Structured Summary
Abstract
Antibiotic macrolide produced by Streptomyces antibioticus.
Chemical Identity
Chemical Information
- Molecular Formula
- C35H61NO12
- Molecular Weight
- 687.9 g/mol
- CAS Registry No.
- 3922-90-5
- IUPAC Name
- (3R,5S,6S,7R,8S,9R,12R,13R,14S,15R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-hydroxy-8-[(2R,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,7,9,12,13,15-hexamethyl-1,11-dioxaspiro[2.13]hexadecane-10,16-dione
- InChIKey
- RZPAKFUAFGMUPI-QESOVKLGSA-N
- SMILES
- C[C@@H]1C[C@@H]([C@H]([C@@H](O1)O[C@H]2[C@H](C[C@@]3(CO3)C(=O)[C@@H]([C@H]([C@H]([C@H](OC(=O)[C@@H]([C@H]([C@@H]2C)O[C@H]4C[C@@H]([C@H]([C@@H](O4)C)O)OC)C)C)C)O)C)C)O)N(C)C
- MeSH Unique ID
- D009827
- Source
- PubChem CID 72493
MeSH Record
Classification
Broader headings
Narrower headings
Related Concepts
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Drug Class
Pharmacological Action
MeSH Record
Synonyms
2 entry terms
- Oleandomycin Phosphate
- Phosphate, Oleandomycin
MeSH Record
Aspects Covered
26 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analogs & derivatives, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, economics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, urine.
MeSH Hierarchy
Tree Number
AMA Style
References
- National Library of Medicine. Oleandomycin. Medical Subject Headings (MeSH). 2026. Unique ID D009827. http://id.nlm.nih.gov/mesh/2026/D009827
- Oleandomycin. In: Wikipedia. https://en.wikipedia.org/wiki/Oleandomycin
- Oleandomycin. In: Wikidata. https://www.wikidata.org/wiki/Q1076248
- Oleandomycin. In: PubChem Compound. CID 72493. https://pubchem.ncbi.nlm.nih.gov/compound/72493