General Information of the Drug (ID: M6APDG01176)
Name
N-hydroxy-2,3-bis(phenylsulfonamido)propanamide
Synonyms
CHEMBL496717; N-hydroxy-2,3-bis(phenylsulfonamido)propanamide
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Status
Investigative
Structure
Formula
C15H17N3O6S2
InChI
1S/C15H17N3O6S2/c19-15(17-20)14(18-26(23,24)13-9-5-2-6-10-13)11-16-25(21,22)12-7-3-1-4-8-12/h1-10,14,16,18,20H,11H2,(H,17,19)
InChIKey
WBWFDDZAXKMHEG-UHFFFAOYSA-N
PubChem CID
24857837
TTD Drug ID
D07SPC
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-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 N-hydroxy-2,3-bis(phenylsulfonamido)propanamide. The E3 ubiquitin-protein ligase Hakai (CBLL1) has potential in affecting the response of N-hydroxy-2,3-bis(phenylsulfonamido)propanamide through regulating the expression of Matrix metalloproteinase-9 (MMP-9). [1], [2]
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 N-hydroxy-2,3-bis(phenylsulfonamido)propanamide. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of N-hydroxy-2,3-bis(phenylsulfonamido)propanamide through regulating the expression of Matrix metalloproteinase-9 (MMP-9). [2], [3]
References
Ref 1 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 2 Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhibitors. J Med Chem. 2009 Oct 22;52(20):6347-61. doi: 10.1021/jm900335a.
Ref 3 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.