25B-NBOH
| 25B-NBOH | |
|---|---|
 | |
| Общие | |
| Систематическое наименование |
2-({[2-(4-бром-2,5-диметоксифенил)этил]амино}метил)фенол |
| Хим. формула | C17H20BrNO3 |
| Физические свойства | |
| Молярная масса | 366,255 г/моль |
| Классификация | |
| Рег. номер CAS | 1335331-46-8 |
| PubChem | 125181394 |
| SMILES | |
| InChI |
[http://chemapps.stolaf.edu/jmol/jmol.php?&model=InChI=InChI%3D1S%2FC17H20BrNO3%2Fc1-21-16-10-14%2818%2917%2822-2%299-12%2816%297-8-19-11-13-5-3-4-6-15%2813%2920%2Fh3-6%2C9-10%2C19-20H%2C7-8%2C11H2%2C1-2H3%0A%20%20%20%20Key%3ARSUNJYKZRKIBNB-UHFFFAOYSA-N InChI=1S/C17H20BrNO3/c1-21-16-10-14(18)17(22-2)9-12(16)7-8-19-11-13-5-3-4-6-15(13)20/h3-6,9-10,19-20H,7-8,11H2,1-2H3
Key:RSUNJYKZRKIBNB-UHFFFAOYSA-N] |
| ChemSpider | 58191433 |
| Приведены данные для стандартных условий (25 °C, 100 кПа), если не указано иное. | |
25B-NBOH (2C-B-NBOH, NBOH-2C-B) — психоактивное вещество из класса фенилэтиламинов, производное от 2C-B. Он действует как мощный агонист серотониновых рецепторов 5-HT2A и 5-HT2C.[1][2][3][4]
Правовой статус
Это пустой раздел, который ещё не написан.
Примечания
- ↑ Martin Hansen, Karina Phonekeo, James S. Paine, Sebastian Leth-Petersen, Mikael Begtrup, Hans Bräuner-Osborne, Jesper L. Kristensen. Synthesis and Structure–Activity Relationships of N -Benzyl Phenethylamines as 5-HT 2A/2C Agonists (англ.) // ACS Chemical Neuroscience. — 2014-03-19. — Vol. 5, iss. 3. — P. 243–249. — ISSN 1948-7193. — doi:10.1021/cn400216u. Архивировано 16 июля 2024 года.
- ↑ Martin Hansen. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain (англ.). — 2010. — doi:10.13140/RG.2.2.33671.14245.
- ↑ Anders Ettrup, Martin Hansen, Martin A. Santini, James Paine, Nic Gillings, Mikael Palner, Szabolcs Lehel, Matthias M. Herth, Jacob Madsen, Jesper Kristensen, Mikael Begtrup, Gitte M. Knudsen. Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT2A agonist PET tracers (англ.) // European Journal of Nuclear Medicine and Molecular Imaging. — 2011-04. — Vol. 38, iss. 4. — P. 681–693. — ISSN 1619-7070. — doi:10.1007/s00259-010-1686-8.
- ↑ Michael R. Braden, Jason C. Parrish, John C. Naylor, David E. Nichols. Molecular Interaction of Serotonin 5-HT 2A Receptor Residues Phe339 (6.51) and Phe340 (6.52) with Superpotent N -Benzyl Phenethylamine Agonists (англ.) // Molecular Pharmacology. — 2006-12. — Vol. 70, iss. 6. — P. 1956–1964. — ISSN 0026-895X. — doi:10.1124/mol.106.028720.
Это заготовка статьи по химии. Помогите Википедии, дополнив её.
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