A8353512
Vinpocetine , 99% , 42971-09-5
Synonym(s):
(3α,16α)-Eburnamenine-14-carboxylic acid ethyl ester;Eburnamenine-14-carboxylic acid ethyl ester
CAS NO.:42971-09-5
Empirical Formula: C22H26N2O2
Molecular Weight: 350.46
MDL number: MFCD00211233
EINECS: 256-028-0
Pack Size | Price | Stock | Quantity |
25MG | RMB23.20 | In Stock |
|
100MG | RMB31.20 | In Stock |
|
1g | RMB50.40 | In Stock |
|
5g | RMB151.20 | In Stock |
|
25g | RMB2079.20 | In Stock |
|
others | Enquire |
Update time: 2022-07-08
PRODUCT Properties
Melting point: | 147-153 °C dec. |
alpha | D20 +114° (c = 1 in pyridine) |
Boiling point: | 484.44°C (rough estimate) |
Density | 1.1260 (rough estimate) |
refractive index | 1.6500 (estimate) |
storage temp. | Sealed in dry,2-8°C |
solubility | DMSO: 5 mg/mL |
form | solid |
pka | 7.87±0.60(Predicted) |
color | white |
optical activity | [α]/D 148.5±5.0°, c = 0.1 in chloroform |
λmax | 315nm(EtOH)(lit.) |
Merck | 14,9991 |
Stability: | Photosensitive |
InChIKey | DDNCQMVWWZOMLN-IRLDBZIGSA-N |
LogP | 5.137 (est) |
Description and Uses
Vinpocetine (42971-09-5) is a phosphodiesterase PDE1 inhibitor (IC50=21 μM).1?Also blocks voltage-gated Na+?channels, IC50=44.2 μM (potency similar to phenytoin), a mechanism which may contribute to its neuroprotective and anticonvulsant activity.2?It reduces inflammatory IL-1β and TNF-α expression in rat hippocampus.3?Displays beneficial effects in a rat model of cerebral ischemia-reperfusion injury.4?Vinpocetine exerts neuroprotective effects by suppressing microglial inflammation.5
A calcium/calmodulin-dependent phosphodiesterase 1 (PDE1) inhibitor
Safety
Symbol(GHS) | GHS07 |
Signal word | Warning |
Hazard statements | H302 |
Precautionary statements | P264-P270-P301+P312-P501 |
Hazard Codes | Xn |
Risk Statements | 22 |
Safety Statements | 36 |
WGK Germany | 3 |
RTECS | JW4792000 |
HS Code | 29399990 |
Toxicity | LD50 in mice, rats (mg/kg): 534, 503 orally; 240, 133.8 i.p.; 58.7, 42.6 i.v. (Pálosi, Szporny), also reported as 161.2 mg/kg i.p. in mice (Cholnoky, Dmk) |