Home Aminos 2H-Oxacyclotetradecino[4,3-d]oxazole-2,6,8,14(1H,7H,9H)-tetrone, 4-ethyloctahydro-11-methoxy-3a,7,9,11,13,15-hexamethyl-1-[4-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl]-10-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-, (3aS,4R,7R,9R,10R,11R,13R,15R,15aR)-

2H-Oxacyclotetradecino[4,3-d]oxazole-2,6,8,14(1H,7H,9H)-tetrone, 4-ethyloctahydro-11-methoxy-3a,7,9,11,13,15-hexamethyl-1-[4-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl]-10-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-, (3aS,4R,7R,9R,10R,11R,13R,15R,15aR)-

CAS No.:
191114-48-4
Catalog Number:
AG002F1S
Molecular Formula:
C43H65N5O10
Molecular Weight:
812.0037
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5mg
95%(HPLC)
In Stock USA
United States
$68
- +
10mg
95%(HPLC)
In Stock USA
United States
$108
- +
25mg
95%(HPLC)
In Stock USA
United States
$198
- +
50mg
95%(HPLC)
In Stock USA
United States
$336
- +
100mg
95%(HPLC)
In Stock USA
United States
$619
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Product Description
Catalog Number:
AG002F1S
Chemical Name:
2H-Oxacyclotetradecino[4,3-d]oxazole-2,6,8,14(1H,7H,9H)-tetrone, 4-ethyloctahydro-11-methoxy-3a,7,9,11,13,15-hexamethyl-1-[4-[4-(3-pyridinyl)-1H-imidazol-1-yl]butyl]-10-[[3,4,6-trideoxy-3-(dimethylamino)-β-D-xylo-hexopyranosyl]oxy]-, (3aS,4R,7R,9R,10R,11R,13R,15R,15aR)-
CAS Number:
191114-48-4
Molecular Formula:
C43H65N5O10
Molecular Weight:
812.0037
MDL Number:
MFCD00943561
IUPAC Name:
(1S,2R,5R,7R,8R,9R,11R,13R,14R)-8-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-9-methoxy-1,5,7,9,11,13-hexamethyl-15-[4-(4-pyridin-3-ylimidazol-1-yl)butyl]-3,17-dioxa-15-azabicyclo[12.3.0]heptadecane-4,6,12,16-tetrone
InChI:
InChI=1S/C43H65N5O10/c1-12-33-43(8)37(48(41(53)58-43)19-14-13-18-47-23-31(45-24-47)30-16-15-17-44-22-30)27(4)34(49)25(2)21-42(7,54-11)38(28(5)35(50)29(6)39(52)56-33)57-40-36(51)32(46(9)10)20-26(3)55-40/h15-17,22-29,32-33,36-38,40,51H,12-14,18-21H2,1-11H3/t25-,26-,27+,28+,29-,32+,33-,36-,37-,38-,40+,42-,43-/m1/s1
InChI Key:
LJVAJPDWBABPEJ-PNUFFHFMSA-N
SMILES:
CC[C@H]1OC(=O)[C@H](C)C(=O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C[C@H](C(=O)[C@@H]([C@@H]2[C@]1(C)OC(=O)N2CCCCn1cnc(c1)c1cccnc1)C)C)(C)OC
UNII:
KI8H7H19WL
Properties
Complexity:
1440  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
13  
Defined Bond Stereocenter Count:
0
Exact Mass:
811.473g/mol
Formal Charge:
0
Heavy Atom Count:
58  
Hydrogen Bond Acceptor Count:
13  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
812.018g/mol
Monoisotopic Mass:
811.473g/mol
Rotatable Bond Count:
11  
Topological Polar Surface Area:
172A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.2  
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Uptake and intracellular activity of ketolide HMR 3647 in human phagocytic and non-phagocytic cells. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010201
Bacteroides fragilis-induced intra-abdominal abscess in an experimental model treated with telithromycin (HMR 3647). Chemotherapy 20010101
In vitro activity of ketolides HMR 3004 and HMR 3647 and seven other antimicrobial agents against Corynebacterium diphtheriae. The Journal of antimicrobial chemotherapy 20010101
HMR 3647 human-like treatment of experimental pneumonia due to penicillin-resistant and erythromycin-resistant Streptococcus pneumoniae. The Journal of antimicrobial chemotherapy 20010101
Telithromycin. Drugs 20010101
Inhibitory and bactericidal effects of telithromycin (HMR 3647, RU 56647) and five comparative antibiotics, used singly and in combination, against vancomycin-resistant and vancomycin-susceptible enterococci. Chemotherapy 20010101
Macrolide resistance in Streptococcus pyogenes isolates from throat infections in the region of Aachen, Germany. Microbial drug resistance (Larchmont, N.Y.) 20010101
Structure-activity relationships of ketolides vs. macrolides. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010101
Safeguarding future antimicrobial options: strategies to minimize resistance. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010101
Microbiological profile of telithromycin, the first ketolide antimicrobial. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010101
Pharmacodynamic and pharmacokinetic considerations in antimicrobial selection: focus on telithromycin. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010101
Community-acquired pneumonia: the evolving challenge. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 20010101
[Ribosomal antibiotics]. Molekuliarnaia biologiia 20010101
Efficacy of short-course therapy with the ketolide telithromycin compared with 10 days of penicillin V for the treatment of pharyngitis/tonsillitis. Scandinavian journal of infectious diseases 20010101
In vitro activity of the new ketolide telithromycin and other antibiotics against Streptococcus pneumoniae in Belgium. Acta clinica Belgica 20010101
In vitro activities of the ketolides telithromycin (HMR 3647) and HMR 3004 compared to those of clarithromycin against slowly growing mycobacteria at pHs 6.8 and 7.4. Antimicrobial agents and chemotherapy 20001001
In vitro susceptibilities of rapidly growing mycobacteria to telithromycin (HMR 3647) and seven other antimicrobials. Antimicrobial agents and chemotherapy 20000101
Use of ketolides in combination with other drugs to treat experimental toxoplasmosis. The Journal of antimicrobial chemotherapy 19981101
The ketolide antibiotics HMR 3647 and HMR 3004 are active against Toxoplasma gondii in vitro and in murine models of infection. Antimicrobial agents and chemotherapy 19971001
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