Structure via PubChem · Public domain (PubChem)
roxithromycin
Sign in to saveAlso known as RU-965, RU-28965, Rulide, (9e)-Erythromycin 9-(O-((2-methoxyethoxy)methyl)oxime), Roxithromycinum, Roxitromicina, Roxithromycine
chemische verbinding
In the Vinony graph
Vinony's link graph records 441 inbound references to roxithromycin, and connects out to valproic acid, phagocyte and neomycin.
It is catalogued under topics including Dimethylamino compounds, Drugboxes which contain changes to watched fields and Drugs with non-standard legal status.
Vinony links it to 27 Wikipedia language editions.
Chemical data
- Formula
- C41H76N2O15
- Molecular weight
- 837 g/mol
- IUPAC name
- (3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-(2-methoxyethoxymethoxyimino)-3,5,7,9,11,13-hexamethyl-oxacyclotetradecan-2-one
- SMILES
- CC[C@@H]1[C@@]([C@@H]([C@H](/C(=N/OCOCCOC)/[C@@H](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2C[C@@]([C@H]([C@@H](O2)C)O)(C)OC)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)C)C)O)(C)O
- InChIKey
- RXZBMPWDPOLZGW-XMRMVWPWSA-N
- XLogP
- 3.1
- Polar surface area
- 217 Ų
- H-bond donors
- 5
- H-bond acceptors
- 17
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 3
- Molecule type
- Small molecule
- Indications
- bacterial disease
via ChEMBL · EBI
Research
1,773 papers- Roxithromycin-Associated Acute Thrombocytopenia.The American journal of case reports · 2021
- Roxithromycin: review of its antimicrobial activity.The Journal of antimicrobial chemotherapy · 1998
- Roxithromycin.Notes from the underground (New York, N.Y.) · 1995
- Roxithromycin. An update of its antimicrobial activity, pharmacokinetic properties and therapeutic use.Drugs · 1994
- [Roxithromycin (Forilin, Surlid)].Ugeskrift for laeger · 1990
via PubMed
Wikidata facts
- Mass
- 836.525
- Has use
- medication
Show 7 more facts
- subject has role
- antibiotic
- defined daily dose
- 0.3
- chemical formula
- C₄₁H₇₆N₂O₁₅
- route of administration
- oral administration
- isomeric SMILES
- CC[C@@H]1[C@@]([C@@H]([C@H](/C(=N/OCOCCOC)/[C@@H](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2C[C@@]([C@H]([C@@H](O2)C)O)(C)OC)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)C)C)O)(C)O
- canonical SMILES
- CCC1C(C(C(C(=NOCOCCOC)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O
- Commons category
- Roxithromycin
via Wikidata · CC0
Connections
valproic acid
Entity
phagocyte
Entity
neomycin
Entity
(RS)-baclofen
Entity
voltage-gated sodium channel
Entity
conotoxin
Entity
voltage-gated calcium channel complex
Entity
cromakalim
Entity
tiapamil
Entity
bacteria
Entity
magnesium
Entity
International Standard Book Number
Entity
barium
Entity
antibiotic
Entity
Mentha
Entity
cocaine
Entity
aspirin
Entity
chemical formula
Entity
ribosome
Entity
blood plasma
Entity