General Information of the Drug (ID: M6APDG00586)
Name
NV-5138
Synonyms
UNII-06CA9QMG6Z; 4-(difluoromethyl)-L-leucine; 2095886-80-7; SCHEMBL18762589; ZINC585143195; HY-114384; N[C@H](C(=O)O)CC(C(F)F)(C)C; CS-0084893; ((S)-2-Amino-5,5-difluoro-4,4-dimethylpentanoic acid; Pentanoic acid, 2-amino-5,5-difluoro-4,4-dimethyl-, (2S)-; K94
    Click to Show/Hide
Status
Phase 1
Structure
Formula
C7H13F2NO2
InChI
1S/C7H13F2NO2/c1-7(2,6(8)9)3-4(10)5(11)12/h4,6H,3,10H2,1-2H3,(H,11,12)/t4-/m0/s1
InChIKey
HRFIMCJTDKEPPV-BYPYZUCNSA-N
PubChem CID
129050791
TTD Drug ID
DAT0U5
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.
Mammalian target of rapamycin complex 1 (mTORC1)
Fat mass and obesity-associated protein (FTO)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The Fat mass and obesity-associated protein (FTO) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [1], [2]
Methyltransferase-like 14 (METTL14)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The Methyltransferase-like 14 (METTL14) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [2], [3]
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [2], [3]
RNA-binding motif protein 15 (RBM15)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The RNA-binding motif protein 15 (RBM15) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [2], [3]
RNA-binding motif protein 15B (RBM15B)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The RNA-binding motif protein 15B (RBM15B) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [2], [3]
Wilms tumor 1-associating protein (WTAP)
In total 1 mechanisms lead to this potential drug response
Response Summary Mammalian target of rapamycin complex 1 (mTORC1) is a therapeutic target for NV-5138. The Wilms tumor 1-associating protein (WTAP) has potential in affecting the response of NV-5138 through regulating the expression of Mammalian target of rapamycin complex 1 (mTORC1). [2], [3]
References
Ref 1 Omeprazole improves chemosensitivity of gastric cancer cells by m6A demethylase FTO-mediated activation of mTORC1 and DDIT3 up-regulation. Biosci Rep. 2021 Jan 29;41(1):BSR20200842. doi: 10.1042/BSR20200842.
Ref 2 Dual mTORC1 and mTORC2 inhibitor Palomid 529 penetrates the blood-brain barrier without restriction by ABCB1 and ABCG2. Int J Cancer. 2013 Sep 1;133(5):1222-33. doi: 10.1002/ijc.28126. Epub 2013 Apr 1.
Ref 3 mTORC1-chaperonin CCT signaling regulates m(6)A RNA methylation to suppress autophagy. Proc Natl Acad Sci U S A. 2021 Mar 9;118(10):e2021945118. doi: 10.1073/pnas.2021945118.