|
|
| | ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Basic information |
| | 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) | | form | Solid | | pka | pK1: 3.81(+1);pK2: 6.17(0) (25°C) | | color | White | | Water Solubility | 0.5g/L(15 ºC) | | Merck | 157 |
| WGK Germany | 3 | | RTECS | AU7480300 | | Toxicity | mouse,LD,intraperitoneal,> 1gm/kg (1000mg/kg),Annals of the New York Academy of Sciences. Vol. 60, Pg. 251, 1954. |
| | ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Usage And Synthesis |
| Chemical Properties | colorless or white to yellowish powder | | Uses | Adenosine 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. | | Definition | ChEBI: 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-). |
| | ADENOSINE 2' -& 3'-MONOPHOSPHATE FREE Preparation Products And Raw materials |
|