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Dihydrotanshinone-I

Cat. No. M4145
Dihydrotanshinone-I Structure
Size Price Availability Quantity
10mg USD 115  USD115 In stock
25mg USD 250  USD250 In stock
50mg USD 365  USD365 In stock
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Quality Control & Documentation
Biological Activity

Dihydrotanshinone I is a natural product isolated from Salvia miltiorrhiza and widely used in the study of cardiovascular diseases. It is a potent inhibitor of HuR:RNA interaction, active in the low nanomole range, mainly by limiting the binding rate of HuR to RNA.

Chemical Information
Molecular Weight 278.30
Formula C18H14O3
CAS Number 87205-99-0
Solubility (25°C) 10 mM in DMSO
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Xiao-Li Jiang, et al. Dihydrotanshinone I inhibits the growth of hepatoma cells by direct inhibition of Src

[2] Yue Wang, et al. Dihydrotanshinone I inhibits aortic valve interstitial cell calcification via the SMAD1/5/8/NF-κB/ERK pathway

[3] Peipei Luo, et al. Dihydrotanshinone I Is Effective against Drug-Resistant Helicobacter pylori In Vitro and In Vivo

[4] Xiaoping Wang, et al. TFEB-NF-κB inflammatory signaling axis: a novel therapeutic pathway of Dihydrotanshinone I in doxorubicin-induced cardiotoxicity

[5] Zhonglei Bao, et al. Dihydrotanshinone I Increase Amyloid-β Clearance and Decrease Tau Phosphorylation via Enhancing Autophagy

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