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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

Alta Scientific Co., Ltd.
Tel
022-6537-8550 15522853686
Fax
022-2532-9655
Email
sales@altasci.com.cn
Country
China
ProdList
4515
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
Advantage
58
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55717
Advantage
58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
Country
China
ProdList
9730
Advantage
58
BOC Sciences
Tel
+16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19743
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11289
Advantage
58

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