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Chemical Structure| 1429054-28-3 Chemical Structure| 1429054-28-3

Structure of IDF-11774
CAS No.: 1429054-28-3

Chemical Structure| 1429054-28-3

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IDF-11774 is a hypoxia-inducible factor (HIF)-1α inhibitor which regulates cancer metabolism, thereby suppressing tumor growth.

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Product Details of IDF-11774

CAS No. :1429054-28-3
Formula : C23H32N2O2
M.W : 368.51
SMILES Code : CN1CCN(C(COC2=CC=C(C34CC5CC(C4)CC(C5)C3)C=C2)=O)CC1
MDL No. :MFCD31619285
InChI Key :QGBBBLPWBSWERZ-UHFFFAOYSA-N
Pubchem ID :71542096

Safety of IDF-11774

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of IDF-11774

epigenetics

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
HT29 cells 5 μM 72 hours To evaluate the synthetic lethal effect of IDF-11774 with ATP6V0C knockdown, results showed that ATP6V0C knockdown significantly enhanced the growth inhibitory effect of IDF-11774 on HT29 cells. Br J Cancer. 2018 Nov;119(11):1347-1357.
WiDr cells 5 μM 72 hours To evaluate the synthetic lethal effect of IDF-11774 with ATP6V0C knockdown, results showed that ATP6V0C knockdown significantly enhanced the growth inhibitory effect of IDF-11774 on WiDr cells. Br J Cancer. 2018 Nov;119(11):1347-1357.
HCT116 cells 5 μM 72 hours To evaluate the synthetic lethal effect of IDF-11774 with ATP6V0C knockdown, results showed that ATP6V0C knockdown significantly enhanced the growth inhibitory effect of IDF-11774 on HCT116 cells. Br J Cancer. 2018 Nov;119(11):1347-1357.
HCT116 human colon cancer cells 10 μM 12 hours IDF-11774 inhibited HIF-1α accumulation and reduced levels of glycolysis and TCA cycle intermediates, leading to an increased AMP/ATP ratio. Cell Death Dis. 2017 Jun 1;8(6):e2843.
MC3T3-E1 cells 10 μM IDF-11774 treatment significantly restored the expression levels of RUNX2 and OPN, which were inhibited by S. aureus infection, and rescued mineralization defects as evidenced by ALP and ARS staining. mSystems. 2022 Aug 30;7(4):e0038022.
B16F10 mouse melanoma cells 2.5 mM and 5.0 mM 48-72 hours IDF-11774 reduced HIF-1α protein expression, decreased cell survival, and increased cytotoxicity under CoCl2-induced hypoxic conditions. Biomol Ther (Seoul). 2022 Sep 1;30(5):465-472.
MKN74 cells 15 µM and 30 µM 4 hours To evaluate the effect of IDF-11774 on HIF-1α expression, results showed that IDF-11774 significantly reduced HIF-1α expression Pharmaceutics. 2023 Dec 13;15(12):2772.
MKN45 cells 15 µM and 30 µM 4 hours To evaluate the effect of IDF-11774 on HIF-1α expression, results showed that IDF-11774 significantly reduced HIF-1α expression Pharmaceutics. 2023 Dec 13;15(12):2772.
K1 cells 15 μM and 30 μM 24 hours To evaluate the effect of IDF-11774 on the proliferation of K1 cells, results showed that IDF-11774 had no significant effect on the proliferation of K1 cells. Pharmaceuticals (Basel). 2020 Aug 24;13(9):208.
BCPAP cells 15 μM and 30 μM 24 hours To evaluate the effect of IDF-11774 on the proliferation of BCPAP cells, results showed that IDF-11774 inhibited the proliferation of BCPAP cells in a dose-dependent manner. Pharmaceuticals (Basel). 2020 Aug 24;13(9):208.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Balb/c nude mice HCT116 human colon cancer xenograft model Oral administration 20 mg/kg/day Once daily for 15 days To evaluate the in vivo anti-tumor activity of IDF-11774, results showed that IDF-11774 significantly inhibited the growth of HCT116 xenograft tumors. Br J Cancer. 2018 Nov;119(11):1347-1357.
Balb/c nude mice HCT116 xenograft model Oral 50 mg/kg Once daily for 15 days IDF-11774 significantly suppressed tumor growth and showed anticancer efficacy in various cancer models. Cell Death Dis. 2017 Jun 1;8(6):e2843.
Mice S. aureus infection-induced osteomyelitis model Oral 20 mg/kg/day Once daily for 7 days IDF-11774 treatment significantly reduced serum levels of IL-6, IL-1β, and CRP, as well as TGF-β1 concentration in infected mice. mSystems. 2022 Aug 30;7(4):e0038022.
Balb/c nude mice B16F10 melanoma transplantation model Oral 0, 10, 30, 60 mg/kg Once daily for 14 days IDF-11774 reduced tumor volume and local invasion, and downregulated HIF-1α expression. Biomol Ther (Seoul). 2022 Sep 1;30(5):465-472.

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.71mL

0.54mL

0.27mL

13.57mL

2.71mL

1.36mL

27.14mL

5.43mL

2.71mL

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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