Misplaced Pages

Piromidic acid

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Chemical compound Pharmaceutical compound
Piromidic acid
Clinical data
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
IUPAC name
  • 8-Ethyl-5-oxo-2-pyrrolidin-1-yl-5,8-dihydropyridopyrimidine-6-carboxylic acid
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard (EPA)
ECHA InfoCard100.039.223 Edit this at Wikidata
Chemical and physical data
FormulaC14H16N4O3
Molar mass288.307 g·mol
3D model (JSmol)
SMILES
  • CCN1C=C(C(=O)C2=CN=C(N=C21)N3CCCC3)C(=O)O
InChI
  • InChI=1S/C14H16N4O3/c1-2-17-8-10(13(20)21)11(19)9-7-15-14(16-12(9)17)18-5-3-4-6-18/h7-8H,2-6H2,1H3,(H,20,21)
  • Key:RCIMBBZXSXFZBV-UHFFFAOYSA-N

Piromidic acid is a quinolone antibiotic.

References

  1. Minami S, Shono T, Matsumoto JI (1971). "Pyrido pyrimidine Antibacterial Agents. II. Piromidic Acid and Related Compounds". Chemical and Pharmaceutical Bulletin. 19 (7): 1426–1432. doi:10.1248/cpb.19.1426.
Antibacterials that inhibit nucleic acid (J01E, J01M)
Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/or DNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins


Stub icon

This systemic antibiotic-related article is a stub. You can help Misplaced Pages by expanding it.

Categories:
Piromidic acid Add topic