m6A-centered Drug Response Information

General Information of the Drug (ID: M6APDG01941)
Name
4-(Quinolin-4-yl)-N-p-tolylpyrimidin-2-amine
Synonyms
CHEMBL1080023
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Status
Investigative
Structure
Formula
C20H16N4
InChI
1S/C20H16N4/c1-14-6-8-15(9-7-14)23-20-22-13-11-19(24-20)17-10-12-21-18-5-3-2-4-16(17)18/h2-13H,1H3,(H,22,23,24)
InChIKey
HFJKLAQBWSUMDJ-UHFFFAOYSA-N
PubChem CID
44820374
TTD Drug ID
D0L5GS
Target Gene(s) and Their Upstream m6A Regulator, Together with the Effect of Target Gene(s) in Drug Response
The target genes involved in drug-target interaction (such as drug-metabolizing enzymes, drug transporters and therapeutic targets) and drug-mediated cell death signaling (including modulating DNA damage and repair capacity, escaping from drug-induced apoptosis, autophagy, cellular metabolic reprogramming, oncogenic bypass signaling, cell microenvironment, cell stemness, etc.) could be regulated by m6A regulator(s) and affected their corresponding drug response. You can browse detailed information on drug-related target gene(s) mediated by m6A regulators.
Cyclin-dependent kinase 1 (CDK1)
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Cyclin-dependent kinase 1 (CDK1) is a therapeutic target for 4-(Quinolin-4-yl)-N-p-tolylpyrimidin-2-amine. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 4-(Quinolin-4-yl)-N-p-tolylpyrimidin-2-amine through regulating the expression of Cyclin-dependent kinase 1 (CDK1). [1], [2]
Protein virilizer homolog (VIRMA)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Cyclin-dependent kinase 1 (CDK1) is a therapeutic target for 4-(Quinolin-4-yl)-N-p-tolylpyrimidin-2-amine. The Protein virilizer homolog (VIRMA) has potential in affecting the response of 4-(Quinolin-4-yl)-N-p-tolylpyrimidin-2-amine through regulating the expression of Cyclin-dependent kinase 1 (CDK1). [2], [3]
References
Ref 1 CircMETTL3, upregulated in a m6A-dependent manner, promotes breast cancer progression. Int J Biol Sci. 2021 Mar 15;17(5):1178-1190. doi: 10.7150/ijbs.57783. eCollection 2021.
Ref 2 Synthesis and cytotoxic activity of 2-methylimidazo[1,2-a]pyridine- and quinoline-substituted 2-aminopyrimidine derivatives. Eur J Med Chem. 2010 Jan;45(1):379-86. doi: 10.1016/j.ejmech.2009.10.002. Epub 2009 Oct 13.
Ref 3 KIAA1429 acts as an oncogenic factor in breast cancer by regulating CDK1 in an N6-methyladenosine-independent manner. Oncogene. 2019 Aug;38(33):6123-6141. doi: 10.1038/s41388-019-0861-z. Epub 2019 Jul 8.