2-アミノグアニジン

Aminoguanidine

HCID 2146CAS 79-17-4

基本情報

標準SMILES
NN=C(N)N
InChIKey
HAMNKKUPIHEESI-UHFFFAOYSA-N
分子式
CH6N4
平均分子量
74.09 g/mol
単同位体質量
74.05924619

概要

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.

名称と識別子

優先名称
Aminoguanidine
IUPAC
2-aminoguanidine
現地名
2-アミノグアニジン
英語名
Aminoguanidine
分子式
CH6N4
分子量
74.09

名称と別名

aminoguanidinePimagedineHydrazinecarboximidamide79-17-4Guanyl hydrazineMonoaminoguanidineAminate baseImino semicarbazide1-aminoguanidinepimagedinaSCQ4EZQ113DTXSID5040964
名称をさらに表示
アミナート塩基アミジノヒドラジンピマゲジンヒドラジンカルボイミドアミドアミノ(イミノ)メチルヒドラジンN-アミノグアニジン1-アミノグアニジンアミノグアニジン2-アミノグアニジンAids030897Aids-030897N-AminoguanidineAminoguanidine (ag)Ribavirin Impurity S
CHEBI:40618pimagedinumRefChem:112042DTXCID3020964201-183-12-aminoguanidinePimagedine [INN]GUANIDINE, AMINO-

データベース識別子

CAS
79-17-4
PubChem CID
2146
DTXSID
DTXSID5040964
ChEMBL
CHEMBL225304
ChEBI
CHEBI:40618
UNII
SCQ4EZQ113
EC Number
201-183-1
Nikkaji
J5.508E

物性

構造計算による物性

XLogP
-1.5
極性表面積
90.4 Ų
水素結合供与体数
3
水素結合受容体数
2
回転可能結合数
0
重原子数
5

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15

物理化学的性質

融点
182 · 182-185 °C (decomp)
沸点
159.5 · 159.5±23.0 °C(Predicted)
比重(密度)
1.72 · 1.72±0.1 g/cm3(Predicted)
屈折率
1.666 · 1.6660 (estimate)
酸解離定数(Pka)
11.08 · 11.08±0.70(Predicted)

化学と産業

薬理情報

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.

応用分野

使用Inhibitor (advanced glycosylation end-product formation).

サプライヤー22 社

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補足説明 · 1 件

定義ChEBI: 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.

関連反応

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関連ノート

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