General Information of the Drug (ID: M6APDG00393)
Name
3-(4-Phenylethynylbenzoyl)nonanoic acid
Synonyms
3-(4-Phenylethynylbenzoyl)nonanoic acid; CHEMBL201298
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Status
Investigative
Structure
Formula
C24H26O3
InChI
1S/C24H26O3/c1-2-3-4-8-11-22(18-23(25)26)24(27)21-16-14-20(15-17-21)13-12-19-9-6-5-7-10-19/h5-7,9-10,14-17,22H,2-4,8,11,18H2,1H3,(H,25,26)
InChIKey
RPSYWEPJQQLLJN-UHFFFAOYSA-N
PubChem CID
11581319
TTD Drug ID
D0A5MV
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.
Matrix metalloproteinase-12 (MMP-12)
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Matrix metalloproteinase-12 (MMP-12) is a therapeutic target for 3-(4-Phenylethynylbenzoyl)nonanoic acid. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 3-(4-Phenylethynylbenzoyl)nonanoic acid through regulating the expression of Matrix metalloproteinase-12 (MMP-12). [1], [2]
Matrix metalloproteinase-2 (MMP-2)
E3 ubiquitin-protein ligase Hakai (CBLL1)
In total 1 mechanisms lead to this potential drug response
Response Summary Matrix metalloproteinase-2 (MMP-2) is a therapeutic target for 3-(4-Phenylethynylbenzoyl)nonanoic acid. The E3 ubiquitin-protein ligase Hakai (CBLL1) has potential in affecting the response of 3-(4-Phenylethynylbenzoyl)nonanoic acid through regulating the expression of Matrix metalloproteinase-2 (MMP-2). [2], [3]
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Matrix metalloproteinase-2 (MMP-2) is a therapeutic target for 3-(4-Phenylethynylbenzoyl)nonanoic acid. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 3-(4-Phenylethynylbenzoyl)nonanoic acid through regulating the expression of Matrix metalloproteinase-2 (MMP-2). [2], [4]
Matrix metalloproteinase-9 (MMP-9)
E3 ubiquitin-protein ligase Hakai (CBLL1)
In total 1 mechanisms lead to this potential drug response
Response Summary Matrix metalloproteinase-9 (MMP-9) is a therapeutic target for 3-(4-Phenylethynylbenzoyl)nonanoic acid. The E3 ubiquitin-protein ligase Hakai (CBLL1) has potential in affecting the response of 3-(4-Phenylethynylbenzoyl)nonanoic acid through regulating the expression of Matrix metalloproteinase-9 (MMP-9). [2], [3]
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Matrix metalloproteinase-9 (MMP-9) is a therapeutic target for 3-(4-Phenylethynylbenzoyl)nonanoic acid. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of 3-(4-Phenylethynylbenzoyl)nonanoic acid through regulating the expression of Matrix metalloproteinase-9 (MMP-9). [1], [2]
References
Ref 1 The aberrant cross-talk of epithelium-macrophages via METTL3-regulated extracellular vesicle miR-93 in smoking-induced emphysema. Cell Biol Toxicol. 2022 Feb;38(1):167-183. doi: 10.1007/s10565-021-09585-1. Epub 2021 Mar 4.
Ref 2 Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids. J Med Chem. 2006 Jan 26;49(2):456-8. doi: 10.1021/jm051101g.
Ref 3 CBLL1 is highly expressed in non-small cell lung cancer and promotes cell proliferation and invasion. Thorac Cancer. 2019 Jun;10(6):1479-1488. doi: 10.1111/1759-7714.13097. Epub 2019 May 23.
Ref 4 RNA m6A methyltransferase METTL3 regulates invasiveness of melanoma cells by matrix metallopeptidase 2. Melanoma Res. 2019 Aug;29(4):382-389. doi: 10.1097/CMR.0000000000000580.