Amoxicillin
Amoxicillin
| Yaɣ sheli | penicillin, carboxylic acid  |
|---|---|
| Di bukaata | tima |
| Stereoisomer of | L-amoxicillin |
| Chemical formula | C₁₆H₁₉N₃O₅S |
| Canonical SMILES | CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)N)C(=O)O)C |
| Isomeric SMILES | CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)C(=O)O)C |
| Active ingredient in | Amoxil, Moxatag |
| Found in taxon | Arundo donax, Guignardia |
| Route of administration | oral administration, intravenous infusion and defusion |
| Pregnancy category | Australian pregnancy category A, US pregnancy category B |
| LiverTox likelihood score | LiverTox toxicity likelihood category B |
| Bachikpani mali tuma | enzyme inhibitor, antibiotic, WHO essential medicines, bactericide |
| WHO Aware Classification | access |
Amoxicillin nyɛla tupaya balishɛli bɛ ni mali n-tibiri "bacteria" binnɛma dɔriti.[1] Ka dɔriti ŋɔ shɛŋa n nyɛ tibili puuni doro bee lɔŋni doro bee "pneumonia" bee ningbuŋ gbaŋ doro bee dulim doro ni din pahi[2][1] Di nyɛla din vaani nɔli ni bee n-chibiri n-niŋdi ʒisɔya ni, amaa ŋa bɛ yɔli.[1][3]
Kundivihira
[mali niŋ | mali mi di yibu sheena n-niŋ]- 1 2 3 Amoxicillin. The American Society of Health-System Pharmacists. Archived 5 Silimin gɔli September 2015 at the Wayback Machine
- ↑ Ritter, James M.; Flower, Rod; Henderson, Graeme; Loke, Yoon Kong; Robinson, Emma; Fullerton, James (2024). "52. Antibacterial drugs". Rang & Dale's Pharmacology (in English) (10th ed.). Elsevier. p. 707. ISBN 978-0-7020-7448-6. Archived from the original on 2024-02-10. Retrieved 2024-01-30.
- ↑ Amoxicillin Sodium for Injection (10 February 2016). Archived 27 Silimin gɔli October 2016 at the Wayback Machine