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Virginiamycin S1

Product Name
Virginiamycin S1
CAS No.
23152-29-6
Chemical Name
Virginiamycin S1
Synonyms
VirginiaMycin coMplex;Antibiotic 899;Staphylomycin S;Verginiamycin S1;Virginiamycin S1;Virginiamycin S?;Antibiotic 1754Z3B;Antibiotic 899, Staphylomycin S;StaphyloMycin S, PA 114B2, 899, A1745Z3B, Factor S;N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]
CBNumber
CB4887230
Molecular Formula
C43H49N7O10
Formula Weight
823.89
MOL File
23152-29-6.mol
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Virginiamycin S1 Property

Melting point:
240-242°
alpha 
D20 -28° (c = 1 in ethanol)
storage temp. 
-20°C
solubility 
methanol: soluble5mg/mL
form 
powder
color 
white
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Safety

WGK Germany 
3
HS Code 
2941900000
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
V4140
Product name
Virginiamycin S1
Purity
≥99% (HPLC)
Packaging
5mg
Price
$471
Updated
2024/03/01
Cayman Chemical
Product number
17455
Product name
Virginiamycin S1
Purity
≥99%
Packaging
5mg
Price
$326
Updated
2024/03/01
Cayman Chemical
Product number
17455
Product name
Virginiamycin S1
Purity
≥99%
Packaging
25mg
Price
$1141
Updated
2024/03/01
TRC
Product number
V673813
Product name
Virginiamycin S1
Packaging
1mg
Price
$255
Updated
2021/12/16
Usbiological
Product number
V2123-59
Product name
Virginiamycin Complex
Packaging
5mg
Price
$523
Updated
2021/12/16
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Virginiamycin S1 Chemical Properties,Usage,Production

Uses

Virginiamycin S1 is a main component of virginiamycin preparations.

Uses

Virginiamycin complex is defined as a mixture of 75% ostreogrycin A (virginamycin M1) and 25% virginiamycin S1, together with the less abundant S analogues. As the two major components have quite different solubilities, these proportions are not readily achieved or used. BioAustralis has isolated and re-combined the individual components to provide the defined components of virginiamycin complex. The composition of the complex is important as Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A.

Uses

Virginiamycin S1 is one of a family of depsipeptide antibiotics co-produced with ostreogrycin A and used as a synergistic mixture. Virginiamycin S1 acts a synergist, binding to the conformational change of the peptidyl transferase centre of the 50S ribosome induced by ostreogrycin A.

Biological Activity

virginiamycin s1 is a macrolide antibiotic that reversibly inhibits protein synthesis [1][2][3].virginiamycin complex contains two antibiotics, virginiamycin m1 and virginiamycin s1. streptogramins are divided into class a and class b based on their structures. virginiamycin s1 is a member of the streptogramin b group of antibiotics, which bind the peptide exit tunnel to inhibit the elongation stage of translation. they show good bactericidal activity against methicillin-resistant s. aureus (mrsa), although resistance in mrsa is conferred by the cfr gene. virginiamycin m1 has activity against gram-positive and in select cases gram-negative bacteria. combination of group a and b streptogramins exhibit bactericidal activity [1]. virginiamycin s1 acted synergistically with virginiamycin m1 to irreversibly inhibit protein synthesis in bacteria. in cell-free systems, virginiamycin m1 and virginiamycin s1 bound to the large ribosomal subunit, and the affinity of ribosomes for vs is increased by vm [2][3].

Contact allergens

Like the other streptogramin, pristinamycin, virginiamycin is made of two subunits, virginiamycin S1 and virginiamycin M1. Dermatitis was quite common in people using the formerly available topical virginiamycin. Occupational dermatitis was observed in the pharmaceutical industry, in breeders, and in a surgeon who used topical virginiamycin on postoperative wounds (personal observation).

References

[1]. fair rj, tor y. antibiotics and bacterial resistance in the 21st century. perspect medicin chem. 2014 aug 28;6:25-64.
[2]. kehrenberg c, cuny c, strommenger b, et al. methicillin-resistant and -susceptible staphylococcus aureus strains of clonal lineages st398 and st9 from swine carry the multidrug resistance gene cfr. antimicrob agents chemother. 2009 feb;53(2):779-81.
[3]. parfait r, cocito c. lasting damage to bacterial ribosomes by reversibly bound virginiamycin m. proc natl acad sci u s a. 1980 sep;77(9):5492-6.

Virginiamycin S1 Preparation Products And Raw materials

Raw materials

Preparation Products

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Virginiamycin S1 Suppliers

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23152-29-6, Virginiamycin S1Related Search:


  • Virginiamycin S1
  • Antibiotic 1754Z3B
  • N-[(3-Hydroxy-2-pyridinyl)carbonyl]cyclo[L-Thr*-D-Abu-L-Pro-N-methyl-L-Phe-4-oxo-L-pipecoloyl-L-phenyl Gly-]
  • N-[(3-Hydroxy-2-pyridyl)carbonyl]cyclo(L-Thr*-D-Abu-L-Pro-N-methyl-L-Phe-4-oxo-L-2-piperidinecarbonyl-L-phenyl Gly-)
  • Staphylomycin S
  • Cebin V, Eskalin V, EskaMicin, Stafac, StephyloMycin, MikaMycin, Ostreogrycin, Patricin, PristinaMycin, StreptograMin, VernaMycin.
  • VirginiaMycin coMplex
  • Antibiotic 899, Staphylomycin S
  • StaphyloMycin S, PA 114B2, 899, A1745Z3B, Factor S
  • Verginiamycin S1
  • Antibiotic 899
  • Virginiamycin S?
  • 23152-29-6
  • C43H49N7O10
  • antibiotic