Acetylspiramycin

For research use only. Not for therapeutic Use.

  • CAT Number: I012985
  • CAS Number: 24916-51-6
  • Molecular Formula: C₄₅H₇₆N₂O₁₅
  • Molecular Weight: 885.09
  • Purity: ≥95%
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Acetylspiramycin(Cat No.:I012985)is a macrolide antibiotic and a semi-synthetic derivative of spiramycin, widely used in pharmaceutical research. It exhibits broad-spectrum antibacterial activity, primarily targeting Gram-positive bacteria by inhibiting bacterial protein synthesis. Acetylspiramycin’s improved bioavailability and stability make it a valuable tool for studying antimicrobial mechanisms and resistance pathways. Its unique properties are also explored in pharmacokinetic and pharmacodynamic studies. As an important compound in developing antibiotic therapies, Acetylspiramycin contributes to advancing research in infectious diseases and antimicrobial drug development.


Catalog Number I012985
CAS Number 24916-51-6
Molecular Formula C₄₅H₇₆N₂O₁₅
Purity ≥95%
Target Antibiotic
Solubility DMSO
IUPAC Name [(4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-[(2S,3R,4R,5S,6R)-5-[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-10-[(2R,5S,6R)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-4-yl] acetate
InChI InChI=1S/C45H76N2O15/c1-25-22-31(20-21-48)41(62-44-39(51)38(47(10)11)40(28(4)58-44)61-37-24-45(7,53)43(52)29(5)57-37)42(54-12)34(59-30(6)49)23-35(50)55-26(2)16-14-13-15-17-33(25)60-36-19-18-32(46(8)9)27(3)56-36/h13-15,17,21,25-29,31-34,36-44,51-53H,16,18-20,22-24H2,1-12H3/b14-13+,17-15+/t25-,26-,27-,28-,29+,31+,32+,33+,34-,36+,37+,38-,39-,40-,41+,42+,43+,44+,45-/m1/s1
InChIKey ZPCCSZFPOXBNDL-ZSTSFXQOSA-N
SMILES C[C@@H]1C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)OC(=O)C)OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)O)N(C)C)O)CC=O)C)O[C@H]4CC[C@@H]([C@H](O4)C)N(C)C
Reference

[1]. Huang MZ, et al. Therapeutic effects of acetylspiramycin and garlicin on cryptosporidiosis among drug users. Int J Parasitol Drugs Drug Resist. 2015 Dec;5(3):185-90.

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