research use only
Cat.No.S3881
| Related Targets | PD-1/PD-L1 CXCR STING AhR CD markers Interleukins Anti-infection Antioxidant COX Histamine Receptor |
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| Other Immunology & Inflammation related Inhibitors | Cl-amidine Bestatin (Ubenimex) Tempol Tranilast Sinomenine Geniposidic acid GI254023X (GI4023) CORM-3 Acacetin Germacrone |
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In vitro |
DMSO
: 38 mg/mL
(197.74 mM)
Ethanol : 10 mg/mL Water : Insoluble |
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In vivo |
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Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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| Molecular Weight | 192.17 | Formula | C10H8O4 |
Storage (From the date of receipt) | |
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| CAS No. | 92-61-5 | Download SDF | Storage of Stock Solutions |
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| Synonyms | Esculetin 6-methyl ether, Gelseminic acid, 6-Methylesculetin, Chrysatropic acid | Smiles | COC1=C(C=C2C(=C1)C=CC(=O)O2)O | ||
| In vitro |
Scopoletin (1-50 μg/ml) inhibits the release of PGE2, TNF-a, IL-1b and IL-6 and suppresses the expression of COX-2 in a concentration-dependent manner. In vitro studies reveal that this compound lessens rotenone-induced apoptosis in SH-SY5Y cells through preventing oxidative injury. Particularly, it markedly up-regulates DJ-1, which then promotes the nuclear translocation of Nrf2 and transactivation of antioxidant genes. This chemical prevents the nuclear exportation of Nrf2 by reducing the levels of Keap1 and thereby enhancing the neuronal defence system.
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| In vivo |
Scopoletin expressively represses the aortic oxido-lipidemic stress and thereby upholding normal morphology of the aorta, and thus minimizing the peril of CVD.
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References |
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