Synonyms |
Azitro; CP 62993; CP-62993; CP62993; Goxal; Odaz; Ribotrex; Toraseptol; Ultreon; XZ-450; XZ450; XZ 450; Zenstavion; Zithromax; Zmax |
IUPAC Name |
(2R,3S,4R,5R,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,6,8,10,12,14-heptamethyl-1-oxa-6-azacyclopentadecan-15-one;dihydrate |
Molecular Weight |
785.02 |
Molecular Formula |
C38H72N2O12.2H2O |
Canonical SMILES |
CCC1C(C(C(N(CC(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)C)O)(C)O.O.O |
InChI |
InChI=1S/C38H72N2O12.2H2O/c1-15-27-38(10,46)31(42)24(6)40(13)19-20(2)17-36(8,45)33(52-35-29(41)26(39(11)12)16-21(3)48-35)22(4)30(23(5)34(44)50-27)51-28-18-37(9,47-14)32(43)25(7)49-28;;/h20-33,35,41-43,45-46H,15-19H2,1-14H3;2*1H2/t20-,21-,22+,23-,24-,25+,26+,27-,28+,29-,30+,31-,32+,33-,35+,36-,37-,38-;;/m1./s1 |
InChIKey |
SRMPHJKQVUDLQE-KUJJYQHYSA-N |
Boiling Point |
822.1°C at 760 mmHg |
Melting Point |
113-115°C |
Flash Point |
451°C |
Purity |
>98% |
Density |
1.18 g/cm3 |
Solubility |
Soluble in DMSO |
Appearance |
White Solid |
Application |
Anti-Bacterial Agents |
Storage |
Store at -20°C |
Complexity |
1150 |
Exact Mass |
784.529663 |
In Vitro |
Azithromycin showed resistance to a range of similar spectrums of bacterial activity. It acts in vitro on gram-positive bacteria with slightly less activity than erythromycin, as the susceptible concentration drops to the concentration range of tissue Azithromycin, although this is clinically uncertain. Azithromycin is also anti-clinical isolates of anaerobic gram-positive bacteria cocci and propionibacterium acnes, with MIC90 of 2.3, 0.03 mg/L. |
PSA |
198.54000 |
Target |
Influenza |
Vapor Pressure |
2.51E-31mmHg at 25°C |