m6A-centered Drug Response Information

General Information of the Drug (ID: M6APDG02071)
Name
1-(4-nitro-2-phenoxybenzyl)-1H-imidazole
Synonyms
CHEMBL1083653; 1-(4-nitro-2-phenoxybenzyl)-1H-imidazole
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Status
Investigative
Structure
Formula
C16H13N3O3
InChI
1S/C16H13N3O3/c20-19(21)14-7-6-13(11-18-9-8-17-12-18)16(10-14)22-15-4-2-1-3-5-15/h1-10,12H,11H2
InChIKey
JIPGEBKJKOMJSL-UHFFFAOYSA-N
PubChem CID
46867546
TTD Drug ID
D0V3MV
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.
Aromatase (CYP19A1)
Fat mass and obesity-associated protein (FTO)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Aromatase (CYP19A1) is a therapeutic target for 1-(4-nitro-2-phenoxybenzyl)-1H-imidazole. The Fat mass and obesity-associated protein (FTO) has potential in affecting the response of 1-(4-nitro-2-phenoxybenzyl)-1H-imidazole through regulating the expression of Aromatase (CYP19A1). [1], [2]
References
Ref 1 Increased N6-methyladenosine causes infertility is associated with FTO expression. J Cell Physiol. 2018 Sep;233(9):7055-7066. doi: 10.1002/jcp.26507. Epub 2018 Mar 25.
Ref 2 Novel highly potent and selective nonsteroidal aromatase inhibitors: synthesis, biological evaluation and structure-activity relationships investigation. J Med Chem. 2010 Jul 22;53(14):5347-51. doi: 10.1021/jm100319h.