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(3R,5R,6S,7S,8R,11R,12S,13R,14S,15S)-14-{[(2S,3R,4S,6R)-3-(acetyloxy)-4-(dimethylamino)-6-methyloxan-2-yl]oxy}-12-{[(2R,4S,5S,6S)-5-(acetyloxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,7,8,11,13,15-hexamethyl-4,10-dioxo-1,9-dioxaspiro[2.13]hexadecan-6-yl acetate
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ChemBase ID:
1187
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Molecular Formular:
C41H67NO15
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Molecular Mass:
813.96838
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Monoisotopic Mass:
813.45107045
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SMILES and InChIs
SMILES:
O1[C@]2(C[C@@H]([C@H](O[C@@H]3O[C@@H](C[C@H](N(C)C)[C@H]3OC(=O)C)C)[C@H]([C@H](O[C@@H]3O[C@H]([C@H](OC(=O)C)[C@@H](OC)C3)C)[C@H](C(=O)O[C@@H]([C@@H]([C@H](OC(=O)C)[C@H](C2=O)C)C)C)C)C)C)C1
Canonical SMILES:
CO[C@H]1C[C@@H](O[C@H]([C@@H]1OC(=O)C)C)O[C@H]1[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2OC(=O)C)N(C)C)[C@@H](C)C[C@]2(OC2)C(=O)[C@@H]([C@H]([C@H]([C@H](OC(=O)[C@@H]1C)C)C)OC(=O)C)C
InChI:
InChI=1S/C41H67NO15/c1-19-17-41(18-49-41)38(46)23(5)34(53-27(9)43)21(3)25(7)52-39(47)24(6)35(56-32-16-31(48-14)36(26(8)51-32)54-28(10)44)22(4)33(19)57-40-37(55-29(11)45)30(42(12)13)15-20(2)50-40/h19-26,30-37,40H,15-18H2,1-14H3/t19-,20+,21-,22+,23+,24+,25+,26-,30-,31-,32-,33-,34-,35-,36-,37+,40-,41+/m0/s1
InChIKey:
LQCLVBQBTUVCEQ-QTFUVMRISA-N
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Cite this record
CBID:1187 http://www.chembase.cn/molecule-1187.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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(3R,5R,6S,7S,8R,11R,12S,13R,14S,15S)-14-{[(2S,3R,4S,6R)-3-(acetyloxy)-4-(dimethylamino)-6-methyloxan-2-yl]oxy}-12-{[(2R,4S,5S,6S)-5-(acetyloxy)-4-methoxy-6-methyloxan-2-yl]oxy}-5,7,8,11,13,15-hexamethyl-4,10-dioxo-1,9-dioxaspiro[2.13]hexadecan-6-yl acetate
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IUPAC Traditional name
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Brand Name
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Cyclamycin
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Evramicina
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Matromicina
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Tao
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Treolmicina
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Tribiocillina
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Synonyms
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Triacetyloleandomycin
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Oleandomycin triacetate
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Oleandomycin, triacetate (ester)
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Oleandomycin triacetyl ester
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Oleandocetine
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Troleandomycin
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Troleandomycin
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Oleandomycin triacetate
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CAS Number
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EC Number
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MDL Number
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Beilstein Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
ALOGPS 2.1
Acid pKa
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16.753065
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H Acceptors
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12
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H Donor
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0
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LogD (pH = 5.5)
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1.9603862
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LogD (pH = 7.4)
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3.7044063
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Log P
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4.298515
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Molar Refractivity
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201.147 cm3
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Polarizability
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82.35146 Å3
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Polar Surface Area
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184.19 Å2
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Rotatable Bonds
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12
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Lipinski's Rule of Five
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false
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Log P
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3.76
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LOG S
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-4.63
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Solubility (Water)
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1.92e-02 g/l
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DETAILS
DETAILS
DrugBank
DrugBank -
DB01361
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Item |
Information |
Drug Groups
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approved |
Description
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A macrolide antibiotic that is similar to erythromycin. |
Indication |
For the treatment of Pneumococcal pneumonia due to susceptible strains and group A beta-hemolytic streptococcal infections of the upper respiratory tract. |
Pharmacology |
Troleandomycin is a macrolide antibiotic that is similar to erythromycin. It is active in vitro against the following gram-positive organisms: Streptococcus pyogenes and Diplococcus pneumoniae. |
Toxicity |
Symptoms of overdose include diarrhea, nausea, stomach cramps, and vomiting. |
Affected Organisms |
• |
Enteric bacteria and other eubacteria |
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External Links |
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PATENTS
PATENTS
PubChem Patent
Google Patent