Piperazine citrateProduct ingredient for Piperazine

Name
Piperazine citrate
Drug Entry
Piperazine

Piperazine is an organic compound that consists of a six-membered ring containing two opposing nitrogen atoms. First used as a solvent for uric acid, the use of piperazine as an anthelmintic agent was first introduced in 1953. Upon entry into the systemic circulation, the drug is partly oxidized and partly eliminated as an unchanged compound. Outside the body, piperazine has a remarkable power to dissolve uric acid and producing a soluble urate, but in clinical experience it has not proved equally successful. Piperazine was first introduced as an anthelmintic in 1953. Piperazine compounds mediate their anthelmintic action by generally paralyzing parasites, allowing the host body to easily remove or expel the invading organism.

Accession Number
DBSALT000775
Structure
Synonyms
Not Available
UNII
63KP7FXF2I
CAS Number
41372-10-5
Weight
Average: 278.2591
Monoisotopic: 278.11140094
Chemical Formula
C10H18N2O7
InChI Key
SWDXALWLRYIJHK-UHFFFAOYSA-N
InChI
InChI=1S/C6H8O7.C4H10N2/c7-3(8)1-6(13,5(11)12)2-4(9)10;1-2-6-4-3-5-1/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);5-6H,1-4H2
IUPAC Name
2-hydroxypropane-1,2,3-tricarboxylic acid; piperazine
SMILES
C1CNCCN1.OC(=O)CC(O)(CC(O)=O)C(O)=O
PubChem Compound
114763
ChemSpider
102744
ChEBI
774793
ChEMBL
CHEMBL1200842
Wikipedia
Piperazine
Predicted Properties
PropertyValueSource
Water Solubility106.0 mg/mLALOGPS
logP-1.3ALOGPS
logP-1.3Chemaxon
logS-0.26ALOGPS
pKa (Strongest Acidic)3.05Chemaxon
pKa (Strongest Basic)-4.2Chemaxon
Physiological Charge-3Chemaxon
Hydrogen Acceptor Count7Chemaxon
Hydrogen Donor Count4Chemaxon
Polar Surface Area132.13 Å2Chemaxon
Rotatable Bond Count5Chemaxon
Refractivity35.62 m3·mol-1Chemaxon
Polarizability15.5 Å3Chemaxon
Number of Rings1Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon