Name | corydaline |
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Synonyms |
13aβ-Berbine, 2,3,9,10-tetramethoxy-13α-methyl-
(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline d-Corydalin (13S,13aR)-2,3,9,10-Tetramethoxy-13-methyl-5,8,13,13a-tetrahydro-6H-isoquinolino[3,2-a]isoquinoline (13S-trans )-5,8,13,13a-Tetrahydro-2,3,9,10-tetramethoxy-13-methyl-6H-dibenzo[a,g]quinolizine Corydaline (+) 6H-Dibenzo[a,g]quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-13-methyl-, (13S,13aR)- Berbine,2,3,9,10-tetramethoxy-13-methyl 2,3,9,10-Tetramethoxy-13a-methyl-13ab-berbine (13S,13aR)-2,3,9,10-Tetramethoxy-13-methyl-5,8,13,13a-tetrahydro-6H-isoquino[3,2-a]isoquinoline Corydalin Corydaline |
Description | Corydaline is an acetylcholinesterase inhibitor isolated from Corydalis yanhusuo. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 482.3±45.0 °C at 760 mmHg |
Melting Point | 135° |
Molecular Formula | C22H27NO4 |
Molecular Weight | 369.454 |
Flash Point | 135.7±25.9 °C |
Exact Mass | 369.194000 |
PSA | 40.16000 |
LogP | 4.19 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.600 |
Storage condition | -20°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
~% 518-69-4 |
Literature: Manske Journal of the American Chemical Society, 1953 , vol. 75, p. 4928 |
~% 518-69-4 |
Literature: CVI PHARMACEUTICALS LIMITED; LIU, Haiyan; LI, Gaoping; WANG, Junbo; LIU, Jingwen Patent: WO2010/75469 A1, 2010 ; Location in patent: Page/Page column 62 ; WO 2010/075469 A1 |
~% 518-69-4 |
Literature: Dobbie; Lauder; Paliatseas Journal of the Chemical Society, 1901 , vol. 79, p. 89 |
~% 518-69-4 |
Literature: Gadamer; Wagner Archiv der Pharmazie (Weinheim, Germany), 1902 , vol. 240, p. 36 |
~% 518-69-4 |
Literature: Gadamer; Wagner Archiv der Pharmazie (Weinheim, Germany), 1902 , vol. 240, p. 36 |
Precursor 5 | |
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DownStream 3 | |