MG 624 structure
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Common Name | MG 624 | ||
|---|---|---|---|---|
| CAS Number | 77257-42-2 | Molecular Weight | 324.48000 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C22H30NO+ | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
Use of MG 624MG624 is a potent and selective neuronal α7 nAChR antagonist with a Ki of 106 nM[1]. |
| Name | MG 624,N,N,N-Triethyl-2-[4-(2-phenylethenyl)phenoxy]ethanaminiumiodide |
|---|---|
| Synonym | More Synonyms |
| Description | MG624 is a potent and selective neuronal α7 nAChR antagonist with a Ki of 106 nM[1]. |
|---|---|
| Related Catalog | |
| References |
| Molecular Formula | C22H30NO+ |
|---|---|
| Molecular Weight | 324.48000 |
| Exact Mass | 324.23300 |
| PSA | 9.23000 |
| LogP | 5.11230 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Safety Phrases | S43 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | BS4305000 |
|
~%
MG 624 CAS#:77257-42-2 |
| Literature: Al-Hassan, Mohammed I. Journal of Organometallic Chemistry, 1990 , vol. 386, # 3 p. 395 - 397 |
|
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MG 624 CAS#:77257-42-2 |
| Literature: Al-Hassan, Mohammed I. Journal of Organometallic Chemistry, 1990 , vol. 386, # 3 p. 395 - 397 |
|
~%
MG 624 CAS#:77257-42-2 |
| Literature: Al-Hassan, Mohammed I. Journal of Organometallic Chemistry, 1990 , vol. 386, # 3 p. 395 - 397 |
|
~%
MG 624 CAS#:77257-42-2 |
| Literature: Al-Hassan, Mohammed I. Journal of Organometallic Chemistry, 1990 , vol. 386, # 3 p. 395 - 397 |
|
~%
MG 624 CAS#:77257-42-2 |
| Literature: Al-Hassan, Mohammed I. Journal of Organometallic Chemistry, 1990 , vol. 386, # 3 p. 395 - 397 |
|
~%
MG 624 CAS#:77257-42-2 |
| Literature: Cavallini et al. Farmaco, Edizione Scientifica, 1953 , vol. 8, p. 317,322 |
|
4-Oxystilbene compounds are selective ligands for neuronal nicotinic alphaBungarotoxin receptors.
Br. J. Pharmacol. 124 , 1197, (1998) 1. Starting from the structure of an old 4-oxystilbene derivate with ganglioplegic activity (MG624), we synthesized two further derivates (F2 and F3) and two stereoisomers of F3 (F3A and F3B), and stu... |
| Stilonium |
| Stilonium iodide |
| CCK Octapeptide,non-sulfated |