Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Within Vinony's link graph, Propicillin is referenced by 186 other articles, and connects out to antibiotic, ceftolozane/tazobactam and International Standard Book Number.
Vinony files it under Chemical pages without DrugBank identifier, Drugboxes which contain changes to verified fields and Drugboxes which contain changes to watched fields.
Its subject is documented across 10 Wikipedia language editions.
Chemical data
- Formula
- C18H22N2O5S
- Molecular weight
- 378.4 g/mol
- IUPAC name
- (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenoxybutanoylamino)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
68 papers- [Propicillin-Baycillin].Arzneimittel-Forschung · 1962
- Pharmacokinetics in the elderly.Clinical pharmacokinetics · 1976
- Propicillin in general practice.The Practitioner · 1962
- Effects of propicillin on mixed continuous cultures of periodontal bacteria.Antimicrobial agents and chemotherapy · 1991
- [Propicillin in dental practice].Zahnarztliche Praxis · 1987
via PubMed
Wikidata facts
- Subclass of
- penicillin
- Mass
- 378.124943
Show 5 more facts
- chemical formula
- C₁₈H₂₂N₂O₅S
- canonical SMILES
- CCC(C(=O)NC1C2N(C1=O)C(C(S2)(C)C)C(=O)O)OC3=CC=CC=C3
- subject has role
- antibiotic
- isomeric SMILES
- CCC(C(=O)N[C@H]1[C@@H]2N(C1=O)[C@H](C(S2)(C)C)C(=O)O)OC3=CC=CC=C3
- Commons category
- Propicillin
Sources (2)
via Wikidata · CC0
Article · Deutsch
Propicillin ist eine organisch-chemische Verbindung der Gruppe der β-Lactam-Antibiotika, genauer der semisynthetischen β-Lactam-Antibiotika. Es zählt zu den Penicillin-Derivaten und wird in Form des Monokaliumsalzes eingesetzt. Patentiert wurde es 1961 von Beecham (jetzt GlaxoSmithKline). Es ist ähnlich wie Benzylpenicillin (Penicillin G) gegen einige Gram-positive Bakterien wirksam.
Abstract from DBpedia / Wikipedia · CC BY-SA