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2751-09-9 molecular structure
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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

ChemBase ID: 1187
Molecular Formular: C41H67NO15
Molecular Mass: 813.96838
Monoisotopic Mass: 813.45107045
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

Cite this record

CBID:1187 http://www.chembase.cn/molecule-1187.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(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
IUPAC Traditional name
troleandomycin
Brand Name
Cyclamycin
Evramicina
Matromicina
Tao
Treolmicina
Tribiocillina
Synonyms
Triacetyloleandomycin
Oleandomycin triacetate
Oleandomycin, triacetate (ester)
Oleandomycin triacetyl ester
Oleandocetine
Troleandomycin
Troleandomycin
Oleandomycin triacetate
CAS Number
2751-09-9
EC Number
220-392-9
MDL Number
MFCD00871198
Beilstein Number
1418238
PubChem SID
160964649
46508062
PubChem CID
202225

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
T6514 external link Add to cart Please log in.

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 16.753065  H Acceptors 12 
H Donor LogD (pH = 5.5) 1.9603862 
LogD (pH = 7.4) 3.7044063  Log P 4.298515 
Molar Refractivity 201.147 cm3 Polarizability 82.35146 Å3
Polar Surface Area 184.19 Å2 Rotatable Bonds 12 
Lipinski's Rule of Five false 
Log P 3.76  LOG S -4.63 
Solubility (Water) 1.92e-02 g/l 

PROPERTIES

PROPERTIES

Safety Information Bioassay(PubChem)
RTECS
RJ9900000 expand Show data source
German water hazard class
2 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source

DETAILS

DETAILS

DrugBank DrugBank
DrugBank - DB01361 external link
Item Information
Drug Groups approved
Description 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
External Links
Wikipedia
RxList
Drugs.com

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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