Benzylamine, m-iodo-, hydrochloride
Benzylamine, m-iodo-, hydrochloride structure
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Common Name | Benzylamine, m-iodo-, hydrochloride | ||
|---|---|---|---|---|
| CAS Number | 3718-88-5 | Molecular Weight | 269.510 | |
| Density | N/A | Boiling Point | 272.5ºC at 760 mmHg | |
| Molecular Formula | C7H9ClIN | Melting Point | 188-190 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 118.6ºC | |
| Symbol |
GHS07, GHS08 |
Signal Word | Danger | |
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2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.
J. Med. Chem. 37(21) , 3614-21, (1994) Adenosine derivatives bearing an N6-(3-iodobenzyl) group, reported to enhance the affinity of adenosine-5'-uronamide analogues as agonists at A3 adenosine receptors (J. Med. Chem. 1994, 37, 636-646), were synthesized starting from methyl beta-D-ribofuranoside... |
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Synthesis, biological evaluation, and molecular modeling of ribose-modified adenosine analogues as adenosine receptor agonists.
J. Med. Chem. 48 , 1550-62, (2005) A number of 3'-C-methyl analogues of selective adenosine receptor agonists such as CPA, CHA, CCPA, 2'-Me-CCPA, NECA, and IB-MECA was synthesized to further investigate the subdomain of the receptor that binds the ribose moiety of the ligands. Affinity data at... |
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