| Name | rauwolscine |
|---|---|
| Synonyms |
isoyohimbine
17a-Hydroxy-20a-yohimban-16b-carboxylic Acid Methyl Ester KEOXIFENE Corynanthidine a-Yohimbine α-Yohimbine EINECS 205-006-9 20α-Yohimban-16β-carboxylic acid, 17α-hydroxy-, methyl ester (8CI) Rauwolscine RALOXIFENE HCL KEOXIFENE HYDROCHLORIDE Yohimban-16-carboxylic acid, 17-hydroxy-, methyl ester, (16β,17α,20α)- Methyl (16β,17α,20α)-17-hydroxyyohimban-16-carboxylate |
| Description | Rauwolscine is a selective α2-adrenoceptor antagonist that inhibits tumor growth and induces apoptosis[1]. |
|---|---|
| Related Catalog | |
| In Vivo | Rauwolscine (0.5 mg/kg, daily) 通过增强细胞凋亡和减少细胞增殖来减少 Balb/c 雌性小鼠的肿瘤生长[1]。 Rauwolscine (i.v., 2.24 mg/kg) 能明显释放大鼠的舔食冲突反应,类似于α受体激动剂 clonidine (0.022 mg/kg) 和benzodiazepine diazepam (0.5 mg/kg)[2]。 |
| References |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 543.0±50.0 °C at 760 mmHg |
| Melting Point | 270-280ºC |
| Molecular Formula | C21H26N2O3 |
| Molecular Weight | 354.443 |
| Flash Point | 282.2±30.1 °C |
| Exact Mass | 354.194336 |
| PSA | 65.56000 |
| LogP | 2.20 |
| Vapour Pressure | 0.0±1.5 mmHg at 25°C |
| Index of Refraction | 1.661 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
| Hazard Codes | Xi |
|---|---|
| Risk Phrases | 23/24/25 |
| Safety Phrases | 22-36/37/39-45 |
| RIDADR | UN 1544 6.1/PG 2 |
| Packaging Group | II |
| Hazard Class | 6.1(a) |