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Chemical Structure| 1020149-73-8 Chemical Structure| 1020149-73-8

Structure of SGI-1027
CAS No.: 1020149-73-8

Chemical Structure| 1020149-73-8

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SGI-1027 is a DNA methyltransferase (DNMT) inhibitor with IC50 values of 7.5 μM, 8 μM, and 12.5 μM for DNMT3B, DNMT3A, and DNMT1, respectively, using poly(dI-dC) as a substrate.

Synonyms: DNA Methyltransferase Inhibitor II

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Product Details of SGI-1027

CAS No. :1020149-73-8
Formula : C27H23N7O
M.W : 461.52
SMILES Code : O=C(NC1=CC=C(NC2=NC(N)=NC(C)=C2)C=C1)C3=CC=C(NC4=CC=NC5=CC=CC=C45)C=C3
Synonyms :
DNA Methyltransferase Inhibitor II
MDL No. :MFCD27937047
InChI Key :QSYLKMKIVWJAAK-UHFFFAOYSA-N
Pubchem ID :24858111

Safety of SGI-1027

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Related Pathways of SGI-1027

epigenetics

Isoform Comparison

Biological Activity

Target
  • DNA Methyltransferase

    DNMT1, IC50:6 μM

    DNMT3A, IC50:7.5 μM

In Vitro:

Cell Line
Concentration Treated Time Description References
DNMT3Acat 0.8 µM (IC50) To study the inhibitory activity of SGI-1027 against DNMT3Acat PMC4358266
DNMT1 10 µM (IC50) 2 hours To study the mechanism of inhibition of DNMT1 by SGI-1027, results showed it as a DNA-competitive and AdoMet non-competitive inhibitor PMC4358266
DNMT1 10 µM (IC50) 2 hours To study the mechanism of inhibition of DNMT1 by SGI-1027, results showed it as a DNA-competitive and AdoMet non-competitive inhibitor PMC4358266
HEK293 cells 10 µM 20 minutes Evaluate the inhibitory effect of SGI-1027 and its derivatives on Rlig1-AMP, results showed that SGI-1027 and some of its derivatives effectively inhibited Rlig1-AMP activity PMC11747885
HeLa cells 1 μM 24 hours To evaluate the effect of SGI-1027 in combination with AH057 on cell cycle in HeLa cells, results showed that the combined treatment increased the proportion of cells in G1 phase. PMC7476923
HeLa cells 1 μM 24 hours To evaluate the effect of SGI-1027 in combination with AH057 on apoptosis in HeLa cells, results showed that the combined treatment significantly increased the percentage of apoptotic cells. PMC7476923
Leukemia KG-1 cells 1-10 μM 24 hours To test the ability of the compounds to reactivate the luciferase reporter gene controlled by a methylated CMV promoter. Results showed that SGI-1027 induced a 16-fold luciferase expression at 5 μM, but at 10 μM, the signal decreased due to cytotoxicity. PMC4506529
MDA-MB-231 breast cancer cells 0.9 μM 48 hours To evaluate cell viability and proliferation, results showed that MC3353 significantly inhibited cell viability and proliferation PMC6501426
PC-3 prostate cancer cells 0.9 μM 48 hours To evaluate cell viability and proliferation, results showed that MC3353 significantly inhibited cell viability and proliferation PMC6501426
RAJI Burkitt’s lymphoma cells 0.4 μM 48 hours To evaluate cell viability and proliferation, results showed that MC3353 significantly inhibited cell viability and proliferation PMC6501426
U-937 acute myeloid leukemia cells 0.4 μM 48 hours To evaluate cell viability and proliferation, results showed that MC3353 significantly inhibited cell viability and proliferation PMC6501426
HCT116 colon cancer cells 0.5 μM 48 hours To evaluate antiproliferative activity, results showed that MC3353 significantly inhibited cell proliferation PMC6501426
HK-2 cells 3.916 μM 48 hours To evaluate the cytotoxicity of SGI-1027 on renal cancer cells and HK-2 cells, it was found that SGI-1027 inhibited the cell viability of all tested cell lines in a dose-dependent manner PMC11481186
Caki-1 cells 2.965 μM 48 hours To evaluate the cytotoxicity of SGI-1027 on renal cancer cells and HK-2 cells, it was found that SGI-1027 inhibited the cell viability of all tested cell lines in a dose-dependent manner PMC11481186
A-498 cells 1.702 μM 48 hours To evaluate the cytotoxicity of SGI-1027 on renal cancer cells and HK-2 cells, it was found that SGI-1027 inhibited the cell viability of all tested cell lines in a dose-dependent manner PMC11481186
786-O cells 1.121 μM 48 hours To evaluate the cytotoxicity of SGI-1027 on renal cancer cells and HK-2 cells, it was found that SGI-1027 inhibited the cell viability of all tested cell lines in a dose-dependent manner PMC11481186
Primary osteoblasts 10 μM 48 hours SGI-1027 alleviated the ferroptotic changes caused by FAC, but not by a GPX4 inactivator RSL3 PMC11609303
Osteoblasts 10 μM 48 hours SGI-1027 reversed titanium particle (TP)-induced GPX4 repression and ferroptotic changes, restoring GPX4 expression and reducing the lipid peroxidation marker 4-HNE. PMC11331012
SMB cells 50 nM (IC50) 5 days Evaluate the effect of SGI-1027 on PrPSc elimination, results showed that SGI-1027 effectively eliminated PrPSc PMC6804459
ScN2a cells 50 nM (IC50) 5 days Evaluate the effect of SGI-1027 on PrPSc elimination, results showed that SGI-1027 effectively eliminated PrPSc PMC6804459
KG-1 acute myeloid leukemia cells 1 μM 5 hours To evaluate CMV promoter-driven luciferase reporter system, results showed that MC3353 significantly enhanced luciferase expression PMC6501426
HK2 cells 10 μM 60 hours Evaluate the restorative effect of SGI-1027 on KLOTHO and NRF2 expression PMC8761007
N2a cells 1 μM 96 hours Evaluate the effect of SGI-1027 on prion infection prevention, results showed that SGI-1027 effectively prevented prion infection PMC6804459
DNMT3Acat 0.8 µM (IC50) To study the inhibitory activity of SGI-1027 against DNMT3Acat PMC4358266
HEK293T cells 0-100 µM SGI-1027 inhibits the interaction between GST-MKK3 and VF-MYC PMC8456368
MDA-MB-468 triple-negative breast cancer cells 0-50 µM SGI-1027 reduces MYC protein level and expression of its target genes CDK4 and PD-L1 PMC8456368
HCT116 colon cancer cells 0-50 µM SGI-1027 inhibits MKK3-MYC protein-protein interaction, reduces MYC protein level and expression of its target genes CDK4 and PD-L1 PMC8456368

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice NMDA-induced retinal injury model Intravitreal injection 10 µM Single injection, lasting 24 hours SGI-1027 induced Oct4 expression in MG at 24hpi after retinal injury. PMC5108807
Mice Ovariectomy-induced osteoporosis model Intraperitoneal injection 2.5 mg/kg Once daily for 6 weeks SGI-1027 reversed promoter hypermethylation, GPX4 suppression and ferroptotic osteoporosis PMC11609303
Mice Calvarial osteolysis model Intraperitoneal injection 2.5 mg/kg Once daily for 2 weeks SGI-1027 significantly reversed TP-induced Gpx4 promoter hypermethylation and GPX4 repression, improving ferroptotic osteolysis to a similar extent as the ferroptosis inhibitor liproxstatin-1. PMC11331012
ICR mice D-galactose-induced accelerated aging model Intraperitoneal injection 2.5 mg/kg Daily for 8 weeks Evaluate the protective effect of SGI-1027 on D-gal-induced renal aging PMC8761007
Nude mice A-498 cell subcutaneous xenograft model Oral gavage 30 mg/kg/day (SGI-1027) and 2 mg/kg/day (everolimus) Once daily for 16 days To evaluate the in vivo anti-tumor effect of SGI-1027 in combination with everolimus, the results showed that the combination treatment significantly inhibited tumor growth and induced GSDME-dependent pyroptosis PMC11481186
BALB/c nude mice HeLa cell xenograft model Oral gavage 50 mg/kg/day Once daily for 30 consecutive days To evaluate the effect of SGI-1027 in combination with AH057 on tumor volume, results showed that the combined treatment significantly reduced tumor volume. PMC7476923

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.17mL

0.43mL

0.22mL

10.83mL

2.17mL

1.08mL

21.67mL

4.33mL

2.17mL

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

[1]Garcia-Dominguez P, Dell'aversana C, et al. Synthetic approaches to DNMT inhibitor SGI-1027 and effects on the U937 leukemia cell line. Bioorg Med Chem Lett. 2013 Mar 15;23(6):1631-5.

[2]Datta J, Ghoshal K, et al. A new class of quinoline-based DNA hypomethylating agents reactivates tumor suppressor genes by blocking DNA methyltransferase 1 activity and inducing its degradation. Cancer Res. 2009 May 15;69(10):4277-85.

[3]Holliday R, Pugh JE. DNA modification mechanisms and gene activity during development. Science. 1975 Jan 24;187(4173):226-32.

[4]Gros C, Fleury L, Nahoum V, Faux C, Valente S, Labella D, Cantagrel F, Rilova E, Bouhlel MA, David-Cordonnier MH, Dufau I, Ausseil F, Mai A, Mourey L, Lacroix L, Arimondo PB. New insights on the mechanism of quinoline-based DNA Methyltransferase inhibitors. J Biol Chem. 2015 Mar 6;290(10):6293-302.

[5]Datta J, Ghoshal K, Denny WA, Gamage SA, Brooke DG, Phiasivongsa P, Redkar S, Jacob ST. A new class of quinoline-based DNA hypomethylating agents reactivates tumor suppressor genes by blocking DNA methyltransferase 1 activity and inducing its degradation. Cancer Res. 2009 May 15;69(10):4277-85.

[6]Sun N, Zhang J, Zhang C, Zhao B, Jiao A. DNMTs inhibitor SGI-1027 induces apoptosis in Huh7 human hepatocellular carcinoma cells. Oncol Lett. 2018 Nov;16(5):5799-5806.

[7]Reyes-Aguirre LI, Lamas M. Oct4 Methylation-Mediated Silencing As an Epigenetic Barrier Preventing Müller Glia Dedifferentiation in a Murine Model of Retinal Injury. Front Neurosci. 2016 Nov 15;10:523.

 

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