Basic information
- Standard SMILES
NN=C(N)N- InChIKey
HAMNKKUPIHEESI-UHFFFAOYSA-N- Molecular formula
- CH6N4
- Average molar mass
- 74.09 g/mol
- Monoisotopic mass
- 74.05924619
Overview
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.
Names & identifiers
- Preferred name
- Aminoguanidine
- IUPAC
- 2-aminoguanidine
- English name
- Aminoguanidine
- Molecular formula
- CH6N4
- Molecular weight
- 74.09
Names & synonyms
aminoguanidinePimagedineHydrazinecarboximidamide79-17-4Guanyl hydrazineMonoaminoguanidineAminate baseImino semicarbazide1-aminoguanidinepimagedinaSCQ4EZQ113DTXSID5040964
Show more names
Aids030897Aids-030897N-AminoguanidineAminoguanidine (ag)Ribavirin Impurity S
CHEBI:40618pimagedinumRefChem:112042DTXCID3020964201-183-12-aminoguanidinePimagedine [INN]GUANIDINE, AMINO-
Database identifiers
- CAS
79-17-4- PubChem CID
- 2146
- DTXSID
DTXSID5040964- ChEMBL
CHEMBL225304- ChEBI
CHEBI:40618- UNII
- SCQ4EZQ113
- EC Number
- 201-183-1
- Nikkaji
- J5.508E
Properties
Computed structural properties
- XLogP
- -1.5
- Topological polar surface area
- 90.4 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 0
- Heavy atoms
- 5
- Formal charge
- 0
- Complexity
- 41.6
Experimental & physicochemical properties
DrugsPharmaceuticals -> Listed in ZINC15
Physicochemical properties
- Melting point
- 182 · 182-185 °C (decomp)
- Boiling point
- 159.5 · 159.5±23.0 °C(Predicted)
- Density
- 1.72 · 1.72±0.1 g/cm3(Predicted)
- refractive index
- 1.666 · 1.6660 (estimate)
- pka
- 11.08 · 11.08±0.70(Predicted)
- FDA UNII
- 4 EZQ113 · SCQ4EZQ113
Chemistry & industry
Pharmacology
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.
Applications
UsesInhibitor (advanced glycosylation end-product formation).
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers22 total
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]
Additional notes
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.
Related reactions
5 records
Linked notes
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