Grundinformationen
- 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
Anbieter22 Anbieter
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
武汉丰泰威远科技有限公司+86-27-8746-5837 +86-18627785180 · [email protected]
武汉丰泰威远科技有限公司027-87465837 19945049750 · [email protected]
上海遐瑞医药科技有限公司+86 21 61551611
深圳振强药物研发有限公司0755-66853366 13670046396 · [email protected]
PT CHEM GROUP LIMITED+86-85511178; +86-85511178 · [email protected]
湖北源梦生物科技有限公司027-68897569 18120462897 · [email protected]
南通全益生物科技有限公司0513-66337626 18051384581 · [email protected]
湖北源梦生物科技有限公司027-68897569 18120462897 · [email protected]
嘉兴市浙嘉生物科技有限公司0573-85609002 · [email protected]
Shaanxi Didu New Materials Co. Ltd+86-86-17392712779 +86-13289823923 · [email protected]
湖州浦瑞生物医药技术有限公司0572-2745768-1 13167223168;13167223168 · [email protected]
麻城市进鑫生物科技有限公司18271582018 · [email protected]
陕西缔都医药化工有限公司029-029-029-81148696 18161915376 · [email protected]
青岛浩海安杰医药科技有限公司156-6622-8711 18639325623 · [email protected]
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.+8618950047208 · [email protected]
湖州浦瑞生物医药技术有限公司+86-0572-2745768 +86-13816075732 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
天门恒昌化工有限公司027-59322316 15172518801 · [email protected]
Hefei TNJ Chemical Industry Co.,Ltd.+86-0551-65418671 +86-189 4982 3763 · [email protected]
AFINE CHEMICALS LIMITED+86-571-85134551 +86-18958018566 · [email protected]
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
Verknüpfte Notizen
Wird geladen…