loading...| Preferred Name | piperazine | |
| Synonyms |
C4H10N2 piperazine |
|
| ID |
http://purl.obolibrary.org/obo/dinto_DB00592 |
|
| activates | ||
| AHFScode |
92:02.00* 08:08.00 |
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| ATCCode |
R03DA09 P02CB01 |
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| binds | ||
| CASRN |
110-85-0 |
|
| DBBrand |
pipersol multifuge asca-trol no. 3 tensofin tasnon lumbrical vermizine moditen antepar pacinol dispermine permitil omca upixon worm-away worm-a-ton dapotum uvilon anatensol wurmirazin vermidol vermex piperazidine eraverm antiren |
|
| DBSynonym |
piperazin piperazin [germany] diethyleneimine piperazine hexahydrate hexahydropyrazine diethylenediamine piperazine hydrate fluphenazine dihydrochloride |
|
| Definition |
Piperazine is an organic compound that consists of a six-membered ring containing two opposing nitrogen atoms. Piperazine exists as small alkaline deliquescent crystals with a saline taste. Piperazine was introduced to medicine as a solvent for uric acid. When taken into the body the drug is partly oxidized and partly eliminated unchanged. 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. A large number of piperazine compounds have anthelmintic action. Their mode of action is generally by paralysing parasites, which allows the host body to easily remove or expel the invading organism. |
|
| has pharmacological target | ||
| InChI |
InChI=1S/C4H10N2/c1-2-6-4-3-5-1/h5-6H,1-4H2 |
|
| InChIKey |
InChIKey=GLUUGHFHXGJENI-UHFFFAOYSA-N |
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| is metabolised by | ||
| is substrate of | ||
| label |
piperazine |
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| modulates | ||
| prefixIRI |
obo2:dinto_DB00592 |
|
| prefLabel |
piperazine |
|
| SMILES |
C1CNCCN1 |
|
| Synonym |
C4H10N2 piperazine |
|
| xref |
Wikipedia:http://en.wikipedia.org/wiki/Piperazine PubChem Substance:46507642 PubChem Compound:4837 PharmGKB:PA450977 Drugs Product Database (DPD):97128 ChEBI:28568 PDB:169 ChemSpider:13835459 |
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| subClassOf |