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Chemical Structure| 1893415-00-3 Chemical Structure| 1893415-00-3

Structure of Mizacorat
CAS No.: 1893415-00-3

Chemical Structure| 1893415-00-3

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Mizacorat is an effective, orally active non-steroidal selective glucocorticoid receptor modulator (SGRM) with an IC50 of 3.8 nM. In models of inflammation with SCW, Mizacorat shows significant anti-inflammatory efficacy, suitable for chronic inflammatory disease research.

Synonyms: AZD9567

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Product Details of Mizacorat

CAS No. :1893415-00-3
Formula : C27H28F2N4O3
M.W : 494.53
SMILES Code : CN1C(C=CC(N2N=CC3=CC(O[C@@H]([C@@H](NC(C(F)(C)F)=O)C(C)C)C4=CC=CC=C4)=CC=C32)=C1)=O
Synonyms :
AZD9567
MDL No. :MFCD31619227

Safety of Mizacorat

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
primary CD4+ T cells 0.01 µM–10 µM 24 hours and 48 hours AZD9567 triggered luciferase expression even at the lowest concentration tested (0.01 µM) J Virol. 2025 Feb 25;99(2):e0188624
U1 cells 0.01 µM–10 µM 48 hours and 96 hours AZD9567 consistently reactivated HIV-1 in all cell lines tested J Virol. 2025 Feb 25;99(2):e0188624
ACH-2 cells 0.01 µM–10 µM 48 hours and 96 hours AZD9567 consistently reactivated HIV-1 in all cell lines tested J Virol. 2025 Feb 25;99(2):e0188624
J-Lat 10.6 cells 0.01 µM–10 µM 48 hours and 96 hours AZD9567 consistently reactivated HIV-1 in all cell lines tested J Virol. 2025 Feb 25;99(2):e0188624
Hela cells 10 μM 18 hours GR ligand binding test, 16 compounds at 10 μM exhibit good inhibition activities (>70%) Adv Sci (Weinh). 2022 Jan;9(3):e2102435
Raw264.7 cells 25 μM 48 hours Cytotoxicity test, 72 compounds do not affect cell viability at 25 μM Adv Sci (Weinh). 2022 Jan;9(3):e2102435

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.02mL

0.40mL

0.20mL

10.11mL

2.02mL

1.01mL

20.22mL

4.04mL

2.02mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

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