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SGI-1027

CAS No.
1020149-73-8
Chemical Name:
SGI-1027
Synonyms
CS-1144;SGI-1027;SGI1027; SGI 1027;SGI-1027 USP/EP/BP;DNA Methyltransferase Inhibitor II;N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide;N-[4-[(2-amino-6-methylpyrimidin-4-yl)amino]phenyl]-4-(quinolin-4-ylamino)benzamide;Benzamide, N-[4-[(2-amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)-;N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide SGI-1027;SGI-1027 N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide
CBNumber:
CB42663344
Molecular Formula:
C27H23N7O
Molecular Weight:
461.52
MDL Number:
MFCD27937047
MOL File:
1020149-73-8.mol
MSDS File:
SDS
Last updated:2024-06-30 15:45:59

SGI-1027 Properties

Melting point >280℃
Density 1.387±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 35 mg/ml)
pka 13.31±0.70(Predicted)
form powder
color white to light brown
Stability Stable for 2 years as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.

SGI-1027 price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1358 SGI-1027 ≥98% (HPLC) 1020149-73-8 5MG $142 2024-06-20 Buy
Sigma-Aldrich SML1358 SGI-1027 ≥98% (HPLC) 1020149-73-8 25MG $564 2024-06-20 Buy
Cayman Chemical 11165 SGI-1027 ≥98% 1020149-73-8 1mg $37 2025-03-01 Buy
Cayman Chemical 11165 SGI-1027 ≥98% 1020149-73-8 5mg $108 2025-03-01 Buy
Cayman Chemical 11165 SGI-1027 ≥98% 1020149-73-8 10mg $178 2025-03-01 Buy
Product number Packaging Price Buy
SML1358 5MG $142 Buy
SML1358 25MG $564 Buy
11165 1mg $37 Buy
11165 5mg $108 Buy
11165 10mg $178 Buy

SGI-1027 Chemical Properties,Uses,Production

Description

SGI-1027 is a DNMT inhibitor with IC50 of 6, 8, 7.5 μM for DNMT1, DNMT3A, and DNMT3B in cell-free assays, respectively.

Features

Potential for use in epigenetic cancer therapy.

In vitro

SGI-1027 inhibits DNA methylation by directly inhibiting DNMTs, and results in selective degradation of DNMT1 in a wide variety of human cancer cell lines. SGI-1027 exhibits minimal or no cytotoxic effect in rat hepatoma H4IIE cells.  SGI-1027 (0-100 μM) exhibits a moderate pro-apoptotic effect on U937 human leukemia cell line with no relevant changes on the cell cycle.

Description

SGI-1027 (1020149-73-8) is a potent and selective inhibitor of DNA methyl transferase inhibiting DNMT1, DNMT3A and DNMT3B with comparable potency (IC50=12.5, 8.0 and 7.5 mM respectively).1? Treatment of various cancer cell lines with SGI-1027 results in selective degradation of DNMT1 (MG-132 sensitive) with minimal effect on DNMT3A and 3B at 2.5-5 mM.1 Prolonged treatment of RKO cells resulted in reexpression of silenced tumor suppressor genes.1 Synergizes with doxorubicin at growth inhibition in neuroblastoma cell lines.2 Disrupts the MKK3-MYC complex in cells and inhibits MYC transcriptional activity in colon and breast cancer cells.3

Uses

SGI-1027 is a quinoline derivative and a potent inhibitor of DNA methyltransferase (DNMT). SGI-1027 can be used as a potential therapeutic agent for the treatment of cancer and other diseases and also as a research tool to investigate the role of DNMTs in epigenetic events.

Biochem/physiol Actions

SGI-1027 is a DNA methyltransferase (DNMT) inhibitor with IC50 values of 6-13 μM for DNMT3B, DNMT3A and DNMT1. SGI-1027 directly inhibits DNMT activity by competing with the cofactor, S-adenosylmethionine (SAM) in the methylation reaction. SGI-1027 treatment of cancer cell lines induced degradation of DNMT1, but not DNMT3A or DNMT3B, and in RKO cells caused re-expression of the silenced tumor supressor genes p16, MLH1 and TIMP3.

target

DNMT1

storage

Store at -20°C

References

Datta et al. (2009), 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., 69 4277 Penter et al. (2015) A rapid screening system evaluates novel inhibitors of DNA methylation and suggests F-box proteins as potential therapeutic targets for high-risk neuroblastoma; Target Oncol., 10 523 Yang et al. (2021), Discovery of the first chemical tools to regulate MKK3-mediated MYC activation in cancer; Bioorg. Chem., 45 116324
611-35-8
1020150-22-4
1020149-73-8
Synthesis of SGI-1027 from 4-Chloroquinoline and 4-aMino-N-(4-(2-aMino-6-MethylpyriMidin-4-ylaMino)phenyl)benzaMide
Global( 88)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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InvivoChem
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Coresyn Pharmatech Co., Ltd.
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ShenZhen Trendseen Biological Technology Co.,Ltd.
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LEAPCHEM CO., LTD.
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SGI-1027 Spectrum

N-[4-[(2-amino-6-methylpyrimidin-4-yl)amino]phenyl]-4-(quinolin-4-ylamino)benzamide SGI-1027 N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide DNA Methyltransferase Inhibitor II Benzamide, N-[4-[(2-amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)- N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide SGI-1027 SGI-1027 N-[4-[(2-Amino-6-methyl-4-pyrimidinyl)amino]phenyl]-4-(4-quinolinylamino)benzamide CS-1144 SGI1027; SGI 1027 SGI-1027 USP/EP/BP 1020149-73-8 C27H23N7O Inhibitors
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