Shopping Cart
- Remove All
- Your shopping cart is currently empty
Dehydrocrenatidine (Kumujian G) is an inhibitor of JAK and induces cell apoptosis.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
25 mg | $2,650 | 10-14 weeks | |
50 mg | $3,450 | 10-14 weeks | |
100 mg | $5,240 | 10-14 weeks |
Description | Dehydrocrenatidine (Kumujian G) is an inhibitor of JAK and induces cell apoptosis. |
In vitro | In DU145 and MDA-MB-468 cells, Dehydrocrenatidine inhibits cell survival and induces cell apoptosis in a JAK-STAT3-dependent manner. Dehydrocrenatidine reduces the STAT3 phosphorylation stimulated by IL-6, IFN-α, and IFN-γ[1]. Dehydrocrenatidine reduces tetrodotoxin-resistant and sensitive voltage-gated sodium channel currents with IC50 values of 12.36 µM and 4.87 µM, respectively[2]. |
In vivo | Dehydrocrenatidine inhibits voltage-gated sodium channels and ameliorates mechanic allodia in a rat model of neuropathic pain[2]. |
Alias | TOP-3, TOP3, TOP 3, O-Methylpicrasidine I, Kumujian G |
Molecular Weight | 254.28 |
Formula | C15H14N2O2 |
Cas No. | 65236-62-6 |
Smiles | O(C)C1=C2C=3C(NC2=C(C=C)N=C1)=C(OC)C=CC3 |
Relative Density. | 1.251 g/cm3 |
Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
Solubility Information | DMSO: Soluble |
Copyright © 2015-2024 TargetMol Chemicals Inc. All Rights Reserved.