기본 정보
- 표준 SMILES
NN=C(N)N- InChIKey
HAMNKKUPIHEESI-UHFFFAOYSA-N- 분자식
- CH6N4
- 평균 분자량
- 74.09 g/mol
- 단동위원소 질량
- 74.05924619
개요
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.
이름 및 식별자
- 우선 이름
- Aminoguanidine
- IUPAC
- 2-aminoguanidine
- 현지명
- 피마게딘
- 영어명
- Aminoguanidine
- 분자식
- CH6N4
- 분자량
- 74.09
이름 및 동의어
aminoguanidinePimagedineHydrazinecarboximidamide79-17-4Guanyl hydrazineMonoaminoguanidineAminate baseImino semicarbazide1-aminoguanidinepimagedinaSCQ4EZQ113DTXSID5040964
이름 더 보기
피마게딘Aids030897Aids-030897N-AminoguanidineAminoguanidine (ag)Ribavirin Impurity S
CHEBI:40618pimagedinumRefChem:112042DTXCID3020964201-183-12-aminoguanidinePimagedine [INN]GUANIDINE, AMINO-
데이터베이스 식별자
- CAS
79-17-4- PubChem CID
- 2146
- DTXSID
DTXSID5040964- ChEMBL
CHEMBL225304- ChEBI
CHEBI:40618- UNII
- SCQ4EZQ113
- EC Number
- 201-183-1
- Nikkaji
- J5.508E
물성
구조 계산 물성
- XLogP
- -1.5
- 극성 표면적
- 90.4 Ų
- 수소 결합 공여자 수
- 3
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 0
- 무거운 원자 수
- 5
- 형식 전하
- 0
- 복잡도
- 41.6
실험 및 물리화학적 성질
DrugsPharmaceuticals -> Listed in ZINC15
물리화학적 성질
- 녹는점
- 182 · 182-185 °C (decomp)
- 끓는 점
- 159.5 · 159.5±23.0 °C(Predicted)
- 밀도
- 1.72 · 1.72±0.1 g/cm3(Predicted)
- 굴절률
- 1.666 · 1.6660 (estimate)
- 산도 계수 (pKa)
- 11.08 · 11.08±0.70(Predicted)
화학 및 산업
약리 정보
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.
응용 분야
용도Inhibitor (advanced glycosylation end-product formation).
상·하류 제품 정보
상류 원료
하류 제품
공급사22 곳
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추가 설명
정의ChEBI: 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.
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