Structure via PubChem · Public domain (PubChem)
テリスロマイシン
Sign in to saveAlso known as HMR-3647, Telithromycin
Telithromycin is the first ketolide antibiotic to enter clinical use and is sold under the brand name of Ketek. It is used to treat community acquired pneumonia of mild to moderate severity. After significant safety concerns, the US Food and Drug Administration sharply curtailed the approved uses of the drug in early 2007.
In the Vinony graph
Vinony's link graph records 125 inbound references to テリスロマイシン, and connects out to neomycin, liver and bacteria.
It sits within the topics 3-Pyridyl compounds, Carbamates and CYP3A4 inhibitors.
Vinony links it to 17 Wikipedia language editions.
Chemical data
- Formula
- C43H65N5O10
- Molecular weight
- 812 g/mol
- 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
- SMILES
- CC[C@@H]1[C@@]2([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H](C(=O)[C@H](C(=O)O1)C)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)OC)C)C)N(C(=O)O2)CCCCN4C=C(N=C4)C5=CN=CC=C5)C
- InChIKey
- LJVAJPDWBABPEJ-PNUFFHFMSA-N
- XLogP
- 4.2
- Polar surface area
- 172 Ų
- H-bond donors
- 1
- H-bond acceptors
- 13
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Approved
- Molecule type
- Small molecule
- First approval
- 2001
- Admin. routes
- oral
- Indications
- infection, pneumonia, Otitis media, maxillary sinusitis
via ChEMBL · EBI
Research
1,019 papers- Telithromycin.Drugs · 2004
- Telithromycin.Expert review of anti-infective therapy · 2004
- [Telithromycin].Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2004
- Telithromycin.Drugs · 2001
- Telithromycin.Annals of internal medicine · 2006
via PubMed
Wikidata facts
- Subclass of
- ketolides
- Mass
- 811.473
- Has use
- medication
Show 8 more facts
- chemical formula
- C₄₃H₆₅N₅O₁₀
- canonical SMILES
- CCC1C2(C(C(C(=O)C(CC(C(C(C(=O)C(C(=O)O1)C)C)OC3C(C(CC(O3)C)N(C)C)O)(C)OC)C)C)N(C(=O)O2)CCCCN4C=C(N=C4)C5=CN=CC=C5)C
- isomeric SMILES
- CC[C@@H]1[C@@]2([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H](C(=O)[C@H](C(=O)O1)C)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)OC)C)C)N(C(=O)O2)CCCCN4C=C(N=C4)C5=CN=CC=C5)C
- defined daily dose
- 0.8
- subject has role
- antibiotic
- native label
- Telithromycinum
- Commons category
- Telithromycin
- legal status (medicine)
- boxed warning
Sources (8)
via Wikidata · CC0