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Synonyms: OJV-II, Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside
![L-Borneol 7-O-[β-D-apiofuranosyl-(1→6)]-β-D-glucopyranoside](https://cdn.targetmol.com/group6/procas/20260611/p/8sbulp1pxg5phlupx6pp8fceb.png)
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $73 | - | In Stock | |
| 5 mg | $185 | - | In Stock | |
| 10 mg | $273 | - | In Stock | |
| 25 mg | $463 | - | In Stock |
| Description | L-Borneol 7-O-[β-D-apiofuranosyl-(1→6)]-β-D-glucopyranoside alleviates myocardial ischemia-reperfusion injury in rats and hypoxic/reoxygenated injured myocardial cells via regulating the PI3K/AKT/mTOR signaling pathway. L-Borneol 7-O-[β-D-apiofuranosyl-(1→6)]-β-D-glucopyranoside is therefore studied in cardiovascular ischemia–reperfusion experimental models to investigate PI3K/AKT/mTOR pathway modulation, cellular stress response regulation, and cardiomyocyte injury-associated signaling dynamics in hypoxia/reoxygenation systems. |
| In vivo | Method: Cardiac histopathological analysis using HE staining and TTC staining was performed in IR rats with L-Borneol 7-O-[β-D-apiofuranosyl-(1→6)]-β-D-glucopyranoside (LBAG) or Ver pretreatment. Result: IR group showed irregular myocardial cell arrangement, partial lysis in the infarct border zone, and cardiac muscle fiber breakage. LBAG or Ver pretreatment partially reversed these histological changes. TTC staining showed increased myocardial infarction size in MIRI rats, while LBAG or Ver pretreatment significantly reduced infarct areas compared with the IR group. |
| Synonyms | OJV-II, Borneol 7-O-[beta-D-apiofuranosyl-(1->6)]-beta-D-glucopyranoside |
| Molecular Weight | 448.50 |
| Formula | C21H36O10 |
| Cas No. | 88700-35-0 |
| Smiles | O([C@H]1[C@]2(C)C(C)(C)[C@](C1)(CC2)[H])[C@@H]3O[C@H](CO[C@H]4[C@H](O)[C@](CO)(O)CO4)[C@@H](O)[C@H](O)[C@H]3O |
| Relative Density. | 1.43 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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