Name | Hirsuteine |
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Synonyms |
Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethenyl-1,2,3,4,6,7,12,12b-octahydro-α-(methoxymethylene)-, methyl ester, (αZ,2S,3R,12bS)-
delta18-Hirsutine (E)-16,17,18,19-Tetradehydro-17-methoxy-17,18-secoyohimban-16-carboxylic AcidMethyl Ester methyl (3beta,16E)-16-(methoxymethylidene)coryn-18-en-17-oate Methyl (16Z)-16-(methoxymethylene)coryn-18-en-17-oate methyl (E)-2-[(2S,3R,12bR)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate |
Description | Hirsuteine is an indole alkaloid extracted from Uncaria genus. Hirsuteine non-competitively antagonizes nicotine-mediated dopamine release by blocking ion permeation through nicotinic receptor channel complexes[1]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 533.2±50.0 °C at 760 mmHg |
Molecular Formula | C22H26N2O3 |
Molecular Weight | 366.453 |
Flash Point | 276.3±30.1 °C |
Exact Mass | 366.194336 |
PSA | 54.56000 |
LogP | 3.75 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.623 |
Hazard Codes | Xi |
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