Penicillin G Potassium
Grundinformationen
- CAS
113-98-4- Standard-SMILES
CC1(C)S[C@@H]2[C@H](NC(=O)Cc3ccccc3)C(=O)N2[C@H]1C(=O)[O-].[K+]- InChIKey
IYNDLOXRXUOGIU-LQDWTQKMSA-M- Summenformel
- C16H17KN2O4S
- Durchschnittliche Molmasse
- 372,5 g/mol
- Monoisotopische Masse
- 372,0546097
Überblick
Benzylpenicillin potassium is organic potassium salt of benzylpenicillin. It contains a benzylpenicillin(1-).
Namen und Bezeichner
- Bevorzugter Name
- Penicillin G Potassium
- IUPAC
- potassium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
- Englischer Name
- Penicillin G potassium salt
- Summenformel
- C16H17KN2O4S
- Molmasse
- 373.49
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
113-98-4- PubChem CID
- 23664709
- DTXSID
DTXSID7045106- ChEMBL
CHEMBL1223- ChEBI
CHEBI:7963- UNII
- VL775ZTH4C
- EC Number
- 204-038-0
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 115 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 4
- Schwere Atome
- 24
- Formalladung
- 0
- Komplexität
- 536
Experimentelle und physikochemische Eigenschaften
Human Drugs
FDA approved drugs -> Active ingredient
FDA approved drugs -> Active ingredient
Physikochemische Eigenschaften
- Schmelzpunkt
- 214 · 214-217 C
- Brechungsindex
- 294 ° · 294 ° (C=1, H2O)
- storage temp.
- -20 °C · Sealed in dry,Store in freezer, under -20°C
- Löslichkeit
- 2 O: · H2O: 100 mg/mL
- Aggregatzustand
- powder
- Farbe
- Needles from butanol (aq)
- PH
- pH (10g/L, 25℃) : 5.0~7.5
- Wasserlöslichkeit
- Soluble in water (100 mg/ml), methanol, ethanol (sparingly), and alcohol. Insoluble in chloroform.
- Merck
- 14 · 14,7094
- BRN
- 3832841 · 3832841
- Stabilität
- Hygroscopic
- InChIKey
- IYNDLOXRXUOGIU-LQDWTQKMSA-M
- SMILES
- N12C([C@@H](NC(=O)CC3=CC=CC=C3)[C@@]1([H])SC(C)(C)[C@@H]2C([O-])=O)=O.[K+] |&1:2,13,19,r|
- EPA chemische Informationen
- Penicillin G Potassium (113-98-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H315 (16.2%): Causes skin irritation [Warning Skin corrosion/irritation]
P233, P260, P261, P264, P264+P265, P271, P272, P280, P284, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P333+P317, P337+P317, P342+P316, P362+P364, P403, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 80 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Status: Active Update: 30-05-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/22421
Penicillin g potassium: Does not have an individual approval but may be used under an appropriate group standard
Sicherheitsdaten
- F
- 10-23
- wgk
- 2
- tsca
- TSCA listed
- hs_code
- 29411000
- RTECS-Nr.
- XH9700000
- risk_code
- 42/43-34-11
- Toxizität
- LD50 oral in rabbit: 5848mg/kg
- hazard_code
- Xn,C,F
- safety_code
- 36/37-45-36/37/39-26-16-60-37-24-22
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Skin Sens. 1
Chemie und Industrie
Pharmakologische Informationen
FDA Pharmacological Classification
BUFFERED PENICILLIN G POTASSIUM
Penicillin-class Antibacterial [EPC]; Penicillins [CS]
PENICILLIN G POTASSIUM
Penicillins [CS]; Penicillin-class Antibacterial [EPC]
Verwendung und Herstellung
Anwendungen
VerwendenPenicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. Penicillin G potassium salt is used as a cell culture additive as an antibiotics. Use to inhibit the synthesis of bacterial cell walls by inhibition of the cell wall peptidoglycan chain cross-lining. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans.
Darstellung
synthetischePenicillin G potassium salt is a highly effective and low toxicity antibiotic, which is obtained by salt formation of Chlorpheniramine maleate and maleic acid.
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Ergänzende Hinweise
DefinitionChEBI: Penicillin G potassium salt is organic potassium salt of benzylpenicillin. It is an antibiotic substance produced by Penicillium sp. Antibacterial. It contains a benzylpenicillin(1-).
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