CM-272
- CAS No.
- 1846570-31-7
- Chemical Name:
- CM-272
- Synonyms
- CM-272;CM-272; CM 272; CM272;6-Methoxy-2-(5-methylfuran-2-yl)-N-(1-methylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinolin-4-amine;4-Quinolinamine, 6-methoxy-2-(5-methyl-2-furanyl)-N-(1-methyl-4-piperidinyl)-7-[3-(1-pyrrolidinyl)propoxy]-;DNMT1,anti-tumour,DNMTs,immunogenic,DNA MTases,CM272,DNMT3A,CM 272,G9a,H3K9me2,Inhibitor,epigenetics,Histone Methyltransferase,GLP,Apoptosis,inhibit,substrate-competitive,CM-272,DNMT3B,DNA Methyltransferase
- CBNumber:
- CB14632529
- Molecular Formula:
- C28H38N4O3
- Molecular Weight:
- 478.63
- MDL Number:
- MFCD31812316
- MOL File:
- 1846570-31-7.mol
Boiling point | 631.9±55.0 °C(Predicted) |
---|---|
Density | 1.164±0.06 g/cm3(Predicted) |
storage temp. | Store at -20°C |
solubility |
DMSO:84.0(Max Conc. mg/mL);179.5(Max Conc. mM) Ethanol:63.0(Max Conc. mg/mL);131.63(Max Conc. mM) |
form | A crystalline solid |
pka | 10.09±0.20(Predicted) |
color | Light brown to brown |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
---|---|
Signal word | Warning |
Hazard statements | H302-H315-H319-H335 |
Precautionary statements | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
CM-272 price
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Axon Medchem | Axon2812 | CM-272 98% | 1846570-31-7 | 5mg | $137.5 | 2021-12-16 | Buy |
ChemScene | CS-0022181 | CM-272 98.13% | 1846570-31-7 | 5mg | $220 | 2021-12-16 | Buy |
ChemScene | CS-0022181 | CM-272 98.13% | 1846570-31-7 | 10mg | $375 | 2021-12-16 | Buy |
ChemScene | CS-0022181 | CM-272 98.13% | 1846570-31-7 | 50mg | $950 | 2021-12-16 | Buy |
ChemScene | CS-0022181 | CM-272 98.13% | 1846570-31-7 | 100mg | $1350 | 2021-12-16 | Buy |
CM-272 Chemical Properties,Uses,Production
Biological Activity
CM272 is a novel, first-in-class dual reversible inhibitor of G9a (GLP) and DNMTs with IC50 values of 8 nM, 382 nM, 85 nM, 1200 nM, and 2 nM for G9a, DNMT1, DNMT3A, DNMT3B, and GLP, respectively. CM272 prolongs survival in in vivo models of hematological malignancies by at least partially inducing immunogenic cell death.
in vitro
CM-272 (100-1000 nM; 12-72 hours; CEMO-1, MV4-11 and OCI-Ly10 cell lines) treatment inhibits cell proliferation in a dose- and time-dependent manner.
CM-272 (100-1000 nM; 24 hours; CEMO-1, MV4-11 and OCI-Ly10 cell lines) treatment blocks cell cycle progression.
CM-272 (100-1000 nM; 12-72 hours; CEMO-1, MV4-11 and OCI-Ly10 cell lines) treatment induces apoptosis in ALL, AML and DLBCL cell lines in a dose- and time-dependent manner.
CM-272 after 48 h of treatment CEMO -1 acute lymphoblastic leukaemia (ALL) cell line, MV4-11 acute myeloid leukaemia (AML) cell line and OCI-Ly10 diffuse large B-cell lymphoma (DLBCL) cell line, the GI 50 values of 218 nM, 269 nM and 455 nM, respectively, and is associated with a decrease in global levels of H3K9me2 and 5mC.
The therapeutic activity of CM-272 relies on the early activation of the type I IFN response in tumour cells , potentially leading to the induction of cell autonomous immunogenic death in tumou r cells.
Cell Proliferation Assay
Cell Line: | CEMO-1, MV4-11 and OCI-Ly10 cell lines |
Concentration: | 125 nM, 250 nM, 500 nM (CEMO-1 cells); 135 nM, 270 nM, 540 nM (MV4-11 cells); 100 nM, 400 nM, 1000 nM (OCI-Ly10 cells) |
Incubation Time: | 12 hours, 24 hours, 48 hours and 72 hours |
Result: | Inhibited cell proliferation in a dose- and time-dependent manner. |
Cell Cycle Analysis
Cell Line: | CEMO-1, MV4-11 and OCI-Ly10 cell lines |
Concentration: | |
Concentration: td> | 125 nM, 250 nM, 500 nM (CEMO-1 cells); 135 nM, 270 nM, 540 nM (MV4-11 cells); 100 nM, 400 nM, 1000 nM (OCI-Ly10 cells) |
Incubation Time: | 24 hours |
Result: | Blocked cell cycle progression. |
Apoptosis Analysis
Cell Line: | CEMO-1, MV4-11 and OCI-Ly10 cell lines |
Concentration: | 125 nM, 250 nM, 500 nM (CEMO-1 cells); 135 nM, 270 nM, 540 nM (MV4-11 cells); 100 nM, 400 nM, 1000 nM (OCI-Ly10 cells) |
Incubation Time: | 12 hours, 24 hours, 48 hours and 72 hours | Result: | Induced apoptosis in ALL, AML and DLBCL cell lines in a dose- and time-dep endent manner. |
in vivo
CM-272 (2.5 mg/kg; injection; daily; for 28 days; female Rag2 intravenous ?/? γc ?/? mice) treatment significantly prolongs survival of CEMO-1 cells xenogeneic models.
Animal Model: | Female BALB/Ca-Rag2 ?/? γc ?/? mice (6–8-week-old) with CEMO-1 cells |
Dosage: | 2.5 mg/kg |
Administration: | Intravenous injection; daily; for 28 days |
Result: | Induced a statistically significant increase in overall survival (OS) in mice. |
target
Target | Value |
G9a (Cell-free assay) | 8 nM |
DNMT3A (Cell-free assay) | 85 nM |
382 nM | |
DNMT3B (Cell-free assay) td> | 1200 nM |
CM-272 Preparation Products And Raw materials
Raw materials
Preparation Products
CM-272 Suppliers
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32760 | 60 |
HANGZHOU CLAP TECHNOLOGY CO.,LTD | 86-571-88216897,88216896 13588875226 | sales@hzclap.com | CHINA | 6313 | 58 |
Zhejiang J&C Biological Technology Co.,Limited | +1-2135480471 +1-2135480471 | sales@sarms4muscle.com | China | 10522 | 58 |
InvivoChem | +1-708-310-1919 +1-13798911105 | sales@invivochem.cn | United States | 6393 | 58 |
TargetMol Chemicals Inc. | +1-781-999-5354 | support@targetmol.com | United States | 19973 | 58 |
LEAPCHEM CO., LTD. | +86-852-30606658 | market18@leapchem.com | China | 43348 | 58 |
Aladdin Scientific | +1-+1(833)-552-7181 | sales@aladdinsci.com | United States | 57511 | 58 |
Shanghai Lollane Biological Technology Co.,Ltd. | 021-52996696,15000506266 15000506266 | China | 4264 | 55 | |
Shanghai Beckham Medical Technology Co., Ltd | 021-13816613772 13816613772 | huahero21@sina.com | China | 382 | 55 |
Shanghai EFE Biological Technology Co., Ltd. | 021-65675885 18964387627 | info@efebio.com | China | 9707 | 58 |