General Information of the Drug (ID: M6APDG01977)
Name
1-(2-nitrophenethyl)-1H-pyrrolo[3,2-b]pyridine
Synonyms
CHEMBL540744; 1-(2-nitrophenethyl)-1H-pyrrolo[3,2-b]pyridine
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Status
Investigative
Structure
Formula
C15H13N3O2
InChI
1S/C15H13N3O2/c19-18(20)14-5-2-1-4-12(14)7-10-17-11-8-13-15(17)6-3-9-16-13/h1-6,8-9,11H,7,10H2
InChIKey
CEHGVNIFTRLUOI-UHFFFAOYSA-N
PubChem CID
45272467
TTD Drug ID
D0S1II
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.
Proto-oncogene c-Met (MET)
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Proto-oncogene c-Met (MET) is a therapeutic target for 1-(2-nitrophenethyl)-1H-pyrrolo[3,2-b]pyridine. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 1-(2-nitrophenethyl)-1H-pyrrolo[3,2-b]pyridine through regulating the expression of Proto-oncogene c-Met (MET). [1], [2]
References
Ref 1 RNA m(6) A methylation regulates uveal melanoma cell proliferation, migration, and invasion by targeting c-Met. J Cell Physiol. 2020 Oct;235(10):7107-7119. doi: 10.1002/jcp.29608. Epub 2020 Feb 4.
Ref 2 Emerging drugs for chemotherapy-induced mucositis. Expert Opin Emerg Drugs. 2008 Sep;13(3):511-22. doi: 10.1517/14728214.13.3.511.