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MI-136

Cat. No. M9149
MI-136 Structure
Size Price Availability Quantity
5mg USD 115  USD115 In stock
10mg USD 190  USD190 In stock
50mg USD 700  USD700 In stock
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Quality Control & Documentation
Biological Activity

MI-136 inhibits DHT-induced expression of androgen receptor (AR) target genes. MI-136 treatment inhibits the expression of genes that were bound to ASH2L after AR stimulation.

In vivo, treatment of VCaP tumor-bearing mice with MI-136 (40 mg/kg) led to a modest but significant reduction in tumor volume with no effect on mouse body weight.

Chemical Information
Molecular Weight 470.51
Formula C23H21F3N6S
CAS Number 1628316-74-4
Solubility (25°C) DMSO: ≥ 30 mg/mL
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] Jingyao Chen, et al. An organoid-based drug screening identified a menin-MLL inhibitor for endometrial cancer through regulating the HIF pathway

[2] Dmitry Borkin, et al. Property Focused Structure-Based Optimization of Small Molecule Inhibitors of the Protein-Protein Interaction between Menin and Mixed Lineage Leukemia (MLL)

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Keywords: MI-136 supplier, Androgen Receptor, inhibitors, activators


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