparency and homeostasis. By forming gap junction channels, connexin 46 enables the diffusion of essential nutrients and the removal of metabolic waste products, ensuring proper cellular function within the lens. Structurally, connexin 46 inhibitors are diverse and can include small molecules or peptides specifically designed to interfere with the assembly, opening, or functioning of connexin 46 channels. These inhibitors can bind to specific sites on the connexin 46 protein, preventing it from forming functional gap junctions or blocking the channels once they are formed. This inhibition can disrupt intercellular communication and alter the homeostatic balance maintained by gap junctions in tissues expressing connexin 46. The study of connexin 46 inhibitors provides valuable insights into the mechanisms of gap junction regulation and the role of connexin 46 in cellular communication and tissue homeostasis. By understanding how these inhibitors affect connexin 46 function, researchers can explore the broader implications of gap junction modulation on cellular processes, including ion transport, metabolic coordination, and overall tissue health. Research into these inhibitors thus contributes to a deeper understanding of the physiological and biochemical pathways influenced by gap junctions and connexin 46 specifically.


Spiramycin I (CAS 24916-50-5) References

  1. Analysis of spiramycin by capillary electrophoresis.  |  González-Hernández, R., et al. 1999. Electrophoresis. 20: 2407-11. PMID: 10499332
  2. Simultaneous determination of metronidazole and spiramycin I in human plasma, saliva and gingival crevicular fluid by LC-MS/MS.  |  Sagan, C., et al. 2005. J Pharm Biomed Anal. 38: 298-306. PMID: 15925222
  3. [Deletion of spiramycin 3-O-acyltransferase gene from Streptomyces spiramyceticus F21 resulting in the production of spiramycin I as major component].  |  Wu, LZ., et al. 2007. Sheng Wu Gong Cheng Xue Bao. 23: 612-7. PMID: 17849607
  4. Hydroxylation and hydrolysis: two main metabolic ways of spiramycin I in anaerobic digestion.  |  Zhu, P., et al. 2014. Bioresour Technol. 153: 95-100. PMID: 24345568
  5. Anaerobic biodegradation of spiramycin I and characterization of its new metabolites.  |  Yao, J., et al. 2017. Biosci Biotechnol Biochem. 81: 1051-1054. PMID: 28095730
  6. Stimulatory Effects of Methyl-β-cyclodextrin on Spiramycin Production and Physical-Chemical Characterization of Nonhost@Guest Complexes.  |  Calcagnile, M., et al. 2018. ACS Omega. 3: 2470-2478. PMID: 30221219
  7. Structure activity relationships of spiramycins.  |  Omura, S., et al. 1985. J Antimicrob Chemother. 16 Suppl A: 1-11. PMID: 3902764
  8. Chemical modification of spiramycins. V. Synthesis and antibacterial activity of 3'- or 4''-de-N-methylspiramycin I and their N-substituted derivatives.  |  Sano, H., et al. 1985. J Antibiot (Tokyo). 38: 186-96. PMID: 3997666
  9. Chemical modification of spiramycins. VI. Synthesis and antibacterial activities of 3,3''-di-O-acyl-4''-O-sulfonyl and 3,3''-di-O-acyl-4''-O-alkyl derivatives of spiramycin I.  |  Sano, M., et al. 1985. J Antibiot (Tokyo). 38: 1350-8. PMID: 4066488
  10. Chemical modification of spiramycins. III. Synthesis and antibacterial activities of 4''-sulfonates and 4''-alkylethers of spiramycin I.  |  Sano, H., et al. 1984. J Antibiot (Tokyo). 37: 750-9. PMID: 6469869
  11. Chemical modification of spiramycins. IV. Synthesis and in vitro and in vivo activities of 3'',4''-diacylates and 3,3'',4''-triacylates of spriamycin I.  |  Sano, H., et al. 1984. J Antibiot (Tokyo). 37: 760-72. PMID: 6469870
  12. Chemical modification of spiramycins. I. Synthesis of the acetal derivatives of neospiramycin I.  |  Sano, H., et al. 1983. J Antibiot (Tokyo). 36: 1336-44. PMID: 6643282
  13. Biosynthesis and the metabolic fate of carbon-14 labeled spiramycin I.  |  Inoue, A., et al. 1983. J Antibiot (Tokyo). 36: 442-4. PMID: 6853373

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Spiramycin I, 2.5 g

sc-220129
2.5 g
$331.00