Natrium-[2S-(2α,5α,6β)]-6-[(1,3-dioxo-3-phenoxy-2-phenylpropyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylat
Carbenicillin Phenyl Sodium
Grundinformationen
- CAS
21649-57-0- Standard-SMILES
CC1(C)S[C@@H]2[C@H](NC(=O)C(C(=O)Oc3ccccc3)c3ccccc3)C(=O)N2[C@H]1C(=O)[O-].[Na+]- InChIKey
JXSBZDNBNJTHBJ-JPZUGYNPSA-M- Summenformel
- C23H21N2NaO6S
- Durchschnittliche Molmasse
- 476,5 g/mol
- Monoisotopische Masse
- 476,10180185
Überblick
Carfecillin sodium is an organic sodium salt. It contains a carfecillin(1-).
Namen und Bezeichner
- Bevorzugter Name
- Carbenicillin Phenyl Sodium
- IUPAC
- sodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(3-oxo-3-phenoxy-2-phenylpropanoyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- Lokaler Name
- Natrium-[2S-(2α,5α,6β)]-6-[(1,3-dioxo-3-phenoxy-2-phenylpropyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-2-carboxylat
- Englischer Name
- sodium [2S-(2alpha,5alpha,6beta)]-6-[(1,3-dioxo-3-phenoxy-2-phenylpropyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- Summenformel
- C23H22N2O6S.Na
- Molmasse
- 477.49
Namen und Synonyme
Carfecillin sodiumCarbenicillin phenyl sodiumcarfecilina sodicaUticillinBRL-347518N5JP36GYCHEBI:34612DTXSID401760364-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 6-((1,3-dioxo-3-phenoxy-2-phenylpropyl)amino)-3,3-dimethyl-7-oxo-, monosodium salt, (2S-(2alpha,5alpha,6beta))RefChem:123511DTXCID3098527244-496-9
Weitere Namen anzeigen
CARFECILLINSODIUMSALT(6R)-6-(2-Phenoxycarbonyl-2-phenylacetylamino)penicillanic acid sodium saltN-[(2S,5R,6R)-2-Sodiooxycarbonyl-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptan-6-yl]-2-phenylmalonamidic acid phenyl estersodium [2S-(2alpha,5alpha,6beta)]-6-[(1,3-dioxo-3-phenoxy-2-phenylpropyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
21649-57-0Carfecillin SodiumCarfecillin (Sodium)Carfecillin Sodium [JAN]Carbenicillin Phenyl Sodium [USAN]Carfecillin Sodium (JAN)sodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(3-oxo-3-phenoxy-2-phenylpropanamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylateCarbenicillin phenyl sodium (USAN)
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 141 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 7
- Frei drehbare Bindungen
- 7
- Schwere Atome
- 33
- Formalladung
- 0
- Komplexität
- 781
Physikochemische Eigenschaften
- storage temp.
- Sealed in dry,Room Temperature
- Löslichkeit
- 0 · DMSO:0.0(Max Conc. mg/mL);0.0(Max Conc. mM)
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Substances capable of killing agents causing urinary tract infections or of preventing them from spreading.
Substances that inhibit the growth or reproduction of BACTERIA.
Anwendungen
BeschreibungCarbenicillin phenyl was synthesized by Beecham Research Laboratories in 1966 as an orally active carbenicillin. It is hydrolyzed to carbenicillin by intestinal esterase and thus acts the same when administered orally. The phenol produced by the hydrolysis is conjugated and excreted in urine.
VerwendenAntibacterial.
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