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Lupanine
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Catalog No. TMA0805Cas No. 550-90-3
Alias D-Lupanine, (+)-Lupanine
Lupanine ((+)-Lupanine), a naturally occurring quinolizidine alkaloid, potently affinity and activates nicotinic acetylcholine receptor (nAChR) (Ki=500 nM), and shows significant neuroprotection against soluble amyloid β-oligomers (SO-Aβ) toxicity in cellular models in association with the anti-apoptotic PI3K/ Akt/Bcl-2 signaling pathway with anti-Alzheimer's disease potential. Improves glucose homeostasis by affecting KATP channels and enhancing insulin secretion with therapeutic potential for type 2 diabetes.
Lupanine
😃Good
Catalog No. TMA0805Alias D-Lupanine, (+)-LupanineCas No. 550-90-3
Lupanine ((+)-Lupanine), a naturally occurring quinolizidine alkaloid, potently affinity and activates nicotinic acetylcholine receptor (nAChR) (Ki=500 nM), and shows significant neuroprotection against soluble amyloid β-oligomers (SO-Aβ) toxicity in cellular models in association with the anti-apoptotic PI3K/ Akt/Bcl-2 signaling pathway with anti-Alzheimer's disease potential. Improves glucose homeostasis by affecting KATP channels and enhancing insulin secretion with therapeutic potential for type 2 diabetes.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $1,309 | 6-8 weeks | |
| 25 mg | Inquiry | 6-8 weeks | |
| 50 mg | Inquiry | 6-8 weeks | |
| 100 mg | Inquiry | 6-8 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | Lupanine ((+)-Lupanine), a naturally occurring quinolizidine alkaloid, potently affinity and activates nicotinic acetylcholine receptor (nAChR) (Ki=500 nM), and shows significant neuroprotection against soluble amyloid β-oligomers (SO-Aβ) toxicity in cellular models in association with the anti-apoptotic PI3K/ Akt/Bcl-2 signaling pathway with anti-Alzheimer's disease potential. Improves glucose homeostasis by affecting KATP channels and enhancing insulin secretion with therapeutic potential for type 2 diabetes. |
| In vitro | Lupanine (0-100 μM) treats SH-SY5Y cells with EC50 and DC50 values of 10.7 μM and 28.2 μM, respectively. [2] |
| In vivo | Methods: Lupanine (20 mg/kg, orally) was administered to non-diabetic and diabetic rats, and an oral glucose tolerance test was performed 30 minutes later. Results: Lupanine reduced blood glucose concentrations and improved glycemic control in an in vivo diabetic rat model. [3] |
| Alias | D-Lupanine, (+)-Lupanine |
| Molecular Weight | 248.36 |
| Formula | C15H24N2O |
| Cas No. | 550-90-3 |
| Smiles | O=C1N2[C@@]([C@]3(C[C@@](C2)([C@]4(N(C3)CCCC4)[H])[H])[H])(CCC1)[H] |
| Relative Density. | 1.16g/cm3 |
Storage & Solubility Information
| Storage | keep away from direct sunlight | store at 4°C | Shipping with blue ice. |
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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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