N6-(2-Phenylethyl)adenosine
N6-(2-Phenylethyl)adenosine structure
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Common Name | N6-(2-Phenylethyl)adenosine | ||
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| CAS Number | 20125-39-7 | Molecular Weight | 371.39000 | |
| Density | 1.57g/cm3 | Boiling Point | 723.5ºC at 760 mmHg | |
| Molecular Formula | C18H21N5O4 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 391.3ºC | |
Use of N6-(2-Phenylethyl)adenosineN6-(2-Phenylethyl)adenosine is a selective A1 adenosine receptor agonist. |
| Name | N6-(2-Phenylethyl)adenosine |
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| Synonym | More Synonyms |
| Description | N6-(2-Phenylethyl)adenosine is a selective A1 adenosine receptor agonist. |
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| Related Catalog |
| Density | 1.57g/cm3 |
|---|---|
| Boiling Point | 723.5ºC at 760 mmHg |
| Molecular Formula | C18H21N5O4 |
| Molecular Weight | 371.39000 |
| Flash Point | 391.3ºC |
| Exact Mass | 371.15900 |
| PSA | 125.55000 |
| LogP | 0.16540 |
| Vapour Pressure | 5.72E-22mmHg at 25°C |
| Index of Refraction | 1.741 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| RIDADR | NONH for all modes of transport |
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~94%
N6-(2-Phenyleth... CAS#:20125-39-7 |
| Literature: METHYLGENE INC. Patent: US2008/132525 A1, 2008 ; Location in patent: Page/Page column 13 ; |
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~92%
N6-(2-Phenyleth... CAS#:20125-39-7 |
| Literature: Nishikawa, Shiro; Kumazawa, Zenzaburo; Kashimura, Naoki; Nishimiki, Yoshio; Uemura, Shoji Agricultural and Biological Chemistry, 1986 , vol. 50, # 9 p. 2243 - 2250 |
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~%
N6-(2-Phenyleth... CAS#:20125-39-7 |
| Literature: Schering Aktiengesellschaft Patent: US3983104 A1, 1976 ; |
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~%
N6-(2-Phenyleth... CAS#:20125-39-7 |
| Literature: Schering Aktiengesellschaft Patent: US3983104 A1, 1976 ; |
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Not1 mediates recruitment of the deadenylase Caf1 to mRNAs targeted for degradation by tristetraprolin.
Nucleic Acids Res. 39 , 4373-86, (2011) The carbon catabolite repressor protein 4 (Ccr4)-Negative on TATA (Not) complex controls gene expression at two levels. In the nucleus, it regulates the basal transcription machinery, nuclear receptor... |
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Exploring distal regions of the A3 adenosine receptor binding site: sterically constrained N6-(2-phenylethyl)adenosine derivatives as potent ligands.
Bioorg. Med. Chem. 12 , 2021-2034, (2004) We synthesized phenyl ring-substituted analogues of N(6)-(1S,2R)-(2-phenyl-1-cyclopropyl)adenosine, which is highly potent in binding to the human A(3)AR with a Ki value of 0.63 nM. The effects of the... |
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Effects of adenosine receptor agonists and antagonists on audiogenic seizure-sensible DBA/2 mice.
Eur. J. Pharmacol. 371 , 137-145, (1999) We have studied the effects of selective and non-selective adenosine receptor agonists and antagonists in audiogenic-seizure-sensitive DBA/2 mice, an animal model of generalized reflex epilepsy. With ... |
| 2-(hydroxymethyl)-5-[6-(2-phenylethylamino)purin-9-yl]oxolane-3,4-diol |