Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C25H30N4O9S2
- Molecular weight
- 594.7 g/mol
- IUPAC name
- [(2S,5R)-3,3-dimethyl-4,4,7-trioxo-4lambda6-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl]oxymethyl (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- SMILES
- CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)OCOC(=O)[C@H]4C(S(=O)(=O)[C@H]5N4C(=O)C5)(C)C)C
- InChIKey
- OPYGFNJSCUDTBT-PMLPCWDUSA-N
- XLogP
- 0.7
- Polar surface area
- 216 Ų
- H-bond donors
- 2
- H-bond acceptors
- 11
- Formal charge
- 0
via PubChem
Research
659 papers- Sultamicillin. A review of its antibacterial activity, pharmacokinetic properties and therapeutic use.Drugs · 1989
- The pharmacokinetics of sultamicillin.APMIS. Supplementum · 1989
- Worldwide clinical experience with sultamicillin.APMIS. Supplementum · 1989
- Use of ampicillin/sulbactam and sultamicillin in pediatric infections: a re-evaluation.The Journal of international medical research · 2001
- Role of sultamicillin and ampicillin/sulbactam in the treatment of upper and lower bacterial respiratory tract infections.International journal of antimicrobial agents · 2001
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 594.145421
Show 5 more facts
- isomeric SMILES
- CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)OCOC(=O)[C@H]4C(S(=O)(=O)[C@H]5N4C(=O)C5)(C)C)C
- chemical formula
- C₂₅H₃₀N₄O₉S₂
- canonical SMILES
- CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)OCOC(=O)C4C(S(=O)(=O)C5N4C(=O)C5)(C)C)C
- subject has role
- antibiotic
- Commons category
- Sultamicillin
Sources (2)
via Wikidata · CC0
Gallery (2)
Available in 10 languages
via Wikidata sitelinks · CC0