| Weight | 388.486 g/mol |
|---|---|
| Formula | C16H17KN2O5S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
Penicillin V potassium salt (132-98-9)
Penicillin V · Penicillin V Potassium · Phenoxymethyl Penicillin
Score:
#175 in Microbiology
,
#645 in Biochemistry
,
#1830 in Biology
,
#2188 in Chemistry
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- Penicillin V for Group A Streptococcal Pharyngotonsillitis: A Randomized Trial of Seven vs Ten Days' Therapy (JAMA, 1981)
- The Total Synthesis of Penicillin V (Journal of the American Chemical Society, 1957)
- Randomised, double blind, placebo controlled trial of penicillin V and amoxycillin in treatment of acute sinus infections in adults. (BMJ, 1996)
- Unexplained Reduced Microbiological Efficacy of Intramuscular Benzathine Penicillin G and of Oral Penicillin V in Eradication of Group A Streptococci From Children With Acute Pharyngitis (Pediatrics, 2001)
- Folate-targeted enzyme prodrug cancer therapy utilizing penicillin-V amidase and a doxorubicin prodrug. (Journal of Drug Targeting, 1999)
- Five vs Ten Days of Penicillin V Therapy for Streptococcal Pharyngitis (JAMA Pediatrics, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Penicillin V
- Penicillin V Potassium
- Phenoxymethyl Penicillin
- Penicillin VK
- Phenoxymethylpenicillin
- Betapen
- Pen VK
- Penicillin Berromycin
- Beromycin
- V Cillin K
- Penicillin V Sodium
- Vegacillin
- VCillin K
- Apocillin
- V-Cillin K
- Fenoxymethylpenicillin
- Penicillin Beromycin
-
SMILESCC1(C(N2C(S1)C(C2=O)NC(=O)COC3=CC=CC=C3)C(=O)[O-])C.[K+]
-
InChIKeyHCTVWSOKIJULET-UHFFFAOYSA-M
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Synthesis
Phenoxyacetyl 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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Penicillin V potassium salt
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