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아데노신

아데노신
아데노신 구조식 이미지
카스 번호:
58-61-7
한글명:
아데노신
동의어(한글):
아데노신
상품명:
Adenosine
동의어(영문):
AR;Myocol;Adesine;Boniton;Adrekar;Adenocor;Adenosin;Sandesin;NSC 7652;ADENOSINE
CBNumber:
CB7304660
분자식:
C10H13N5O4
포뮬러 무게:
267.24
MOL 파일:
58-61-7.mol

아데노신 속성

녹는점
234-236 °C(lit.)
알파
D11 -61.7° (c = 0.706 in water); 9D -58.2° (c = 0.658 in water)
끓는 점
410.43°C (rough estimate)
밀도
1.3382 (rough estimate)
굴절률
1.7610 (estimate)
저장 조건
2-8°C
용해도
Slightly soluble in water, soluble in hot water, practically insoluble in ethanol (96 per cent) and in methylene chloride. It dissolves in dilute mineral acids.
물리적 상태
Crystalline Powder
산도 계수 (pKa)
3.6, 12.4(at 25℃)
색상
White
optical activity
[α]20/D 70±3°, c = 2% in 5% NaOH
수용성
Soluble in water, ammonium hydroxide and dimethyl sulfoxide. Insoluble in ethanol.
Merck
14,153
BRN
93029
안정성
Stable. Incompatible with strong oxidizing agents.
InChIKey
OIRDTQYFTABQOQ-KQYNXXCUSA-N
CAS 데이터베이스
58-61-7(CAS DataBase Reference)
NIST
adenosine(58-61-7)

안전

위험 카페고리 넘버 36/37/38
안전지침서 24/25-36/37/39-26
WGK 독일 2
RTECS 번호 AU7175000
F 고인화성물질 10-23
TSCA Yes
HS 번호 29389090

아데노신 MSDS


Adenosine

아데노신 C화학적 특성, 용도, 생산

존재

아데노신은 핵염기인 아데닌과 5탄당인 리보스가 β-N9-글리코사이드 결합으로 연결된 퓨린 뉴클레오사이드이다. 아데노신의 유도체는 자연계에서 널리 발견되며, 아데노신 삼인산(ATP)과 아데노신 이인산(ADP)이 관여하는 에너지 전달 과정 뿐만 아니라 고리형 아데노신 일인산(cAMP)이 관여하는 신호 전달 과정과 같은 생화학적 과정에서 중요한 역할을 한다. 아데노신 자체는 신경조절물질(neuromodulator)이며, 수면을 촉진시키고 각성을 억제하는 역할을 한다고 여겨진다. 아데노신은 또한 혈관 확장을 통해 다양한 기관으로의 혈류 조절에 역할을 한다.

물성

아데노신(영어: adenosine)은 많은 생명체에서 발견되는 화합물로 의약품으로 사용되는 물질이다. 의약품으로서 아데노신은 미주신경 자극법으로 개선되지 않는 특정 형태의 심실상빈맥을 치료하는데 사용된다.

용도

아데노신은 식품의약품 안전청 고시 기능성 주름개선 화장품 재료입니다.아데닌(Adenine)과 리보스(Robose) 성분이 결합한 화합물로 RNA나 많은 조효소의 구성성분으로 동물, 식물, 미생물 등 모든 생명체의 세포에 존재하는 아미노산 계열의 단백질 성분입니다. 그리고 피부세포의 재생을 촉진하거나 손상을 방지하며 피부노화를 방지하는데 도움을 줍니다.

화학적 성질

White or almost white, crystalline powder.

용도

antiarrhythmic, cardiac depressant

용도

Nucleotide.

용도

adenosine is an amino acid. Studies indicate anti-wrinkle and skinsmoothing capacities. Although little is written about its direct skin benefit, adenosine plays an important role in biochemical processes. As adenosine triphosphate (ATP) and adenosine diphosphate (ADP), it is involved in energy transfer, and as cyclic adenosine monophosphate (cAMP) in signal transduction.

정의

adenosine: A nucleoside comprisingone adenine molecule linked to ad-ribose sugar molecule. The phosphate-ester derivatives of adenosine,AMP, ADP, and ATP, are of fundamentalbiological importance as carriersof chemical energy.

정의

ChEBI: A ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a beta1N9-glycosidic bond.

상표명

Adenocard (Astellas); Adenoscan (Astellas).

생물학적 활성

Neurotransmitter that acts as the preferred endogenous agonist at all adenosine receptor subtypes.

Clinical Use

Adenosine (Adenocard) is an endogenous nucleoside that is a product of the metabolism of adenosine triphosphate. It is used for the rapid termination of supraventricular arrhythmias following rapid bolus dosing.
Adenosine is approved for the acute management and termination of supraventricular tachyarrhythmias, including A-V nodal reentrant tachycardia and A-V reciprocating tachycardia. Adenosine may be helpful in the diagnosis of atrial flutter.

부작용

Adverse reactions to the administration of adenosine are fairly common; however, the short half-life of the drug limits the duration of such events.The most common adverse effects are flushing, chest pain, and dyspnea. Adenosine may induce profound bronchospasm in patients with known reactive airway disease. The mechanism for bronchospasm is unclear, and the effect may last for up to 30 minutes despite the short half-life of the drug.

Drug interactions

Metabolism of adenosine is slowed by dipyridamole, indicating that in patients stabilized on dipyridamole the therapeutically effective dose of adenosine may have to be increased. Methylxanthines antagonize the effects of adenosine via blockade of the adenosine receptors.

Purification Methods

Crystallise adenosine from distilled water and dry it at 110o. It has been purified via the picrate, where ethanolic picric acid is added to adenosine and the picrate is filtered off and recrystallised from EtOH. It has m 180-185o(dec). Adenosine is recovered by dissolving 0.4g of the picrate in 80mL of hot H2O, treated with a small quantity of Dowex 1 anion exchange resin in the chloride form, and the resin is filtered off. The filtrate is treated with more resin and filtered again. One equivalent of aqueous NaOH is added to the colourless filtrate which is evaporated to 4mL and cooled to give 0.176g of adenosine m 236o. [Davoll et al. J Chem Soc 967 1948, Davoll & Lowy J Am Chem Soc 73 1650 1951, Beilstein 26 III/IV 3598.]

주의 사항

Patients with second- or third-degree A-V block should not receive adenosine. As indicated previously, the use of adenosine in asthmatic patients may exacerbate the asthmatic symptoms.

아데노신 준비 용품 및 원자재

원자재

준비 용품


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