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About This Item
Empirical Formula (Hill Notation):
C28H45NO5S
CAS Number:
Molecular Weight:
507.73
UNSPSC Code:
51101500
NACRES:
NA.21
Quality Level
assay
≥98% (HPLC)
form
powder
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
application(s)
advanced drug delivery
mode of action
protein synthesis | inhibits
shipped in
ambient
storage temp.
2-8°C
SMILES string
CC1CCC23CCC(=O)C2C1(C(CC(C(C3C)O)(C)C=C)OC(=O)CSC4CCC(CC4O)N)C
InChI
1S/C28H45NO5S/c1-6-26(4)14-22(34-23(32)15-35-21-8-7-18(29)13-20(21)31)27(5)16(2)9-11-28(17(3)25(26)33)12-10-19(30)24(27)28/h6,16-18,20-22,24-25,31,33H,1,7-15,29H2,2-5H3/t16-,17+,18-,20-,21-,22-,24+,25+,26-,27+,28+/m1/s1
InChI key
KPVIXBKIJXZQJX-FCEONZPQSA-N
General description
Lefamulin is an antibiotic which belongs to a class of coumpounds known as pleuromutilins. It is a semisynthetic derivative of the naturally occurring antibiotic pleuromutilin, and it is used for the treatment of bacterial infections.
Biochem/physiol Actions
Lefamulin inhibits bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome. Specifically, it binds to the peptidyl transferase center of the ribosome and inhibits the transfer of amino acids to growing polypeptide chains, which leads to the inhibition of bacterial protein synthesis and bacterial death. Lefamulin is active against a wide range of Gram-positive bacteria, including Streptococcus pneumoniae, Staphylococcus aureus, and methicillin-resistant S. aureus (MRSA), as well as some atypical bacteria such as Legionella species. It has also been shown to have activity against some Gram-negative bacteria, including Haemophilus influenzae and Moraxella catarrhalis.
signalword
Warning
hcodes
Hazard Classifications
STOT SE 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Global Trade Item Number
| SKU | GTIN |
|---|---|
| SBR00096-5MG | 04065271975330 |
