Aminoguanidin
Aminoguanidine
Grundinformationen
- CAS
79-17-4- Standard-SMILES
NN=C(N)N- InChIKey
HAMNKKUPIHEESI-UHFFFAOYSA-N- Summenformel
- CH6N4
- Durchschnittliche Molmasse
- 74,09 g/mol
- Monoisotopische Masse
- 74,05924619
Überblick
Aminoguanidine is a one-carbon compound whose unique structure renders it capable of acting as a derivative of hydrazine, guanidine or formamide. It has a role as an EC 1.4.3.4 (monoamine oxidase) inhibitor and an EC 1.14.13.39 (nitric oxide synthase) inhibitor. It is a member of guanidines and a one-carbon compound.
Namen und Bezeichner
- Bevorzugter Name
- Aminoguanidine
- IUPAC
- 2-aminoguanidine
- Lokaler Name
- Aminoguanidin
- Englischer Name
- Aminoguanidine
- Summenformel
- CH6N4
- Molmasse
- 74.09
Namen und Synonyme
aminoguanidinePimagedineHydrazinecarboximidamide79-17-4Guanyl hydrazineMonoaminoguanidineAminate baseImino semicarbazide1-aminoguanidinepimagedinaSCQ4EZQ113DTXSID5040964
Weitere Namen anzeigen
Aids030897Aids-030897N-AminoguanidineAminoguanidine (ag)Ribavirin Impurity S
CHEBI:40618pimagedinumRefChem:112042DTXCID3020964201-183-12-aminoguanidinePimagedine [INN]GUANIDINE, AMINO-
Datenbank-Bezeichner
- CAS
79-17-4- PubChem CID
- 2146
- DTXSID
DTXSID5040964- ChEMBL
CHEMBL225304- ChEBI
CHEBI:40618- UNII
- SCQ4EZQ113
- EC Number
- 201-183-1
- Nikkaji
- J5.508E
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -1,5
- Polarare Oberfläche (TPSA)
- 90,4 Ų
- H-Brücken-Donoren
- 3
- H-Brücken-Akzeptoren
- 2
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 5
- Formalladung
- 0
- Komplexität
- 41,6
Experimentelle und physikochemische Eigenschaften
DrugsPharmaceuticals -> Listed in ZINC15
Physikochemische Eigenschaften
- Schmelzpunkt
- 182 · 182-185 °C (decomp)
- Siedepunkt
- 159.5 · 159.5±23.0 °C(Predicted)
- Dichte
- 1.72 · 1.72±0.1 g/cm3(Predicted)
- Brechungsindex
- 1.666 · 1.6660 (estimate)
- pka
- 11.08 · 11.08±0.70(Predicted)
Chemie und Industrie
Pharmakologische Informationen
Mechanism of ActionPimagedine reportedly inhibits the formation of glycosylated proteins (advanced glycosylation end-products) and has other actions including inhibition of aldose reductase.
MeSH Pharmacological ClassificationCompounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.
Anwendungen
VerwendenInhibitor (advanced glycosylation end-product formation).
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Nachgelagerte Produkte
Ergänzende Hinweise
DefinitionChEBI: Aminoguanidine is a one-carbon compound whose unique structure renders it capable of acting as a derivative of hydrazine, guanidine or formamide. It has a role as an EC 1.4.3.4 (monoamine oxidase) inhibitor and an EC 1.14.13.39 (nitric oxide synthase) inhibitor. It is a member of guanidines and a one-carbon compound.
Zugehörige Reaktionen
5
Notizen zur Verbindung
Wird geladen…