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ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE

ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Suppliers list
Company Name: Guangzhou Younan Technology Co., Ltd  Gold
Tel: 020-82000279 18988941452
Email: YN_research@163.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
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Company Name: Hongene Biotech Corporation  
Tel: 021-64757213
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Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
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ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE manufacturers

ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Basic information
Product Name:ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE
Synonyms:-MONOPHOSPHATE FREE;adenosine2’-phosphoricacid;Adenosine 2'(3')-Monophosphate(2',3'mixed);2'-, and 3'-adenylic acid, mixed isomers;Ado-2'-P;Adenylic Acid Hydrate;Adenosine-2'(3')-monophosphoric acid (mixed isomers);adenosine 2'-phosphate hemihydrate
CAS:130-49-4
MF:C10H14N5O7P
MW:347.22
EINECS:204-990-7
Product Categories:Biochemistry;Nucleosides, Nucleotides & Related Reagents;Nucleotides and their analogs
Mol File:130-49-4.mol
ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Structure
ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Chemical Properties
Melting point 183 °C
Boiling point 815.5±75.0 °C(Predicted)
density 2.3200 (rough estimate)
refractive index 1.9050 (estimate)
storage temp. -20°C
solubility <3mg/ml in PBS(pH7.2)
pkapK1: 3.81(+1);pK2: 6.17(0) (25°C)
form Solid
color White
biological sourceyeast
Water Solubility 0.5g/L(15 ºC)
Merck 157
InChIInChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(22-23(18,19)20)6(17)4(1-16)21-10/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6+,7,10-/m1/s1
InChIKeyQDFHPFSBQFLLSW-PKJMTWSGSA-N
SMILESN1=C(N)C2N=CN([C@]3([H])O[C@]([H])(CO)[C@]([H])(O)C3([H])OP(O)(=O)O)C=2N=C1
Safety Information
WGK Germany 3
RTECS AU7480300
Storage Class11 - Combustible Solids
Toxicitymouse,LD,intraperitoneal,> 1gm/kg (1000mg/kg),Annals of the New York Academy of Sciences. Vol. 60, Pg. 251, 1954.
MSDS Information
ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Usage And Synthesis
Chemical Propertiescolorless or white to yellowish powder
UsesAdenosine 2′-monophosphate (2′-AMP) is a metabolite produced from hydrolysis of 2′,3′-cAMP. 2′-AMP inhibits proliferation of preglomerular vascular smooth muscle cells and glomerular mesangial cells via A2B receptors. 2′-AMP is used in the synthesis of a new photoaffinity lable for the coenzyme site of porcine NADP-specific isocitrate dehydrogenase. 2′,3′-cAMP and 2′-AMP represent a new unexplored pathway for adenosine-based cell regulation.
DefinitionChEBI: Adenosine 2'-phosphate is a purine ribonucleoside 2'-monophosphate. It has a role as a Saccharomyces cerevisiae metabolite. It is a conjugate acid of an adenosine 2'-phosphate(2-).
Biological ActivityAMP serves as a key component of several compounds, including coenzyme A, which plays an essential role in energy metabolism, as well as certain key redox cofactors such as NAD+, NADP+, and FAD. Furthermore, AMP is one of the key components of RNA, which is essential for protein synthesis and other biological processes in cells.
IC 50A2A adenosine receptor; A2B adenosine receptor; Human Endogenous Metabolite
ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Preparation Products And Raw materials
Tag:ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE(130-49-4) Related Product Information
c-di-AMP ADENOSINE-2':3'-CYCLIC MONOPHOSPHATE, SODIUM SALT INDEX NAME NOT YET ASSIGNED [5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxy-oxolan-2-yl]methoxyphosphonic acid 2'-O-Methyladenosine ADP [(2R,5R)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxy-oxolan-2-yl]me thoxyphosphonic acid 2'-Deoxyadenosine P1,P2-di(adenosine-5')pyrophosphate sodium salt 2-amino-2-deoxy-beta-arabinofuranosyladenine 2'-Deoxyadenosine-5'-triphosphate, trisodiuM salt 2'-Adenylic acid, 3',5'-bis(dihydrogen phosphate) (9CI) Adenosine 5'-monophosphate 3'-Adenylic acid 6-Methylaminopurine 9-ribofuranoside Adenosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-[1-(dimethylamino)ethylidene]- (9CI) Triphosphopyridine nucleotide Nadph tetrasodium salt