Oleandomycin hydrochlorideProduct ingredient for Oleandomycin
- Name
- Oleandomycin hydrochloride
- Drug Entry
- Oleandomycin
Oleandomycin is a macrolide antibiotic, though it is less effective than erythromycin. It is synthesized from strains of Streptomyces antibioticus.
- Accession Number
- DBSALT002276
- Structure
Structure for Oleandomycin hydrochloride (DBSALT002276)
- Synonyms
- Oleandomycin HCl
- UNII
- 0SEZ96A40Y
- CAS Number
- 6696-47-5
- Weight
- Average: 724.33
Monoisotopic: 723.3960541 - Chemical Formula
- C35H62ClNO12
- InChI Key
- CWYHZGJSHPPEHY-UOBLTHIJSA-N
- InChI
- InChI=1S/C35H61NO12.ClH/c1-16-14-35(15-43-35)32(40)19(4)27(37)18(3)22(7)46-33(41)21(6)31(47-26-13-25(42-11)28(38)23(8)45-26)20(5)30(16)48-34-29(39)24(36(9)10)12-17(2)44-34;/h16-31,34,37-39H,12-15H2,1-11H3;1H/t16-,17+,18-,19+,20+,21+,22+,23-,24-,25-,26-,27-,28-,29+,30-,31-,34-,35+;/m0./s1
- IUPAC Name
- (3R,5R,6S,7R,8R,11R,12S,13R,14S,15S)-14-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-6-hydroxy-12-{[(2R,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-5,7,8,11,13,15-hexamethyl-1,9-dioxaspiro[2.13]hexadecane-4,10-dione hydrochloride
- SMILES
- Cl.CO[C@H]1C[C@H](O[C@H]2[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@@H](C)C[C@@]3(CO3)C(=O)[C@H](C)[C@@H](O)[C@@H](C)[C@@H](C)OC(=O)[C@@H]2C)O[C@@H](C)[C@@H]1O
- External Links
- ChemSpider
- 21252073
- Predicted Properties
Property Value Source Water Solubility 0.407 mg/mL ALOGPS logP 1.46 ALOGPS logP 2.98 Chemaxon logS -3.2 ALOGPS pKa (Strongest Acidic) 12.67 Chemaxon pKa (Strongest Basic) 9 Chemaxon Physiological Charge 1 Chemaxon Hydrogen Acceptor Count 12 Chemaxon Hydrogen Donor Count 3 Chemaxon Polar Surface Area 162.68 Å2 Chemaxon Rotatable Bond Count 6 Chemaxon Refractivity 173.69 m3·mol-1 Chemaxon Polarizability 73.85 Å3 Chemaxon Number of Rings 4 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule No Chemaxon MDDR-like Rule Yes Chemaxon