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Lexithromycin

Product Name
Lexithromycin
CAS No.
53066-26-5
Chemical Name
Lexithromycin
Synonyms
Wy 48314;Lexithromycin;Erythromycin A-E-oxime;Azithromycin Impurity 4;erythromycin A methoxime;Azithromycin Impurity 31;Erythromycin A 9-Methoxime;Erythromycin, 9-(O-methyloxime);9-(Methoxyimino)-9-deoxoerythromycin;ErythroMycin A 9-MethoxiMe, Wy 48314
CBNumber
CB41327717
Molecular Formula
C38H70N2O13
Formula Weight
762.97
MOL File
53066-26-5.mol
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Lexithromycin Property

Melting point:
>115°C (dec.)
Boiling point:
824.6±75.0 °C(Predicted)
Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility 
Chloroform (Slightly), DMSO (Slightly)
pka
13.19±0.70(Predicted)
form 
Solid
color 
White to Off-White
Stability:
Hygroscopic
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
22002
Product name
Lexithromycin
Purity
≥98%
Packaging
5mg
Price
$171
Updated
2024/03/01
Cayman Chemical
Product number
22002
Product name
Lexithromycin
Purity
≥98%
Packaging
25mg
Price
$760
Updated
2024/03/01
ChemScene
Product number
CS-0026970
Product name
Lexithromycin
Purity
98.80%
Packaging
100mg
Price
$1650
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0011780
Product name
LEXITHROMYCIN
Purity
95.00%
Packaging
5MG
Price
$502.99
Updated
2021/12/16
ChemScene
Product number
CS-0026970
Product name
Lexithromycin
Purity
98.80%
Packaging
25mg
Price
$550
Updated
2021/12/16
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Lexithromycin Chemical Properties,Usage,Production

Description

Lexithromycin is a semisynthetic antibiotic derived from erythromycin . Lexithromycin has improved absorption in vivo over erythromycin due to increased hydrophopicity and pH stability. As with other macrolides, lexithromycin prevents protein synthesis by binding the ribosome at the polypeptide exit tunnel. Formulations containing lexithromycin were tested in clinical trials as treatment for HIV but were discontinued.

Uses

Lexithromycin is an early semi-synthetic erythromycin, prepared by reaction of the 9-keto moiety to methyl oxime. The structural change improves the pH stability profile and hydrophobicity of lexithromycin for better in vivo absorption. This same rationale was used to greater effect with roxithromycin and, as a result, lexithromycin was quickly superseded and has not been not extensively studied. Like all tetracyclines, lexithromycin shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal sub-units, blocking protein synthesis.

Uses

Lexithromycin is a semi-synthetic erythromycin with improved pH stability and hydrophobicity. It is used in compositions and methods for treating viral infections.

Lexithromycin Preparation Products And Raw materials

Raw materials

Preparation Products

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Lexithromycin Suppliers

BOC Sciences
Tel
16314854226; +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
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6393
Advantage
58
Standardpharm Co. Ltd.
Tel
86-714-3992388
Email
overseasales1@yongstandards.com
Country
United States
ProdList
14336
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10413
Advantage
58

53066-26-5, LexithromycinRelated Search:


  • erythromycin A methoxime
  • 9-(Methoxyimino)-9-deoxoerythromycin
  • 9-Deoxo-9-[[methyloxy]imino]erythromycin
  • ErythroMycin A 9-MethoxiMe, Wy 48314
  • Erythromycin A-E-oxime
  • Erythromycin A-E-oxime LEXITHROMYCIN.
  • Erythromycin A 9-Methoxime
  • Azithromycin Impurity 4
  • Azithromycin Impurity 31
  • Lexithromycin
  • Wy 48314
  • Erythromycin, 9-(O-methyloxime)
  • 53066-26-5