Name | Tabersonine |
Synonyms | C09244 tabersonin TABERSONINE Tabersonine TABERSONINE(SH) ,12-beta,19-alpha)- methyl (5alpha,19alpha)-2,3,6,7-tetradehydroaspidospermidine-3-carboxylate aspidospermidine-3-carboxylicacid,2,3,6,7-tetrahydro-,methylester,(5-alpha methyl (5alpha,12beta,19alpha)-2,3,6,7-tetradehydroaspidospermidine-3-carboxylate Aspidospermidine-3-carboxylic acid, 2,3,6,7-tetradehydro-, methyl ester, (5alpha,12beta,19alpha)- |
CAS | 4429-63-4 |
EINECS | 224-615-0 |
InChI | InChI=1/C21H24N2O2/c1-3-20-9-6-11-23-12-10-21(19(20)23)15-7-4-5-8-16(15)22-17(21)14(13-20)18(24)25-2/h4-9,19,22H,3,10-13H2,1-2H3/t19-,20-,21+/m0/s1 |
Molecular Formula | C21H24N2O2 |
Molar Mass | 336.44 |
Density | 1.27±0.1 g/cm3(Predicted) |
Melting Point | 196 °C |
Boling Point | 488.7±45.0 °C(Predicted) |
Specific Rotation(α) | -310 (c, 0.13 in MeOH) (hydrochloride) |
Flash Point | 249.4°C |
Solubility | Soluble in methanol, ethanol, DMSO and other organic solvents |
Vapor Presure | 1.06E-09mmHg at 25°C |
Appearance | Powder |
Color | Light Yellow to Dark Yellow |
pKa | 7?+-.0.60(Predicted) |
Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
Stability | Light Sensitive |
Refractive Index | 1.651 |
MDL | MFCD28140545 |
Physical and Chemical Properties | White crystalline powder, soluble in methanol, ethanol, DMSO and other organic solvents, derived from the leaves of the water licorice leaves, oval leaf water licorice seeds, African wokanga tree seeds, Vinca seeds. |
use | has anti-tumor, antihypertensive, hypoglycemic, diuretic and other effects. Clinically, it is mainly used for the treatment and prevention of lymphosarcoma, leukemia, rhabdomyosarcoma, melanoma, spermatoblastoma, teratoma, and the treatment and prevention of hypertension and hyperglycemia. Glycyrrhizine has the effect of lowering blood pressure. used for content determination/identification/pharmacological experiment, etc. |
biological activity | Tabersonine is an indole alkaloid mainly isolated from rose. Tabersonine can destroy the polymerization of Aβ(1-42) and improve the cytotoxicity induced by Aβ polymerization. Tabersonine has anti-inflammatory activity and can be used for ALI/ARDS research. |