| Weight | 372.487 g/mol |
|---|---|
| Formula | C16H17KN2O4S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Penicillin G potassium (113-98-4, 1406-05-9)
Penicillin G · Benzylpenicillin · Penicillin G Sodium
Score:
#352 in Microbiology
,
#2853 in Biology
,
#3571 in Chemistry
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- Sigma-Aldrich - Penicillin G potassium15.40 - 338.10 USD
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- TCI - Penicillin G potassium32.00 USD
- Studies on the distribution and fate of S35-labelled benzylpenicillin in the body. (Acta Radiologica, 1954)
- Biodegradability of Cefotiam, Ciprofloxacin, Meropenem, Penicillin G, and Sulfamethoxazole and Inhibition of Waste Water Bacteria (Archives of Environmental Contamination and Toxicology, 1999)
- STUDIES ON THE MECHANISM OF THE FORMATION OF THE PENICILLIN ANTIGEN III. THE N-(D--BENZYLPENICILLOYL) GROUP AS AN ANTIGENIC DETERMINANT RESPONSIBLE FOR HYPERSENSITIVITY TO PENICILLIN G (Journal of Experimental Medicine, 1961)
- Single-Dose Azithromycin versus Penicillin G Benzathine for the Treatment of Early Syphilis (The New England Journal of Medicine, 2005)
- Evaluation of penicillin hypersensitivity: Value of clinical history and skin testing with penicilloyl-polylysine and penicillin G: A cooperative prospective study of the penicillin study group of the American Academy of Allergy (The Journal of Allergy and Clinical Immunology, 1977)
- Transmissible resistance to penicillin G, neomycin, and chloramphenicol in Rhizobium japonicum. (Antimicrobial Agents and Chemotherapy, 1973)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Penicillin G
- Benzylpenicillin
- Penicillin G Sodium
- Sodium Penicillin
- Pfizerpen
- Crystapen
- Benzylpenicillin Potassium
- Sodium Benzylpenicillin
- Sodiopen
- Or-pen
- Penilevel
- Coliriocilina
- Sodipen
- Penicillin Grnenthal
- Penibiot
- Penicillin G Jenapharm
- Penicilina G Llorente
- Ursopen
- Van-Pen-G
- Peniroger
- Parcillin
- Benpen
- Pengesod
- Pekamin
- Unicilina
-
SMILESCC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[K+]
-
InChIKeyIYNDLOXRXUOGIU-UHFFFAOYSA-M
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Most-cited Publications
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Alternate Names
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Synthesis
PHENYLACETYL CHLORIDE
+
(2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
(Schotten-Baumann amide from acid)
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