ChemicalBook > CAS DataBase List > Adenosine

Adenosine

Defination In the body Medical uses Mechanism of action

Product Name: Adenosine
CAS No.: 58-61-7
Chemical Name: Adenosine
Synonyms: AR;(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol;Adenosin;ADENINENUCLEOSIDE;Androgen receptor;2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol;Adesine;Adenocard;Adenoscan;(2R,3R,4S,5R)-2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
CBNumber: CB7304660
Molecular Formula: C10H13N5O4
Formula Weight: 267.24
MOL File: 58-61-7.mol

Less

Adenosine Property

Melting point:: 234-236 °C (lit.)
Boiling point:: 410.43°C (rough estimate)
alpha: D11 -61.7° (c = 0.706 in water); 9D -58.2° (c = 0.658 in water)
Density: 1.3382 (rough estimate)
refractive index: 1.7610 (estimate)
storage temp.: 2-8°C
solubility: 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.
form: Crystalline Powder
pka: 3.6, 12.4(at 25℃)
color: White
PH: 3.59；12.5
biological source: synthetic (organic)
optical activity: [α]20/D 70±3°, c = 2% in 5% NaOH
Water Solubility: Soluble in water, ammonium hydroxide and dimethyl sulfoxide. Insoluble in ethanol.
λmax: 257 (pH 1)；260 (pH 6)
Merck: 14,153
BRN: 93029
Stability:: Stable. Incompatible with strong oxidizing agents.
InChIKey: OIRDTQYFTABQOQ-KQYNXXCUSA-N
LogP: -0.755 (est)
CAS DataBase Reference: 58-61-7(CAS DataBase Reference)
NIST Chemistry Reference: adenosine(58-61-7)
EPA Substance Registry System: Adenosine (58-61-7)

Less

Safety

Risk Statements: 36/37/38
Safety Statements: 24/25-36/37/39-26
WGK Germany: 2
RTECS: AU7175000
F: 10-23
TSCA: Yes
HS Code: 29389090
Hazardous Substances Data: 58-61-7(Hazardous Substances Data)
Toxicity: LD50 oral in mouse: > 20gm/kg

Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Less

N-Bromosuccinimide Price

Sigma-Aldrich

Product number: SAB1306176
Product name: ANTI-ANDROGEN RECEPTOR (ANDR) antibody produced in rabbit
Purity: affinity isolated antibody, buffered aqueous solution
Packaging: 400 μL
Price: $496
Updated: 2025/07/31

Sigma-Aldrich

Product number: RAB0019
Product name: Human Amphiregulin ELISA Kit
Purity: for serum, plasma, cell culture supernatant and urine
Packaging: 1 kit
Price: $569
Updated: 2025/07/31

Sigma-Aldrich

Product number: PHL80977
Product name: Adenosine
Purity: phyproof? Reference Substance
Packaging: 100MG
Price: $239
Updated: 2025/07/31

Sigma-Aldrich

Product number: A0230200
Product name: Adenosine
Purity: European Pharmacopoeia (EP) Reference Standard
Packaging: 50 mg
Price: $236
Updated: 2025/07/31

Sigma-Aldrich

Product number: 01890
Product name: Adenosine
Packaging: 5g
Price: $48.3
Updated: 2025/07/31

Less

Adenosine Chemical Properties,Usage,Production

Defination

Adenosine is a natural nucleotide, which is the intermediate product of metabolism, chemically 6-amino-9-beta-D-ribofuranosyl-9-H-purine. Adenosine is one of the important active components in the body, helps in cellular energy transfer by forming molecules like adenosine triphosphate (ATP) and adenosine diphosphate (ADP). It also plays a role in signaling various pathways and functions in the body by forming signally molecules like cyclic adenosine monophosphate (cAMP).

In the body

Adenosine in the body

Function

Brain

Promoting sleep and suppresses arousal acting as a central nervous system depressant.

Heart

Causing dilation of the coronary blood vessels that Improving blood circulation to the heart; Increasing the diameter of blood vessels in the peripheral organs; Decreasing heart rate

Blood

Broken down by adenosine deaminase. By taking medicine like Dipyridamole(inhibitor of adenosine deaminase), it can improve blood flow through the coronary blood vessels that supply the heart muscles.

Kidneys, lungs and liver

In the kidneys adenosine decreases renal blood flow and decrease the production of rennin from the kidneys. In the lungs it causes constriction of airways and in the liver it leads to constriction of blood vessels and increases breakdown of glycogen to form glucose.

Medical uses

Adenosine has a role in the expansion of coronary artery and myocardial contractility, is clinically applied in the treatment of angina, hypertension, cerebrovascular disorders, stroke sequelae, muscular atrophy, etc. It is also given intravenously (by IV) for treating supraventricular tachycardia and Tl myocardial imaging. It is also used for cardiac stress tests. Side effects:
Since the half-life of this compound is less than 10 seconds, its side effects are usually transient. However, side effects are common, and include flushing, headache, chest discomfort, bronchoconstriction, and occasionally hypotension. Hepatic and renal failure and other drugs except dipyridamole seem to have little effect on the action of adenosine. Adenosine dose

Mechanism of action

Its function is realized through the activation of the adenosine receptor (A receptor). Adenosine activates G protein coupled potassium channels by binding to the A receptor which makes increasing the outflow of K+ and cell membrane hyperpolarization so as to decrease the automaticity in the atrium, sinoatrial node and atrioventricular node. It can also significantly increase the level of cGMP , prolong ERP of the atrioventricular node and slowing of atrioventricular, depress sympathetic nervous or early and delayed after depolarization induced by isoproterenol and then plays an effective role in arrhythmia. This product has not been classified in I~IV anti arrhythmia medicine.

Adenosine receptor

A1 receptors, which are found in cardiomyocytes and which are responsible for the inhibition of adenylyl cylase activity which lowers cyclic adenosine monophosphate (AMP) results in sinus slowing, increase in AV node conduction delay, and antagonism of the effects of catecholamines;
A2 receptors, which are found in endothelial cells and vascular smooth muscle and are responsible for the enhancement of adenylyl cylase activity and increased cyclic AMP which relaxes smooth muscle. Both negative chronotropic and dromotropic effects of adenosine are cyclic AMP independent (direct action) as well cyclic AMP dependent (indirect action).

Description

Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety via a β-N9-glycosidic bond. Adenosine works in the energy transfer-as adenosine triphosphate (ATP) and adenosine diphosphate (ADP)-as well as in signal transduction as cyclic adenosine monophosphate, cAMP. It shows neuromodulatory, cytoprotective, anti-inflammatory and cardioprotective actions.

Chemical Properties

Adenosine is an important nucleoside composed of adenine and ribose. White, crystalline, odorless powder, mild, saline, or bitter taste, quite soluble in hot water, practically insoluble in alcohol. Formed by isolation following hydrolysis of yeast nucleic acid.

Uses

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.

Application

Adenosine can serve as a diagnostic or therapeutic agent. Diagnostically, adenosine is one pharmaceutical agent used in a myocardial perfusion stress imaging study for its vasodilatory effects. Therapeutically, adenosine is used for its antiarrhythmic properties in supraventricular tachycardia (SVT) and can function as a diagnostic tool, depending on the type of SVT.

Definition

ChEBI: Adenosine is a ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a beta-N(9)-glycosidic bond. It has a role as an anti-arrhythmia drug, a vasodilator agent, an analgesic, a human metabolite and a fundamental metabolite. It is a purines D-ribonucleoside and a member of adenosines. It is functionally related to an adenine.

brand name

Adenocard (Astellas); Adenoscan (Astellas).

Origin

Adenosine may be generated intracellularly in the central nervous system from degradation of AMP or from the hydrolysis of S-adenosyl homocysteine, and then exit via bi-directional nucleoside transporters, or extracellularly by the metabolism of released nucleotides. Inactivation of extracellular adenosine occurs by transport into neurons or neighboring cells, followed by either phosphorylation to AMP by adenosine kinase or deamination to inosine by adenosine deaminase[1].

Biological Functions

Adenosine regulates multiple physiological and pathophysiological processes, by acting both through G-protein coupled adenosine receptors and intracellularly. It modulates neuronal plasticity, astrocytic activity , learning and memory, food intake, motor function, sleep/wake cycle, pain, immunosupression, proliferation, and aging. Adenosine is involved in ischemia and stroke, epilepsy, and neurodegenerative pathologies such as Parkinson's disease (PD), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and Huntington's disease (HD). Extracellular adenosine, interacting with P1 receptors (A1R, A2AR, A2BR, and A3R) regulates metabolism through different signaling pathways[1].

Biological Functions

[1] Mercedes Garcia-Gil. “Metabolic Aspects of Adenosine Functions in the Brain.” Frontiers in Pharmacology (2021): 672182.

General Description

Adenosine is a purine nucleoside and a building block of RNA and many other biomolecules such as adenosine triphosphate and nicotinamide adenine dinucleotide. In the extracellular space, ecto-5′-nucleotidase (CD73) dephosphorylates adenosine triphosphate (ATP) to produce adenosine. Adenosine has four receptors namely A1R, A2AR A2BR and A3R. Adenosine plays a key role in the osteogenic differentiation. A1R induces osteoclast differentiation and A2AR induces osteoblast differentiation.

Biological Activity

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

Biochem/physiol Actions

Endogenous neurotransmitter at adenosine receptors. Cardioprotective effects may relate to activation of A1 adenosine receptors. The antiplatelet and anti?inflammatory actions of adenosine appear to be mediated via the A2 adenosine receptor. In contrast, adenosine appears to be a pro-inflammatory mediator in asthma and chronic obstructive pulmonary disease (COPD).

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.

Side effects

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.

Metabolism

It is impossible to study adenosine in classical pharmacokinetic studies, since it is present in various forms in all the cells of the body. An efficient salvage and recycling system exists in the body, primarily in erythrocytes and blood vessel endothelial cells. The halflife in vitro is estimated to be less than 10 seconds, and may be even shorter in vivo.

storage

-20°C

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.]

Precautions

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.

Adenosine Preparation Products And Raw materials

Raw materials

Preparation Products

Vidarabine Calcium 5'-ribonucleotide

Less

Adenosine Suppliers

Americas 1 Belgium 2 Brazil 6 Canada 4 China 993 Czech Republic 1 Europe 4 France 3 Germany 16 India 42 Italy 3 Japan 7 Poland 1 Slovakia 1 Switzerland 3 The Netherlands 2 United Kingdom 24 United States 100 Venezuela 1 Global 1215

LoongZe (NanJing) Medicine Chemical Industry CO.,LTD

Tel: 025-58392866-05 17766083849
Email: 3696999150@qq.com
Country: China
ProdList: 28
Advantage: 58

WeiTai BioPharmaceutical Co.,Ltd(Hangzhou?)

Tel: 0571-82358004 13588879771
Email: info@weitai-pharmaceutical.com
Country: China
ProdList: 68
Advantage: 58

Spec-Chem Industry Inc.

Tel: 025-84523390 13505162978
Email: sc@specchemind.com
Country: China
ProdList: 116
Advantage: 58

Jiangsu Huayu Chemical Co., Ltd.

Tel: 25-83241163
Fax: +86-25-83241173
Email: sales@elegantnutri.com
Country: China
ProdList: 55
Advantage: 55

Nanjing UltraPure Biotech Co., Ltd.

Tel: 025-82263158 13851993283
Fax: 025-82263168
Email: 2842979086@qq.com
Country: China
ProdList: 241
Advantage: 58

Shanghai Bojing Chemical Co., Ltd

Tel: 021-37199966 13681836088
Fax: 021-37597788
Email: bj@bj-chem.com
Country: China
ProdList: 463
Advantage: 58

Shanghai Xianggeng Technology Development Co. Ltd.

Tel: 021-021-56152668 18116302010
Fax: 18116300787
Email: sharing@sharingtechcn.com
Country: China
ProdList: 506
Advantage: 58

Zheng zhou nine potential chemical products co,.ltd.

Tel: +86-0371-55215939 +86-17319721973
Email: foreignsales@jiushichem.com
Country: China
ProdList: 31
Advantage: 58

Wuxi Jingyao Bio-Technology Co., Ltd.

Tel: 0510-88770633 13961738808
Email: jingyaobiotech@126.com
Country: China
ProdList: 346
Advantage: 55

Xinxiang Yicheng Biotechnology Co.,LTD

Tel: 0373-6014999 18937330588
Email: xxycswsale@163.com
Country: China
ProdList: 70
Advantage: 58

Anhui Chnbio Technology Co., Ltd.

Tel: 18969017660
Email: 2424422732@qq.com
Country: China
ProdList: 85
Advantage: 58

Shanghai Tuolei Chemical Reagents Co., Ltd.

Tel: 86-021-50318510
Fax: 021-58650104
Country: China
ProdList: 69
Advantage: 55

J & K SCIENTIFIC LTD.

Tel: 18210857532; 18210857532
Fax: 86-10-82849933
Email: jkinfo@jkchemical.com
Country: China
ProdList: 96815
Advantage: 76

Meryer (Shanghai) Chemical Technology Co., Ltd.

Tel: 4006356688 18621169109
Fax: 86-21-61259102
Email: market03@meryer.com
Country: China
ProdList: 40228
Advantage: 62

3B Pharmachem (Wuhan) International Co.,Ltd.

Tel: 821-50328103-801 18930552037
Fax: 86-21-50328109
Email: 3bsc@sina.com
Country: China
ProdList: 15838
Advantage: 69

future industrial shanghai co., ltd

Tel: 400-0066400 13621662912
Fax: 021-55660885
Email: sales@jonln.com
Country: China
ProdList: 1995
Advantage: 65

Hongene Biotech Corporation

Tel: 021-64757213
Fax: 86-21-64700613
Email: info@hongene.com
Country: China
ProdList: 672
Advantage: 61

Chembest Research Laboratories Limited

Tel: +86-21-20908456
Fax: 021-58180499
Email: sales@BioChemBest.com
Country: China
ProdList: 6003
Advantage: 61

Alfa Aesar

Tel: 400-6106006
Fax: 021-67582001/03/05
Email: saleschina@alfa-asia.com
Country: China
ProdList: 30123
Advantage: 84

TAIYUAN RHF CO.,LTD.

Tel: +86 351 7031519
Fax: +86 351 7031519
Email: sales@RHFChem.com
Country: China
ProdList: 2338
Advantage: 56

TCI (Shanghai) Development Co., Ltd.

Tel: 021-67121386
Fax: 021-67121385
Email: Sales-CN@TCIchemicals.com
Country: China
ProdList: 24529
Advantage: 81

ShangHai DEMO Chemical Co.,Ltd

Tel: 400-021-7337 2355568890
Fax: 0086-21-50182339
Email: sales@demochem.com
Country: China
ProdList: 2572
Advantage: 57

Beijing HwrkChemical Technology Co., Ltd

Tel: 18515581800 18501085097
Fax: 010-89508210
Email: sales.bj@hwrkchemical.com
Country: China
ProdList: 9400
Advantage: 55

Energy Chemical

Tel: 021-021-58432009 400-005-6266
Fax: 021-58436166
Email: sales8178@energy-chemical.com
Country: China
ProdList: 44801
Advantage: 61

Capot Chemical Co., Ltd

Tel: +86 (0) 571 85 58 67 18
Fax: 0086-571-85864795
Country: China
ProdList: 18207
Advantage: 66

Beijing Ouhe Technology Co., Ltd

Tel: 010-010-82967028 13522913783
Fax: +86-10-82967029
Email: 2355560935@qq.com
Country: China
ProdList: 12000
Advantage: 60

JinYan Chemicals(ShangHai) Co.,Ltd.

Tel: 13817811078
Fax: 86-021-50426522,50426273
Email: sales@jingyan-chemical.com
Country: China
ProdList: 9976
Advantage: 60

Jia Xing Isenchem Co.,Ltd

Tel: 0573-85285100 18627885956
Fax: 0573-85285100
Email: isenchem@163.com
Country: China
ProdList: 9310
Advantage: 66

Wuhu Huaren Science and Technology Co., Ltd.

Tel: 0553-5842013-801 18155347026
Fax: 086-553-5843138
Email: jinhuaren@huarensh.com
Country: China
ProdList: 255
Advantage: 64

Adamas Reagent, Ltd.

Tel: 400-6009262 16621234537
Fax: 021-64823266
Email: chenyj@titansci.com
Country: China
ProdList: 14101
Advantage: 59

Accela ChemBio Co.,Ltd.

Tel: 021-50795510 4000665055
Fax: 021-50795055
Email: sales@accelachem.com
Country: China
ProdList: 11035
Advantage: 64

Shanghai Hanhong Scientific Co.,Ltd.

Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Country: China
ProdList: 42934
Advantage: 64

Chemsky（shanghai）International Co.,Ltd.

Tel: 021-50135380
Email: shchemsky@sina.com
Country: China
ProdList: 32321
Advantage: 50

China DongFan Chemical Co.,LTD

Tel: 86-0571-85151182
Fax: 86-0571-85151182
Country: China
ProdList: 5691
Advantage: 66

XiaoGan ShenYuan ChemPharm co,ltd

Tel: 15527768836
Email: 1791901229@qq.com
Country: China
ProdList: 6950
Advantage: 52

Beijing Isomersyn Technology CO;LTD

Tel: 010-82954736 13391601435
Email: sales@isomersyn.com
Country: China
ProdList: 3295
Advantage: 57

Shandong Xiya Chemical Co., Ltd

Tel: 4009903999 13355009207
Fax: 0539-6365991
Email: 3007715519@qq.com
Country: China
ProdList: 18729
Advantage: 57

Syntechem Co.,Ltd

Tel
Fax: E-Mail Inquiry
Email: info@syntechem.com
Country: China
ProdList: 12984
Advantage: 57

Sichuan Kulinan Technology Co., Ltd

Tel: 400-1166-196 18981987031
Fax: 028-84555506 800101999
Email: cdhxsj@163.com
Country: China
ProdList: 11705
Advantage: 57

China Langchem Inc.

Tel: 0086-21-58956006
Fax: 0086-21-58956100
Country: China
ProdList: 7811
Advantage: 57

Tianjin heowns Biochemical Technology Co., Ltd.

Tel: 400 638 7771
Email: sales@heowns.com
Country: China
ProdList: 14435
Advantage: 57

Sinopharm Chemical Reagent Co,Ltd.

Tel: 86-21-63210123
Fax: 86-21-63290778 86-21-63218885
Email: sj_scrc@sinopharm.com
Country: China
ProdList: 9815
Advantage: 79

Hunan Hui Bai Shi Biotechnology Co., Ltd.

Tel: 0731-85526065 13308475853
Email: ivy@hnhbsj.com
Country: China
ProdList: 7247
Advantage: 62

Maya High Purity Chemicals

Tel: +86 (573) 82222445 (0)18006601000 452520369
Fax: +86 (573) 82222643
Email: sales@maya-r.com
Country: China
ProdList: 11707
Advantage: 57

Aktin Chemicals, Inc.

Tel: 86-28-85159085
Fax: 86-28-85152372
Email: info@aktinchem.com
Country: China
ProdList: 297
Advantage: 62

ZhengZhou HuaWen Chemical Co.Ltd

Tel: 0370-2785118 17550508557
Fax: QQ：3470079902
Email: 675141927@qq.com
Country: China
ProdList: 3199
Advantage: 55

Spectrum Chemical Manufacturing Corp.

Tel: 021-021-021-67601398-809-809-809 15221380277
Fax: 021-57711696
Email: marketing_china@spectrumchemical.com
Country: China
ProdList: 9658
Advantage: 60

Wuhan Fortuna Chemical Co., Ltd

Tel: 027-59207852 13308628970
Fax: QQ3130921841
Email: buy@fortunachem.com
Country: China
ProdList: 2744
Advantage: 58

Dalian Meilun Biotech Co., Ltd.

Tel: 0411-62910999 13889544652
Email: sales@meilune.com
Country: China
ProdList: 4747
Advantage: 58

BioBioPha Co., Ltd.

Tel: 0871-65217109 13211707573;
Fax: 0871-65215563
Email: y.liu@mail.biobiopha.com
Country: China
ProdList: 5653
Advantage: 65

Less

View Lastest Price from Adenosine manufacturers

WeiTai BioPharmaceutical Co.,Ltd(Hangzhou?)

Product: Adenosine Ar 58-61-7
Price: US $0.00-0.00/kg
Min. Order: 25kg
Purity: ≥99%
Supply Ability: 2tons
Release date: 2025-08-19

WUHAN FORTUNA CHEMICAL CO., LTD

Product: Adenosine 58-61-7
Price: US $0.00-0.00/kg
Min. Order: 1kg
Purity: 98%min
Supply Ability: 10 Tons
Release date: 2025-07-15

Anhuyan (Hainan) Biotechnology Co., LTD

Product: Adenosine 58-61-7
Price: US $0.00/G/KG
Min. Order: 1G/KG
Purity: 99%
Supply Ability: 100000000KG
Release date: 2025-04-23

58-61-7, AdenosineRelated Search:

Adenine Sulfate ADENOSINE 3':5'-CYCLIC MONOPHOSPHATE,ADENOSINE 3'-,5'-CYCLIC MONOPHOSPHATE,(-)-ADENOSINE 3',5'-CYCLIC MONOPHOSPHATE Adenine Adenine phosphate salt（1：1） PUROMYCIN AMINONUCLEOSIDE Guanosine Adenine phosphate(1:x) NUCLEOSIDE PHOSPHORYLASE BACTERIAL Adenosine5'-(tetrahydrogen triphosphate), disodiuM salt, trihydrate (9CI) 6-Chloropurine ribonucleoside Adenine hydrochloride hemihydrate ATP disodium salt Cytidine ADENOSINE-5'-DIPHOSPHOGLUCOSE Adenine hydrochloride 5'-Guanylic acid Adenosine 5'-monophosphate S-Adenosyl-L-methionine

D-ADENOSINE

(2R,3R,4S,5R)-2-(6-AMINO-PURIN-9-YL)-5-HYDROXYMETHYL-TETRAHYDRO-FURAN-3,4-DIOL

9-BETA-D-RIBOFURANOSYLADENINE

Adenine riboside, Adenine-9-beta-ribofuranoside

ADENOSINE extrapure for biochemistry

9-β-D-Ribofuranosyladenine, Adenine riboside, Adenine-9-β-D-ribofuranoside

ADENINENUCLEOSIDE

ADENINE RIBOSIDE

ADENOSINE

ADENINE-9-BETA-D-RIBOFURANOSIDE

6-Amino-9-β-D-ribofuranosyl-[9H]-purine

2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

ADENOSINE(FREE BASE)(RG)

adenine-9-1'-β-ribofuranoside

vidarabine，ara-A

9-D-Ribofuranosyl sdenine

ADENOSINE[9-BETA-D-RIBOFURANOSYLADENINE]

Adenoside

(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

(2R,3R,4S,5R)-2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

ADENOSINE (Ado)

adenosin (german)

Adesine

MONOCLONAL ANTI-ANDROGEN RECEPTOR PROTEIN antibody produced in mouse

Adenosine Vetec(TM) reagent grade, 98%

ATP DISODIUM TRIHYDRATE ULTRA PURE GRADE

Adenine riboside, low endotoxins

Adenine-9-β-D-ribofuranoside, low endotoxis

Adenosine free base, low endotoxinsCell culture grade, ≥ 99.5% (HPLC)

Adenosine, 99%, substrate of adenosine deaminase

Adenosine - Endotoxin level below 100 EU/g

Adenosine - Endotoxin level below 1000 EU/g

2,3,5-Tri-O-acetyl &alpha

NanoLiposomal Adenosine, Water-Soluble Adenosine

ADENINE-9-D-RIBOFURANOSIDE

Adenine-9-B-D-Ribofuranoside

(-)-ADENOSINE, 99+%

ADENOSINE FREE BASE CELL CULTURE TESTED

Adenine-9-β-D-ribofur

AdenosineForBiochemistry

Adenosine,>98%

9-bate-D-Ribofuranosyladenine free base

Adenosine,9-β-D-Ribofuranosyladenine, Adenine riboside, Adenine-9-β-D-ribofuranoside

Adenosine (200 mg)

6-amino-9-beta-d-ribofuranosyl-9h-purine

6-Amino-9beta-D-ribofuranosyl-9H-purine

9-beta-D-Ribofuranosidoadenine

9-beta-D-Ribofuranosyl-9H-purin-6-amine

9H-Purin-6-amine, 9-beta-d-ribofuranosyl-

Adenocard

Adenocor

Adenoscan

Adenosin

beta-Adenosine

beta-d-Adenosine

beta-d-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1-deoxy-

beta-d-Ribofuranoside, adenine-9