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M1001

Cat. No. M11025
M1001  Structure
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Biological Activity

M1001 is a weaker HIF-2α agonist that binds directly to the HIF-2α PAS-B domain.Kd The value is 667 nM. The M1001 enhances stability between HIF-2α-ARNT complexes.

Chemical Information
Molecular Weight 327.4
Formula C17H17N3O2S
CAS Number 874590-32-6
Solubility (25°C) DMSO ≥ 60 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] Rong Zhang, et al. Front Plant Sci. Combining Metabolomics and Transcriptomics to Reveal the Mechanism of Coloration in Purple and Cream Mutant of Sweet Potato ( Ipomoea batatas L.)

[2] Yancheng Yu, et al. Eur J Med Chem. Insight into the binding mode of HIF-2 agonists through molecular dynamic simulations and biological validation

[3] Aliakbar Dehno Khalaji, et al. Acta Crystallogr Sect E Struct Rep Online. [4-Bromo-N-(pyridin-2-yl-methyl-idene)aniline-κ(2)N,N']iodido(triphenyl-phosphane-κP)copper(I)

[4] Muhammad Mufakkar, et al. Acta Crystallogr Sect E Struct Rep Online. Dichloridobis(N,N'-diethyl-thio-urea-κS)mercury(II)

[5] Yong-Hong Liu, et al. Acta Crystallogr Sect E Struct Rep Online. (E)-1-Ferrocenyl-3-phenyl-prop-2-en-1-one

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