Pipemidic acid

CAS : 51940-44-4

Ref. 3D-FP52512

Informations sur le produit

• Nom: Pipemidic acid
• Synonymes: 8-Ethyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)pyrido(2,3-d)pyrimidine-6-carboxylic acid, 1489Rb, 8-Ethyl-2-(piperazin-1-yl)-5-oxo-5,8-dihydropyrido[2,3-d]pyrimidine-6-carboxylic acid, 8-Ethyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)pyrido[2,3-d]pyrimidine-6-carboxylic acid, 8-Ethyl-5-Oxo-2-(Piperazin-1-Yl)-5,8-Dihydropyrido[2,3-D]Pyrimidine-6-Carboxylic Acid, Deblaston, Dolcol, Filtrax, Memento 400, Palin, Pi-Coli, Pipeacid, Pipedac, Pipemid, Pipemidic Acid Anhydrous, Pipurin, Pyrido[2,3-d]pyrimidine-6-carboxylic acid, 8-ethyl-5,8-dihydro-5-oxo-2-(1-piperazinyl)-, Tractur, Uromidin, Uropimid, Urosten, Uroval

Description

Pipemidic acid is an experimental drug that inhibits bacterial growth by binding to the gyrase enzyme. It has been shown to be effective against a wide range of Gram-positive and Gram-negative bacteria, as well as fungi and protozoa. Pipemidic acid has low toxicity in animal studies, but has not yet been tested in humans. Pipemidic acid is also an inhibitor molecule for other antimicrobial agents. The electrochemical impedance spectroscopy (EIS) method can be used to detect the presence of pipemidic acid in wastewater samples, which can help with wastewater treatment processes. Pipemidic acid may have potential use as a new analytical method for the detection of drugs or other molecules, since it can be detected using a matrix effect or chemiluminescence method. Pipemidic acid belongs to the coordination geometry class and its structure consists of two fused six-membered rings with carboxyl groups at each end. This drug

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 303.32 g/mol
• Formule: C₁₄H₁₇N₅O₃
• Degré de pureté: (%) Min. 98%
• Couleur/Forme: Off-White To Light (Or Pale) Yellow Solid
• InChI: InChI=1S/C14H17N5O3/c1-2-18-8-10(13(21)22)11(20)9-7-16-14(17-12(9)18)19-5-3-15-4-6-19/h7-8,15H,2-6H2,1H3,(H,21,22)
• Code InChI: InChIKey=JOHZPMXAZQZXHR-UHFFFAOYSA-N
• SMILES: CCn1cc(C(=O)O)c(=O)c2cnc(N3CCNCC3)nc21