General Information of the Drug (ID: M6APDG02041)
Name
2-(4-(methylsulfonyl)phenyl)-3-phenylquinoline
Synonyms
CHEMBL598330; 2-(4-(methylsulfonyl)phenyl)-3-phenylquinoline
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Status
Investigative
Structure
Formula
C22H17NO2S
InChI
1S/C22H17NO2S/c1-26(24,25)19-13-11-17(12-14-19)22-20(16-7-3-2-4-8-16)15-18-9-5-6-10-21(18)23-22/h2-15H,1H3
InChIKey
OPLJPOZQZWTQDV-UHFFFAOYSA-N
PubChem CID
46232132
TTD Drug ID
D0V2QP
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.
Prostaglandin G/H synthase 2 (COX-2)
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Prostaglandin G/H synthase 2 (COX-2) is a therapeutic target for 2-(4-(methylsulfonyl)phenyl)-3-phenylquinoline. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 2-(4-(methylsulfonyl)phenyl)-3-phenylquinoline through regulating the expression of Prostaglandin G/H synthase 2 (COX-2). [1], [2]
References
Ref 1 METTL3 promotes experimental osteoarthritis development by regulating inflammatory response and apoptosis in chondrocyte. Biochem Biophys Res Commun. 2019 Aug 13;516(1):22-27. doi: 10.1016/j.bbrc.2019.05.168. Epub 2019 Jun 8.
Ref 2 Discovery of 3-(4-bromophenyl)-6-nitrobenzo[1.3.2]dithiazolium ylide 1,1-dioxide as a novel dual cyclooxygenase/5-lipoxygenase inhibitor that also inhibits tumor necrosis factor-alpha production. Bioorg Med Chem. 2010 Jan 15;18(2):597-604. doi: 10.1016/j.bmc.2009.12.008. Epub 2009 Dec 6.